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
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.