Cloning and analysis of axolotl ISL2 and LHX2 LIM-homeodomain transcription factors

We cloned and characterized the ISL2 and LHX2 LIM‐homeodomain transcription factors of the Mexican salamander, or axolotl, Ambystoma mexicanum. Using a degenerate PCR approach, partial cDNAs representing five LIM‐homeodomain genes were cloned, indicating conservation of this class of transcription f...

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Published inGenesis (New York, N.Y. : 2000) Vol. 38; no. 3; pp. 110 - 121
Main Authors Showalter, Aaron D., Yaden, Benjamin C., Chernoff, Ellen A.G., Rhodes, Simon J.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.03.2004
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Summary:We cloned and characterized the ISL2 and LHX2 LIM‐homeodomain transcription factors of the Mexican salamander, or axolotl, Ambystoma mexicanum. Using a degenerate PCR approach, partial cDNAs representing five LIM‐homeodomain genes were cloned, indicating conservation of this class of transcription factors in urodeles. Full‐length cDNAs for Isl2 and Lhx2 were identified and sequenced. The predicted ISL2 and LHX2 proteins are well conserved, especially in the LIM and DNA‐binding domains. The Isl2 and Lhx2 genes are expressed at all examined stages of embryogenesis and display tissue‐restricted expression patterns in adults. In functional tests, axolotl LHX2 was inactive compared to homologous mammalian factors and adopted unusual DNA/protein complexes. However, axolotl ISL2 bound and induced transcription from the rat insulin gene. These experiments demonstrate conservation of key developmental regulatory proteins in salamanders and will allow future studies of their potential roles in the molecular regulation of tissue regeneration in such species. genesis 38:110–121, 2004. © 2004 Wiley‐Liss, Inc.
Bibliography:National Science Foundation (NSF)
ark:/67375/WNG-GM26LQ39-K
NIH and NSF
Indiana 21st Century Research and Technology Fund
istex:4B559F7467866DEADF069DB1751886B8AEBE9EC0
ArticleID:GENE20007
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
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ISSN:1526-954X
1526-968X
DOI:10.1002/gene.20007