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PMID: 9486792 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

The Hox gene lin-39 is required during C. elegans vulval induction to select the outcome of Ras signaling.

Development (Cambridge, England) ·Vol. 125 ·No. 2 ·1998-01-00 ·Pages 181-90

Maloof JN, Kenyon C

Abstract

The Ras signaling pathway specifies a variety of cell fates in many organisms. However, little is known about the genes that function downstream of the conserved signaling cassette, or what imparts the specificity necessary to cause Ras activation to trigger different responses in different tissues. In C. elegans, activation of the Ras pathway induces cells in the central body region to generate the vulva. Vulval induction takes place in the domain of the Hox gene lin-39. We have found that lin-39 is absolutely required for Ras signaling to induce vulval development. During vulval induction, the Ras pathway, together with basal lin-39 activity, up-regulates lin-39 expression in vulval precursor cells. We find that if lin-39 function is absent at this time, no vulval cell divisions occur. Furthermore, if lin-39 is replaced with the posterior Hox gene mab-5, then posterior structures are induced instead of a vulva. Our findings suggest that in addition to permitting vulval cell divisions to occur, lin-39 is also required to specify the outcome of Ras signaling by selectively activating vulva-specific genes.

MeSH Terms
Animals Caenorhabditis elegans/embryology,genetics Caenorhabditis elegans Proteins Disorders of Sex Development Embryonic Induction/genetics Female Gene Expression Genes, Homeobox/physiology Genes, ras/physiology Homeodomain Proteins/analysis,genetics,physiology Hot Temperature Male Mutation Signal Transduction/genetics Transcription Factors/genetics Vulva/cytology,embryology
Chemicals
Caenorhabditis elegans Proteins Homeodomain Proteins Mab-5 protein, C elegans Transcription Factors lin-39 protein, C elegans
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Maloof J N
Department of Biochemistry and Biophysics, University of California, San Francisco, 94143-0554, USA.
Kenyon C
Article Info
Journal
Development (Cambridge, England)
Abbr.
Development
ISSN
0950-1991
Published
1998-01-00
Pages
181-90
Language
English
Region
England
NLM ID
8701744
Subset
IM
Grants
NIGMS NIH HHS · R01 GM37053 · United States
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