Identification of tightly regulated groups of genes during Drosophila melanogaster embryogenesis

被引:56
作者
Hooper, Sean D.
Boue, Stephanie
Krause, Roland
Jensen, Lars J.
Mason, Christopher E.
Ghanim, Murad
White, Kevin P.
Furlong, Eileen E. M.
Bork, Peer
机构
[1] European Mol Biol Lab, Struct & Computat Biol Unit, D-69117 Heidelberg, Germany
[2] Max Planck Inst Mol Genet, Dept Vingron, Berlin, Germany
[3] Max Planck Inst Infect Biol, Dept Zychlinsky, Berlin, Germany
[4] Yale Univ, Sch Med, Dept Genet, New Haven, CT 06510 USA
关键词
Drosophila embryogenesis; Notch pathway; supervised clustering; transient expression; EXPRESSION; NETWORKS; GENOME; CYCLE; MAP;
D O I
10.1038/msb4100112
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Time-series analysis of whole-genome expression data during Drosophila melanogaster development indicates that up to 86% of its genes change their relative transcript level during embryogenesis. By applying conservative filtering criteria and requiring 'sharp' transcript changes, we identified 1534 maternal genes, 792 transient zygotic genes, and 1053 genes whose transcript levels increase during embryogenesis. Each of these three categories is dominated by groups of genes where all transcript levels increase and/or decrease at similar times, suggesting a common mode of regulation. For example, 34% of the transiently expressed genes fall into three groups, with increased transcript levels between 2.5-12, 11-20, and 15-20 h of development, respectively. We highlight common and distinctive functional features of these expression groups and identify a coupling between downregulation of transcript levels and targeted protein degradation. By mapping the groups to the protein network, we also predict and experimentally confirm new functional associations.
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页数:11
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