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Analysis of mRNA associated factors during bovine oocyte maturation and early embryonic development
Author(s) -
Siemer Corinna,
Smiljakovic Tatjana,
Bhojwani Monika,
Leiding Claus,
Kanitz Wilhelm,
Kubelka Michal,
Tomek Wolfgang
Publication year - 2009
Publication title -
molecular reproduction and development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.745
H-Index - 105
eISSN - 1098-2795
pISSN - 1040-452X
DOI - 10.1002/mrd.21096
Subject(s) - biology , eif4g , eif4e , microbiology and biotechnology , oocyte , phosphorylation , translational regulation , messenger rna , translational efficiency , kinase , embryo , translation (biology) , genetics , gene
Abstract Regulation of gene expression at the translational level is particularly essential during developmental periods, when transcription is impaired. According to the closed‐loop model of translational initiation, we have analyzed components of the 5´‐mRNA cap‐binding complex eIF4F (eIF4E, eIF4G, eIF4A), the eIF4E repressor 4E‐BP1, and 3´‐mRNA poly‐(A) tail‐associated proteins (PABP1 and 3, PAIP1 and 2, CPEB1, Maskin) during in vitro maturation of bovine oocytes and early embryonic development up to the 16‐cell stage. Furthermore, we have elucidated the activity of distinct kinases which are potentially involved in their phosphorylation. Major phosphorylation of specific target sequences of PKA, PKB, PKC, CDKs, ATM/ATR, and MAPK were observed in M II stage oocytes. Furthermore, main changes in the abundance and/or phosphorylation of distinct mRNA‐binding factors occur at the transition from M II stage oocytes to 2‐cell embryos. In conclusion, the results indicate that, at the transition from oocyte to embryonic development, translational initiation is regulated by striking differences in the abundance and/or phosphorylation of 5´‐end and 3´‐end mRNA associated factors, mainly the poly‐(A) bindings proteins PABP1 and 3, their repressor PAIP2 and a Maskin‐like protein with distinct eIF4E‐binding properties which prevents eIF4E/cap binding and eIF4F formation in vitro. Nevertheless, from the M II stage to 16‐cell embryos a substantial amount of eIF4E and, to a lesser extent, of eIF4G was precipitated by 7 m‐GTP‐Separose indicating eIF4F complex formation. Therefore, it is likely that in general the reduction in PABP1 and 3 abundance represses overall translation during early embryonic development. Mol. Reprod. Dev. 76: 1208–1219, 2009. © 2009 Wiley‐Liss, Inc.