Gene expression during minor genome activation in preimplantation bovine development

Theriogenology

Volumn 72, Issue 4, 2009, Pages 572-583

  Kanka J ^a   Kepkova K ^a   Nemcova L ^a  

^a INSTITUTE OF ANIMAL PHYSIOLOGY AND GENETICS   (Czech Republic)

Author keywords

Developmental biology; Embryo; Gene expression; Real time RT PCR; SSH

Indexed keywords

COMPLEMENTARY DNA;

ANIMAL; ARTICLE; BLASTOCYST; CATTLE; CHEMISTRY; EMBRYO DEVELOPMENT; GENE EXPRESSION; GENE EXPRESSION PROFILING; GENETICS; GENOME; NUCLEIC ACID HYBRIDIZATION; PRENATAL DEVELOPMENT; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION;

ANIMALS; BLASTOCYST; CATTLE; DNA, COMPLEMENTARY; EMBRYONIC DEVELOPMENT; GENE EXPRESSION; GENE EXPRESSION PROFILING; GENOME; NUCLEIC ACID HYBRIDIZATION; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION;

BOVINAE;

EID: 67651172792     PISSN: 0093691X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.theriogenology.2009.04.014     Document Type: Article

References (62)

1. Schultz R.M., Davis W., Stein P., and Svoboda P. Reprogramming of gene expression during preimplantation development. J Exp Zool 285 (1999) 276-282
2. Latham K.E., and Schultz R.M. Embryonic genome activation. Front Biosci 6 (2001) D748-759
3. Kanka J. Gene expression and chromatin structure in the pre-implantation embryo. Theriogenology 59 (2003) 3-19
4. Bettegowda A., Lee K.B., and Smith G.W. Cytoplasmic and nuclear determinants of the maternal-to-embryonic transition. Reprod Fertil Dev 20 (2008) 45-53
5. Clegg K.B., and Piko L. Poly(A) length, cytoplasmic adenylation and synthesis of poly(A)+ RNA in early mouse embryos. Dev Biol 95 (1983) 331-341
6. Bensaude O., Babinet C., Morange M., and Jacob F. Heat shock proteins, first major products of zygotic gene activity in mouse embryo. Nature 305 (1983) 331-333
7. Conover J.C., Temeles G.L., Zimmermann J.W., Burke B., and Schultz R.M. Stage-specific expression of a family of proteins that are major products of zygotic gene activation in the mouse embryo. Dev Biol 144 (1991) 392-404
8. Latham K.E., Solter D., and Schultz R.M. Activation of a 2-cell stage-specific gene following transfer of heterologous nuclei into enucleated mouse embryos. Mol Reprod Dev 30 (1991) 182-186
9. Bouniol C., Nguyen E., and Debey P. Endogenous transcription occurs at the 1-cell stage in the mouse embryo. Exp Cell Res 218 (1995) 57-62
10. Aoki F., Worrad D.M., and Schultz R.M. Regulation of transcriptional activity during the first and second cell cycles in the preimplantation mouse embryo. Dev Biol 181 (1997) 296-307
11. Christians E., Campion E., Thompson E.M., and Renard J.P. Expression of the HSP 70.1 gene, a landmark of early zygotic activity in the mouse embryo, is restricted to the first burst of transcription. Development 121 (1995) 113-122
12. Zeng F., and Schultz R.M. RNA transcript profiling during zygotic gene activation in the preimplantation mouse embryo. Dev Biol 283 (2005) 40-57
13. Svoboda P., Stein P., Anger M., Bernstein E., Hannon G.J., and Schultz R.M. RNAi and expression of retrotransposons MuERV-L and IAP in preimplantation mouse embryos. Dev Biol 269 (2004) 276-285
14. Ma L., Zhao X., and Zhu X. Mitosin/CENP-F in mitosis, transcriptional control, and differentiation. J Biomed Sci 13 (2006) 205-213
15. Zeng F.Y., Baldwin D.A., and Schultz R.M. Transcript profiling during preimplantation mouse development. Dev Biol 272 (2004) 483-496
16. Hamatani T., Carter M.G., Sharov A.A., and Ko M.S. Dynamics of global gene expression changes during mouse preimplantation development. Dev Cell 6 (2004) 117-131
17. Wang Q.T., Piotrowska K., Ciemerych M.A., Milenkovic L., Scott M.P., Davis R.W., and Zernicka-Goetz M. A genome-wide study of gene activity reveals developmental signaling pathways in the preimplantation mouse embryo. Dev Cell 6 (2004) 133-144
18. Potireddy S., Vassena R., Patel B.G., and Latham K.E. Analysis of polysomal mRNA populations of mouse oocytes and zygotes: dynamic changes in maternal mRNA utilization and function. Dev Biol 298 (2006) 155-166
19. Hara K.T., Oda S., Naito K., Nagata M., Schultz R.M., and Aoki F. Cyclin A2-CDK2 regulates embryonic gene activation in 1-cell mouse embryos. Dev Biol 286 (2005) 102-113
20. Philipsen S., and Suske G. A tale of three fingers: the family of mammalian Sp/XKLF transcription factors. Nucleic Acids Res 27 (1999) 2991-3000
21. Bultman S.J., Gebuhr T.C., Pan H., Svoboda P., Schultz R.M., and Magnuson T. Maternal BRG1 regulates zygotic genome activation in the mouse. Genes Dev 20 (2006) 1744-1754
22. Camous S., Kopecny V., and Flechon J.E. Autoradiographic detection of the earliest stage of [3/H]-uridine incorporation into the cow embryo. Biol Cell 58 (1986) 195-200
23. Frei R.E., Schultz G.A., and Church R.B. Qualitative and quantitative changes in protein synthesis occur at the 8-16-cell stage of embryogenesis in the cow. J Reprod Fertil 86 (1989) 637-641
24. DeLouis C., Bonnerot C., Vernet M., and Nicolas J.F. Expression of microinjected DNA and RNA in early rabbit embryos: changes in permissiveness for expression and transcriptional selectivity. Exp Cell Res 201 (1992) 284-291
25. Viuff D., Avery B., Greve T., King W.A., and Hyttel P. Transcriptional activity in in vitro produced bovine two- and four-cell embryos. Mol Reprod Dev 43 (1996) 171-179
26. Memili E., Dominko T., and First N.L. Onset of transcription in bovine oocytes and preimplantation embryos. Mol Reprod Dev 51 (1998) 36-41
27. Memili E., and First N.L. Control of gene expression at the onset of bovine embryonic development. Biol Reprod 61 (1999) 1198-1207
28. Liu Z.S., and Foote R.H. Effects of amino acids and alpha-amanitin on bovine embryo development in a simple protein-free medium. Mol Reprod Dev 46 (1997) 278-285
29. Natale D.R., Kidder G.M., Westhusin M.E., and Watson A.J. Assessment by differential display-RT-PCR of mRNA transcript transitions and alpha-amanitin sensitivity during bovine preattachment development. Mol Reprod Dev 55 (2000) 152-163
30. Kanka J., Bryova A., Duranthon V., Oudin J.F., Peynot N., and Renard J.P. Identification of differentially expressed mRNAs in bovine preimplantation embryos. Zygote 11 (2003) 43-52
31. Jakobsen A.S., Avery B., Dieleman S.J., Knijn H.M., Vos P.L., and Thomsen P.D. Transcription of ribosomal RNA genes is initiated in the third cell cycle of bovine embryos. Mol Reprod Dev 73 (2006) 196-205
32. Misirlioglu M., Page G.P., Sagirkaya H., Kaya A., Parrish J.J., First N.L., and Memili E. Dynamics of global transcriptome in bovine matured oocytes and preimplantation embryos. Proc Natl Acad Sci USA 103 (2006) 18905-18910
33. Vigneault C., Gravel C., Vallee M., McGraw S., and Sirard M.A. Unveiling the bovine embryo transcriptome during the maternal-to-embryonic transition. Reproduction 137 (2009) 245-257
34. Pavlok A., Lucas-Hahn A., and Niemann H. Fertilization and developmental competence of bovine oocytes derived from different categories of antral follicles. Mol Reprod Dev 31 (1992) 63-67
35. Fair T., Murphy M., Rizos D., Moss C., Martin F., Boland M.P., and Lonergan P. Analysis of differential maternal mRNA expression in developmentally competent and incompetent bovine two-cell embryos. Mol Reprod Dev 67 (2004) 136-144
36. Altschul S.F., Gish W., Miller W., Myers E.W., and Lipman D.J. Basic local alignment search tool. J Mol Biol 215 (1990) 403-410
37. Robert C., McGraw S., Massicotte L., Pravetoni M., Gandolfi F., and Sirard M.A. Quantification of housekeeping transcript levels during the development of bovine preimplantation embryos. Biol Reprod 67 (2002) 1465-1472
38. Vigneault C., Gilbert I., Sirard M.A., and Robert C. Using the histone H2a transcript as an endogenous standard to study relative transcript abundance during bovine early development. Mol Reprod Dev 74 (2007) 703-715
39. Brunet-Simon A., Henrion G., Renard J.P., and Duranthon V. Onset of zygotic transcription and maternal transcript legacy in the rabbit embryo. Mol Reprod Dev 58 (2001) 127-136
40. Brevini T.A.L., Lonergan P., Cillo F., Francisci C., Favetta L.A., Fair T., and Gandolfi F. Evolution of mRNA polyadenylation between oocyte maturation and first embryonic cleavage in cattle and its relation with developmental competence. Mol Reprod Dev 63 (2002) 510-517
41. Pennetier S., Perreau C., Uzbekova S., Thelie A., Delaleu B., Mermillod P., and Dalbies-Tran R. MATER protein expression and intracellular localization throughout folliculogenesis and preimplantation embryo development in the bovine. BMC Dev Biol 6 (2006) 26
42. Bui L.C., Leandri R.D., Renard J.P., and Duranthon V. SSH adequacy to preimplantation mammalian development: scarce specific transcripts cloning despite irregular normalisation. BMC Genomics 6 (2005) 155
43. Mohan M., Ryder S., Claypoo P.L., Geisert R.D., and Malayer J.R. Analysis of gene expression in the bovine blastocyst produced in vitro using suppression-subtractive hybridization. Biol Reprod 67 (2002) 447-453
44. Yao Y.Q., Xu J.S., Lee W.M., Yeung W.S., and Lee K.F. Identification of mRNAs that are up-regulated after fertilization in the murine zygote by suppression subtractive hybridization. Biochem Biophys Res Commun 304 (2003) 60-66
45. Kues W.A., Sudheer S., Herrmann D., Carnwath J.W., Havlicek V., Besenfelder U., et al. Genome-wide expression profiling reveals distinct clusters of transcriptional regulation during bovine preimplantation development in vivo. Proc Natl Acad Sci USA 105 (2008) 19768-19773
46. Nishikimi A., Mukai J., Ikeda S., and Yamada M. Nuclear translocation of a pre-mRNA splicing factor, p100(prp1/zer1/prp6), in mouse 1-cell embryos. J Reprod Dev 48 (2002) 257-263
47. Huang Y., and Steitz J.A. Splicing factors SRp20 and 9G8 promote the nucleocytoplasmic export of mRNA. Mol Cell 7 (2001) 899-905
48. Lou H., Neugebauer K.M., Gagel R.F., and Berget S.M. Regulation of alternative polyadenylation by u1 snRNPs and SRp20. Mol Cell Biol 18 (1998) 4977-4985
49. Jumaa H., Guenet J.L., and Nielsen P.J. Regulated expression and RNA processing of transcripts from the Srp20 splicing factor gene during the cell cycle. Mol Cell Biol 17 (1997) 3116-3124
50. Jumaa H., Wei G., and Nielsen P.J. Blastocyst formation is blocked in mouse embryos lacking the splicing factor SRp20. Curr Biol 9 (1999) 899-902
51. Liao H., Winkfein R.J., Mack G., Rattner J.B., and Yen T.J. CENP-F is protein of the nuclear matrix that assembles onto kinetochores at late G2 and is rapidly degraded after mitosis. J Cell Biol 130 (1995) 507-518
52. Evans H.J., Edwards L., and Goodwin R.L. Conserved C-terminal domains of mCenp-F (LEK1) regulate subcellular localization and mitotic checkpoint delay. Exp Cell Res 313 (2007) 2427-2437
53. Liu S.T., Hittle J.C., Jablonski S.A., Campbell M.S., Yoda K., and Yen T.J. Human CENP-I specifies localization of CENP-F, MAD1 and MAD2 to kinetochores and is essential for mitosis. Nat Cell Biol 5 (2003) 341-345
54. Holt S.V., Vergnolle M.A.S., Hussein D., Wozniak M.J., Allan V.J., and Taylor S.S. Silencing Cenp-F weakens centromeric cohesion, prevents chromosome alignment and activates the spindle checkpoint. J Cell Sci 118 (2005) 4889-4900
55. Varis A., Salmela A.L., and Kallio M.J. Cenp-F (mitosin) is more than a mitotic marker. Chromosoma 115 (2006) 288-295
56. Bustin M. Chromatin unfolding and activation by HMGN chromosomal proteins. Trends Biochem Sci 26 (2001) 431-437
57. Agresti A., and Bianchi M.E. HMGB proteins and gene expression. Curr Opin Genet Dev 13 (2003) 170-178
58. Bustin M., and Reeves R. High-mobility-group chromosomal proteins: architectural components that facilitate chromatin function. Progr Nucleic Acid Res 54 (1996) 35-100
59. Postnikov Y.V., Shick V.V., Belyavsky A.V., Khrapko K.R., Brodolin K.L., Nikolskaya T.A., and Mirzabekov A.D. Distribution of high mobility group preoteins 1/2, E and 14/17 and linker histone-H1 and histone-H5 on transcribed and nontranscribed regions of chicken erythrocyte chromatin. Nucleic Acids Res 19 (1991) 717-725
60. Mohamed O.A., Bustin M., and Clarke H.J. High-mobility group proteins 14 and 17 maintain the timing of early embryonic development in the mouse. Dev Biol 229 (2001) 237-249
61. Raught B., and Gingras A.C. eIF4E activity is regulated at multiple levels. Int J Biochem Cell Biol 31 (1999) 43-57
62. Topisirovic I., Capili A.D., and Borden K.L.B. Gamma interferon and cadmium treatments modulate eukaryotic initiation factor 4E-dependent mRNA transport of cyclin D1 in a PML-dependent manner. Mol Cell Biol 22 (2002) 6183-6198