The cellular and molecular mechanisms of vertebrate lens development
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The ocular lens is a model system for understanding important aspects of embryonic development, such as cell specification and the spatiotemporally controlled formation of a three-dimensional structure. The lens, which is characterized by transparency, refraction and elasticity, is composed of a bulk mass of fiber cells attached to a sheet of lens epithelium. Although lens induction has been studied for over 100 years, recent findings have revealed a myriad of extracellular signaling pathways and gene regulatory networks, integrated and executed by the transcription factor Pax6, that are required for lens formation in vertebrates. This Review summarizes recent progress in the field, emphasizing the interplay between the diverse regulatory mechanisms employed to form lens progenitor and precursor cells and highlighting novel opportunities to fill gaps in our understanding of lens tissue morphogenesis.
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RA signaling is responsible for the formation of the lens placode through the combination of the optic vessel (OV) and prospective lens ectoderm (PLE).
“RA signaling is responsible for the formation of the lens placode through the combination of the optic vessel (OV) and prospective lens ectoderm (PLE).”
From Vitamin A Transporters in Visual Function: A Mini Review on Membrane Receptors for Dietary Vitamin A Uptake, Storage, and Transport to the Eye (2021) · cites this paper as [50]
The section on lens placode formation says RA signaling contributes to lens induction and is active in the prospective lens ectoderm as the placode forms. It also says RA acts alongside BMP signaling and the Pax6, Six3 and Sox2 network; it does not describe RA as solely responsible or the optic vesicle and prospective lens ectoderm as combining to form the placode. No page number is provided in our copy. (LLM, conf=0.86)
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Enhanced autophagy ameliorates cardiac proteinopathy
Bhuiyan, M. S., Pattison, J. S., Osinska, H., James, J., Gulick, J., McLendon, P. M., Hill, J. A., Sadoshima, J., & Robbins, J. (2013) · Journal of Clinical Investigation · doi:10.1172/jci70877 · Cited by 298 · see citing works
Mutation Altering the miR-184 Seed Region Causes Familial Keratoconus with Cataract
Hughes, A. E., Bradley, D. T., Campbell, M., Lechner, J., Dash, D. P., Simpson, D. A., & Willoughby, C. E. (2011) · The American Journal of Human Genetics · doi:10.1016/j.ajhg.2011.09.014 · Cited by 276 · see citing works
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Tuoc, T. C., Boretius, S., Sansom, S. N., Pitulescu, M.-E., Frahm, J., Livesey, F. J., & Stoykova, A. (2013) · Developmental Cell · doi:10.1016/j.devcel.2013.04.005 · Cited by 177 · see citing works
Valapala, M., Wilson, C., Hose, S., Bhutto, I. A., Grebe, R., Dong, A., Greenbaum, S., Gu, L., Sengupta, S., Cano, M., et al. (2014) · Autophagy · doi:10.4161/auto.27292 · Cited by 144 · see citing works
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Yamben, I. F., Rachel, R. A., Shatadal, S., Copeland, N. G., Jenkins, N. A., Warming, S., & Griep, A. E. (2013) · Developmental Biology · doi:10.1016/j.ydbio.2013.09.027 · Cited by 50 · see citing works
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Research works printed but not linked: 242
- Acampora D., Avantaggiato V., Tuorto F., Barone P., Perera M., Choo D., Wu D., Corte G. and Simeone A. (1999). Differential transcriptional control as the major molecular event in generating Otx1-/- and Otx2-/- divergent phenotypes. Development 126, 1417- 1426. 10068635
- Agre P. and Kozono D. (2003). Aquaporin water channels: molecular mechanisms for human diseases. FEBS Lett. 555, 72- 78 10.1016/S0014-5793(03)01083-4 14630322 · DOI
- Ahmad N., Aslam M., Muenster D., Horsch M., Khan M. A., Carlsson P., Beckers J. and Graw J. (2013). Pitx3 directly regulates Foxe3 during early lens development. Int. J. Dev. Biol. 57, 741- 751 10.1387/ijdb.130193jg 24307298 · DOI
- Albert M., Schmitz S. U., Kooistra S. M., Malatesta M., Morales Torres C., Rekling J. C., Johansen J. V., Abarrategui I. and Helin K. (2013). The histone demethylase Jarid1b ensures faithful mouse development by protecting developmental genes from aberrant H3K4me3. PLoS Genet. 9, e1003461 10.1371/journal.pgen.1003461 23637629 PMC3630093 · DOI
- Antosova B., Smolikova J., Borkovcova R., Strnad H., Lachova J., Machon O. and Kozmik Z. (2013). Ectopic activation of Wnt/beta-catenin signaling in lens fiber cells results in cataract formation and aberrant fiber cell differentiation. PLoS ONE 8, e78279 10.1371/journal.pone.0078279 24205179 PMC3813504 · DOI
- Aota S.-i., Nakajima N., Sakamoto R., Watanabe S., Ibaraki N. and Okazaki K. (2003). Pax6 autoregulation mediated by direct interaction of Pax6 protein with the head surface ectoderm-specific enhancer of the mouse Pax6 gene. Dev. Biol. 257, 1- 13 10.1016/S0012-1606(03)00058-7 12710953 · DOI
- Arnold K., Sarkar A., Yram M. A., Polo J. M., Bronson R., Sengupta S., Seandel M., Geijsen N. and Hochedlinger K. (2011). Sox2(+) adult stem and progenitor cells are important for tissue regeneration and survival of mice. Cell Stem Cell 9, 317- 329 10.1016/j.stem.2011.09.001 21982232 PMC3538360 · DOI
- Ashery-Padan R., Marquardt T., Zhou X. and Gruss P. (2000). Pax6 activity in the lens primordium is required for lens formation and for correct placement of a single retina in the eye. Genes Dev. 14, 2701- 2711 10.1101/gad.184000 11069887 PMC317031 · DOI
- Attreed M., Desbois M., van Kuppevelt T. H. and Bülow H. E. (2012). Direct visualization of specifically modified extracellular glycans in living animals. Nat. Methods 9, 477- 479 10.1038/nmeth.1945 22466794 PMC3437987 · DOI
- Avellino R., Carrella S., Pirozzi M., Risolino M., Salierno F. G., Franco P., Stoppelli P., Verde P., Banfi S. and Conte I. (2013). miR-204 targeting of Ankrd13A controls both mesenchymal neural crest and lens cell migration. PLoS ONE 8, e61099 10.1371/journal.pone.0061099 23620728 PMC3631221 · DOI
- Bailey A. P., Bhattacharyya S., Bronner-Fraser M. and Streit A. (2006). Lens specification is the ground state of all sensory placodes, from which FGF promotes olfactory identity. Dev. Cell 11, 505- 517 10.1016/j.devcel.2006.08.009 17011490 · DOI · Paper page
- Barolo S. and Posakony J. W. (2002). Three habits of highly effective signaling pathways: principles of transcriptional control by developmental cell signaling. Genes Dev. 16, 1167- 1181 10.1101/gad.976502 12023297 · DOI
- Bassnett S. (2009). On the mechanism of organelle degradation in the vertebrate lens. Exp. Eye Res. 88, 133- 139 10.1016/j.exer.2008.08.017 18840431 PMC2693198 · DOI
- Bassnett S. and Mataic D. (1997). Chromatin degradation in differentiating fiber cells of the eye lens. J. Cell Biol. 137, 37- 49 10.1083/jcb.137.1.37 9105035 PMC2139849 · DOI
- Bassnett S., Shi Y. and Vrensen G. F. J. M. (2011). Biological glass: structural determinants of eye lens transparency. Philos. Trans. R. Soc. Lond. B Biol. Sci. 366, 1250- 1264 10.1098/rstb.2010.0302 21402584 PMC3061108 · DOI
- Basu S., Rajakaruna S. and Menko A. S. (2012). Insulin-like growth factor receptor-1 and nuclear factor kappaB are crucial survival signals that regulate caspase-3-mediated lens epithelial cell differentiation initiation. J. Biol. Chem. 287, 8384- 8397 10.1074/jbc.M112.341586 22275359 PMC3381865 · DOI
- Basu S., Rajakaruna S., De Arcangelis A., Zhang L., Georges-Labouesse E. and Menko A. S. (2014a). α6 integrin transactivates insulin-like growth factor receptor-1 (IGF-1R) to regulate caspase-3-mediated lens epithelial cell differentiation initiation. J. Biol. Chem. 289, 3842- 3855 10.1074/jbc.M113.515254 24381169 PMC3924254 · DOI
- Basu S., Rajakaruna S., Reyes B., Van Bockstaele E. and Menko A. S. (2014b). Suppression of MAPK/JNK-MTORC1 signaling leads to premature loss of organelles and nuclei by autophagy during terminal differentiation of lens fiber cells. Autophagy 10, 1193- 1211 10.4161/auto.28768 24813396 PMC4203547 · DOI
- Baulmann D. C., Ohlmann A., Flügel-Koch C., Goswami S., Cvekl A. and Tamm E. R. (2002). Pax6 heterozygous eyes show defects in chamber angle differentiation that are associated with a wide spectrum of other anterior eye segment abnormalities. Mech. Dev. 118, 3- 17 10.1016/S0925-4773(02)00260-5 12351165 · DOI
- Bhattacharyya S., Bailey A. P., Bronner-Fraser M. and Streit A. (2004). Segregation of lens and olfactory precursors from a common territory: cell sorting and reciprocity of Dlx5 and Pax6 expression. Dev. Biol. 271, 403- 414 10.1016/j.ydbio.2004.04.010 15223343 · DOI
- Blixt A., Landgren H., Johansson B. R. and Carlsson P. (2007). Foxe3 is required for morphogenesis and differentiation of the anterior segment of the eye and is sensitive to Pax6 gene dosage. Dev. Biol. 302, 218- 229 10.1016/j.ydbio.2006.09.021 17064680 · DOI
- Boswell B. A., Overbeek P. A. and Musil L. S. (2008). Essential role of BMPs in FGF-induced secondary lens fiber differentiation. Dev. Biol. 324, 202- 212 10.1016/j.ydbio.2008.09.003 18848538 PMC2853743 · DOI
- Brady J. P., Garland D., Duglas-Tabor Y., Robison W. G. Jr, Groome A. and Wawrousek E. F. (1997). Targeted disruption of the mouse αA-crystallin gene induces cataract and cytoplasmic inclusion bodies containing the small heat shock protein αB-crystallin. Proc. Natl. Acad. Sci. USA 94, 884- 889 10.1073/pnas.94.3.884 9023351 PMC19608 · DOI
- Brennan L. A., Kantorow W. L., Chauss D., McGreal R., He S., Mattucci L., Wei J., Riazuddin S. A., Cvekl A., Hejtmancik J. F. et al. (2012). Spatial expression patterns of autophagy genes in the eye lens and induction of autophagy in lens cells. Mol. Vis. 18, 1773- 1786. 22815631 PMC3398491
- Cain S., Martinez G., Kokkinos M. I., Turner K., Richardson R. J., Abud H. E., Huelsken J., Robinson M. L. and de Iongh R. U. (2008). Differential requirement for β-catenin in epithelial and fiber cells during lens development. Dev. Biol. 321, 420- 433 10.1016/j.ydbio.2008.07.002 18652817 · DOI
- Cang Y., Zhang J., Nicholas S. A., Bastien J., Li B., Zhou P. and Goff S. P. (2006). Deletion of DDB1 in mouse brain and lens leads to p53-dependent elimination of proliferating cells. Cell 127, 929- 940 10.1016/j.cell.2006.09.045 17129780 · DOI
- Carbe C. and Zhang X. (2011). Lens induction requires attenuation of ERK signaling by Nf1. Hum. Mol. Genet. 20, 1315- 1323 10.1093/hmg/ddr014 21233129 PMC3049355 · DOI
- Cavalheiro G. R., Matos-Rodrigues G. E., Gomes A. L., Rodrigues P. M. G. and Martins R. A. P. (2014). c-myc regulates cell proliferation during lens development. PLoS ONE 9, e87182 10.1371/journal.pone.0087182 24503550 PMC3913586 · DOI
- Chaffee B. R., Shang F., Chang M.-L., Clement T. M., Eddy E. M., Wagner B. D., Nakahara M., Nagata S., Robinson M. L. and Taylor A. (2014). Nuclear removal during terminal lens fiber cell differentiation requires CDK1 activity: appropriating mitosis-related nuclear disassembly. Development 141, 3388- 3398 10.1242/dev.106005 25139855 PMC4199135 · DOI
- Chauhan B. K., Disanza A., Choi S.-Y., Faber S. C., Lou M., Beggs H. E., Scita G., Zheng Y. and Lang R. A. (2009). Cdc42- and IRSp53-dependent contractile filopodia tether presumptive lens and retina to coordinate epithelial invagination. Development 136, 3657- 3667 10.1242/dev.042242 19820184 PMC2761112 · DOI
- Chauhan B. K., Lou M., Zheng Y. and Lang R. A. (2011). Balanced Rac1 and RhoA activities regulate cell shape and drive invagination morphogenesis in epithelia. Proc. Natl. Acad. Sci. USA 108, 18289- 18294 10.1073/pnas.1108993108 22021442 PMC3215052 · DOI
- Chauss D., Basu S., Rajakaruna S., Ma Z., Gau V., Anastas S., Brennan L. A., Hejtmancik J. F., Menko A. S. and Kantorow M. (2014). Differentiation state-specific mitochondrial dynamic regulatory networks are revealed by global transcriptional analysis of the developing chicken lens. G3 (Bethesda) 4, 1515- 1527 10.1534/g3.114.012120 24928582 PMC4132181 · DOI
- Chen Q., Hung F. C., Fromm L. and Overbeek P. A. (2000). Induction of cell cycle entry and cell death in postmitotic lens fiber cells by overexpression of E2F1 or E2F2. Invest. Ophthalmol. Vis. Sci. 41, 4223- 3421. 11095619
- Chen Y., Doughman Y.-q., Gu S., Jarrell A., Aota S.-i., Cvekl A., Watanabe M., Dunwoodie S. L., Johnson R. S., van Heyningen V. et al. (2008a). Cited2 is required for the proper formation of the hyaloid vasculature and for lens morphogenesis. Development 135, 2939- 2948 10.1242/dev.021097 18653562 PMC2654719 · DOI
- Chen Y., Stump R. J. W., Lovicu F. J., Shimono A. and McAvoy J. W. (2008b). Wnt signaling is required for organization of the lens fiber cell cytoskeleton and development of lens three-dimensional architecture. Dev. Biol. 324, 161- 176 10.1016/j.ydbio.2008.09.002 18824165 PMC2651430 · DOI
- Chen J., Ma Z., Jiao X., Fariss R., Kantorow W. L., Kantorow M., Pras E., Frydman M., Pras E., Riazuddin S. et al. (2011). Mutations in FYCO1 cause autosomal-recessive congenital cataracts. Am. J. Hum. Genet. 88, 827- 838 10.1016/j.ajhg.2011.05.008 21636066 PMC3113247 · DOI · Paper page
- Cheng C., Ansari M. M., Cooper J. A. and Gong X. (2013). EphA2 and Src regulate equatorial cell morphogenesis during lens development. Development 140, 4237- 4245 10.1242/dev.100727 24026120 PMC3787762 · DOI
- Choudhuri A., Maitra U. and Evans T. (2013). Translation initiation factor eIF3h targets specific transcripts to polysomes during embryogenesis. Proc. Natl. Acad. Sci. USA 110, 9818- 9823 10.1073/pnas.1302934110 23716667 PMC3683746 · DOI
- Conte I., Carrella S., Avellino R., Karali M., Marco-Ferreres R., Bovolenta P. and Banfi S. (2010). miR-204 is required for lens and retinal development via Meis2 targeting. Proc. Natl. Acad. Sci. USA 107, 15491- 15496 10.1073/pnas.0914785107 20713703 PMC2932609 · DOI · Paper page
- Conte I., Banfi S. and Bovolenta P. (2013). Non-coding RNAs in the development of sensory organs and related diseases. Cell. Mol. Life Sci. 70, 4141- 4155 10.1007/s00018-013-1335-z 23588489 PMC11113508 · DOI
- Cooper M. A., Son A. I., Komlos D., Sun Y., Kleiman N. J. and Zhou R. (2008). Loss of ephrin-A5 function disrupts lens fiber cell packing and leads to cataract. Proc. Natl. Acad. Sci. USA 105, 16620- 16625 10.1073/pnas.0808987105 18948590 PMC2575469 · DOI
- Costello M. J., Brennan L. A., Basu S., Chauss D., Mohamed A., Gilliland K. O., Johnsen S., Menko A. S. and Kantorow M. (2013). Autophagy and mitophagy participate in ocular lens organelle degradation. Exp. Eye Res. 116, 141- 150 10.1016/j.exer.2013.08.017 24012988 PMC3856666 · DOI
- Counis M. F., Chaudun E., Arruti C., Oliver L., Sanwal M., Courtois Y. and Torriglia A. (1998). Analysis of nuclear degradation during lens cell differentiation. Cell Death Differ. 5, 251- 261 10.1038/sj.cdd.4400351 10200471 · DOI
- Crawford S. E., Qi C., Misra P., Stellmach V., Rao M. S., Engel J. D., Zhu Y. and Reddy J. K. (2002). Defects of the heart, eye, and megakaryocytes in peroxisome proliferator activator receptor-binding protein (PBP) null embryos implicate GATA family of transcription factors. J. Biol. Chem. 277, 3585- 3592 10.1074/jbc.M107995200 11724781 · DOI
- Cvekl A. and Duncan M. K. (2007). Genetic and epigenetic mechanisms of gene regulation during lens development. Prog. Retin. Eye Res. 26, 555- 597 10.1016/j.preteyeres.2007.07.002 17905638 PMC2136409 · DOI
- Cvekl A. and Mitton K. P. (2010). Epigenetic regulatory mechanisms in vertebrate eye development and disease. Heredity 105, 135- 151 10.1038/hdy.2010.16 20179734 PMC4228956 · DOI
- Cvekl A. and Tamm E. R. (2004). Anterior eye development and ocular mesenchyme: new insights from mouse models and human diseases. Bioessays 26, 374- 386 10.1002/bies.20009 15057935 PMC2094210 · DOI
- Cvekl A. and Wang W.-L. (2009). Retinoic acid signaling in mammalian eye development. Exp. Eye Res. 89, 280- 291 10.1016/j.exer.2009.04.012 19427305 PMC2756743 · DOI
- Dawes L. J., Sugiyama Y., Tanedo A. S., Lovicu F. J. and McAvoy J. W. (2013). Wnt-frizzled signaling is part of an FGF-induced cascade that promotes lens fiber differentiation. Invest. Ophthalmol. Vis. Sci. 54, 1582- 1590 10.1167/iovs.12-11357 23385791 PMC4601884 · DOI
- Dawes L. J., Sugiyama Y., Lovicu F. J., Harris C. G., Shelley E. J. and McAvoy J. W. (2014). Interactions between lens epithelial and fiber cells reveal an intrinsic self-assembly mechanism. Dev. Biol. 385, 291- 303 10.1016/j.ydbio.2013.10.030 24211762 PMC3947272 · DOI
- Dimanlig P. V., Faber S. C., Auerbach W., Makarenkova H. P. and Lang R. A. (2001). The upstream ectoderm enhancer in Pax6 has an important role in lens induction. Development 128, 4415- 4424. 11714668
- Dincer Z., Piao J., Niu L., Ganat Y., Kriks S., Zimmer B., Shi S.-H., Tabar V. and Studer L. (2013). Specification of functional cranial placode derivatives from human pluripotent stem cells. Cell Rep. 5, 1387- 1402 10.1016/j.celrep.2013.10.048 24290755 PMC3887225 · DOI
- Donner A. L. and Maas R. L. (2004). Conservation and non-conservation of genetic pathways in eye specification. Int. J. Dev. Biol. 48, 743- 753 10.1387/ijdb.041877ad 15558467 · DOI
- Donner A. L., Episkopou V. and Maas R. L. (2007). Sox2 and Pou2f1 interact to control lens and olfactory placode development. Dev. Biol. 303, 784- 799 10.1016/j.ydbio.2006.10.047 17140559 PMC3276313 · DOI
- Duggan C. D., DeMaria S., Baudhuin A., Stafford D. and Ngai J. (2008). Foxg1 is required for development of the vertebrate olfactory system. J. Neurosci. 28, 5229- 5239 10.1523/JNEUROSCI.1134-08.2008 18480279 PMC2706027 · DOI
- Duncan M. K., Cui W., Oh D.-J. and Tomarev S. I. (2002). Prox1 is differentially localized during lens development. Mech. Dev. 112, 195- 198 10.1016/S0925-4773(01)00645-1 11850194 · DOI
- Enwright J. F. III and Grainger R. M. (2000). Altered retinoid signaling in the heads of small eye mouse embryos. Dev. Biol. 221, 10- 22 10.1006/dbio.2000.9652 10772788 · DOI
- Faber S. C., Robinson M. L., Makarenkova H. P. and Lang R. A. (2002). Bmp signaling is required for development of primary lens fiber cells. Development 129, 3727- 3737. 12117821
- Foley J. D., Rosenbaum H. and Griep A. E. (2004). Temporal regulation of VEID-7-amino-4-trifluoromethylcoumarin cleavage activity and caspase-6 correlates with organelle loss during lens development. J. Biol. Chem. 279, 32142- 32150 10.1074/jbc.M313683200 15161922 · DOI
- Fudge D. S., McCuaig J. V., Van Stralen S., Hess J. F., Wang H., Mathias R. T. and FitzGerald P. G. (2011). Intermediate filaments regulate tissue size and stiffness in the murine lens. Invest. Ophthalmol. Vis. Sci. 52, 3860- 3867 10.1167/iovs.10-6231 21345981 PMC3109061 · DOI
- Fujimoto M., Izu H., Seki K., Fukuda K., Nishida T., Yamada S.-i., Kato K., Yonemura S., Inouye S. and Nakai A. (2004). HSF4 is required for normal cell growth and differentiation during mouse lens development. EMBO J. 23, 4297- 4306 10.1038/sj.emboj.7600435 15483628 PMC524399 · DOI
- Fujimoto M., Oshima K., Shinkawa T., Wang B. B., Inouye S., Hayashida N., Takii R. and Nakai A. (2008). Analysis of HSF4 binding regions reveals its necessity for gene regulation during development and heat shock response in mouse lenses. J. Biol. Chem. 283, 29961- 29970 10.1074/jbc.M804629200 18755693 PMC2662063 · DOI
- Furuta Y. and Hogan B. L. M. (1998). BMP4 is essential for lens induction in the mouse embryo. Genes Dev. 12, 3764- 3775 10.1101/gad.12.23.3764 9851982 PMC317259 · DOI
- Garcia C. M., Huang J., Madakashira B. P., Liu Y., Rajagopal R., Dattilo L., Robinson M. L. and Beebe D. C. (2011). The function of FGF signaling in the lens placode. Dev. Biol. 351, 176- 185 10.1016/j.ydbio.2011.01.001 21223962 PMC3053579 · DOI
- Goetz R. and Mohammadi M. (2013). Exploring mechanisms of FGF signalling through the lens of structural biology. Nat. Rev. Mol. Cell Biol. 14, 166- 180 10.1038/nrm3528 23403721 PMC3695728 · DOI
- Gokhin D. S., Nowak R. B., Kim N. E., Arnett E. E., Chen A. C., Sah R. L., Clark J. I. and Fowler V. M. (2012). Tmod1 and CP49 synergize to control the fiber cell geometry, transparency, and mechanical stiffness of the mouse lens. PLoS ONE 7, e48734 10.1371/journal.pone.0048734 23144950 PMC3492431 · DOI
- Golestaneh N., Fan J., Fariss R. N., Lo W.-K., Zelenka P. S. and Chepelinsky A. B. (2004). Lens major intrinsic protein (MIP)/aquaporin 0 expression in rat lens epithelia explants requires fibroblast growth factor-induced ERK and JNK signaling. J. Biol. Chem. 279, 31813- 31822 10.1074/jbc.M403473200 15145928 · DOI
- Gong L., Ji W.-K., Hu X.-H., Hu W.-F., Tang X.-C., Huang Z.-X., Li L., Liu M., Xiang S.-H., Wu E. et al. (2014). Sumoylation differentially regulates Sp1 to control cell differentiation. Proc. Natl. Acad. Sci. USA 111, 5574- 5579 10.1073/pnas.1315034111 24706897 PMC3992630 · DOI
- Gotoh N., Ito M., Yamamoto S., Yoshino I., Song N., Wang Y., Lax I., Schlessinger J., Shibuya M. and Lang R. A. (2004). Tyrosine phosphorylation sites on FRS2α responsible for Shp2 recruitment are critical for induction of lens and retina. Proc. Natl. Acad. Sci. USA 101, 17144- 17149 10.1073/pnas.0407577101 15569927 PMC535393 · DOI
- Goudreau G., Petrou P., Reneker L. W., Graw J., Löster J. and Gruss P. (2002). Mutually regulated expression of Pax6 and Six3 and its implications for the Pax6 haploinsufficient lens phenotype. Proc. Natl. Acad. Sci. USA 99, 8719- 8724 10.1073/pnas.132195699 12072567 PMC124365 · DOI
- Grainger R. M. (1992). Embryonic lens induction: shedding light on vertebrate tissue determination. Trends Genet. 8, 349- 355 10.1016/0168-9525(92)90280-H 1475847 · DOI
- Graw J. (2009). Mouse models of cataract. J. Genet. 88, 469- 486 10.1007/s12041-009-0066-2 20090208 · DOI
- Graw J., Neuhäuser-Klaus A., Klopp N., Selby P. B., Löster J. and Favor J. (2004). Genetic and allelic heterogeneity of Cryg mutations in eight distinct forms of dominant cataract in the mouse. Invest. Ophthalmol. Vis. Sci. 45, 1202- 1213 10.1167/iovs.03-0811 15037589 · DOI
- Greiling T. M., Houck S. A. and Clark J. I. (2009). The zebrafish lens proteome during development and aging. Mol. Vis. 15, 2313- 2325. 19936306 PMC2779061
- Griep A. E. (2006). Cell cycle regulation in the developing lens. Semin. Cell Dev. Biol. 17, 686- 697 10.1016/j.semcdb.2006.10.004 17218126 PMC2570782 · DOI
- Grocott T., Tambalo M. and Streit A. (2012). The peripheral sensory nervous system in the vertebrate head: a gene regulatory perspective. Dev. Biol. 370, 3- 23 10.1016/j.ydbio.2012.06.028 22790010 · DOI
- Grove M., Demyanenko G., Echarri A., Zipfel P. A., Quiroz M. E., Rodriguiz R. M., Playford M., Martensen S. A., Robinson M. R., Wetsel W. C. et al. (2004). ABI2-deficient mice exhibit defective cell migration, aberrant dendritic spine morphogenesis, and deficits in learning and memory. Mol. Cell. Biol. 24, 10905- 10922 10.1128/MCB.24.24.10905-10922.2004 15572692 PMC533973 · DOI · Paper page
- Groves A. K. and LaBonne C. (2014). Setting appropriate boundaries: fate, patterning and competence at the neural plate border. Dev. Biol. 389, 2- 12 10.1016/j.ydbio.2013.11.027 24321819 PMC3972267 · DOI
- Gupta R., Asomugha C. O. and Srivastava O. P. (2011). The common modification in αA-crystallin in the lens, N101D, is associated with increased opacity in a mouse model. J. Biol. Chem. 286, 11579- 11592 10.1074/jbc.M110.148627 21245144 PMC3064212 · DOI
- He S., Pirity M. K., Wang W.-L., Wolf L., Chauhan B. K., Cveklova K., Tamm E. R., Ashery-Padan R., Metzger D., Nakai A. et al. (2010). Chromatin remodeling enzyme Brg1 is required for mouse lens fiber cell terminal differentiation and its denucleation. Epigenetics Chromatin 3, 21 10.1186/1756-8935-3-21 21118511 PMC3003251 · DOI
- Hever A. M., Williamson K. A. and Van Heyningen V. (2006). Developmental malformations of the eye: the role of PAX6, SOX2 and OTX2. Clin. Genet. 69, 459- 470 10.1111/j.1399-0004.2006.00619.x 16712695 · DOI
- Hisa T., Spence S. E., Rachel R. A., Fujita M., Nakamura T., Ward J. M., Devor-Henneman D. E., Saiki Y., Kutsuna H., Tessarollo L. et al. (2004). Hematopoietic, angiogenic and eye defects in Meis1 mutant animals. EMBO J. 23, 450- 459 10.1038/sj.emboj.7600038 14713950 PMC1271748 · DOI
- Hogan B. L., Hirst E. M., Horsburgh G. and Hetherington C. M. (1988). Small eye (Sey): a mouse model for the genetic analysis of craniofacial abnormalities. Development 103 Suppl., 115- 119. 3250848
- Huang J., Rajagopal R., Liu Y., Dattilo L. K., Shaham O., Ashery-Padan R. and Beebe D. C. (2011). The mechanism of lens placode formation: a case of matrix-mediated morphogenesis. Dev. Biol. 355, 32- 42 10.1016/j.ydbio.2011.04.008 21540023 PMC3104088 · DOI
- Inoue M., Kamachi Y., Matsunami H., Imada K., Uchikawa M. and Kondoh H. (2007). PAX6 and SOX2-dependent regulation of the Sox2 enhancer N-3 involved in embryonic visual system development. Genes Cells 12, 1049- 1061 10.1111/j.1365-2443.2007.01114.x 17825048 · DOI
- Jarrin M., Pandit T. and Gunhaga L. (2012). A balance of FGF and BMP signals regulates cell cycle exit and Equarin expression in lens cells. Mol. Biol. Cell 23, 3266- 3274 10.1091/mbc.E12-01-0075 22718906 PMC3418319 · DOI
- Jia J., Lin M., Zhang L., York J. P. and Zhang P. (2007). The Notch signaling pathway controls the size of the ocular lens by directly suppressing p57Kip2 expression. Mol. Cell. Biol. 27, 7236- 7247 10.1128/MCB.00780-07 17709399 PMC2168910 · DOI
- Kallifatidis G., Boros J., Shin E. H. H., McAvoy J. W. and Lovicu F. J. (2011). The fate of dividing cells during lens morphogenesis, differentiation and growth. Exp. Eye Res. 92, 502- 511 10.1016/j.exer.2011.03.012 21440542 PMC3137915 · DOI
- Kamachi Y., Uchikawa M., Tanouchi A., Sekido R. and Kondoh H. (2001). Pax6 and SOX2 form a co-DNA-binding partner complex that regulates initiation of lens development. Genes Dev. 15, 1272- 1286 10.1101/gad.887101 11358870 PMC313803 · DOI
- Kawauchi S., Takahashi S., Nakajima O., Ogino H., Morita M., Nishizawa M., Yasuda K. and Yamamoto M. (1999). Regulation of lens fiber cell differentiation by transcription factor c-Maf. J. Biol. Chem. 274, 19254- 19260 10.1074/jbc.274.27.19254 10383433 · DOI
- Kerr C. L., Zaveri M. A., Robinson M. L., Williams T. and West-Mays J. A. (2014). AP-2α is required after lens vesicle formation to maintain lens integrity. Dev. Dyn. 243, 1298- 1309 10.1002/dvdy.24141 24753151 PMC7962590 · DOI
- Kim J. I., Li T., Ho I.-C., Grusby M. J. and Glimcher L. H. (1999). Requirement for the c-Maf transcription factor in crystallin gene regulation and lens development. Proc. Natl. Acad. Sci. USA 96, 3781- 3785 10.1073/pnas.96.7.3781 10097114 PMC22371 · DOI
- Kioussi C., O'Connell S., St-Onge L., Treier M., Gleiberman A. S., Gruss P. and Rosenfeld M. G. (1999). Pax6 is essential for establishing ventral-dorsal cell boundaries in pituitary gland development. Proc. Natl. Acad. Sci. USA 96, 14378- 14382 10.1073/pnas.96.25.14378 10588713 PMC24444 · DOI
- Klimova L. and Kozmik Z. (2014). Stage-dependent requirement of neuroretinal Pax6 for lens and retina development. Development 141, 1292- 1302 10.1242/dev.098822 24523460 · DOI
- Kowanetz M., Valcourt U., Bergstrom R., Heldin C.-H. and Moustakas A. (2004). Id2 and Id3 define the potency of cell proliferation and differentiation responses to transforming growth factor beta and bone morphogenetic protein. Mol. Cell. Biol. 24, 4241- 4254 10.1128/MCB.24.10.4241-4254.2004 15121845 PMC400464 · DOI
- Kreslova J., Machon O., Ruzickova J., Lachova J., Wawrousek E. F., Kemler R., Krauss S., Piatigorsky J. and Kozmik Z. (2007). Abnormal lens morphogenesis and ectopic lens formation in the absence of beta-catenin function. Genesis 45, 157- 168 10.1002/dvg.20277 17410548 · DOI
- Kuszak J. R., Zoltoski R. K. and Tiedemann C. E. (2004). Development of lens sutures. Int. J. Dev. Biol. 48, 889- 902 10.1387/ijdb.041880jk 15558480 · DOI
- Lachke S. A., Alkuraya F. S., Kneeland S. C., Ohn T., Aboukhalil A., Howell G. R., Saadi I., Cavallesco R., Yue Y., Tsai A. C.-H. et al. (2011). Mutations in the RNA granule component TDRD7 cause cataract and glaucoma. Science 331, 1571- 1576 10.1126/science.1195970 21436445 PMC3279122 · DOI
- Lachke S. A., Ho J. W. K., Kryukov G. V., O'Connell D. J., Aboukhalil A., Bulyk M. L., Park P. J. and Maas R. L. (2012). iSyTE: integrated Systems Tool for Eye gene discovery. Invest. Ophthalmol. Vis. Sci. 53, 1617- 1627 10.1167/iovs.11-8839 22323457 PMC3339920 · DOI
- Lagutin O. V., Zhu C. C., Kobayashi D., Topczewski J., Shimamura K., Puelles L., Russell H. R. C., McKinnon P. J., Solnica-Krezel L. and Oliver G. (2003). Six3 repression of Wnt signaling in the anterior neuroectoderm is essential for vertebrate forebrain development. Genes Dev. 17, 368- 379 10.1101/gad.1059403 12569128 PMC195989 · DOI
- Lampi K. J., Shih M., Ueda Y., Shearer T. R. and David L. L. (2002). Lens proteomics: analysis of rat crystallin sequences and two-dimensional electrophoresis map. Invest. Ophthalmol. Vis. Sci. 43, 216- 224. 11773034
- Lang R. A., Herman K., Reynolds A. B., Hildebrand J. D. and Plageman T. F. Jr (2014). p120-catenin-dependent junctional recruitment of Shroom3 is required for apical constriction during lens pit morphogenesis. Development 141, 3177- 3187 10.1242/dev.107433 25038041 PMC4197547 · DOI
- Le T. T., Conley K. W. and Brown N. L. (2009). Jagged 1 is necessary for normal mouse lens formation. Dev. Biol. 328, 118- 126 10.1016/j.ydbio.2009.01.015 19389370 PMC2674137 · DOI
- Le T. T., Conley K. W., Mead T. J., Rowan S., Yutzey K. E. and Brown N. L. (2012). Requirements for Jag1-Rbpj mediated Notch signaling during early mouse lens development. Dev. Dyn. 241, 493- 504 10.1002/dvdy.23739 22275127 PMC3288604 · DOI
- Lee A., Morrow J. S. and Fowler V. M. (2001). Caspase remodeling of the spectrin membrane skeleton during lens development and aging. J. Biol. Chem. 276, 20735- 20742 10.1074/jbc.M009723200 11278555 · DOI
- Lee H. Y., Wroblewski E., Philips G. T., Stair C. N., Conley K., Reedy M., Mastick G. S. and Brown N. L. (2005). Multiple requirements for Hes1 during early eye formation. Dev. Biol. 284, 464- 478 10.1016/j.ydbio.2005.06.010 16038893 PMC4128414 · DOI
- Leonard M., Zhang L., Bleaken B. M. and Menko A. S. (2013). Distinct roles for N-Cadherin linked c-Src and fyn kinases in lens development. Dev. Dyn. 242, 469- 484 10.1002/dvdy.23935 23361870 PMC3882121 · DOI
- Leung A. W., Kent Morest D. and Li J. Y. H. (2013). Differential BMP signaling controls formation and differentiation of multipotent preplacodal ectoderm progenitors from human embryonic stem cells. Dev. Biol. 379, 208- 220 10.1016/j.ydbio.2013.04.023 23643939 PMC3712508 · DOI
- Li Y. and Piatigorsky J. (2009). Targeted deletion of Dicer disrupts lens morphogenesis, corneal epithelium stratification, and whole eye development. Dev. Dyn. 238, 2388- 2400 10.1002/dvdy.22056 19681134 PMC2787093 · DOI
- Li H., Tao C., Cai Z., Hertzler-Schaefer K., Collins T. N., Wang F., Feng G.-S., Gotoh N. and Zhang X. (2014). Frs2α and Shp2 signal independently of Gab to mediate FGF signaling in lens development. J. Cell Sci. 127, 571- 582 10.1242/jcs.134478 24284065 PMC4007765 · DOI
- Lippens S., Hoste E., Vandenabeele P., Agostinis P. and Declercq W. (2009). Cell death in the skin. Apoptosis 14, 549- 569 10.1007/s10495-009-0324-z 19221876 · DOI
- Litsiou A., Hanson S. and Streit A. (2005). A balance of FGF, BMP and WNT signalling positions the future placode territory in the head. Development 132, 4051- 4062 10.1242/dev.01964 16093325 · DOI
- Liu W., Lagutin O. V., Mende M., Streit A. and Oliver G. (2006). Six3 activation of Pax6 expression is essential for mammalian lens induction and specification. EMBO J. 25, 5383- 5395 10.1038/sj.emboj.7601398 17066077 PMC1636621 · DOI
- Lleras-Forero L., Tambalo M., Christophorou N., Chambers D., Houart C. and Streit A. (2013). Neuropeptides: developmental signals in placode progenitor formation. Dev. Cell 26, 195- 203 10.1016/j.devcel.2013.07.001 23906067 PMC3748341 · DOI
- Lohnes D., Mark M., Mendelsohn C., Dolle P., Dierich A., Gorry P., Gansmuller A. and Chambon P. (1994). Function of the retinoic acid receptors (RARs) during development (I). Craniofacial and skeletal abnormalities in RAR double mutants. Development 120, 2723- 2748. 7607067
- Lovicu F. J. and McAvoy J. W. (2005). Growth factor regulation of lens development. Dev. Biol. 280, 1- 14 10.1016/j.ydbio.2005.01.020 15766743 · DOI
- Luo G., Hofmann C., Bronckers A. L., Sohocki M., Bradley A. and Karsenty G. (1995). BMP-7 is an inducer of nephrogenesis, and is also required for eye development and skeletal patterning. Genes Dev. 9, 2808- 2820 10.1101/gad.9.22.2808 7590255 · DOI
- Madakashira B. P., Kobrinski D. A., Hancher A. D., Arneman E. C., Wagner B. D., Wang F., Shin H., Lovicu F. J., Reneker L. W. and Robinson M. L. (2012). Frs2α enhances fibroblast growth factor-mediated survival and differentiation in lens development. Development 139, 4601- 4612 10.1242/dev.081737 23136392 PMC3509723 · DOI
- Maddala R., Chauhan B. K., Walker C., Zheng Y., Robinson M. L., Lang R. A. and Rao P. V. (2011). Rac1 GTPase-deficient mouse lens exhibits defects in shape, suture formation, fiber cell migration and survival. Dev. Biol. 360, 30- 43. 21945075 PMC3215831
- Maeda A., Moriguchi T., Hamada M., Kusakabe M., Fujioka Y., Nakano T., Yoh K., Lim K.-C., Engel J. D. and Takahashi S. (2009). Transcription factor GATA-3 is essential for lens development. Dev. Dyn. 238, 2280- 2291 10.1002/dvdy.22035 19623612 PMC3408506 · DOI
- Mahon K. A., Chepelinsky A. B., Khillan J. S., Overbeek P. A., Piatigorsky J. and Westphal H. (1987). Oncogenesis of the lens in transgenic mice. Science 235, 1622- 1628 10.1126/science.3029873 3029873 · DOI
- Manthey A. L., Lachke S. A., FitzGerald P. G., Mason R. W., Scheiblin D. A., McDonald J. H. and Duncan M. K. (2014). Loss of Sip1 leads to migration defects and retention of ectodermal markers during lens development. Mech. Dev. 131, 86- 110 10.1016/j.mod.2013.09.005 24161570 PMC4144920 · DOI
- Martinez G. and de Iongh R. U. (2010). The lens epithelium in ocular health and disease. Int. J. Biochem. Cell Biol. 42, 1945- 1963 10.1016/j.biocel.2010.09.012 20883819 · DOI
- Massague J., Seoane J. and Wotton D. (2005). Smad transcription factors. Genes Dev. 19, 2783- 2810 10.1101/gad.1350705 16322555 · DOI
- Mathers P. H., Grinberg A., Mahon K. A. and Jamrich M. (1997). The Rx homeobox gene is essential for vertebrate eye development. Nature 387, 603- 607 10.1038/42475 9177348 · DOI
- Mathias R. T., White T. W. and Gong X. (2010). Lens gap junctions in growth, differentiation, and homeostasis. Physiol. Rev. 90, 179- 206 10.1152/physrev.00034.2009 20086076 PMC4627646 · DOI
- McAvoy J. W. (1980). Cytoplasmic processes interconnect lens placode and optic vesicle during eye morphogenesis. Exp. Eye Res. 31, 527- 534 10.1016/S0014-4835(80)80011-X 7192638 · DOI
- McAvoy J. W. and Chamberlain C. G. (1989). Fibroblast growth factor (FGF) induces different responses in lens epithelial cells depending on its concentration. Development 107, 221- 228. 2632221
- McCabe K. L. and Bronner-Fraser M. (2009). Molecular and tissue interactions governing induction of cranial ectodermal placodes. Dev. Biol. 332, 189- 195 10.1016/j.ydbio.2009.05.572 19500565 PMC2747488 · DOI
- Medina-Martinez O., Brownell I., Amaya-Manzanares F., Hu Q., Behringer R. R. and Jamrich M. (2005). Severe defects in proliferation and differentiation of lens cells in Foxe3 null mice. Mol. Cell. Biol. 25, 8854- 8863 10.1128/MCB.25.20.8854-8863.2005 16199865 PMC1265778 · DOI
- Medina-Martinez O., Shah R. and Jamrich M. (2009). Pitx3 controls multiple aspects of lens development. Dev. Dyn. 238, 2193- 2201 10.1002/dvdy.21924 19334279 PMC2978039 · DOI
- Mic F. A., Molotkov A., Molotkova N. and Duester G. (2004). Raldh2 expression in optic vesicle generates a retinoic acid signal needed for invagination of retina during optic cup formation. Dev. Dyn. 231, 270- 277 10.1002/dvdy.20128 15366004 · DOI
- Mikkola I., Bruun J.-A., Bjorkoy G., Holm T. and Johansen T. (1999). Phosphorylation of the transactivation domain of Pax6 by extracellular signal-regulated kinase and p38 mitogen-activated protein kinase. J. Biol. Chem. 274, 15115- 15126 10.1074/jbc.274.21.15115 10329718 · DOI
- Molotkov A., Molotkova N. and Duester G. (2006). Retinoic acid guides eye morphogenetic movements via paracrine signaling but is unnecessary for retinal dorsoventral patterning. Development 133, 1901- 1910 10.1242/dev.02328 16611695 PMC2833011 · DOI
- Morcillo J., Martínez-Morales J. R., Trousse F., Fermin Y., Sowden J. C. and Bovolenta P. (2006). Proper patterning of the optic fissure requires the sequential activity of BMP7 and SHH. Development 133, 3179- 3190 10.1242/dev.02493 16854970 · DOI
- Morgenbesser S. D., Williams B. O., Jacks T. and DePinho R. A. (1994). p53-dependent apoptosis produced by Rb-deficiency in the developing mouse lens. Nature 371, 72- 74 10.1038/371072a0 8072529 · DOI
- Morozov V. and Wawrousek E. F. (2006). Caspase-dependent secondary lens fiber cell disintegration in αA-/αB-crystallin double-knockout mice. Development 133, 813- 821 10.1242/dev.02262 16439475 · DOI
- Muñoz-Sanjuán I. and Brivanlou A. H. (2002). Neural induction, the default model and embryonic stem cells. Nat. Rev. Neurosci. 3, 271- 280 10.1038/nrn786 11967557 · DOI
- Nakamura T., Pichel J. G., Williams-Simons L. and Westphal H. (1995). An apoptotic defect in lens differentiation caused by human p53 is rescued by a mutant allele. Proc. Natl. Acad. Sci. USA 92, 6142- 6146 10.1073/pnas.92.13.6142 7597093 PMC41658 · DOI
- Neppl R. L., Kataoka M. and Wang D.-Z. (2014). Crystallin-αB regulates skeletal muscle homeostasis via modulation of argonaute2 activity. J. Biol. Chem. 289, 17240- 17248 10.1074/jbc.M114.549584 24782307 PMC4059164 · DOI
- Ng D., Thakker N., Corcoran C. M., Donnai D., Perveen R., Schneider A., Hadley D. W., Tifft C., Zhang L., Wilkie A. O. M. et al. (2004). Oculofaciocardiodental and Lenz microphthalmia syndromes result from distinct classes of mutations in BCOR. Nat. Genet. 36, 411- 416 10.1038/ng1321 15004558 · DOI
- Ninkovic J., Pinto L., Petricca S., Lepier A., Sun J., Rieger M. A., Schroeder T., Cvekl A., Favor J. and Götz M. (2010). The transcription factor Pax6 regulates survival of dopaminergic olfactory bulb neurons via crystallin alphaA. Neuron 68, 682- 694 10.1016/j.neuron.2010.09.030 21092858 PMC4388427 · DOI
- Ninkovic J., Steiner-Mezzadri A., Jawerka M., Akinci U., Masserdotti G., Petricca S., Fischer J., von Holst A., Beckers J., Lie C. D. et al. (2013). The BAF complex interacts with Pax6 in adult neural progenitors to establish a neurogenic cross-regulatory transcriptional network. Cell Stem Cell 13, 403- 418 10.1016/j.stem.2013.07.002 23933087 PMC4098720 · DOI
- Nishimoto S., Kawane K., Watanabe-Fukunaga R., Fukuyama H., Ohsawa Y., Uchiyama Y., Hashida N., Ohguro N., Tano Y., Morimoto T. et al. (2003). Nuclear cataract caused by a lack of DNA degradation in the mouse eye lens. Nature 424, 1071- 1074 10.1038/nature01895 12944971 · DOI
- Ogino H., Fisher M. and Grainger R. M. (2008). Convergence of a head-field selector Otx2 and Notch signaling: a mechanism for lens specification. Development 135, 249- 258 10.1242/dev.009548 18057103 PMC3918164 · DOI
- Oliver G. and Gruss P. (1997). Current views on eye development. Trends Neurosci. 20, 415- 421 10.1016/S0166-2236(97)01082-5 9292971 · DOI
- Ousman S. S., Tomooka B. H., van Noort J. M., Wawrousek E. F., O'Connor K., Hafler D. A., Sobel R. A., Robinson W. H. and Steinman L. (2007). Protective and therapeutic role for αB-crystallin in autoimmune demyelination. Nature 448, 474- 479 10.1038/nature05935 17568699 · DOI
- Overbeek P. A., Chepelinsky A. B., Khillan J. S., Piatigorsky J. and Westphal H. (1985). Lens-specific expression and developmental regulation of the bacterial chloramphenicol acetyltransferase gene driven by the murine αA-crystallin promoter in transgenic mice. Proc. Natl. Acad. Sci. USA 82, 7815- 7819 10.1073/pnas.82.23.7815 3865198 PMC390860 · DOI
- Pan H. and Griep A. E. (1994). Altered cell cycle regulation in the lens of HPV-16 E6 or E7 transgenic mice: implications for tumor suppressor gene function in development. Genes Dev. 8, 1285- 1299 10.1101/gad.8.11.1285 7926731 · DOI
- Pan H. and Griep A. E. (1995). Temporally distinct patterns of p53-dependent and p53-independent apoptosis during mouse lens development. Genes Dev. 9, 2157- 2169 10.1101/gad.9.17.2157 7657167 · DOI
- Pan Y., Woodbury A., Esko J. D., Grobe K. and Zhang X. (2006). Heparan sulfate biosynthetic gene Ndst1 is required for FGF signaling in early lens development. Development 133, 4933- 4944 10.1242/dev.02679 17107998 · DOI
- Petrash J. M. (2013). Aging and age-related diseases of the ocular lens and vitreous body. Invest. Ophthalmol. Vis. Sci. 54, ORSF54- ORSF59 10.1167/iovs.13-12940 24335070 PMC3864378 · DOI
- Piatigorsky J. (1981). Lens differentiation in vertebrates. A review of cellular and molecular features. Differentiation 19, 134- 153 10.1111/j.1432-0436.1981.tb01141.x 7030840 · DOI
- Plageman T. F. Jr, Chung M.-I., Lou M., Smith A. N., Hildebrand J. D., Wallingford J. B. and Lang R. A. (2010). Pax6-dependent Shroom3 expression regulates apical constriction during lens placode invagination. Development 137, 405- 415 10.1242/dev.045369 20081189 PMC2858910 · DOI
- Plageman T. F. Jr, Chauhan B. K., Yang C., Jaudon F., Shang X., Zheng Y., Lou M., Debant A., Hildebrand J. D. and Lang R. A. (2011). A Trio-RhoA-Shroom3 pathway is required for apical constriction and epithelial invagination. Development 138, 5177- 5188 10.1242/dev.067868 22031541 PMC3210497 · DOI
- Pontoriero G. F., Deschamps P., Ashery-Padan R., Wong R., Yang Y., Zavadil J., Cvekl A., Sullivan S., Williams T. and West-Mays J. A. (2008). Cell autonomous roles for AP-2α in lens vesicle separation and maintenance of the lens epithelial cell phenotype. Dev. Dyn. 237, 602- 617 10.1002/dvdy.21445 18224708 PMC2517426 · DOI
- Pontoriero G. F., Smith A. N., Miller L.-A. D., Radice G. L., West-Mays J. A. and Lang R. A. (2009). Co-operative roles for E-cadherin and N-cadherin during lens vesicle separation and lens epithelial cell survival. Dev. Biol. 326, 403- 417 10.1016/j.ydbio.2008.10.011 18996109 PMC3408230 · DOI
- Porter F. D., Drago J., Xu Y., Cheema S. S., Wassif C., Huang S. P., Lee E., Grinberg A., Massalas J. S., Bodine D. et al. (1997). Lhx2, a LIM homeobox gene, is required for eye, forebrain, and definitive erythrocyte development. Development 124, 2935- 2944. 9247336
- Ptashne M. (2013). Epigenetics: core misconcept. Proc. Natl. Acad. Sci. USA 110, 7101- 7103 10.1073/pnas.1305399110 23584020 PMC3645541 · DOI
- Purcell P., Oliver G., Mardon G., Donner A. L. and Maas R. L. (2005). Pax6-dependence of Six3, Eya1 and Dach1 expression during lens and nasal placode induction. Gene Expr. Patterns 6, 110- 118 10.1016/j.modgep.2005.04.010 16024294 · DOI
- Qu X., Hertzler K., Pan Y., Grobe K., Robinson M. L. and Zhang X. (2011). Genetic epistasis between heparan sulfate and FGF-Ras signaling controls lens development. Dev. Biol. 355, 12- 20 10.1016/j.ydbio.2011.04.007 21536023 PMC3104109 · DOI
- Quinn J. C., West J. D. and Hill R. E. (1996). Multiple functions for Pax6 in mouse eye and nasal development. Genes Dev. 10, 435- 446 10.1101/gad.10.4.435 8600027 · DOI
- Rai K., Nadauld L. D., Chidester S., Manos E. J., James S. R., Karpf A. R., Cairns B. R. and Jones D. A. (2006). Zebra fish Dnmt1 and Suv39h1 regulate organ-specific terminal differentiation during development. Mol. Cell. Biol. 26, 7077- 7085 10.1128/MCB.00312-06 16980612 PMC1592902 · DOI
- Rai K., Jafri I. F., Chidester S., James S. R., Karpf A. R., Cairns B. R. and Jones D. A. (2010). Dnmt3 and G9a cooperate for tissue-specific development in zebrafish. J. Biol. Chem. 285, 4110- 4121 10.1074/jbc.M109.073676 19946145 PMC2823551 · DOI
- Rajagopal R., Huang J., Dattilo L. K., Kaartinen V., Mishina Y., Deng C.-X., Umans L., Zwijsen A., Roberts A. B. and Beebe D. C. (2009). The type I BMP receptors, Bmpr1a and Acvr1, activate multiple signaling pathways to regulate lens formation. Dev. Biol. 335, 305- 316 10.1016/j.ydbio.2009.08.027 19733164 PMC2783396 · DOI
- Rao P. V. and Maddala R. (2006). The role of the lens actin cytoskeleton in fiber cell elongation and differentiation. Semin. Cell Dev. Biol. 17, 698- 711 10.1016/j.semcdb.2006.10.011 17145190 PMC1803076 · DOI
- Raviv S., Bharti K., Rencus-Lazar S., Cohen-Tayar Y., Schyr R., Evantal N., Meshorer E., Zilberberg A., Idelson M., Reubinoff B. et al. (2014). PAX6 regulates melanogenesis in the retinal pigmented epithelium through feed-forward regulatory interactions with MITF. PLoS Genet. 10, e1004360 10.1371/journal.pgen.1004360 24875170 PMC4038462 · DOI
- Ring B. Z., Cordes S. P., Overbeek P. A. and Barsh G. S. (2000). Regulation of mouse lens fiber cell development and differentiation by the Maf gene. Development 127, 307- 317. 10603348
- Rivera C., Yamben I. F., Shatadal S., Waldof M., Robinson M. L. and Griep A. E. (2009). Cell-autonomous requirements for Dlg-1 for lens epithelial cell structure and fiber cell morphogenesis. Dev. Dyn. 238, 2292- 2308 10.1002/dvdy.22036 19623611 PMC3016059 · DOI
- Rowan S., Conley K. W., Le T. T., Donner A. L., Maas R. L. and Brown N. L. (2008). Notch signaling regulates growth and differentiation in the mammalian lens. Dev. Biol. 321, 111- 122 10.1016/j.ydbio.2008.06.002 18588871 PMC2593917 · DOI
- Rowan S., Siggers T., Lachke S. A., Yue Y., Bulyk M. L. and Maas R. L. (2010). Precise temporal control of the eye regulatory gene Pax6 via enhancer-binding site affinity. Genes Dev. 24, 980- 985 10.1101/gad.1890410 20413611 PMC2867212 · DOI
- Sandilands A., Hutcheson A. M., Long H. A., Prescott A. R., Vrensen G., Löster J., Klopp N., Lutz R. B., Graw J., Masaki S. et al. (2002). Altered aggregation properties of mutant γ-crystallins cause inherited cataract. EMBO J. 21, 6005- 6014 10.1093/emboj/cdf609 12426373 PMC137201 · DOI
- Sandoval H., Thiagarajan P., Dasgupta S. K., Schumacher A., Prchal J. T., Chen M. and Wang J. (2008). Essential role for Nix in autophagic maturation of erythroid cells. Nature 454, 232- 235 10.1038/nature07006 18454133 PMC2570948 · DOI · Paper page
- Saravanamuthu S. S., Le T. T., Gao C. Y., Cojocaru R. I., Pandiyan P., Liu C., Zhang J., Zelenka P. S. and Brown N. L. (2012). Conditional ablation of the Notch2 receptor in the ocular lens. Dev. Biol. 362, 219- 229 10.1016/j.ydbio.2011.11.011 22173065 PMC3265577 · DOI
- Sawyer J. M., Harrell J. R., Shemer G., Sullivan-Brown J., Roh-Johnson M. and Goldstein B. (2010). Apical constriction: a cell shape change that can drive morphogenesis. Dev. Biol. 341, 5- 19 10.1016/j.ydbio.2009.09.009 19751720 PMC2875788 · DOI
- Semina E. V., Reiter R. S. and Murray J. C. (1997). Isolation of a new homeobox gene belonging to the Pitx/Rieg family: expression during lens development and mapping to the aphakia region on mouse chromosome 19. Hum. Mol. Genet. 6, 2109- 2116 10.1093/hmg/6.12.2109 9328475 · DOI
- Seritrakul P. and Gross J. M. (2014). Expression of the de novo DNA methyltransferases (dnmt3 - dnmt8) during zebrafish lens development. Dev. Dyn. 243, 350- 356 10.1002/dvdy.24077 24123478 · DOI
- Shaham O., Smith A. N., Robinson M. L., Taketo M. M., Lang R. A. and Ashery-Padan R. (2009). Pax6 is essential for lens fiber cell differentiation. Development 136, 2567- 2578 10.1242/dev.032888 19570848 PMC2709063 · DOI
- Shaham O., Menuchin Y., Farhy C. and Ashery-Padan R. (2012). Pax6: a multi-level regulator of ocular development. Prog. Retin. Eye Res. 31, 351- 376 10.1016/j.preteyeres.2012.04.002 22561546 · DOI
- Shaham O., Gueta K., Mor E., Oren-Giladi P., Grinberg D., Xie Q., Cvekl A., Shomron N., Davis N., Keydar-Prizant M. et al. (2013). Pax6 regulates gene expression in the vertebrate lens through miR-204. PLoS Genet. 9, e1003357 10.1371/journal.pgen.1003357 23516376 PMC3597499 · DOI
- Shao W., Zhang S.-z., Tang M., Zhang X.-h., Zhou Z., Yin Y.-q., Zhou Q.-b., Huang Y.-y., Liu Y.-j., Wawrousek E. et al. (2013). Suppression of neuroinflammation by astrocytic dopamine D2 receptors via αB-crystallin. Nature 494, 90- 94 10.1038/nature11748 23242137 · DOI
- Shi Y., Barton K., De Maria A., Petrash J. M., Shiels A. and Bassnett S. (2009). The stratified syncytium of the vertebrate lens. J. Cell Sci. 122, 1607- 1615 10.1242/jcs.045203 19401333 PMC2680101 · DOI
- Shiels A. and Bassnett S. (1996). Mutations in the founder of the MIP gene family underlie cataract development in the mouse. Nat. Genet. 12, 212- 215 10.1038/ng0296-212 8563764 · DOI
- Shiels A. and Hejtmancik J. F. (2013). Genetics of human cataract. Clin. Genet. 84, 120- 127 10.1111/cge.12182 23647473 PMC3991604 · DOI
- Shiels A., Bassnett S., Varadaraj K., Mathias R., Al-Ghoul K., Kuszak J., Donoviel D., Lilleberg S., Friedrich G. and Zambrowicz B. (2001). Optical dysfunction of the crystalline lens in aquaporin-0-deficient mice. Physiol. Genomics 7, 179- 186. 11773604
- Sjödal M., Edlund T. and Gunhaga L. (2007). Time of exposure to BMP signals plays a key role in the specification of the olfactory and lens placodes ex vivo. Dev. Cell 13, 141- 149 10.1016/j.devcel.2007.04.020 17609116 · DOI
- Smith A. N., Miller L.-A. D., Song N., Taketo M. M. and Lang R. A. (2005). The duality of β-catenin function: a requirement in lens morphogenesis and signaling suppression of lens fate in periocular ectoderm. Dev. Biol. 285, 477- 489 10.1016/j.ydbio.2005.07.019 16102745 · DOI
- Smith A. N., Miller L.-A., Radice G., Ashery-Padan R. and Lang R. A. (2009). Stage-dependent modes of Pax6-Sox2 epistasis regulate lens development and eye morphogenesis. Development 136, 2977- 2985 10.1242/dev.037341 19666824 PMC2723069 · DOI
- Song N., Schwab K. R., Patterson L. T., Yamaguchi T., Lin X., Potter S. S. and Lang R. A. (2007). Pygopus 2 has a crucial, Wnt pathway-independent function in lens induction. Development 134, 1873- 1885 10.1242/dev.001495 17428831 · DOI
- Song J. Y., Park R., Kim J. Y., Hughes L., Lu L., Kim S., Johnson R. L. and Cho S.-H. (2014). Dual function of Yap in the regulation of lens progenitor cells and cellular polarity. Dev. Biol. 386, 281- 290 10.1016/j.ydbio.2013.12.037 24384391 PMC3985746 · DOI
- Sorokina E. A., Muheisen S., Mlodik N. and Semina E. V. (2011). MIP/Aquaporin 0 represents a direct transcriptional target of PITX3 in the developing lens. PLoS ONE 6, e21122 10.1371/journal.pone.0021122 21698120 PMC3117865 · DOI
- Steinfeld J., Steinfeld I., Coronato N., Hampel M.-L., Layer P. G., Araki M. and Vogel-Hopker A. (2013). RPE specification in the chick is mediated by surface ectoderm-derived BMP and Wnt signalling. Development 140, 4959- 4969 10.1242/dev.096990 24227655 · DOI
- Steventon B., Mayor R. and Streit A. (2012). Mutual repression between Gbx2 and Otx2 in sensory placodes reveals a general mechanism for ectodermal patterning. Dev. Biol. 367, 55- 65 10.1016/j.ydbio.2012.04.025 22564795 PMC3384001 · DOI
- Sugiyama Y., Akimoto K., Robinson M. L., Ohno S. and Quinlan R. A. (2009). A cell polarity protein aPKClambda is required for eye lens formation and growth. Dev. Biol. 336, 246- 256 10.1016/j.ydbio.2009.10.010 19835853 PMC2806522 · DOI
- Sugiyama Y., Stump R. J. W., Nguyen A., Wen L., Chen Y., Wang Y., Murdoch J. N., Lovicu F. J. and McAvoy J. W. (2010). Secreted frizzled-related protein disrupts PCP in eye lens fiber cells that have polarised primary cilia. Dev. Biol. 338, 193- 201 10.1016/j.ydbio.2009.11.033 19968984 PMC2815166 · DOI
- Sugiyama Y., Lovicu F. J. and McAvoy J. W. (2011). Planar cell polarity in the mammalian eye lens. Organogenesis 7, 191- 201 10.4161/org.7.3.18421 22027540 PMC3243032 · DOI
- Sun M., Hölter S. M., Stepan J., Garrett L., Genius J., Kremmer E., Hrabě de Angelis M., Wurst W., Lie D. C., Bally-Cuif L. et al. (2013). Crybb2 coding for βB2-crystallin affects sensorimotor gating and hippocampal function. Mamm. Genome 24, 333- 348 10.1007/s00335-013-9478-7 24096375 PMC3824278 · DOI
- Tittle R. K., Sze R., Ng A., Nuckels R. J., Swartz M. E., Anderson R. M., Bosch J., Stainier D. Y. R., Eberhart J. K. and Gross J. M. (2011). Uhrf1 and Dnmt1 are required for development and maintenance of the zebrafish lens. Dev. Biol. 350, 50- 63 10.1016/j.ydbio.2010.11.009 21126517 PMC3022120 · DOI
- Turner N. and Grose R. (2010). Fibroblast growth factor signalling: from development to cancer. Nat. Rev. Cancer 10, 116- 129 10.1038/nrc2780 20094046 · DOI
- Upadhya D., Ogata M. and Reneker L. W. (2013). MAPK1 is required for establishing the pattern of cell proliferation and for cell survival during lens development. Development 140, 1573- 1582 10.1242/dev.081042 23482492 PMC3596996 · DOI · Paper page
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“These transcription factors promote the expression of the bone morphogenic protein 4 (BMP4) and bone morphogenic protein 7 (BMP7), which are both responsible for the activation of Six3 and Pax6 in the PLE, leading to the formation of the lens placode [50].”
- Authors
- Cvekl, A., & Ashery-Padan, R.
- Affiliations
- Albert Einstein College of Medicine (US)
- Sackler School of Medicine and Sagol School of Neuroscience, Tel-Aviv University, 69978 Ramat Aviv, Tel Aviv, Israel
- Corresponding author
- Cvekl, Aleš
- ORCID
- Cvekl, Aleš
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2014-12-01
- Volume
- 141
- Issue
- 23
- Pages
- 4432-4447
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- PMC
- PMC4302924
- OpenAlex
- W2131142658
- Cited by
- 227
- References
- 6
- Citations by year
- 2026: 13 · 2025: 16 · 2024: 25 · 2023: 21 · 2022: 22 · 2021: 19 · 2020: 22 · 2019: 21 · 2018: 17 · 2017: 18 · 2016: 19 · 2015: 14
- FWCI
- 1.60
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Locations
- Development (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- HighWire Press Open Archive (submittedVersion)
- Funders
- National Eye Institute (EY014237, R01EY014237, R01EY012200)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Ocular Disorders and Treatments
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Retinal Development and Disorders
- Keywords
- lens development, lens induction, Pax6, lens epithelium, lens fiber cells, lens morphogenesis, gene regulatory networks, cell specification, eye development
- MeSH terms
- PAX6 Transcription Factor, Animals, Cell Cycle, Cell Differentiation, Eye Proteins, Humans, Lens, Crystalline, Models, Biological, Repressor Proteins, Species Specificity, Vertebrates, Signal Transduction, Homeodomain Proteins, Organogenesis, Paired Box Transcription Factors, Gene Regulatory Networks, Neural Plate
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