Author
Listed:
- Pierre Gönczy
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG)
Swiss Institute for Experimental Cancer Research (ISREC))
- Christophe Echeverri
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG)
European Molecular Biology Laboratory (EMBL)
Cenix BioScience GmbH)
- Karen Oegema
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG)
European Molecular Biology Laboratory (EMBL))
- Alan Coulson
(The Sanger Centre, Wellcome Trust Genome Campus)
- Steven J. M. Jones
(Genome Sequence Centre, British Columbia Cancer Research Centre)
- Richard R. Copley
(European Molecular Biology Laboratory (EMBL))
- John Duperon
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG))
- Jeff Oegema
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG))
- Michael Brehm
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG)
Cenix BioScience GmbH)
- Etienne Cassin
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG))
- Eva Hannak
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG))
- Matthew Kirkham
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG))
- Silke Pichler
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG)
European Molecular Biology Laboratory (EMBL))
- Kathrin Flohrs
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG))
- Anoesjka Goessen
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG))
- Sebastian Leidel
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG))
- Anne-Marie Alleaume
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG)
Cenix BioScience GmbH)
- Cécilie Martin
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG)
Cenix BioScience GmbH)
- Nurhan Özlü
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG))
- Peer Bork
(European Molecular Biology Laboratory (EMBL))
- Anthony A. Hyman
(Max-Planck-Institute for Cell Biology and Genetics (MPI-CBG)
European Molecular Biology Laboratory (EMBL))
Abstract
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 ∼96% of the ∼2,300 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 (∼6%) 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 ∼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.
Suggested Citation
Pierre Gönczy & Christophe Echeverri & Karen Oegema & Alan Coulson & Steven J. M. Jones & Richard R. Copley & John Duperon & Jeff Oegema & Michael Brehm & Etienne Cassin & Eva Hannak & Matthew Kirkham, 2000.
"Functional genomic analysis of cell division in C. elegans using RNAi of genes on chromosome III,"
Nature, Nature, vol. 408(6810), pages 331-336, November.
Handle:
RePEc:nat:nature:v:408:y:2000:i:6810:d:10.1038_35042526
DOI: 10.1038/35042526
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