TEAD family transcription factors in development and disease
Open accessAbstract
The balance between stem cell potency and lineage specification entails the integration of both extrinsic and intrinsic cues, which ultimately influence gene expression through the activity of transcription factors. One example of this is provided by the Hippo signalling pathway, which plays a central role in regulating organ size during development. Hippo pathway activity is mediated by the transcriptional co-factors Yes-associated protein (YAP) and transcriptional co-activator with PDZ-binding motif (TAZ), which interact with TEA domain (TEAD) proteins to regulate gene expression. Although the roles of YAP and TAZ have been intensively studied, the roles played by TEAD proteins are less well understood. Recent studies have begun to address this, revealing that TEADs regulate the balance between progenitor self-renewal and differentiation throughout various stages of development. Furthermore, it is becoming apparent that TEAD proteins interact with other co-factors that influence stem cell biology. This Primer provides an overview of the role of TEAD proteins during development, focusing on their role in Hippo signalling as well as within other developmental, homeostatic and disease contexts.
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TEAD4 is a transcription factor involved in the Hippo signaling pathway.
“TEAD4 is a transcription factor involved in the Hippo signaling pathway27, and future work is warranted to further examine its role in cardiac development.”
From Transfer learning enables predictions in network biology (2023) · cites this paper as [27]
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The Hippo Signaling Pathway in Development and Disease
Zheng, Y., & Pan, D. (2019) · Developmental Cell · doi:10.1016/j.devcel.2019.06.003 · Cited by 867 · see citing works
Hippo Pathway Activity Influences Liver Cell Fate
Yimlamai, D., Christodoulou, C., Galli, G. G., Yanger, K., Pepe-Mooney, B., Gurung, B., Shrestha, K., Cahan, P., Stanger, B. Z., & Camargo, F. D. (2014) · Cell · doi:10.1016/j.cell.2014.03.060 · Cited by 857 · see citing works
Wu, S., Liu, Y., Zheng, Y., Dong, J., & Pan, D. (2008) · Developmental Cell · doi:10.1016/j.devcel.2008.01.007 · Cited by 640 · see citing works
YAP/TAZ as mechanosensors and mechanotransducers in regulating organ size and tumor growth
Low, B. C., Pan, C. Q., Shivashankar, G. V., Bershadsky, A., Sudol, M., & Sheetz, M. (2014) · FEBS Letters · doi:10.1016/j.febslet.2014.04.012 · Cited by 412 · see citing works
Autopalmitoylation of TEAD proteins regulates transcriptional output of the Hippo pathway
Chan, P., Han, X., Zheng, B., DeRan, M., Yu, J., Jarugumilli, G. K., Deng, H., Pan, D., Luo, X., & Wu, X. (2016) · Nature Chemical Biology · doi:10.1038/nchembio.2036 · Cited by 313 · see citing works
Regulation of TEAD Transcription Factors in Cancer Biology
Huh, H., Kim, D., Jeong, H.-S., & Park, H. (2019) · Cells · doi:10.3390/cells8060600 · Cited by 259 · see citing works
The Hippo pathway effector YAP is a critical regulator of skeletal muscle fibre size
Watt, K. I., Turner, B. J., Hagg, A., Zhang, X., Davey, J. R., Qian, H., Beyer, C., Winbanks, C. E., Harvey, K. F., & Gregorevic, P. (2015) · Nature Communications · doi:10.1038/ncomms7048 · Cited by 164 · see citing works
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Research works printed but not linked: 155
- Anbanandam, A., Albarado, D. C., Nguyen, C. T., Halder, G., Gao, X. and Veeraraghavan, S. (2006). Insights into transcription enhancer factor 1 (TEF-1) activity from the solution structure of the TEA domain. Proc. Natl Acad. Sci. USA 103, 17225-17230. doi:10.1073/pnas.0607171103 · DOI
- Aragona, M., Panciera, T., Manfrin, A., Giulitti, S., Michielin, F., Elvassore, N., Dupont, S. and Piccolo, S. (2013). A mechanical checkpoint controls multicellular growth through YAP/TAZ regulation by actin-processing factors. Cell 154, 1047-1059. doi:10.1016/j.cell.2013.07.042 · DOI · Paper page
- Belandia, B. and Parker, M. G. (2000). Functional interaction between the p160 coactivator proteins and the transcriptional enhancer factor family of transcription factors. J. Biol. Chem. 275, 30801-30805. doi:10.1074/jbc. · DOI
- C000484200 · DOI
- Beverdam, A., Claxton, C., Zhang, X., James, G., Harvey, K. F. and Key, B. (2013). Yap controls stem/progenitor cell proliferation in the mouse postnatal epidermis. J. Investig. Dermatol. 133, 1497-1505. doi:10.1038/jid.2012.430 · DOI
- Beyer, T. A., Weiss, A., Khomchuk, Y., Huang, K., Ogunjimi, A. A., Varelas, X. and Wrana, J. L. (2013). Switch enhancers interpret TGF-β and hippo signaling to control cell fate in human embryonic stem cells. Cell Rep. 5, 1611-1624. doi:10. 1016/j.celrep.2013.11.021 · DOI
- Bokhovchuk, F., Mesrouze, Y., Izaac, A., Meyerhofer, M., Zimmermann, C., Fontana, P., Schmelzle, T., Erdmann, D., Furet, P., Kallen, J. et al. (2019). Molecular and structural characterization of a TEAD mutation at the origin of Sveinsson's chorioretinal atrophy. FEBS J. 286, 2381-2398. doi:10.1111/febs. 14817 · DOI
- Bokhovchuk, F., Mesrouze, Y., Delaunay, C., Martin, T., Villard, F., Meyerhofer, M., Fontana, P., Zimmermann, C., Erdmann, D., Furet, P. et al. (2020). Identification of FAM181A and FAM181B as new interactors with the TEAD transcription factors. Protein Sci. 29, 509-520. doi:10.1002/pro.3775 · DOI
- Bu ̈rglin, T. R. (1991). The TEA domain: a novel, highly conserved DNA-binding motif. Cell 66, 11-12. doi:10.1016/0092-8674(91)90132-I · DOI
- Cabochette, P., Vega-Lopez, G., Bitard, J., Parain, K., Chemouny, R., Masson, C., Borday, C., Hedderich, M., Henningfeld, K. A., Locker, M. et al. (2015). YAP controls retinal stem cell DNA replication timing and genomic stability. eLife 4, e08488. doi:10.7554/eLife.08488 · DOI
- Calses, P. C., Crawford, J. J., Lill, J. R. and Dey, A. (2019). Hippo pathway in cancer: aberrant regulation and therapeutic opportunities. Trends in Cancer 5, 297-307. doi:10.1016/j.trecan.2019.04.001 · DOI
- Campbell, S. D., Duttaroy, A., Katzen, A. L. and Chovnick, A. (1991). Cloning and characterization of the scalloped region of Drosophila melanogaster. Genetics 127, 367-380. doi:10.1093/genetics/127.2.367 · DOI
- Campbell, S., Inamdar, M., Rodrigues, V., Raghavan, V., Palazzolo, M. and Chovnick, A. (1992). The scalloped gene encodes a novel, evolutionarily conserved transcription factor required for sensory organ differentiation in Drosophila. Genes Dev. 6, 367-379. doi:10.1101/gad.6.3.367 · DOI
- Cao, X., Pfaff, S. L. and Gage, F. H. (2008). YAP regulates neural progenitor cell number via the TEA domain transcription factor. Genes Dev. 22, 3320-3334. doi:10.1101/gad.1726608 · DOI
- Cao, Q., Wang, X., Zhao, M., Yang, R., Malik, R., Qiao, Y., Poliakov, A., Yocum, A. K., Li, Y., Chen, W. et al. (2014). The central role of EED in the orchestration of polycomb group complexes. Nat. Commun. 5, 3127. doi:10.1038/ ncomms4127 · DOI
- Cebola, I., Rodrıǵuez-Seguı, S. A., Cho, C. H.-H., Bessa, J., Rovira, M., Luengo, M., Chhatriwala, M., Berry, A., Ponsa-Cobas, J., Maestro, M. A. et al. (2015). TEAD and YAP regulate the enhancer network of human embryonic pancreatic progenitors. Nat. Cell Biol. 17, 615-626. doi:10.1038/ncb3160 · DOI
- Chen, Z., Friedrich, G. A. and Soriano, P. (1994). Transcriptional enhancer factor 1 disruption by a retroviral gene trap leads to heart defects and embryonic lethality in mice. Genes Dev. 8, 2293-2301. doi:10.1101/gad.8.19.2293 · DOI
- Chen, H.-H., Mullett, S. J. and Stewart, A. F. R. (2004). Vgl-4, a novel member of the vestigial-like family of transcription cofactors, regulates α1-adrenergic activation of gene expression in cardiac myocytes. J. Biol. Chem. 279, 30800-30806. doi:10.1074/jbc. · DOI
- M400154200 · DOI
- Chung, H., Lee, B.-K., Uprety, N., Shen, W., Lee, J. and Kim, J. (2016). Yap1 is dispensable for self-renewal but required for proper differentiation of mouse embryonic stem (ES) cells. EMBO Rep. 17, 519-529. doi:10.15252/embr. 201540933 · DOI
- Davis, J. R. and Tapon, N. (2019). Hippo signalling during development. Development 146, dev167106. doi:10.1242/dev.167106 · DOI
- Deng, H., Hughes, S. C., Bell, J. B. and Simmonds, A. J. (2009). Alternative requirements for Vestigial, Scalloped, and Dmef2 during muscle differentiation in Drosophila melanogaster. Mol. Biol. Cell 20, 256-269. doi:10.1091/mbc.e08-03- 0288 · DOI
- Deshpande, N., Chopra, A., Rangarajan, A., Shashidhara, L. S., Rodrigues, V. and Krishna, S. (1997). The human transcription enhancer factor-1, TEF-1, can substitute for Drosophila scalloped during Wingblade development. J. Biol. Chem. 272, 10664-10668. doi:10.1074/jbc.272.16.10664 · DOI
- Feng, X., Wang, Z., Wang, F., Lu, T., Xu, J., Ma, X., Li, J., He, L., Zhang, W., Li, S. et al. (2019). Dual function of VGLL4 in muscle regeneration. EMBO J. 38, e101051. doi:10.15252/embj.2018101051 · DOI
- Ferguson, G. B. and Martinez-Agosto, J. A. (2014). Yorkie and Scalloped signaling regulates Notch-dependent lineage specification during Drosophila hematopoiesis. Curr. Biol. 24, 2665-2672. doi:10.1016/j.cub.2014.09.081 · DOI
- Figeac, N., Mohamed, A. D., Sun, C., Schönfelder, M., Matallanas, D., Garcia-Munoz, A., Missiaglia, E., Collie-Duguid, E., De Mello, V., Pobbati, A. V. et al. (2019). VGLL3 operates via TEAD1, TEAD3 and TEAD4 to influence myogenesis in skeletal muscle. J. Cell Sci. 132, jcs225946. doi:10.1242/jcs. 225946 · DOI
- Fillatre, J., Fauny, J.-D., Fels, J. A., Li, C., Goll, M., Thisse, C. and Thisse, B. (2019). TEADs, Yap, Taz, Vgll4s transcription factors control the establishment of Left-Right asymmetry in zebrafish. eLife 8, e45241. doi:10.7554/eLife.45241 · DOI
- Fossdal, R., Jonasson, F., Kristjansdottir, G. T., Kong, A., Stefansson, H., Gosh, S., Gulcher, J. R. and Stefansson, K. (2004). A novel TEAD1 mutation is the causative allele in Sveinsson's chorioretinal atrophy (helicoid peripapillary chorioretinal degeneration). Hum. Mol. Genet. 13, 975-981. doi:10.1093/hmg/ ddh106 · DOI
- Frum, T., Watts, J. L. and Ralston, A. (2019). TEAD4, YAP1 and WWTR1 prevent the premature onset of pluripotency prior to the 16-cell stage. Development 146, dev179861. doi:10.1242/dev.179861 · DOI
- Ganesan, K., Kulandaisamy, A., Binny Priya, S. and Gromiha, M. M. (2019). HuVarBase: A human variant database with comprehensive information at gene and protein levels. PLoS ONE 14, e0210475. doi:10.1371/journal.pone.0210475 · DOI
- Garg, A., Srivastava, A., Davis, M. M., O'Keefe, S. L., Chow, L. and Bell, J. B. (2007). Antagonizing scalloped with a novel vestigial construct reveals an important role for scalloped in Drosophila melanogaster leg, eye and optic lobe development. Genetics 175, 659-669. doi:10.1534/genetics.106.063966 · DOI
- Gee, S. T., Milgram, S. L., Kramer, K. L., Conlon, F. L. and Moody, S. A. (2011). Yes-associated protein 65 (YAP) expands neural progenitors and regulates Pax3 expression in the neural plate border zone. PLoS ONE 6, e20309. doi:10.1371/ journal.pone.0020309 · DOI
- Gibault, F., Sturbaut, M., Bailly, F., Melnyk, P. and Cotelle, P. (2018). Targeting Transcriptional Enhanced Associate Domains (TEADs). J. Med. Chem. 61, 5057-5072. doi:10.1021/acs.jmedchem.7b00879 · DOI
- Gnedeva, K., Wang, X., McGovern, M. M., Barton, M., Tao, L., Trecek, T., Monroe, T. O., Llamas, J., Makmura, W., Martin, J. F. et al. (2020). Organ of Corti size is governed by Yap/Tead-mediated progenitor self-renewal. Proc. Natl. Acad. Sci. USA 117, 13552-13561. doi:10.1073/pnas.2000175117 · DOI
- Goodman, C. A., Dietz, J. M., Jacobs, B. L., McNally, R. M., You, J.-S. and Hornberger, T. A. (2015). Yes-associated protein is up-regulated by mechanical overload and is sufficient to induce skeletal muscle hypertrophy. FEBS Lett. 589, 1491-1497. doi:10.1016/j.febslet.2015.04.047 · DOI · Paper page
- Goulev, Y., Fauny, J. D., Gonzalez-Marti, B., Flagiello, D., Silber, J. and Zider, A. (2008). SCALLOPED Interacts with YORKIE, the nuclear effector of the hippo tumor-suppressor pathway in Drosophila. Curr. Biol. 18, 435-441. doi:10.1016/j. cub.2008.02.034 · DOI
- Guo, T., Lu, Y., Li, P., Yin, M.-X., Lv, D., Zhang, W., Wang, H., Zhou, Z., Ji, H., Zhao, Y. et al. (2013). A novel partner of Scalloped regulates Hippo signaling via antagonizing Scalloped-Yorkie activity. Cell Res. 23, 1201-1214. doi:10.1038/cr. 2013.120 · DOI
- Gupta, M. P., Kogut, P. and Gupta, M. (2000). Protein kinase-A dependent phosphorylation of transcription enhancer factor-1 represses its DNA-binding activity but enhances its gene activation ability. Nucleic Acids Res. 28, 3168-3177. doi:10.1093/nar/28.16.3168 · DOI
- Gupta, M., Kogut, P., Davis, F. J., Belaguli, N. S., Schwartz, R. J. and Gupta, M. P. (2001). Physical interaction between the MADS box of serum response factor and the TEA/ATTS DNA-binding domain of transcription enhancer factor. J. Biol. Chem. 276, 10413-10422. doi:10.1074/jbc. · DOI
- M008625200 · DOI
- Guss, K. A., Nelson, C. E., Hudson, A., Kraus, M. E. and Carroll, S. B. (2001). Control of a genetic regulatory network by a selector gene. Science 292, 1164-1167. doi:10.1126/science.1058312 · DOI
- Guss, K. A., Benson, M., Gubitosi, N., Brondell, K., Broadie, K. and Skeath, J. B. (2013). Expression and function of scalloped during Drosophila development. Dev. Dyn. 242, 874-885. doi:10.1002/dvdy.23942 · DOI
- Hagenbeek, T. J., Webster, J. D., Kljavin, N. M., Chang, M. T., Pham, T., Lee, H.-J., Klijn, C., Cai, A. G., Totpal, K., Ravishankar, B. et al. (2018). The Hippo pathway effector TAZ induces TEAD-dependent liver inflammation and tumors. Sci. Signal. 11, eaaj1757. doi:10.1126/scisignal. · DOI
- aaj1757 · DOI
- Halder, G. and Carroll, S. B. (2001). Binding of the Vestigial co-factor switches the DNA-target selectivity of the Scalloped selector protein. Development 128, 3295-3305. doi:10.1242/dev.128.17.3295 · DOI
- Halder, G., Polaczyk, P., Kraus, M. E., Hudson, A., Kim, J., Laughon, A. and Carroll, S. (1998). The Vestigial and Scalloped proteins act together to directly regulate wing-specific gene expression in Drosophila. Genes Dev. 12, 3900-3909. doi:10.1101/gad.12.24.3900 · DOI
- Hamon, A., Masson, C., Bitard, J., Gieser, L., Roger, J. E. and Perron, M. (2017). Retinal degeneration triggers the activation of YAP/TEAD in reactive müller cells. Invest. Opthalmol. Vis. Sci. 58, 1941. doi:10.1167/iovs.16-21366 · DOI
- Han, D., Byun, S.-H., Park, S., Kim, J., Kim, I., Ha, S., Kwon, M. and Yoon, K. (2015). YAP/TAZ enhance mammalian embryonic neural stem cell characteristics in a Tead-dependent manner. Biochem. Biophys. Res. Commun. 458, 110-116. doi:10.1016/j.bbrc.2015.01.077 · DOI
- Hashimoto, M. and Sasaki, H. (2019). Epiblast formation by TEAD-YAP- dependent expression of pluripotency factors and competitive elimination of unspecified cells. Dev. Cell 50, 139-154.e5. doi:10.1016/j.devcel.2019.05.024 · DOI
- Hillmer, R. E. and Link, B. A. (2019). The roles of hippo signaling transducers Yap and Taz in chromatin remodeling. Cells 8, 502. doi:10.3390/cells8050502 · DOI
- Holden, J. K. and Cunningham, C. N. (2018). Targeting the hippo pathway and cancer through the TEAD family of transcription factors. Cancers 10, 81. doi:10. 3390/cancers10030081 · DOI
- Holden, J. K., Crawford, J. J., Noland, C. L., Schmidt, S., Zbieg, J. R., Lacap, J. A., Zang, R., Miller, G. M., Zhang, Y., Beroza, P. et al. (2020). Small molecule Dysregulation of TEAD lipidation induces a dominant-negative inhibition of hippo pathway signaling. Cell Rep. 31, 107809. doi:10.1016/j.celrep.2020. 107809 · DOI
- Honda, M., Tsuchimochi, H., Hitachi, K. and Ohno, S. (2019). Transcriptional cofactor Vgll2 is required for functional adaptations of skeletal muscle induced by chronic overload. J. Cell. Physiol. 234, 15809-15824. doi:10.1002/jcp.28239 · DOI
- Hong, L., Li, X., Zhou, D., Geng, J. and Chen, L. (2018). Role of Hippo signaling in regulating immunity. Cell. Mol. Immunol. 15, 1003-1009. doi:10.1038/s41423- 018-0007-1 · DOI
- Huang, J., Wu, S., Barrera, J., Matthews, K. and Pan, D. (2005). The hippo signaling pathway coordinately regulates cell proliferation and apoptosis by inactivating yorkie, the Drosophila homolog of YAP. Cell 122, 421-434. doi:10. 1016/j.cell.2005.06.007 · DOI
- Imajo, M., Ebisuya, M. and Nishida, E. (2015). Dual role of YAP and TAZ in renewal of the intestinal epithelium. Nat. Cell Biol. 17, 7-19. doi:10.1038/ncb3084 · DOI
- Inamdar, M., Vijayraghavan, K. and Rodrigues, V. (1993). The Drosophila homolog of the human transcription factor TEF-1, Scalloped, is essential for normal taste behavior. J. Neurogenet. 9, 123-139. doi:10.3109/ 01677069309083454 · DOI
- Jacquemin, P. and Davidson, I. (1997). The role of the TEF transcription factors in cardiogenesis and other developmental processes. Trends Cardiovasc. Med. 7, 192-197. doi:10.1016/S1050-1738(97)00052-2 · DOI
- Jacquemin, P., Sapin, V., Alsat, E., Evain-Brion, D., Dolle, P. and Davidson, I. (1998). Differential expression of the TEF family of transcription factors in the murine placenta and during differentiation of primary human trophoblasts in vitro. Dev. Dyn. 212, 423-436. doi:10.1002/(SICI)1097-0177(199807)212:3<423::AID- AJA10>3.0.CO;2-1 · DOI · Paper page
- Jiang, S.-W., Dong, M., Trujillo, M. A., Miller, L. J. and Eberhardt, N. L. (2001). DNA binding of TEA/ATTS domain factors is regulated by protein Kinase C Phosphorylation in human choriocarcinoma cells. J. Biol. Chem. 276, 23464-23470. doi:10.1074/jbc. · DOI
- M010934200 · DOI
- Jiang, Q., Liu, D., Gong, Y., Wang, Y., Sun, S., Gui, Y. and Song, H. (2009). yap is required for the development of brain, eyes, and neural crest in zebrafish. Biochem. Biophys. Res. Commun. 384, 114-119. doi:10.1016/j.bbrc.2009.04.070 · DOI
- Johnson, C. W., Hernandez-Lagunas, L., Feng, W., Melvin, V. S., Williams, T. and Artinger, K. B. (2011). Vgll2a is required for neural crest cell survival during zebrafish craniofacial development. Dev. Biol. 357, 269-281. doi:10.1016/j.ydbio. 2011.06.034 · DOI
- Jonasson, F., Hardarson, S., Olafsson, B. M. and Klintworth, G. K. (2007). Sveinsson Chorioretinal Atrophy/Helicoid Peripapillary Chorioretinal degeneration: first histopathology report. Ophthalmology 114, 1541-1546. doi:10.1016/j.ophtha.2006.11.016 · DOI
- Kaan, H. Y. K., Sim, A. Y. L., Tan, S. K. J., Verma, C. and Song, H. (2017). Targeting YAP/TAZ-TEAD protein-protein interactions using fragment-based and computational modeling approaches. PLoS ONE 12, e0178381. doi:10.1371/ journal.pone.0178381 · DOI
- Kanai, F., Marignani, P. A., Sarbassova, D., Yagi, R., Hall, R. A., Donowitz, M., Hisaminato, A., Fujiwara, T., Ito, Y., Cantley, L. C. et al. (2000). TAZ: a novel transcriptional co-activator regulated by interactions with 14-3-3 and PDZ domain proteins. EMBO J. 19, 6778-6791. doi:10.1093/emboj/19.24.6778 · DOI
- Kaneko, K. J., Kohn, M. J., Liu, C. and DePamphilis, M. L. (2007). Transcription factor TEAD2 is involved in neural tube closure. Genesis 45, 577-587. doi:10. 1002/dvg.20330 · DOI
- Karczewski, K. J., Francioli, L. C., Tiao, G., Cummings, B. B., Alföldi, J., Wang, Q., Collins, R. L., Laricchia, K. M., Ganna, A., Birnbaum, D. P. et al. (2020). The mutational constraint spectrum quantified from variation in 141,456 humans. Nature 581, 434-443. doi:10.1038/s41586-020-2308-7 · DOI · Paper page
- Kim, N.-G. and Gumbiner, B. M. (2019). Cell contact and Nf2/Merlin-dependent regulation of TEAD palmitoylation and activity. Proc. Natl Acad. Sci. USA 116, 9877-9882. doi:10.1073/pnas.1819400116 · DOI
- Kim, J., Sebring, A., Esch, J. J., Kraus, M. E., Vorwerk, K., Magee, J. and Carroll, S. B. (1996). Integration of positional signals and regulation of wing formation and identity by Drosophila vestigial gene. Nature 382, 133-138. doi:10. 1038/382133a0 · DOI
- Kim, M., Kim, T., Johnson, R. L. and Lim, D.-S. (2015). Transcriptional co- repressor function of the hippo pathway transducers YAP and TAZ. Cell Reports 11, 270-282. doi:10.1016/j.celrep.2015.03.015 · DOI
- Kim, M.-K., Jang, J.-W. and Bae, S.-C. (2018). DNA binding partners of YAP/TAZ. BMB Rep. 51, 126-133. doi:10.5483/BMBRep.2018.51.3.015 · DOI
- Kimura, M., Horie, T., Baba, O., Ide, Y., Tsuji, S., Ruiz Rodriguez, R., Watanabe, T., Yamasaki, T., Otani, C., Xu, S. et al. (2020). Homeobox A4 suppresses vascular remodeling by repressing YAP/TEAD transcriptional activity. EMBO Rep. 21, e48389. doi:10.15252/embr.201948389 · DOI
- Kitagawa, M. (2007). A Sveinsson's chorioretinal atrophy-associated missense mutation in mouse Tead1 affects its interaction with the co-factors YAP and TAZ. Biochem. Biophys. Res. Commun. 361, 1022-1026. doi:10.1016/j.bbrc.2007.07. 129 · DOI
- Koontz, L. M., Liu-Chittenden, Y., Yin, F., Zheng, Y., Yu, J., Huang, B., Chen, Q., Wu, S. and Pan, D. (2013). The Hippo effector Yorkie controls normal tissue growth by antagonizing scalloped-mediated default repression. Dev. Cell 25, 388-401. doi:10.1016/j.devcel.2013.04.021 · DOI
- Landin-Malt, A., Benhaddou, A., Zider, A. and Flagiello, D. (2016). An evolutionary, structural and functional overview of the mammalian TEAD1 and TEAD2 transcription factors. Gene 591, 292-303. doi:10.1016/j.gene.2016.07. 028 · DOI
- Legent, K., Dutriaux, A., Delanoue, R. and Silber, J. (2006). Cell cycle genes regulate vestigial and scalloped to ensure normal proliferation in the wing disc of Drosophila melanogaster. Genes Cells 11, 907-918. doi:10.1111/j.1365-2443. 2006.00993.x · DOI
- Li, Q., Han, G., Liu, D. and Zhou, Y. (2019). Force-induced decline of TEA domain family member 1 contributes to osteoclastogenesis via regulation of Osteoprotegerin. Arch. Oral Biol. 100, 23-32. doi:10.1016/j.archoralbio.2019.01. 020 · DOI
- Lian, I., Kim, J., Okazawa, H., Zhao, J., Zhao, B., Yu, J., Chinnaiyan, A., Israel, M. A., Goldstein, L. S. B., Abujarour, R. et al. (2010). The role of YAP transcription coactivator in regulating stem cell self-renewal and differentiation. Genes Dev. 24, 1106-1118. doi:10.1101/gad.1903310 · DOI
- Lin, Z., Guo, H., Cao, Y., Zohrabian, S., Zhou, P., Ma, Q., VanDusen, N., Guo, Y., Zhang, J., Stevens, S. M. et al. (2016). Acetylation of VGLL4 regulates Hippo- YAP signaling and postnatal cardiac growth. Dev. Cell 39, 466-479. doi:10.1016/j. devcel.2016.09.005 · DOI
- Lin, K. C., Moroishi, T., Meng, Z., Jeong, H.-S., Plouffe, S. W., Sekido, Y., Han, J., Park, H. W. and Guan, K.-L. (2017). Regulation of Hippo pathway transcription factor TEAD by p38 MAPK-induced cytoplasmic translocation. Nat. Cell Biol. 19, 996-1002. doi:10.1038/ncb3581 · DOI
- Liu, X., Grammont, M. and Irvine, K. D. (2000). Roles for scalloped and vestigial in regulating cell affinity and interactions between the wing blade and the wing hinge. Dev. Biol. 228, 287-303. doi:10.1006/dbio.2000.9939 · DOI
- Liu, C.-Y., Zha, Z.-Y., Zhou, X., Zhang, H., Huang, W., Zhao, D., Li, T., Chan, S. W., Lim, C. J., Hong, W. et al. (2010). The hippo tumor pathway promotes TAZ degradation by Phosphorylating a Phosphodegron and recruiting the SCFβ-TrCP E3 Ligase. J. Biol. Chem. 285, 37159-37169. doi:10.1074/jbc.M110.152942 · DOI · Paper page
- Liu, F., Wang, X., Hu, G., Wang, Y. and Zhou, J. (2014). The transcription factor TEAD1 represses smooth muscle-specific gene expression by abolishing myocardin function. J. Biol. Chem. 289, 3308-3316. doi:10.1074/jbc.M113. 515817 · DOI
- Liu, X., Li, H., Rajurkar, M., Li, Q., Cotton, J. L., Ou, J., Zhu, L. J., Goel, H. L., Mercurio, A. M., Park, J.-S. et al. (2016). Tead and AP1 coordinate transcription and motility. Cell Rep. 14, 1169-1180. doi:10.1016/j.celrep.2015.12.104 · DOI
- Liu, R., Lee, J., Kim, B. S., Wang, Q., Buxton, S. K., Balasubramanyam, N., Kim, J. J., Dong, J., Zhang, A., Li, S. et al. (2017). Tead1 is required for maintaining adult cardiomyocyte function, and its loss results in lethal dilated cardiomyopathy. JCI Insight 2, e93343. doi:10.1172/jci.insight.93343 · DOI
- Liu, X., Kong, C. and Zhang, Z. (2018). miR-130b promotes bladder cancer cell proliferation, migration and invasion by targeting VGLL4. Oncol. Rep. 39, 2324-2332. doi:10.3892/or.2018.6300 · DOI
- Liu, R., Jagannathan, R., Li, F., Lee, J., Balasubramanyam, N., Kim, B. S., Yang, P., Yechoor, V. K. and Moulik, M. (2019). Tead1 is required for perinatal cardiomyocyte proliferation. PLoS ONE 14, e0212017. doi:10.1371/journal.pone. 0212017 · DOI
- Liu-Chittenden, Y., Huang, B., Shim, J. S., Chen, Q., Lee, S.-J., Anders, R. A., Liu, J. O. and Pan, D. (2012). Genetic and pharmacological disruption of the TEAD-YAP complex suppresses the oncogenic activity of YAP. Genes Dev. 26, 1300-1305. doi:10.1101/gad.192856.112 · DOI · Paper page
- Lopez-Anido, C., Poitelon, Y., Gopinath, C., Moran, J. J., Ma, K. H., Law, W. D., Antonellis, A., Feltri, M. L. and Svaren, J. (2016). Tead1 regulates the expression of Peripheral Myelin Protein 22 during Schwann cell development. Hum. Mol. Genet. 25, 3055-3069. doi:10.1093/hmg/ddw158 · DOI
- Lunde, K., Trimble, J. L., Guichard, A., Guss, K. A., Nauber, U. and Bier, E. (2003). Activation of the knirps locus links patterning to morphogenesis of the second wing vein in Drosophila. Development 130, 235-248. doi:10.1242/dev. 00207 · DOI
- Ma, S., Meng, Z., Chen, R. and Guan, K.-L. (2019). The Hippo pathway: biology and pathophysiology. Annu. Rev. Biochem. 88, 577-604. doi:10.1146/annurev- biochem-013118-111829 · DOI · Paper page
- Maeda, T., Chapman, D. L. and Stewart, A. F. R. (2002a). Mammalian Vestigial-like 2, a Cofactor of TEF-1 and MEF2 transcription factors that promotes skeletal muscle differentiation. J. Biol. Chem. 277, 48889-48898. doi:10.1074/jbc. · DOI
- M206858200 · DOI
- Maeda, T., Gupta, M. P. and Stewart, A. F. R. (2002b). TEF-1 and MEF2 transcription factors interact to regulate muscle-specific promoters. Biochem. Biophys. Res. Commun. 294, 791-797. doi:10.1016/S0006-291X(02)00556-9 · DOI
- Mammoto, T., Muyleart, M. and Mammoto, A. (2019). Endothelial YAP1 in regenerative lung growth through the Angiopoietin-Tie2 pathway. Am. J. Respir. Cell Mol. Biol. 60, 117-127. doi:10.1165/rcmb.2018-0105OC · DOI
- Mann, R. S. and Carroll, S. B. (2002). Molecular mechanisms of selector gene function and evolution. Curr. Opin. Genet. Dev. 12, 592-600. doi:10.1016/S0959- 437X(02)00344-1 · DOI
- Manning, S. A., Kroeger, B. and Harvey, K. F. (2020). The regulation of Yorkie, YAP and TAZ: new insights into the hippo pathway. Development 147, dev179069. doi:10.1242/dev.179069 · DOI
- Marks, M., Pennimpede, T., Lange, L., Grote, P., Herrmann, B. G. and Wittler, L. (2016). Analysis of the Fam181 gene family during mouse development reveals distinct strain-specific expression patterns, suggesting a role in nervous system development and function. Gene 575, 438-451. doi:10.1016/j.gene.2015.09.035 · DOI
- Miesfeld, J. B., Gestri, G., Clark, B. S., Flinn, M. A., Poole, R. J., Bader, J. R., Besharse, J. C., Wilson, S. W. and Link, B. A. (2015). Yap and Taz regulate retinal pigment epithelial cell fate. Development 142, 3021-3032. doi:10.1242/ dev.119008 · DOI · Paper page
- Mueller, K. A., Glajch, K. E., Huizenga, M. N., Wilson, R. A., Granucci, E. J., Dios, A. M., Tousley, A. R., Iuliano, M., Weisman, E., LaQuaglia, M. J. et al. (2018). Hippo signaling pathway dysregulation in human Huntington's disease brain and neuronal stem cells. Sci. Rep. 8, 11355. doi:10.1038/s41598-018-29319-4 · DOI
- Mukhtar, T., Breda, J., Grison, A., Karimaddini, Z., Grobecker, P., Iber, D., Beisel, C., van Nimwegen, E. and Taylor, V. (2020). Tead transcription factors differentially regulate cortical development. Sci. Rep. 10, 4625. doi:10.1038/ s41598-020-61490-5 · DOI
- Nakajima, H., Yamamoto, K., Agarwala, S., Terai, K., Fukui, H., Fukuhara, S., Ando, K., Miyazaki, T., Yokota, Y., Schmelzer, E. et al. (2017). Flow-dependent endothelial YAP regulation contributes to vessel maintenance. Dev. Cell 40, 523-536.e6. doi:10.1016/j.devcel.2017.02.019 · DOI
- Nishioka, N., Inoue, K.-i., Adachi, K., Kiyonari, H., Ota, M., Ralston, A., Yabuta, N., Hirahara, S., Stephenson, R. O., Ogonuki, N. et al. (2009). The hippo signaling pathway components lats and Yap pattern Tead4 activity to distinguish mouse trophectoderm from inner cell mass. Dev. Cell 16, 398-410. doi:10.1016/j. devcel.2009.02.003 · DOI
- Noland, C. L., Gierke, S., Schnier, P. D., Murray, J., Sandoval, W. N., Sagolla, M., Dey, A., Hannoush, R. N., Fairbrother, W. J. and Cunningham, C. N. (2016). Palmitoylation of TEAD transcription factors is required for their stability and function in hippo pathway signaling. Structure 24, 179-186. doi:10.1016/j.str.2015. 11.005 · DOI
- Osman, I., He, X., Liu, J., Dong, K., Wen, T., Zhang, F., Yu, L., Hu, G., Xin, H., Zhang, W. et al. (2019). TEAD1 (TEA Domain Transcription Factor 1) promotes smooth muscle cell proliferation through upregulating SLC1A5 (solute carrier family 1 member 5)-mediated glutamine uptake. Circ. Res. 124, 1309-1322. doi:10.1161/CIRCRESAHA.118.314187 · DOI
- Panciera, T., Azzolin, L., Fujimura, A., Di Biagio, D., Frasson, C., Bresolin, S., Soligo, S., Basso, G., Bicciato, S., Rosato, A. et al. (2016). Induction of expandable tissue-specific stem/progenitor cells through transient expression of YAP/TAZ. Cell Stem Cell 19, 725-737. doi:10.1016/j.stem.2016.08.009 · DOI
- Panciera, T., Azzolin, L., Cordenonsi, M. and Piccolo, S. (2017). Mechanobiology of YAP and TAZ in physiology and disease. Nat. Rev. Mol. Cell Biol. 18, 758-770. doi:10.1038/nrm.2017. · DOI · Paper page
- Paumard-Rigal, S., Zider, A., Vaudin, P. and Silber, J. (1998). Specific interactions between vestigial and scalloped are required to promote wing tissue proliferation in Drosophila melanogaster. Dev. Genes Evol. 208, 440-446. doi:10.1007/s004270050201 · DOI
- Plouffe, S. W., Lin, K. C., Moore, J. L., Tan, F. E., Ma, S., Ye, Z., Qiu, Y., Ren, B. and Guan, K.-L. (2018). The hippo pathway effector proteins YAP and TAZ have both distinct and overlapping functions in the cell. J. Biol. Chem. 293, 11230-11240. doi:10.1074/jbc.RA118.002715 · DOI
- Pobbati, A. V. and Hong, W. (2013). Emerging roles of TEAD transcription factors and its coactivators in cancers. Cancer Biol. Ther. 14, 390-398. doi:10.4161/cbt. 23788 · DOI
- Qin, H., Blaschke, K., Wei, G., Ohi, Y., Blouin, L., Qi, Z., Yu, J., Yeh, R.-F., Hebrok, M. and Ramalho-Santos, M. (2012). Transcriptional analysis of pluripotency reveals the Hippo pathway as a barrier to reprogramming. Hum. Mol. Genet. 21, 2054-2067. doi:10.1093/hmg/dds023 · DOI
- Ralston, A., Cox, B. J., Nishioka, N., Sasaki, H., Chea, E., Rugg-Gunn, P., Guo, G., Robson, P., Draper, J. S. and Rossant, J. (2010). Gata3 regulates trophoblast development downstream of Tead4 and in parallel to Cdx2. Development 137, 395-403. doi:10.1242/dev.038828 · DOI
- Ribas, R., Moncaut, N., Siligan, C., Taylor, K., Cross, J. W., Rigby, P. W. J. and Carvajal, J. J. (2011). 'Members of the TEAD family of transcription factors regulate the expression of Myf5 in ventral somitic compartments', Dev. Biol. 355, 372-380. doi:10.1016/j.ydbio.2011.04.005 · DOI
- Rohith, B. N. and Shyamala, B. V. (2017). Scalloped a member of the Hippo tumor suppressor pathway controls mushroom body size in Drosophila brain by non- canonical regulation of neuroblast proliferation. Dev. Biol. 432, 203-214. doi:10. 1016/j.ydbio.2017.10.016 · DOI
- Saha, B., Ganguly, A., Home, P., Bhattacharya, B., Ray, S., Ghosh, A., Rumi, M. A. K., Marsh, C., French, V. A., Gunewardena, S. et al. (2020). TEAD4 ensures postimplantation development by promoting trophoblast self-renewal: an implication in early human pregnancy loss. Proc. Natl Acad. Sci. USA 117, 17864. doi:10.1073/pnas.2002449117 · DOI
- Saito, K., Kawasoe, R., Sasaki, H., Kawaguchi, A. and Miyata, T. (2018). Neural progenitor cells undergoing Yap/tead-mediated enhanced self-renewal form heterotopias more easily in the diencephalon than in the telencephalon. Neurochem. Res. 43, 180-189. doi:10.1007/s11064-017-2390-x · DOI
- Salah, Z., Alian, A. and Aqeilan, R. I. (2012). WW domain-containing proteins: retrospectives and the future. Front. Biosci. 17, 331-348. doi:10.2741/3930 · DOI
- Sawada, A., Kiyonari, H., Ukita, K., Nishioka, N., Imuta, Y. and Sasaki, H. (2008). Redundant roles of Tead1 and Tead2 in notochord development and the regulation of cell proliferation and survival. Mol. Cell. Biol. 28, 3177-3189. doi:10. 1128/MCB.01759-07 · DOI
- Schlegelmilch, K., Mohseni, M., Kirak, O., Pruszak, J., Rodriguez, J. R., Zhou, D., Kreger, B. T., Vasioukhin, V., Avruch, J., Brummelkamp, T. R. et al. (2011). Yap1 acts downstream of α-catenin to control epidermal proliferation. Cell 144, 782-795. doi:10.1016/j.cell.2011.02.031 · DOI · Paper page
- Schrauwen, I., Szelinger, S., Siniard, A. L., Corneveaux, J. J., Kurdoglu, A., Richholt, R., De Both, M., Malenica, I., Swaminathan, S., Rangasamy, S. et al. (2015). A de novo mutation in TEAD1 causes non-X-linked Aicardi syndrome. Invest. Ophthalmol. Vis. Sci. 56, 3896-3904. doi:10.1167/iovs.14-16261 · DOI
- Simmonds, A. J., Liu, X., Soanes, K. H., Krause, H. M., Irvine, K. D. and Bell, J. B. (1998). Molecular interactions between vestigial and scalloped promote wing formation in Drosophila. Genes Dev. 12, 3815-3820. doi:10.1101/gad.12.24.3815 · DOI
- Simon, E., Faucheux, C., Zider, A., Theźe, N. and Thiebaud, P. (2016). From vestigial to vestigial-like: the Drosophila gene that has taken wing. Dev. Genes Evol. 226, 297-315. doi:10.1007/s00427-016-0546-3 · DOI
- Simon, E., Theźe, N., Fedou, S., Thiebaud, P. and Faucheux, C. (2017). Vestigial- like 3 is a novel Ets1 interacting partner and regulates trigeminal nerve formation and cranial neural crest migration. Biology Open 6, 1528-1540. doi:10.1242/bio. 026153 · DOI
- Su, T., Bondar, T., Zhou, X., Zhang, C., He, H. and Medzhitov, R. (2015). Two- signal requirement for growth-promoting function of Yap in hepatocytes. eLife 4, e02948. doi:10.7554/eLife.02948 · DOI · Paper page
- Sun, C., De Mello, V., Mohamed, A., Ortuste Quiroga, H. P., Garcia-Munoz, A., Al Bloshi, A., Tremblay, A. M., von Kriegsheim, A., Collie-Duguid, E., Vargesson, N. et al. (2017). Common and distinctive functions of the hippo effectors Taz and Yap in skeletal muscle stem cell function. Stem Cells 35, 1958-1972. doi:10.1002/stem.2652 · DOI
- Suo, J., Feng, X., Li, J., Wang, J., Wang, Z., Zhang, L. and Zou, W. (2020). VGLL4 promotes osteoblast differentiation by antagonizing TEADs-inhibited Runx2 transcription. Sci. Adv. 6, eaba4147. doi:10.1126/sciadv.aba4147 · DOI
- Tamm, C., Bo ̈wer, N. and Annereń, C. (2011). Regulation of mouse embryonic stem cell self-renewal by a Yes-YAP-TEAD2 signaling pathway downstream of LIF. J. Cell Sci. 124, 1136-1144. doi:10.1242/jcs.075796 · DOI
- Tremblay, A. M., Missiaglia, E., Galli, G. G., Hettmer, S., Urcia, R., Carrara, M., Judson, R. N., Thway, K., Nadal, G., Selfe, J. L. et al. (2014). The hippo transducer YAP1 transforms activated satellite cells and is a potent effector of embryonal rhabdomyosarcoma formation. Cancer Cell 26, 273-287. doi:10.1016/ j.ccr.2014.05.029 · DOI · Paper page
- Tsika, R. W., Schramm, C., Simmer, G., Fitzsimons, D. P., Moss, R. L. and Ji, J. (2008). Overexpression of TEAD-1 in transgenic mouse striated muscles produces a slower skeletal muscle contractile phenotype. J. Biol. Chem. 283, 36154-36167. doi:10.1074/jbc.M807461200 · DOI · Paper page
- Tsika, R. W., Ma, L., Kehat, I., Schramm, C., Simmer, G., Morgan, B., Fine, D. M., Hanft, L. M., McDonald, K. S., Molkentin, J. D. et al. (2010). TEAD-1 overexpression in the mouse heart promotes an age-dependent heart dysfunction. J. Biol. Chem. 285, 13721-13735. doi:10.1074/jbc.M109.063057 · DOI
- Vissers, J. H. A., Froldi, F., Schro ̈der, J., Papenfuss, A. T., Cheng, L. Y. and Harvey, K. F. (2018). The scalloped and Nerfin-1 transcription factors cooperate to maintain neuronal cell fate. Cell Reports 25, 1561-1576.e7. doi:10.1016/j. celrep.2018.10.038 · DOI
- Voltes, A., Hevia, C. F., Engel-Pizcueta, C., Dingare, C., Calzolari, S., Terriente, J., Norden, C., Lecaudey, V. and Pujades, C. (2019). Yap/Taz-TEAD activity links mechanical cues to progenitor cell behavior during zebrafish hindbrain segmentation. Development 146, dev176735. doi:10.1242/dev.176735 · DOI
- Wang, L., Xia, J., Li, J., Hagemann, T. L., Jones, J. R., Fraenkel, E., Weitz, D. A., Zhang, S.-C., Messing, A. and Feany, M. B. (2018). Tissue and cellular rigidity and mechanosensitive signaling activation in Alexander disease. Nat. Commun. 9:, 1899. doi:10.1038/s41467-018-04269-7 · DOI
- Wen, T., Yin, Q., Yu, L., Hu, G., Liu, J., Zhang, W., Huang, L., Su, H., Wang, M. and Zhou, J. (2017). Characterization of mice carrying a conditional TEAD1 allele. Genesis 55, e23085. doi:10.1002/dvg.23085 · DOI
- Wen, T., Liu, J., He, X., Dong, K., Hu, G., Yu, L., Yin, Q., Osman, I., Peng, J., Zheng, Z. et al. (2019). Transcription factor TEAD1 is essential for vascular development by promoting vascular smooth muscle differentiation. Cell Death Differ. 26, 2790-2806. doi:10.1038/s41418-019-0335-4 · DOI
- Williams, J. A., Bell, J. B. and Carroll, S. B. (1991). Control of Drosophila wing and haltere development by the nuclear vestigial gene product. Genes Dev. 5, 2481-2495. doi:10.1101/gad.5.12b.2481 · DOI
- Williamson, K. A., Rainger, J., Floyd, J. A. B., Ansari, M., Meynert, A., Aldridge, K. V., Rainger, J. K., Anderson, C. A., Moore, A. T., Hurles, M. E. et al. (2014). Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects. Am. J. Hum. Genet. 94, 295-302. doi:10.1016/j.ajhg.2014.01.001 · DOI
- Wong, B. K. Y., Sutton, V. R., Lewis, R. A. and Van den Veyver, I. B. (2017). Independent variant analysis of TEAD1 and OCEL1 in 38 Aicardi syndrome patients. Mol. Genet. Genomic Med. 5, 117-121. doi:10.1002/mgg3.250 · DOI
- Xu, J., Wu, R.-C. and O'Malley, B. W. (2009). Normal and cancer-related functions of the p160 steroid receptor co-activator (SRC) family. Nat. Rev. Cancer 9, 615-630. doi:10.1038/nrc2695 · DOI
- Yagi, R., Kohn, M. J., Karavanova, I., Kaneko, K. J., Vullhorst, D., DePamphilis, M. L. and Buonanno, A. (2007). Transcription factor TEAD4 specifies the trophectoderm lineage at the beginning of mammalian development. Development 134, 3827-3836. doi:10.1242/dev.010223 · DOI
- Yamaguchi, N. (2020). Multiple roles of vestigial-like family members in tumor development. Front. Oncol. 10, 1266. doi:10.3389/fonc.2020.01266 · DOI
- Yasunami, M., Suzuki, K. and Ohkubo, H. (1996). A novel family of TEA domain- containing transcription factors with distinct spatiotemporal expression patterns. Biochem. Biophys. Res. Commun. 228, 365-370. doi:10.1006/bbrc.1996.1667 · DOI
- Yuan, Y., Park, J., Feng, A., Awasthi, P., Wang, Z., Chen, Q. and Iglesias- Bartolome, R. (2020). YAP1/TAZ-TEAD transcriptional networks maintain skin homeostasis by regulating cell proliferation and limiting KLF4 activity. Nat. Commun. 11, 1472. doi:10.1038/s41467-020-15301-0 · DOI · Paper page
- Zanconato, F., Forcato, M., Battilana, G., Azzolin, L., Quaranta, E., Bodega, B., Rosato, A., Bicciato, S., Cordenonsi, M. and Piccolo, S. (2015). Genome-wide association between YAP/TAZ/TEAD and AP-1 at enhancers drives oncogenic growth. Nat. Cell Biol. 17, 1218-1227. doi:10.1038/ncb3216 · DOI · Paper page
- Zeng, Y., Stauffer, S., Zhou, J., Chen, X., Chen, Y. and Dong, J. (2017). Cyclin- dependent kinase 1 (CDK1)-mediated mitotic phosphorylation of the transcriptional co-repressor Vgll4 inhibits its tumor-suppressing activity. J. Biol. Chem. 292, 15028-15038. doi:10.1074/jbc.M117.796284 · DOI
- Zhang, L., Ren, F., Zhang, Q., Chen, Y., Wang, B. and Jiang, J. (2008). The TEAD/ TEF family of transcription factor Scalloped mediates hippo signaling in organ size control. Dev. Cell 14, 377-387. doi:10.1016/j.devcel.2008.01.006 · DOI · Paper page
- Zhang, H., Pasolli, H. and Fuchs, E. (2011). Yes-associated protein (YAP) transcriptional coactivator functions in balancing growth and differentiation in skin. Proc. Natl. Acad. Sci. USA 108, 2270-2275. doi:10.1073/pnas.1019603108 · DOI · Paper page
- Zhang, W., Gao, Y., Li, P., Shi, Z., Guo, T., Li, F., Han, X., Feng, Y., Zheng, C., Wang, Z. et al. (2014). VGLL4 functions as a new tumor suppressor in lung cancer by negatively regulating the YAP-TEAD transcriptional complex. Cell Res. 24, 331-343. doi:10.1038/cr.2014. · DOI
- Zhang, W., Xu, J., Li, J., Guo, T., Jiang, D., Feng, X., Ma, X., He, L., Wu, W., Yin, M. et al. (2018). The TEA domain family transcription factor TEAD4 represses murine adipogenesis by recruiting the cofactors VGLL4 and CtBP2 into a transcriptional complex. J. Biol. Chem. 293, 17119-17134. doi:10.1074/jbc.RA118.003608 · DOI
- Zhang, C., Wang, F., Gao, Z., Zhang, P., Gao, J. and Wu, X. (2020). Regulation of hippo signaling by mechanical signals and the cytoskeleton. DNA Cell Biol. 39, 159-166. doi:10.1089/dna.2019.5087 · DOI
- Zhao, B., Li, L., Tumaneng, K., Wang, C.-Y. and Guan, K.-L. (2010). A coordinated phosphorylation by Lats and CK1 regulates YAP stability through SCF β -TRCP. Genes Dev. 24, 72-85. doi:10.1101/gad.1843810 · DOI · Paper page
- Zhao, Y., Fei, X., Guo, J., Zou, G., Pan, W., Zhang, J., Huang, Y., Liu, T. and Cheng, W. (2017). Induction of reprogramming of human amniotic epithelial cells into iPS cells by overexpression of Yap, Oct4, and Sox2 through the activation of the hippo-Yap pathway. Exp. Ther. Med. 14, 199-206. doi:10.3892/etm.2017. 4512 · DOI
- Zhou, Z., Hu, T., Xu, Z., Lin, Z., Zhang, Z., Feng, T., Zhu, L., Rong, Y., Shen, H., Luk, J. M. et al. (2015). Targeting Hippo pathway by specific interruption of YAP- TEAD interaction using cyclic YAP-like peptides. FASEB J. 29, 724-732. doi:10. 1096/fj.14-262980 · DOI
- Zhu, C., Li, L., Zhang, Z., Bi, M., Wang, H., Su, W., Hernandez, K., Liu, P., Chen, J., Chen, M. et al. (2019). A non-canonical role of YAP/TEAD is required for activation of estrogen-regulated enhancers in breast cancer. Mol. Cell 75, 791-806.e8. doi:10.1016/j.molcel.2019.06.010 · DOI
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Therapeutic targeting of TEAD transcription factors in cancer
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- Authors
- Currey, L., Thor, S., & Piper, M.
- Affiliations
- The University of Queensland (AU)
- Venue
- Development
- Publisher
- The Company of Biologists
- Published
- 2021-06-15
- Volume
- 148
- Issue
- 12
- ISSN
- 0950-1991 (ISSN-L)
- 1477-9129
- OpenAlex
- W3167338135
- Cited by
- 120
- References
- 7
- Citations by year
- 2026: 24 · 2025: 33 · 2024: 33 · 2023: 18 · 2022: 9 · 2021: 3
- FWCI
- 2.18
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Development (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Australian Research Council (DP180100017)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Hippo pathway signaling and YAP/TAZ
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Congenital heart defects research
- Keywords
- TEAD transcription factors, Hippo signaling pathway, YAP, TAZ, stem cell potency, lineage specification, progenitor self-renewal, organ size control, transcriptional cofactors, developmental homeostasis, disease
- MeSH terms
- Animals, Cell Differentiation, Disease Susceptibility, DNA-Binding Proteins, Multigene Family, Homeostasis, Humans, Organ Specificity, Regeneration, Species Specificity, Stem Cells, Transcription Factors, Vertebrates, Biomarkers, Trans-Activators, Gene Expression Regulation, Developmental, Embryonic Development, Molecular Targeted Therapy
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