We are engaged in reversion study of par-2III, a maternal gene we reported earlier (WBG 9:2 p. 72). The ts mutation
it5 is used to screen for suppressors. Homozygous
it5 worms at 25 C give rise to 96% dead embryos. Less than 1% of the survivors are fertile. At 16 C, however, they produce 74% living progeny with 24% being fertile. Thus, the
it5 homozygous strain can be maintained at 16 C but is genetically lethal at 25 C. For suppressor hunting,
it5 worms are grown synchronously at 16 C on large plates with concentrated bacteria. The young hermaphrodites are collected and treated with EMS. Four to twelve hours after the treatment, they are hypochlorited to obtain a synchronous F1 population. The F1 embryos are distributed onto large plates and the number of L1's is estimated after hatching. When the F1's grow to adults, the worms are pooled and hypochlorited to obtain F2 embryos. The F2's are shifted to 25 C before they reach L4 stage (prior to oogenesis). After two generations at 25 C, F4's are cloned as putative revertant stocks. We have recovered seven putative revertants after screening about 67, 000 chromosomes, in eight independent mutageneses. The frequency of 1/10,000 is probably an underestimate of actual frequency, because we kept only one revertant from each successful mutagenesis. The healthiest revertant among the seven was chosen for further analysis. This revertant carries a new mutation,
it76, that is a dominant, extragenic suppressor to
it5. It maps to chromosome II to the left of
dpy-10, but we do not yet know its precise map position.
it76 restores viability and fertility of
it5 to nearly wild-type level. But unfortunately,
it76 alone has no obvious phenotype. We have tested the suppression specificities of
it76. It suppresses five par- 2 mutations thus far tested (
e2030,
it5,
it49,
it53 and
it58). However, it does not suppress
par-1(
b274), 2), 7) and
par-5(
it55). Therefore, the suppression of
it76 is gene specific to
par-2, but is allele nonspecific. Thus,
it76 is unlikely to be an informations suppressor and it may identify a gene that can be mutated to replace the wild-type function of
par-2.