CGC Bibliography Paper 5557

The Caenorhabditis elegans presenilin sel-12 is required for mesodermal patterning and muscle function.

Eimer S, Donhauser R, Baumeister R

Medline:
12413907
Citation:
Developmental Biology 251: 178-192 2002
Type:
ARTICLE
Genes:
cog-2 egl-15 hlh-8 hop-1 lin-12 myo-3 sel-12 ttx-3 unc-54
Abstract:
Mutations in presenilin genes impair Notch signalling and, in humans, have been implicated in the development of familial Alzheimer's disease. We show here that a reduction of the activity of the Caenorhabditis elegans presenilin sel-12 results in a late defect during sex muscle development. The morphological abnormalities and functional deficits in the sex muscles contribute to the egg-laying defects seen in sel-12 hermaphrodites and to the severely reduced mating efficiency of sel-12 males. Both defects can be rescued by expressing sel-12 from the h1h-8 promoter that is active during the development of the sex muscle-specific M lineage, but not by expressing sel-12 from late muscle-specific promoters. Both weak and strong sel-12 mutations cause defects in the sex muscles that resemble the defects we found in lin-12 hypomorphic alleles, suggesting a previously uncharacterised LIN-12 signalling event late in postembryonic mesoderm development. Together with a previous study indicating a role of lin-12 and sel-12 during the specification of the pi cell lineage required for proper vulva-uterine connection, our data suggest that the failure of sel-12 animals to lay eggs properly is caused by defects in at least two independent signalling events in different