Identification of transforming growth factor-β- regulated genes in Caenorhabditis elegans by differential hybridization of arrayed cDNAs
Author(s) -
Makoto Mochii,
Satoru Yoshida,
Kiyokazu Morita,
Yuji Kohara,
Naoto Ueno
Publication year - 1999
Publication title -
proceedings of the national academy of sciences
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.011
H-Index - 771
eISSN - 1091-6490
pISSN - 0027-8424
DOI - 10.1073/pnas.96.26.15020
Subject(s) - biology , caenorhabditis elegans , gene , in situ hybridization , microbiology and biotechnology , differential display , gene expression , genetics
Members of the transforming growth factor-β family play critical roles in body patterning, in both vertebrates and invertebrates. One transforming growth factor-β-related gene,dbl-1, has been shown to regulate body length and male ray patterning inCaenorhabditis elegans . We screened arrayed cDNAs to identify downstream target genes for the DBL-1 signaling by using differential hybridization.C. elegans cDNAs representing 7,584 independent genes were arrayed on a nylon membrane at high density and hybridized with33 P-labeled DNA probes synthesized from the mRNAs of wild-type,dbl-1 ,sma-2, andlon-2 worms. Signals for all the spots representing hybridized DNA were quantified and compared among strains. The screening identified 22 and 2 clones, which were positively and negatively regulated, respectively, by the DBL-1 signal. Northern hybridization confirmed the expression profiles of most of the clones, indicating good reliability of the differential hybridization using arrayed cDNAs.In situ hybridization analysis revealed the spatial and temporal expression patterns of each clone and showed that at least four genes, including the gene for the type I receptor for DBL-1,sma-6 , were transcriptionally regulated by the DBL-1 signal.
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