Cited by 235RNA Research and SplicingReproductive Biology and FertilityRNA and protein synthesis mechanisms

The DOI matches its Crossref record; 55 of the 58 references it cites were found in a registry or an index.

Translational control by cytoplasmic polyadenylation of c‐mos mRNA is necessary for oocyte maturation in the mouse.

Open access

Gebauer, F., Xu, W., Cooper, G.M., Richter, J.D.·1994·The EMBO Journal

DOI 10.1002/j.1460-2075.1994.tb06909.xPMC PMC395537

Open this paper in CoChat — free account Open PDF

Abstract

The c-mos proto-oncogene product is a key element in the cascade of events leading to meiotic maturation of vertebrate oocytes. We have investigated the role of cytoplasmic polyadenylation in the translational control of mouse c-mos mRNA and its contribution to meiosis. Using an RNase protection assay we show that optimal cytoplasmic polyadenylation of c-mos mRNA requires three cis elements in the 3' UTR: the polyadenylation hexanucleotide AAUAAA and two U-rich cytoplasmic polyadenylation elements (CPEs) located 4 and 51 nucleotides upstream of the hexanucleotide. When fused to CAT coding sequences, the wild-type 3' UTR of c-mos mRNA, but not a 3' UTR containing mutations in both CPEs, confers translational recruitment during maturation. This recruitment coincides with maximum polyadenylation. To assess whether c-mos mRNA polyadenylation is necessary for maturation of mouse oocytes, we have ablated endogenous c-mos mRNA by injecting an antisense oligonucleotide, which results in a failure to progress to meiosis II after emission of the first polar body. Such antisense oligonucleotide-injected oocytes could be efficiently rescued by co-injection of a c-mos mRNA carrying a wild-type 3' UTR. However, co-injection of a c-mos mRNA lacking functional CPEs substantially lowered the rescue activity. These results demonstrate that translational control of c-mos mRNA by cytoplasmic polyadenylation is necessary for normal development.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Integrity signals

Registry

Crossref · 10.1002/j.1460-2075.1994.tb06909.x

Cites

55 of 55 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

DNA sequencing with chain-terminating inhibitors
Sanger, F., Nicklen, S., & Coulson, A. R. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.12.5463 · Cited by 68,572
Single-Step Method of RNA Isolation by Acid Guanidinium Thiocyanate–Phenol–Chloroform Extraction
Chomczynski, P., & Sacchi, N. (1987) · Analytical Biochemistry · doi:10.1006/abio.1987.9999 · Cited by 65,515
The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14
Lee, R. C., Feinbaum, R. L., & Ambros, V. (1993) · Cell · doi:10.1016/0092-8674(93)90529-y · Cited by 12,948
Posttranscriptional regulation of the heterochronic gene lin-14 by lin-4 mediates temporal pattern formation in C. elegans
Wightman, B., Ha, I., & Ruvkun, G. (1993) · Cell · doi:10.1016/0092-8674(93)90530-4 · Cited by 4,292
The c-mos proto-oncogene product is a cytostatic factor responsible for meiotic arrest in vertebrate eggs
Sagata, N., Watanabe, N., Woude, G. F. V., & Ikawa, Y. (1989) · Nature · doi:10.1038/342512a0 · Cited by 642
Function of c-mos proto-oncogene product in meiotic maturation in Xenopus oocytes
Sagata, N., Oskarsson, M. K., Copeland, T., Brumbaugh, J. A., & Woude, G. F. V. (1988) · Nature · doi:10.1038/335519a0 · Cited by 611
Disruption of c-mos causes parthenogenetic development of unfertilized mouse eggs
Colledge, W. H., Carlton, M. B. L., Udy, G. B., & Evans, M. J. (1994) · Nature · doi:10.1038/370065a0 · Cited by 480
Parthenogenetic activation of oocytes in c-mos-deficient mice
Hashimoto, N., Watanabe, N., Furuta, Y., Tamemoto, H., Sagata, N., Yokoyama, M., Okazaki, K., Nagayoshi, M., Takedat, N., Ikawatll, Y., et al. (1994) · Nature · doi:10.1038/370068a0 · Cited by 442
Mos stimulates MAP kinase in Xenopus oocytes and activates a MAP kinase kinase in vitro.
Posada, J. A., Yew, N. S., Ahn, N. G., Woude, G. F. V., & Cooper, J. A. (1993) · Molecular and Cellular Biology · doi:10.1128/mcb.13.4.2546 · Cited by 410
Poly(A) elongation during Xenopus oocyte maturation is required for translational recruitment and is mediated by a short sequence element.
McGrew, L. L., Dworkin-Rastl, E., Dworkin, M. B., & Richter, J. D. (1989) · Genes & Development · doi:10.1101/gad.3.6.803 · Cited by 403
Self-citation

Show all 58 references

Research works printed but not linked: 8

Goldman,D.S., Kiessling,A.A., Millette,C.F. and Cooper,G.M. (1987) Proc. Natl Acad. Sci. USA, 84, 4509-4513.
Kanki,J.P. and Donoghue,D.J. (1991) Proc. Natl Acad. Sci. USA, 88, 5794-5798.
Mutter,G.L. and Wolgemuth,D.J. (1987) Proc. Natl Acad. Sci. USA, 84, 7869-7872.
O'Keefe,S., Wolfes,H., Kiessling,A. and Cooper,G. (1989) Proc. Natl Acad. Sci. USA, 86, 7038-7042.
O'Keefe,S., Kiessling,A. and Cooper,G. (1991) Proc. Natl Acad. Sci. USA, 88, 7869-7872.
Paules,R., Buccione,R., Moschel,R. and Vande Woude,G.F. (1989) Proc. Natl Acad. Sci. USA, 86, 5395-5399.
Sanger,F., Nicklen,S. and Coulson,A.R. (1977) Proc. Natl Acad. Sci. USA, 74, 5463-5467.
Serta,R.T., Seibel,M.M. and Kiessling,A.A. (1995) Hum. Reprod., in press.

Sorted by citations

Signal Transduction through MAP Kinase Cascades
Lewis, T. S., Shapiro, P. S., & Ahn, N. G. (1998) · Advances in cancer research · doi:10.1016/s0065-230x(08)60765-4 · Cited by 1,759
Initiation of Protein Synthesis in Eukaryotic Cells
Pain, V. M. (1996) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1996.00747.x · Cited by 718
Poly(A)-tail profiling reveals an embryonic switch in translational control
Subtelny, A. O., Eichhorn, S. W., Chen, G. R., Sive, H., & Bartel, D. P. (2014) · Nature · doi:10.1038/nature13007 · Cited by 664
Translational control by CPEB: a means to the end
Méndez, R., & Richter, J. D. (2001) · Nature Reviews Molecular Cell Biology · doi:10.1038/35080081 · Cited by 609
Self-citation
CONTROL OF TRANSLATION INITIATION IN ANIMALS
Gray, N. K., & Wickens, M. (1998) · Annual Review of Cell and Developmental Biology · doi:10.1146/annurev.cellbio.14.1.399 · Cited by 500
CPEB-Mediated Cytoplasmic Polyadenylation and the Regulation of Experience-Dependent Translation of α-CaMKII mRNA at Synapses
Wu, L., Wells, D., Tay, J., Mendis, D., Abbott, M.-A., Barnitt, A., Quinlan, E., Heynen, A., Fallon, J. R., & Richter, J. D. (1998) · Neuron · doi:10.1016/s0896-6273(00)80630-3 · Cited by 488
Self-citation
CPEB is a specificity factor that mediates cytoplasmic polyadenylation during Xenopus oocyte maturation
Hake, L. E., & Richter, J. D. (1994) · Cell · doi:10.1016/0092-8674(94)90547-9 · Cited by 454
Self-citation
Translational regulation in development
Curtis, D., Lehmann, R., & Zamore, P. D. (1995) · Cell · doi:10.1016/0092-8674(95)90325-9 · Cited by 395
Acquisition of oocyte competence to develop as an embryo: integrated nuclear and cytoplasmic events
Conti, M., & Franciosi, F. (2017) · Human Reproduction Update · doi:10.1093/humupd/dmx040 · Cited by 380
Life and death in the cytoplasm: messages from the 3′ end
Wickens, M., Anderson, P., & Jackson, R. J. (1997) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(97)80132-3 · Cited by 332
Mos is required for MAP kinase activation and is involved in microtubule organization during meiotic maturation in the mouse
Verlhac, M., Kubiak, J. Z., Weber, M., Géraud, G., Colledge, W. H., Evans, M. J., & Maro, B. (1996) · Development · doi:10.1242/dev.122.3.815 · Cited by 320
Involvement of Mitogen-Activated Protein Kinase Cascade During Oocyte Maturation and Fertilization in Mammals1
Fan, H., & Sun, Q. (2004) · Biology of Reproduction · doi:10.1095/biolreprod.103.022830 · Cited by 318
Selective degradation of transcripts during meiotic maturation of mouse oocytes
Su, Y., Sugiura, K., Woo, Y., Wigglesworth, K., Kamdar, S. J., Affourtit, J. P., & Eppig, J. J. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.09.008 · Cited by 324
Cytoplasmic Polyadenylation in Development and Beyond
Richter, J. D. (1999) · Microbiology and Molecular Biology Reviews · doi:10.1128/mmbr.63.2.446-456.1999 · Cited by 299
Self-citation
Chromosomal elements conferring epigenetic inheritance
Lyko, F., & Paro, R. (1999) · BioEssays · doi:10.1002/(sici)1521-1878(199910)21:10 · Cited by 79
CPEB controls the cytoplasmic polyadenylation of cyclin, Cdk2 and c‐mos mRNAs and is necessary for oocyte maturation in Xenopus.
Stebbins‐Boaz, B., Hake, L. E., & Richter, J. D. (1996) · The EMBO Journal · doi:10.1002/j.1460-2075.1996.tb00616.x · Cited by 283
Self-citation
The maternal legacy to the embryo: cytoplasmic components and their effects on early development
Brevini, T. A. L., & Gandolfi, F. (2001) · Theriogenology · doi:10.1016/s0093-691x(01)00481-2 · Cited by 239
Germ Cell Differentiation and Synaptonemal Complex Formation Are Disrupted in CPEB Knockout Mice
Tay, J., & Richter, J. D. (2001) · Developmental Cell · doi:10.1016/s1534-5807(01)00025-9 · Cited by 231
Self-citation
Polyadenylation of c-mos mRNA as a control point in Xenopus meiotic maturation
Sheets, M. D., Wu, M., & Wickens, M. (1995) · Nature · doi:10.1038/374511a0 · Cited by 229
Translational repressorbruno plays multiple roles in development and is widely conservedPreprint
Webster, P. J., Liang, L., Berg, C. A., Lasko, P. F., & Macdonald, P. M. (1997) · Genes & Development · doi:10.1101/gad.11.19.2510 · Cited by 211
Cytoplasmic polyadenylation elements mediate masking and unmasking of cyclin B1 mRNA
de Moor, C. H., & Richter, J. D. (1999) · The EMBO Journal · doi:10.1093/emboj/18.8.2294 · Cited by 205
Self-citation
Beneficial effect of resveratrol on bovine oocyte maturation and subsequent embryonic development after in vitro fertilization
Wang, F., Tian, X., Zhang, L., He, C., Ji, P., Li, Y., Tan, D. X., & Liu, G. (2013) · Fertility and Sterility · doi:10.1016/j.fertnstert.2013.10.041 · Cited by 201
Ultrasensitive Ribo-seq reveals translational landscapes during mammalian oocyte-to-embryo transition and pre-implantation development
Xiong, Z., Xu, K., Lin, Z., Kong, F., Wang, Q., Quan, Y., Sha, Q., Li, F., Zou, Z., Liu, L., et al. (2022) · Nature Cell Biology · doi:10.1038/s41556-022-00928-6 · Cited by 199
Translational control by cytoplasmic polyadenylation in Xenopus oocytes
Radford, H. E., Meijer, H. A., & de Moor, C. H. (2008) · Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms · doi:10.1016/j.bbagrm.2008.02.002 · Cited by 200
Meiotic Maturation of the Mouse Oocyte Requires an Equilibrium between Cyclin B Synthesis and Degradation
Ledan, E., Polański, Z., Terret, M., & Maro, B. (2001) · Developmental Biology · doi:10.1006/dbio.2001.0188 · Cited by 182
The Control of Cyclin B1 mRNA Translation during Mouse Oocyte Maturation
Tay, J., Hodgman, R., & Richter, J. D. (2000) · Developmental Biology · doi:10.1006/dbio.2000.9669 · Cited by 174
Self-citation
Cracking the egg: molecular dynamics and evolutionary aspects of the transition from the fully grown oocyte to embryoPreprint
Evsikov, A. V., Graber, J. H., Brockman, J. M., Hampl, A., Holbrook, A. E., Singh, P., Eppig, J. J., Solter, D., & Knowles, B. B. (2006) · Genes & Development · doi:10.1101/gad.1471006 · Cited by 171
Specificity of RNA Binding by CPEB: Requirement for RNA Recognition Motifs and a Novel Zinc Finger
Hake, L. E., Méndez, R., & Richter, J. D. (1998) · Molecular and Cellular Biology · doi:10.1128/mcb.18.2.685 · Cited by 170
Self-citation
Timely translation during the mouse oocyte-to-embryo transition
Oh, B., Hwang, S.-Y., McLaughlin, J., Solter, D., & Knowles, B. B. (2000) · Development · doi:10.1242/dev.127.17.3795 · Cited by 169
Circadian control of mRNA polyadenylation dynamics regulates rhythmic protein expressionPreprint
Kojima, S., Sher-Chen, E. L., & Green, C. B. (2012) · Genes & Development · doi:10.1101/gad.208306.112 · Cited by 170
Specificity factors in cytoplasmic polyadenylation
Charlesworth, A. G., Meijer, H. A., & de Moor, C. H. (2013) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1171 · Cited by 167
CPEB controls oocyte growth and follicle development in the mouse
Racki, W. J., & Richter, J. D. (2006) · Development · doi:10.1242/dev.02651 · Cited by 153
Self-citation
The roles of cytoplasmic poly(A)-binding proteins in regulating gene expression: A developmental perspective
Gorgoni, B. (2004) · Briefings in Functional Genomics and Proteomics · doi:10.1093/bfgp/3.2.125 · Cited by 158
Spindlin, a major maternal transcript expressed in the mouse during the transition from oocyte to embryo
Oh, B., Hwang, S., Solter, D., & Knowles, B. B. (1997) · Development · doi:10.1242/dev.124.2.493 · Cited by 151
The Mos Pathway Regulates Cytoplasmic Polyadenylation in Xenopus Oocytes
de Moor, C. H., & Richter, J. D. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.11.6419 · Cited by 150
Self-citation
Loss of Maternal CTCF Is Associated with Peri-Implantation Lethality of Ctcf Null Embryos
Moore, J. M., Rabaia, N. A., Smith, L. E., Fagerlie, S. R., Gurley, K. E., Loukinov, D., Distèche, C. M., Collins, S. J., Kemp, C. J., Lobanenkov, V. V., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0034915 · Cited by 133
Widespread Changes in the Posttranscriptional Landscape at the Drosophila Oocyte-to-Embryo Transition
Kronja, I., Yuan, B., Eichhorn, S. W., Dzeyk, K., Krijgsveld, J., Bartel, D. P., & Orr‐Weaver, T. L. (2014) · Cell Reports · doi:10.1016/j.celrep.2014.05.002 · Cited by 132
3′-End cleavage and polyadenylation of mRNA precursors
Wahle, E. (1995) · Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression · doi:10.1016/0167-4781(94)00248-2 · Cited by 135
Translational control of dosage compensation in Drosophila by Sex‐lethal: cooperative silencing via the 5′ and 3′ UTRs of msl‐2 mRNA is independent of the poly(A) tail
Gebauer, F., Corona, D. F. V., Preiß, T., Becker, P. B., & Hentze, M. W. (1999) · The EMBO Journal · doi:10.1093/emboj/18.21.6146 · Cited by 134
Self-citation
Revisiting the Closed-Loop Model and the Nature of mRNA 5′–3′ Communication
Vicens, Q., Kieft, J. S., & Rissland, O. S. (2018) · Molecular Cell · doi:10.1016/j.molcel.2018.10.047 · Cited by 140
Expression of MSY2 in Mouse Oocytes and Preimplantation Embryos1
Yu, J., Hecht, N. B., & Schultz, R. M. (2001) · Biology of Reproduction · doi:10.1095/biolreprod65.4.1260 · Cited by 126
Quantitative analysis of messenger RNA abundance for ribosomal protein L-15, cyclophilin-A, phosphoglycerokinase, β-glucuronidase, glyceraldehyde 3-phosphate dehydrogenase, β-actin, and histone H2A during bovine oocyte maturation and early embryogenesis in vitro
Bettegowda, A., PATEL, O. V., Ireland, J. J., & Smith, G. W. (2005) · Molecular Reproduction and Development · doi:10.1002/mrd.20333 · Cited by 123
New member of the Snf1/AMPK kinase family, Melk, is expressed in the mouse egg and preimplantation embryo
Heyer, B. S., Warsowe, J., Solter, D., Knowles, B. B., & Ackerman, S. L. (1997) · Molecular Reproduction and Development · doi:10.1002/(sici)1098-2795(199706)47:2 · Cited by 122
Redox Control in Mammalian Embryo Development
Ufer, C., Wang, C. C., Borchert, A., Heydeck, D., & Kühn, H. (2010) · Antioxidants and Redox Signaling · doi:10.1089/ars.2009.3044 · Cited by 121
Synthesis and function of mos: The control switch of vertebrate oocyte meiosis
Gebauer, F., & Richter, J. D. (1997) · BioEssays · doi:10.1002/bies.950190106 · Cited by 118
Self-citation
Portrait of an oocyte: our obscure origin
Gosden, R. G., & Lee, B. (2010) · Journal of Clinical Investigation · doi:10.1172/jci41294 · Cited by 122
Mouse cytoplasmic polyadenylylation element binding protein: An evolutionarily conserved protein that interacts with the cytoplasmic polyadenylylation elements of c- mos mRNA
Gebauer, F., & Richter, J. D. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.25.14602 · Cited by 115
Self-citation
Cyclin synthesis controls the progression of meiotic maturation in mouse oocytes
Polański, Z., Ledan, E., Brunet, S., Louvet‐Vallée, S., Verlhac, M., Kubiak, J. Z., & Maro, B. (1998) · Development · doi:10.1242/dev.125.24.4989 · Cited by 112
Mechanisms of maternal mRNA regulation: implications for mammalian early embryonic development
Bettegowda, A. (2007) · Frontiers in bioscience · doi:10.2741/2346 · Cited by 110
CPEB phosphorylation and cytoplasmic polyadenylation are catalyzed by the kinase IAK1/Eg2 in maturing mouse oocytes
Hodgman, R., Tay, J., Méndez, R., & Richter, J. D. (2001) · Development · doi:10.1242/dev.128.14.2815 · Cited by 110
Self-citation
Cytoplasmic polyadenylation in mammalian oocyte maturation
Reyes, J. M., & Ross, P. J. (2015) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1316 · Cited by 114
The DAZL and PABP families: RNA-binding proteins with interrelated roles in translational control in oocytes
Brook, M., Smith, J. W. S., & Gray, N. K. (2009) · Reproduction · doi:10.1530/rep-08-0524 · Cited by 109
Masking, unmasking, and regulated polyadenylation cooperate in the translational control of a dormant mRNA in mouse oocytesPreprint
Stutz, A., Conne, B., Huarte, J., Gubler, P., Völkel, V., Flandin, P., & Vassalli, J. (1998) · Genes & Development · doi:10.1101/gad.12.16.2535 · Cited by 108
Cytoplasmic 3′ poly(A) addition induces 5′ cap ribose methylation: implications for translational control of maternal mRNA.
Kuge, H., & Richter, J. D. (1995) · The EMBO Journal · doi:10.1002/j.1460-2075.1995.tb00320.x · Cited by 107
Self-citation
Transcriptome dynamics and molecular cross-talk between bovine oocyte and its companion cumulus cells
Regassa, A., Rings, F., Hoelker, M., Cinar, U., Tholen, E., Looft, C., Schellander, K., & Tesfaye, D. (2011) · BMC Genomics · doi:10.1186/1471-2164-12-57 · Cited by 104
Cytoplasmic Polyadenylation Element (CPE)- and CPE-binding Protein (CPEB)-independent Mechanisms Regulate Early Class Maternal mRNA Translational Activation in Xenopus Oocytes
Charlesworth, A. G., Cox, L. L., & MacNicol, A. M. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m313837200 · Cited by 101
Translational control in vertebrate development
de Moor, C. H., & Richter, J. D. (2001) · International review of cytology · doi:10.1016/s0074-7696(01)03017-0 · Cited by 102
Self-citation
Comparative Analysis of Protein Synthesis, Transcription and Cytoplasmic Polyadenylation of mRNA during Maturation of Bovine Oocytes in vitro
Tomek, W., Torner, H., & KANITZ, W. (2002) · Reproduction in Domestic Animals · doi:10.1046/j.1439-0531.2002.00336.x · Cited by 97
Cap ribose methylation of c-mos mRNA stimulates translation and oocyte maturation in Xenopus laevis
Kuge, H. (1998) · Nucleic Acids Research · doi:10.1093/nar/26.13.3208 · Cited by 96
Global gene expression analysis during bovine oocyte in vitro maturation
Fair, T., Carter, F., Park, S.-Y., Evans, A. C. O., & Lonergan, P. (2007) · Theriogenology · doi:10.1016/j.theriogenology.2007.04.018 · Cited by 96
A dependent pathway of cytoplasmic polyadenylation reactions linked to cell cycle control by c-mos and CDK1 activation.
Ballantyne, S. M., Daniel, D., & Wickens, M. (1997) · Molecular Biology of the Cell · doi:10.1091/mbc.8.8.1633 · Cited by 96
Diversity in translational regulation
Macdonald, P. M. (2001) · Current Opinion in Cell Biology · doi:10.1016/s0955-0674(00)00215-5 · Cited by 96
Mechanisms of translational control in early development
Seydoux, G. (1996) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(96)80083-9 · Cited by 94
Meiotic maturation in Xenopus requires polyadenylation of multiple mRNAs
Barkoff, A., Ballantyne, S., & Wickens, M. (1998) · The EMBO Journal · doi:10.1093/emboj/17.11.3168 · Cited by 93
Maternal factors required for oocyte developmental competence in mice: Transcriptome analysis of non-surrounded nucleolus (NSN) and surrounded nucleolus (SN) oocytes
Ma, J., Li, M., Luo, Y., Song, S., Tian, D., Yang, J., Zhang, B., Hou, Y., Schatten, H., Liu, Z., et al. (2013) · Cell Cycle · doi:10.4161/cc.24991 · Cited by 92
The Mitogen-Activated Protein Kinase Signaling Pathway Stimulates Mos mRNA Cytoplasmic Polyadenylation during Xenopus Oocyte Maturation
Howard, E. L., Charlesworth, A. G., Welk, J. F., & MacNicol, A. M. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.3.1990 · Cited by 89
An embryonic poly(A)-binding protein (ePAB) is expressed in mouse oocytes and early preimplantation embryos
Seli, E. U., Lalioti, M. D., Flaherty, S. M., Sakkas, D., Çizmecioğlu, N. T., & STEITZ, J. A. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0408378102 · Cited by 88
Single-cell quantification of ribosome occupancy in early mouse development
Özadam, H., Tonn, T., Han, C. M., Segura, A., Hoskins, I., Rao, S. J., Ghatpande, V., Tran, D., Catoe, D., Salit, M., et al. (2023) · Nature · doi:10.1038/s41586-023-06228-9 · Cited by 85
Metazoan oocyte and early embryo development program: a progression through translation regulatory cascadesPreprint
Vasudevan, S., Seli, E. U., & STEITZ, J. A. (2006) · Genes & Development · doi:10.1101/gad.1398906 · Cited by 86
Embryonic poly(A)-binding protein (EPAB) is required for oocyte maturation and female fertility in mice
Guzeloglu‐Kayisli, O., Lalioti, M. D., Aydıner, F., Sasson, I. E., Ilbay, O., Sakkas, D., Lowther, K. M., Mehlmann, L. M., & Seli, E. U. (2012) · Biochemical Journal · doi:10.1042/bj20120467 · Cited by 84
Two Xenopus Proteins That Bind the 3′ End of Histone mRNA: Implications for Translational Control of Histone Synthesis during Oogenesis
Wang, Z.-F., Ingledue, T. C., Domiński, Z., Sànchez, R., & Marzluff, W. F. (1999) · Molecular and Cellular Biology · doi:10.1128/mcb.19.1.835 · Cited by 85
Mutations that perturb poly(A)-dependent maternal mRNA activation block the initiation of development
Lieberfarb, M. E., Chu, T., Wreden, C. C., Theurkauf, W. E., Gergen, J. P., & Strickland, S. (1996) · Development · doi:10.1242/dev.122.2.579 · Cited by 83
RNA-Binding Proteins in Early Development
Colegrove-Otero, L. J., Minshall, N., & Standart, N. (2005) · Critical Reviews in Biochemistry and Molecular Biology · doi:10.1080/10409230590918612 · Cited by 81
Translational regulation of maternal mRNAs
Macdonald, P. M., & Smibert, C. A. (1996) · Current Opinion in Genetics & Development · doi:10.1016/s0959-437x(96)80060-8 · Cited by 78
Post-transcriptional Control of Gene Expression During Mouse Oogenesis
Clarke, H. J. (2012) · Results and problems in cell differentiation · doi:10.1007/978-3-642-30406-4_1 · Cited by 78
Translational regulation during oogenesis and early development: The cap-poly(A) tail relationship
Piccioni, F., Zappavigna, V., & Verrotti, A. C. (2005) · Comptes Rendus Biologies · doi:10.1016/j.crvi.2005.05.006 · Cited by 76
Analysis of polysomal mRNA populations of mouse oocytes and zygotes: Dynamic changes in maternal mRNA utilization and function
Potireddy, S., Vassena, R., Patel, B. G., & Latham, K. E. (2006) · Developmental Biology · doi:10.1016/j.ydbio.2006.06.024 · Cited by 74
A new role for Mos inXenopusoocyte maturation: targeting Myt1 independently of MAPK
Peter, M., Labbé, J., Dorée, M., & Mandart, E. (2002) · Development · doi:10.1242/dev.129.9.2129 · Cited by 74
The organization and regulation of mRNA –protein complexes
Rissland, O. S. (2016) · Wiley Interdisciplinary Reviews - RNA · doi:10.1002/wrna.1369 · Cited by 73
Evolutionary conservation of sequence elements controlling cytoplasmic polyadenylylation.
Verrotti, A. C., Thompson, S. R., Wreden, C. C., Strickland, S., & Wickens, M. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.17.9027 · Cited by 71
From Transcript to Protein
Dreyfuss, G., Hentze, M. W., & Lamond, A. I. (1996) · Cell · doi:10.1016/s0092-8674(00)81298-2 · Cited by 70
miR-181a Regulates Cap-Dependent Translation of p27kip1 mRNA in Myeloid Cells
Cuesta, R., Martínez-Sánchez, A., & Gebauer, F. (2009) · Molecular and Cellular Biology · doi:10.1128/mcb.01971-08 · Cited by 69
Self-citation
Hsp90 is required for c‐Mos activation and biphasic MAP kinase activation in Xenopus oocytes
Fisher, D., Mandart, E., & Dorée, M. (2000) · The EMBO Journal · doi:10.1093/emboj/19.7.1516 · Cited by 68
RNA‐Seq profiling of single bovine oocyte transcript abundance and its modulation by cytoplasmic polyadenylation
Reyes, J. M., Chitwood, J. L., & Ross, P. J. (2015) · Molecular Reproduction and Development · doi:10.1002/mrd.22445 · Cited by 69
Ovarian follicle development in vitro and oocyte competence: advances and challenges for farm animals
Silva, J. R. V., Hurk, R. V. D., & Figueiredo, J. R. (2016) · Domestic Animal Endocrinology · doi:10.1016/j.domaniend.2015.12.006 · Cited by 67
A novel regulatory element determines the timing of Mos mRNA translation during Xenopus oocyte maturation
Charlesworth, A. G., Ridge, J. A., King, L. A., MacNicol, M. C., & MacNicol, A. M. (2002) · The EMBO Journal · doi:10.1093/emboj/21.11.2798 · Cited by 67
Translational regulation of oskar mRNA occurs independent of the cap and poly(A) tail in Drosophila ovarian extracts
Lie, Y. S., & Macdonald, P. M. (1999) · Development · doi:10.1242/dev.126.22.4989 · Cited by 66
A genome-wide survey of maternal and embryonic transcripts during Xenopus tropicalis development
Paranjpe, S. S., Jacobi, U. G., van Heeringen, S. J., & Veenstra, G. J. C. (2013) · BMC Genomics · doi:10.1186/1471-2164-14-762 · Cited by 68
A pollen-, ovule-, and early embryo-specific poly(A) binding protein from Arabidopsis complements essential functions in yeast.
Belostotsky, D. A., & Meagher, R. B. (1996) · The Plant Cell · doi:10.1105/tpc.8.8.1261 · Cited by 65
Mos in the Oocyte: How to Use MAPK Independently of Growth Factors and Transcription to Control Meiotic Divisions
Dupré, A., Haccard, O., & Jessus, C. (2010) · Journal of Signal Transduction · doi:10.1155/2011/350412 · Cited by 63
Large T antigen on the simian virus 40 origin of replication: a 3D snapshot prior to DNA replication
Gómez-Lorenzo, M. G., Valle, M., Frank, J., Gruss, C. B., Sorzano, C. Ó. S., Chen, X. S., Donate, L. E., & Carazo, J. M. (2003) · The EMBO Journal · doi:10.1093/emboj/cdg612 · Cited by 63
Posttranscriptional Regulation of Cyclin A1 and Cyclin A2 During Mouse Oocyte Meiotic Maturation and Preimplantation Development1
Fuchimoto, D., Mizukoshi, A., Schultz, R. M., Sakai, S., & Aoki, F. (2001) · Biology of Reproduction · doi:10.1095/biolreprod65.4.986 · Cited by 62
Possible role of mouse poly(A) polymerase mGLD-2 during oocyte maturation
Nakanishi, T., Kubota, H., Ishibashi, N., Kumagai, S., Watanabe, H., Yamashita, M., Kashiwabara, S., Miyado, K., & Baba, T. (2005) · Developmental Biology · doi:10.1016/j.ydbio.2005.10.017 · Cited by 60
Regulation of Translation During In Vitro Maturation of Bovine Oocytes: The Role of MAP Kinase, eIF4E (Cap Binding Protein) Phosphorylation, and eIF4E-BP11
Tomek, W., Melo-Sterza, F. D. A., Kubelka, M., Wollenhaupt, K., Torner, H., Anger, M., & KANITZ, W. (2002) · Biology of Reproduction · doi:10.1095/biolreprod66.5.1274 · Cited by 60
Phosphatidylinositol 3-Kinase in Cumulus Cells and Oocytes Is Responsible for Activation of Oocyte Mitogen-Activated Protein Kinase During Meiotic Progression Beyond the Meiosis I Stage in Pigs
Shimada, M., & Terada, T. (2001) · Biology of Reproduction · doi:10.1095/biolreprod64.4.1106 · Cited by 60
The 36-Kilodalton Embryonic-Type Cytoplasmic Polyadenylation Element-Binding Protein in Xenopus laevis Is ElrA, a Member of the ELAV Family of RNA-Binding Proteins
Wu, L., Good, P. J., & Richter, J. D. (1997) · Molecular and Cellular Biology · doi:10.1128/mcb.17.11.6402 · Cited by 59
Self-citation
Regulated CPEB phosphorylation during meiotic progression suggests a mechanism for temporal control of maternal mRNA translationPreprint
Tay, J., Hodgman, R., Sarkissian, M., & Richter, J. D. (2003) · Genes & Development · doi:10.1101/gad.1071403 · Cited by 59
Self-citation
Synonymous codon usage regulates translation initiation
Barrington, C. L., Galindo, G., Koch, A., Horton, E. R., Morrison, E. J., Tisa, S., Stasevich, T. J., & Rissland, O. S. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.113413 · Cited by 64
Cytoplasmic Prep1 Interacts with 4EHP Inhibiting Hoxb4 Translation
Villaescusa, C., Buratti, C., Penkov, D., Mathiasen, L., Planagumà, J., Ferretti, E., & Blasi, F. (2009) · PLoS ONE · doi:10.1371/journal.pone.0005213 · Cited by 55
4E-T-bound mRNAs are stored in a silenced and deadenylated formPreprint
Räsch, F., Weber, R., Izaurralde, E., & Igreja, C. (2020) · Genes & Development · doi:10.1101/gad.336073.119 · Cited by 55

Authors: Gebauer, F., Xu, W., Cooper, G. M., & Richter, J. D.
ORCID: Gebauer, F.
Xu, W.
Richter, J.D.
Venue: The EMBO Journal
Publisher: Springer Science and Business Media LLC
Published: 1994-12-01
Volume: 13
Issue: 23
Pages: 5712-5720
ISSN: 0261-4189 (ISSN-L)
1460-2075
DOI: 10.1002/j.1460-2075.1994.tb06909.x
PMC: PMC395537
OpenAlex: W126837237
Cited by: 235
References: 58
Citations by year: 2025: 3 · 2024: 2 · 2023: 6 · 2022: 2 · 2021: 4 · 2020: 5 · 2019: 5 · 2018: 5 · 2017: 3 · 2016: 5 · 2015: 5 · 2014: 6 · 2013: 9 · 2012: 5
FWCI: 5.30
Type: journal article
Language: en
Open access: bronze
doi.org
Licence: www.springer.com/tdm (tdm)
www.springer.com/tdm (vor)
Locations: The EMBO Journal (publishedVersion)
PubMed Central (publishedVersion)
PubMed (publishedVersion)
Funders: March of Dimes Foundation
National Institutes of Health (7r01ca040189-14, 5r01hd026594-09)
National Cancer Institute (CA-40189)
National Institute of General Medical Sciences (GM46779, R01GM046779)
Eunice Kennedy Shriver National Institute of Child Health and Human Development (HD26594)
Topics: Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA Research and Splicing
Health Sciences › Medicine › Reproductive Medicine › Reproductive Biology and Fertility
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › RNA and protein synthesis mechanisms
Keywords: c-mos, cytoplasmic polyadenylation, oocyte maturation, translational regulation, 3' untranslated region, cytoplasmic polyadenylation element, meiotic maturation, antisense oligonucleotides, mouse oocytes, meiosis II
MeSH terms: Adenosine Monophosphate, Amino Acid Sequence, Animals, Base Sequence, Cytoplasm, Kinetics, Meiosis, Molecular Sequence Data, Oogenesis, RNA, Messenger, Protein Biosynthesis, Proto-Oncogene Proteins c-mos, Mice

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Translational control by cytoplasmic polyadenylation of c‐mos mRNA is necessary for oocyte maturation in the mouse.

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Self-check

Citations

Cites

Cited by

Related

Metadata

Record

About these checks