Functional genomic analysis of cell division in C-elegans using RNAi of genes on chromosome III

被引:675
|
作者
Gönczy, P
Echeverri, C
Oegema, K
Coulson, A
Jones, SJM
Copley, RR
Duperon, J
Oegema, J
Brehm, M
Cassin, E
Hannak, E
Kirkham, M
Pichler, S
Flohrs, K
Goessen, A
Leidel, S
Alleaume, AM
Martin, C
Özlü, N
Bork, P
Hyman, AA
机构
[1] European Mol Biol Lab, D-69117 Heidelberg, Germany
[2] Sanger Ctr, Cambridge CB10 1SA, England
[3] British Columbia Canc Res Ctr, Genome Sequence Ctr, Vancouver, BC V5Z 4E6, Canada
[4] Max Planck Inst Cell Biol & Genet, D-01307 Dresden, Germany
关键词
D O I
10.1038/35042526
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Genome sequencing projects generate a wealth of information; however, the ultimate goal of such projects is to accelerate the identification of the biological function of genes. This creates a need for comprehensive studies to fill the gap between sequence and function. Here we report the results of a functional genomic screen to identify genes required for cell division in Caenorhabditis elegans. We inhibited the expression of similar to 96% of the similar to2,300 predicted open reading frames on chromosome III using RNA-mediated interference (RNAi). By using an in vivo time-lapse differential interference contrast microscopy assay, we identified 133 genes (similar to6%) necessary for distinct cellular processes in early embryos. Our results indicate that these genes represent most of the genes on chromosome III that are required for proper cell division in C. elegans embryos. The complete data set, including sample time-lapse recordings, has been deposited in an open access database. We found that similar to 47% of the genes associated with a differential interference contrast phenotype have clear orthologues in other eukaryotes, indicating that this screen provides putative gene functions for other species as well.
引用
收藏
页码:331 / 336
页数:6
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