Identification of transforming growth factor-beta-regulated genes in Caenorhabditis elegans by differential hybridization of arrayed cDNAs

Citation
M. Mochii et al., Identification of transforming growth factor-beta-regulated genes in Caenorhabditis elegans by differential hybridization of arrayed cDNAs, P NAS US, 96(26), 1999, pp. 15020-15025
Citations number
19
Categorie Soggetti
Multidisciplinary
Journal title
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
ISSN journal
00278424 → ACNP
Volume
96
Issue
26
Year of publication
1999
Pages
15020 - 15025
Database
ISI
SICI code
0027-8424(199912)96:26<15020:IOTGFG>2.0.ZU;2-7
Abstract
Members of the transforming growth factor-beta family play critical roles i n body patterning, in both vertebrates and invertebrates. One transforming growth factor-beta-related gene, dbl-1, has been shown to regulate body len gth and male ray patterning in Caenorhabditis 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 with P-33-labeled DNA probes synthesized from the mRNAs of wild-type, dbl-1, sm a-2 and Ion-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 hyb ridization 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 DBL1, sma- 6 were transcriptionally regulated by the DBL-1 signal.