The influence of follicle size, FSH‐enriched maturation medium, and early cleavage on bovine oocyte maternal mRNA levels

Transcription is arrested in the bovine oocyte within the first few hours of in vitro maturation, thus the stored maternal mRNAs accumulated in the oocyte are essential to sustain development until the Maternal‐Zygotic Transition. In vivo matured oocytes have superior blastocyst formation rates than in vitro matured oocytes, suggesting that the mRNA content of these oocytes is of higher quality. To determine which transcripts may be associated with developmental competence, a Suppressive Subtractive Hybridization was performed between oocytes collected by ovariectomy at 6 hr post‐LH surge and oocytes from slaughterhouse collected after 6 hr of maturation, resulting in a library enriched in these functionally important mRNAs. The clones were spotted onto a cDNA microarray and transcripts potentially associated with developmental competence were hybridized onto these slides. Hybridizations were performed with transcripts up‐regulated in oocytes cultured for 6 hr in the presence or absence of rFSH in vitro, and secondly with transcripts up regulated in early‐cleaving embryos versus those at the one‐cell stage at 36 hr postfertilization. From these hybridizations, 13 candidates were selected. Their functional association with embryonic competence was validated by measuring their relative transcript levels by quantitative real‐time PCR in eight different conditions: oocytes cultured with or without rFSH, early—versus late‐cleaving embryos, and oocytes from different follicle sizes (1–3, 3–5, 5–8, and >8 mm of diameter). The gene candidates CCNB2, PTTG1, H2A, CKS1, PSMB2, SKIIP, CDC5L, RGS16, and PRDX1 showed a significant quantitative association with competence compared to BMP15, GDF9, CCNB1, and STK6. Mol. Reprod. Dev. 73: 1367–1379, 2006. © 2006 Wiley‐Liss, Inc.

[1]  P. Chidiac,et al.  RGS proteins have a signalling complex: interactions between RGS proteins and GPCRs, effectors, and auxiliary proteins. , 2006, Cellular signalling.

[2]  M. Sirard,et al.  Protein kinases influence bovine oocyte competence during short-term treatment with recombinant human follicle stimulating hormone. , 2005, Reproduction.

[3]  K. Tremblay,et al.  Expression of Cyclin B1 Messenger RNA Isoforms and Initiation of Cytoplasmic Polyadenylation in the Bovine Oocyte1 , 2005, Biology of reproduction.

[4]  M. Sirard,et al.  Effect of serum and cumulus cell expansion on marker gene transcripts in bovine cumulus-oocyte complexes during maturation in vitro. , 2005, Fertility and sterility.

[5]  P. Greengard,et al.  Spinophilin regulates Ca2+ signalling by binding the N-terminal domain of RGS2 and the third intracellular loop of G-protein-coupled receptors , 2005, Nature Cell Biology.

[6]  P. Mermillod,et al.  Influence of antral follicle size on oocyte characteristics and embryo development in the bovine. , 2005, Theriogenology.

[7]  C. Robert,et al.  RNA interference as a tool to study gene function in bovine oocytes , 2005, Molecular reproduction and development.

[8]  S. Reed,et al.  A kinase-independent function of Cks1 and Cdk1 in regulation of transcription. , 2005, Molecular cell.

[9]  C. Robert,et al.  Potential and limitations of bovine-specific arrays for the analysis of mRNA levels in early development: preliminary analysis using a bovine embryonic array. , 2005, Reproduction, fertility, and development.

[10]  P. Mermillod,et al.  Several signaling pathways are involved in the control of cattle oocyte maturation , 2004, Molecular reproduction and development.

[11]  P. Pfeffer,et al.  Isolation of Genes Associated with Developmentally Competent Bovine Oocytes and Quantitation of Their Levels During Development1 , 2004, Biology of reproduction.

[12]  M. Herbert,et al.  Maintenance of sister chromatid attachment in mouse eggs through maturation-promoting factor activity. , 2004, Developmental biology.

[13]  B. Knoops,et al.  Expression of peroxiredoxins in bovine oocytes and embryos produced in vitro , 2004, Molecular reproduction and development.

[14]  J. Juengel,et al.  The oocyte and its role in regulating ovulation rate: a new paradigm in reproductive biology. , 2004, Reproduction.

[15]  B. Pintado,et al.  Effect of speed of development on mRNA expression pattern in early bovine embryos cultured in vivo or in vitro , 2004, Molecular reproduction and development.

[16]  S. McGraw,et al.  Transcription Factor Expression Patterns in Bovine In Vitro-Derived Embryos Priorto Maternal-Zygotic Transition1 , 2004, Biology of reproduction.

[17]  R. Rajmon,et al.  Effect of proteasome inhibitor MG132 on in vitro maturation of pig oocytes , 2004, Zygote.

[18]  H. Schatten,et al.  Aurora-A Is a Critical Regulator of Microtubule Assembly and Nuclear Activity in Mouse Oocytes, Fertilized Eggs, and Early Embryos1 , 2004, Biology of reproduction.

[19]  Takashi Ito,et al.  SKIP modifies gene expression by affecting both transcription and splicing. , 2004, Biochemical and biophysical research communications.

[20]  F. Romero,et al.  Securin Is a Target of the UV Response Pathway in Mammalian Cells , 2004, Molecular and Cellular Biology.

[21]  P. Lonergan,et al.  Analysis of differential maternal mRNA expression in developmentally competent and incompetent bovine two‐cell embryos , 2004, Molecular reproduction and development.

[22]  A. Gutiérrez-Adán,et al.  Relative messenger RNA abundance in bovine oocytes collected in vitro or in vivo before and 20 hr after the preovulatory luteinizing hormone surge , 2003, Molecular reproduction and development.

[23]  A. Lamond,et al.  Identification of peptide inhibitors of pre-mRNA splicing derived from the essential interaction domains of CDC5L and PLRG1. , 2003, Nucleic acids research.

[24]  A. Castro,et al.  Cdc2-Cyclin B Triggers H3 Kinase Activation of Aurora-A in Xenopus Oocytes* , 2003, Journal of Biological Chemistry.

[25]  W. Yeung,et al.  Identification of mRNAs that are up-regulated after fertilization in the murine zygote by suppression subtractive hybridization. , 2003, Biochemical and biophysical research communications.

[26]  W. Hwang,et al.  Effects of protein source and energy substrates on the in vitro development of bovine embryos in a two-step culture system. , 2003, Journal of veterinary science.

[27]  R. Duronio,et al.  Histone mRNA expression: multiple levels of cell cycle regulation and important developmental consequences. , 2002, Current opinion in cell biology.

[28]  S. McGraw,et al.  Quantification of Cyclin B1 and p34cdc2 in Bovine Cumulus-Oocyte Complexes and Expression Mapping of Genes Involved in the Cell Cycle by Complementary DNA Macroarrays1 , 2002, Biology of reproduction.

[29]  S. McGraw,et al.  Quantification of Housekeeping Transcript Levels During the Development of Bovine Preimplantation Embryos1 , 2002, Biology of reproduction.

[30]  C. Wrenzycki,et al.  Effects of oocyte maturation regimen on the relative abundance of gene transcripts in bovine blastocysts derived in vitro or in vivo. , 2002, Reproduction.

[31]  M. Sirard,et al.  Effect of the Absence or Presence of Various Protein Supplements on Further Development of Bovine Oocytes During In Vitro Maturation1 , 2002, Biology of reproduction.

[32]  W. Tomek,et al.  Comparative analysis of protein synthesis, transcription and cytoplasmic polyadenylation of mRNA during maturation of bovine oocytes in vitro. , 2002, Reproduction in domestic animals = Zuchthygiene.

[33]  A. Gutiérrez-Adán,et al.  Analysis of Differential Messenger RNA Expression Between Bovine Blastocysts Produced in Different Culture Systems: Implications for Blastocyst Quality1 , 2002, Biology of reproduction.

[34]  R. Braw-Tal The initiation of follicle growth: the oocyte or the somatic cells? , 2002, Molecular and Cellular Endocrinology.

[35]  M. Matzuk,et al.  Functional analysis of oocyte-expressed genes using transgenic models , 2002, Molecular and Cellular Endocrinology.

[36]  M. Sirard,et al.  The effects of 17β-estradiol and protein supplement on the response to purified and recombinant follicle stimulating hormone in bovine oocytes , 2002, Zygote.

[37]  P. Lonergan,et al.  Consequences of bovine oocyte maturation, fertilization or early embryo development in vitro versus in vivo: Implications for blastocyst yield and blastocyst quality , 2002, Molecular reproduction and development.

[38]  M. Sirard,et al.  Manipulation of Follicular Development to Produce Developmentally Competent Bovine Oocytes1 , 2002, Biology of reproduction.

[39]  C. Wrenzycki,et al.  Effects of in vivo prematuration and in vivo final maturation on developmental capacity and quality of pre-implantation embryos. , 2002, Theriogenology.

[40]  H. Wang,et al.  Pds1 phosphorylation in response to DNA damage is essential for its DNA damage checkpoint function. , 2001, Genes & development.

[41]  M. Sirard Resumption of meiosis: mechanism involved in meiotic progression and its relation with developmental competence. , 2001, Theriogenology.

[42]  X. Shen,et al.  Human Cdc5, a regulator of mitotic entry, can act as a site-specific DNA binding protein. , 2000, Journal of cell science.

[43]  C. Robert,et al.  Subtractive hybridization used to identify mRNA associated with the maturation of bovine oocytes , 2000, Molecular reproduction and development.

[44]  E. Memili,et al.  Zygotic and embryonic gene expression in cow: a review of timing and mechanisms of early gene expression as compared with other species , 2000, Zygote.

[45]  E. Memili,et al.  Control of gene expression at the onset of bovine embryonic development. , 1999, Biology of reproduction.

[46]  P. Lonergan,et al.  Effect of time interval from insemination to first cleavage on the developmental characteristics, sex ratio and pregnancy rate after transfer of bovine embryos. , 1999, Journal of reproduction and fertility.

[47]  M. Mendenhall,et al.  Regulation of Cdc28 Cyclin-Dependent Protein Kinase Activity during the Cell Cycle of the Yeast Saccharomyces cerevisiae , 1998, Microbiology and Molecular Biology Reviews.

[48]  E. Zeinstra,et al.  Follicle‐stimulating hormone and growth hormone act differently on nuclear maturation while both enhance developmental competence of in vitro matured bovine oocytes , 1998, Molecular reproduction and development.

[49]  T. Hunt,et al.  Cyclin B2-null mice develop normally and are fertile whereas cyclin B1-null mice die in utero. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[50]  H. Callesen,et al.  OOCYTE GROWTH, CAPACITATION AND FINAL MATURATION IN CATTLE , 1997 .

[51]  W. B. Currie,et al.  Dynamics of maturation-promoting factor and its constituent proteins during in vitro maturation of bovine oocytes. , 1997, Biology of reproduction.

[52]  M. Sirard,et al.  Resumption of meiosis is initiated by the accumulation of cyclin B in bovine oocytes. , 1996, Biology of reproduction.

[53]  P. Hyttel,et al.  Bovine oocyte diameter in relation to maturational competence and transcriptional activity , 1995, Molecular reproduction and development.

[54]  M. Sirard,et al.  Oocyte and follicular morphology as determining characteristics for developmental competence in bovine oocytes , 1995, Molecular reproduction and development.

[55]  P. Lonergan,et al.  Effect of follicle size on bovine oocyte quality and developmental competence following maturation, fertilization, and culture in vitro , 1994, Molecular reproduction and development.

[56]  R. Schultz Regulation of zygotic gene activation in the mouse , 1993, BioEssays : news and reviews in molecular, cellular and developmental biology.

[57]  A. Lucas-Hahn,et al.  Fertilization and developmental competence of bovine oocytes derived from different categories of antral follicles , 1992, Molecular reproduction and development.

[58]  N. First,et al.  Embryonic transcription in in vitro cultured bovine embryos , 1991, Molecular reproduction and development.

[59]  S. Dieleman,et al.  Changes in oestradiol, progesterone and testosterone concentrations in follicular fluid and in the micromorphology of preovulatory bovine follicles relative to the peak of luteinizing hormone. , 1983, The Journal of endocrinology.

[60]  R. Moor,et al.  10 – REGULATION OF OOCYTE MATURATION IN MAMMALS , 1978 .