Published February 15, 2010 | Version Accepted Version
Journal Article Open

C. elegans BED domain transcription factor BED-3 controls lineage-specific cell proliferation during organogenesis

  • 1. ROR icon National University of Singapore
  • 2. ROR icon California Institute of Technology

Abstract

The control of cell division is critical to organogenesis, but how this control is achieved is not fully understood. We found that mutations in bed-3, encoding a BED Zn-finger domain transcription factor, confer a phenotype where a specific set of cell divisions during vulval organogenesis is lost. Unlike general cell cycle regulators in Caenorhabditis elegans, the function of bed-3 is restricted to specific lineages. Transcriptional reporters suggest that bed-3 is expressed in a limited number of cell types including vulval cells whose divisions are affected in bed-3 mutants. A bed-3 mutation also affects the expression pattern of the cdh-3 cadherin gene in the vulva. The phenotype of bed-3 mutants is similar to the phenotype caused by mutations in cog-1 (Nkx6), a component of a gene regulatory network controlling cell type specific gene expression in the vulval lineage. These results suggest that bed-3 is a key component linking the gene regulatory network controlling cell-type specification to control of cell division during vulval organogenesis.

Additional Information

© 2009 Elsevier Inc. Received 22 April 2009; revised 9 November 2009; accepted 4 December 2009. Available online 17 December 2009. We thank J. Gruber, Ng L.F., B. Halliwell, Shen Y.Q. and Fu X.Y. for assistance and resources at NUS. We thank J. Fernandes and T. Ririe for comments on the manuscript, and members of the Sternberg laboratory for helpful discussions. T.I. was supported by fellowship DRG-1646 from the Damon Runyon Cancer Research Foundation. This work was supported by the HHMI, with which P.W.S. is an investigator. Some nematode strains used in this work were provided by the Caenorhabditis Genetics Center, which is funded by the NIH National Center for Research Resources (NCRR).

Attached Files

Accepted Version - nihms177815.pdf

Files

nihms177815.pdf

Files (1.6 MB)

Name Size
md5:20141ec35e101f2329372936a1144fa6
1.6 MB Preview Download

Additional details

Identifiers

PMCID
PMC2862168
Eprint ID
17638
DOI
10.1016/j.ydbio.2009.12.005
Resolver ID
CaltechAUTHORS:20100303-094838992

Related works

Funding

Damon Runyon Cancer Research Foundation
DRG-1646
Howard Hughes Medical Institute (HHMI)
NIH

Dates

Created
2010-03-11
Created from EPrint's datestamp field
Updated
2021-11-08
Created from EPrint's last_modified field