Literature DB >> 14660442

A cell-specific enhancer that specifies lin-3 expression in the C. elegans anchor cell for vulval development.

Byung Joon Hwang1, Paul W Sternberg.   

Abstract

During C. elegans vulval development, the anchor cell (AC) in the somatic gonad expresses lin-3, activating the EGF receptor signaling pathway in vulval precursor cells (VPCs) and thereby inducing and patterning VPCs. Previous studies with lin-3 mutants and transgene expression have revealed that the level of LIN-3 in the AC must be precisely regulated for proper vulval development. To understand how lin-3 expression is achieved in the AC, we identified a 59 bp lin-3 enhancer sufficient to activate lin-3 transcription solely in the AC. The enhancer contains two E-box elements, and one FTZ-F1 nuclear hormone receptor (NHR) binding site that is mutated in a vulvaless mutant, lin-3(e1417). Mutagenesis studies show that both E-boxes and the NHR binding site are necessary to express lin-3 in the AC. In vitro DNA-binding studies and in vivo functional assays indicate that distinct trans-acting factors, including the E-protein/Daughterless homolog HLH-2 and unidentified nuclear hormone receptor(s), are necessary for lin-3 transcription in the AC and thus are involved in vulval development.

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Year:  2003        PMID: 14660442     DOI: 10.1242/dev.00924

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  49 in total

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7.  Evolution of Transcriptional Repressors Impacts Caenorhabditis Vulval Development.

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8.  LIN-12/Notch regulates lag-1 and lin-12 expression during anchor cell/ventral uterine precursor cell fate specification.

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9.  The Caenorhabditis elegans nuclear receptor gene nhr-25 regulates epidermal cell development.

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10.  The roles of EGF and Wnt signaling during patterning of the C. elegans Bgamma/delta Equivalence Group.

Authors:  Adeline Seah; Paul W Sternberg
Journal:  BMC Dev Biol       Date:  2009-12-31       Impact factor: 1.978

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