Pleiotropy refers to the phenomenon in which a single gene controls several distinct, and seemingly unrelated, phenotypic effects. We use C. elegans early embryogenesis as a model to conduct systematic studies of pleiotropy. We analyze high-throughput RNA interference (RNAi) data from C. elegans and identify “phenotypic signatures”, which are sets of cellular defects indicative of certain biological functions. By matching phenotypic profiles to our identified signatures, we assign genes with complex phenotypic profiles to multiple functional classes. Overall, we observe that pleiotropy occurs extensively among genes involved in early embryogenesis, and a small proportion of these genes are highly pleiotropic. We hypothesize that genes involved in early embryogenesis are organized into partially overlapping functional modules, and that pleiotropic genes represent “connectors” between these modules. In support of this hypothesis, we find that highly pleiotropic genes tend to reside in central positions in protein-protein interaction networks, suggesting that pleiotropic genes act as connecting points between different protein complexes or pathways.
Systematic Analysis of Pleiotropy in C. elegans Early Embryogenesis
L. Zou,Sira Sriswasdi,B. Ross,Patrycja Vasilyev Missiuro,Jun S. Liu,Hui Ge
Published 2008 in PLoS Comput. Biol.
ABSTRACT
PUBLICATION RECORD
- Publication year
2008
- Venue
PLoS Comput. Biol.
- Publication date
2008-02-01
- Fields of study
Biology, Medicine, Computer Science
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
CITATION MAP
EXTRACTION MAP
CLAIMS
- No claims are published for this paper.
CONCEPTS
- No concepts are published for this paper.
REFERENCES
Showing 1-26 of 26 references · Page 1 of 1
CITED BY
Showing 1-31 of 31 citing papers · Page 1 of 1