TY - JOUR
T1 - Structure and expression of daf-12
T2 - A nuclear hormone receptor with three isoforms that are involved in development and aging in Caenorhabditis elegans
AU - Snow, Mark I.
AU - Larsen, Pamela L.
N1 - Funding Information:
We would like to thank Patricia Herd for technical assistance, Yuji Kohara for the yk104e5 clone, Andy Fire for the pPD95.73 GFP vector, Paul Sternberg for use of injection and photography equipment, Aidyl Gonzalez-Serricchio for advice on injections, Chieh Chang for help with photography, Mark Viney for advice on isolating RNA, Michael Stallcup and Hui Yu for critical reading of the manuscript, and Paul Sternberg and members of his and our laboratory for discussions and advice. This work was supported by a subcontract from University of Missouri on R01 AG12689-03 to P.L. and a Glenn/AFAR Fellowship to M.S.
PY - 2000/11/15
Y1 - 2000/11/15
N2 - During Caenorhabditis elegans early larval development environmental conditions promote a cascade of signaling molecules to direct growth to the reproductive adult or to arrest development as a dauer larva. Two parallel chemosensory signal transduction pathways, one of which is transforming growth factor (TGF)-β-like, converge on the daf-12 gene to regulate dauer formation. A third insulin-like signaling pathway interacts with the daf-12 pathway to regulate both dauer formation and adult longevity. To further understand the role of daf-12 in these processes, we have molecularly characterized this gene. We establish rescue of the mutant dauer defective phenotype with a genomic clone. We show that three transcripts of different lengths, due to differential splicing, are made from the daf-12 gene. The deduced protein isoforms are similar to both DNA- and ligand-binding domains of nuclear hormone receptors. The three daf-12 transcripts are produced throughout development and expression increases during the preparation for and execution of dauer formation. Analysis of various daf mutant strains suggests that the isoform ratios of daf-12 steady-state mRNA are not changed by reduction of function in the TGF-β and insulin signaling components of the dauer pathway. The daf-12 promoter directs expression of GFP in the pharynx. daf-12 is a C. elegans nuclear hormone receptor with multiple isoforms, is expressed throughout development in distinct cells, and functions under a variety of environmental conditions. Copyright (C) 2000 Elsevier Science B.V.
AB - During Caenorhabditis elegans early larval development environmental conditions promote a cascade of signaling molecules to direct growth to the reproductive adult or to arrest development as a dauer larva. Two parallel chemosensory signal transduction pathways, one of which is transforming growth factor (TGF)-β-like, converge on the daf-12 gene to regulate dauer formation. A third insulin-like signaling pathway interacts with the daf-12 pathway to regulate both dauer formation and adult longevity. To further understand the role of daf-12 in these processes, we have molecularly characterized this gene. We establish rescue of the mutant dauer defective phenotype with a genomic clone. We show that three transcripts of different lengths, due to differential splicing, are made from the daf-12 gene. The deduced protein isoforms are similar to both DNA- and ligand-binding domains of nuclear hormone receptors. The three daf-12 transcripts are produced throughout development and expression increases during the preparation for and execution of dauer formation. Analysis of various daf mutant strains suggests that the isoform ratios of daf-12 steady-state mRNA are not changed by reduction of function in the TGF-β and insulin signaling components of the dauer pathway. The daf-12 promoter directs expression of GFP in the pharynx. daf-12 is a C. elegans nuclear hormone receptor with multiple isoforms, is expressed throughout development in distinct cells, and functions under a variety of environmental conditions. Copyright (C) 2000 Elsevier Science B.V.
KW - Aging
KW - Dauer development
KW - Nuclear hormone receptor
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U2 - 10.1016/S0167-4781(00)00224-4
DO - 10.1016/S0167-4781(00)00224-4
M3 - Article
C2 - 11072073
AN - SCOPUS:0034670132
SN - 0167-4781
VL - 1494
SP - 104
EP - 116
JO - Biochimica et Biophysica Acta - Gene Structure and Expression
JF - Biochimica et Biophysica Acta - Gene Structure and Expression
IS - 1-2
ER -