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Article . 2007 . Peer-reviewed
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A novel eIF4G homolog, Off-schedule, couples translational control to meiosis and differentiation inDrosophilaspermatocytes

Authors: Tina M. Franklin-Dumont; Steven A. Wasserman; Stephen DiNardo; Chandrima Chatterjee;

A novel eIF4G homolog, Off-schedule, couples translational control to meiosis and differentiation inDrosophilaspermatocytes

Abstract

During spermatogenesis, cells coordinate differentiation with the meiotic cell cycle to generate functional gametes. We identified a novel gene, which we named off-schedule (ofs), as being essential for this coordinated control. During the meiotic G2 phase, Drosophila ofs mutant germ cells do not reach their proper size and fail to execute meiosis or significant differentiation. The accumulation of four cell cycle regulators-Cyclin A, Boule, Twine and Roughex-is altered in these mutants,indicating that ofs reveals a novel branch of the pathway controlling meiosis and differentiation. Ofs is homologous to eukaryotic translation initiation factor eIF4G. The level of ofs expression in spermatocytes is much higher than for the known eIF4G ortholog (known as eIF-4G or eIF4G),suggesting that Ofs substitutes for this protein. Consistent with this, assays for association with mRNA cap complexes, as well as RNA-interference and phenotypic-rescue experiments, demonstrate that Ofs has eIF4G activity. Based on these studies, we speculate that spermatocytes monitor G2 growth as one means to coordinate the initiation of meiotic division and differentiation.

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Keywords

Male, Sequence Homology, Amino Acid, Gene Expression Regulation, Developmental, Cell Differentiation, Cyclin A, Spermatids, Animals, Genetically Modified, Meiosis, Gene Expression Regulation, Spermatocytes, Protein Biosynthesis, Animals, Drosophila Proteins, Drosophila, Tissue Distribution, Eukaryotic Initiation Factor-4G, Eye Proteins, Cells, Cultured

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    citations
    This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    37
    popularity
    This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
    Top 10%
    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
    Top 10%
    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
    Top 10%
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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
37
Top 10%
Top 10%
Top 10%
bronze