Worm Breeder's Gazette 5(1): 8

These abstracts should not be cited in bibliographies. Material contained herein should be treated as personal communication and should be cited as such only with the consent of the author.

Genetic Studies of unc-93 III

I. Greenwald, B. Horvitz

Figure 1

We have been studying unc-93 III, a muscle mutant that reverts 
spontaneously (Newsletter, January 1979).  We have analyzed over 120 
spontaneous and mutagen-induced revertants and have found that they 
define three sites, two extragenic (sup-9 II and sup-10 X) and one 
intragenic (within .01%).  These studies have suggested that, although 
the e1500 mutation confers a striking phenotype, the phenotype that 
results from complete elimination of unc-93 gene product is wild-type. 
This hypothesis was originally based on three observations.  (1) 
Intragenic revertants are obtained after EMS treatment at a frequency 
of about 4 x 10+E4, which is the frequency at which mutations due to 
complete elimination of gene function arise in wild-type animals after 
EMS mutagenesis (Brenner, 1974).  (2) Only two visible alleles of unc-
93 have been detected (Nancy Tsung in this laboratory recently 
isolated n200, which is similar in phenotype to e1500 but weaker); 
thus, mutations in unc-93 that result in a detectable phenotype may be 
rare.  (3) All of the intragenic revertants are recessive, suggesting 
that they do not simply restore gene function: e1500/+ is essentially 
wild-type in phenotype, whereas heterozygotes for these intragenic 
revertants are uncoordinated and egg-laying defective.  Additional 
evidence now supports this model.  Like e1500/intragenic revertant, 
e1500/Df(unc-93) is uncoordinated and egg-laying defective; thus, 
intragenic revertants are genetically equivalent to deficiencies of 
unc-93, which are null alleles by definition.  We have also identified 
an intragenic revertant that is suppressed by sup-7(st5) X (a null 
allele suppressor; R.  Waterston, personal communication) to restore 
the mutant phenotype.  The two extragenic suppressors, sup-9 II and 
sup-10 X, are recessive and also arise with a frequency of about 4 x 
10+E4; they also appear to represent complete elimination of gene 
function and are candidates for regulatory loci.  Both of these fail 
to complement deficiencies for suppressor activity.  Studies with the 
null allele suppressor sup-5(e1464) III (Waterston and Brenner, 1978) 
are in progress.
[See Figure 1]

Figure 1