Worm Breeder's Gazette 11(2): 115

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.

A Screen for Male-Specific Uncs Yields a New Ray Mutation

Marie E. Sutherlin and Scott W. Emmons

We have isolated a new T-ray defective mutation, bx59, in a screen 
for male-specific Uncs.  bx59 is a recessive mutation that results in 
loss of rays 7-9 and ray 5.  The mutant phenotype is fully penetrant, 
but has variable expressivity.  Thus, every homozygous male exhibits 
some ray loss.  Other rays are missing a low percentage of the time.  
An Unc phenotype (male-specific coiling, starting from the tail) has 
segregated with the Mab defect.  bx59 has been localized to the left 
of dpy-17 on LGIII.  We are currently investigating the nature of this 
mutation (i.e.  lineage defect, ray attachment defect, etc.), but we 
have no data on this at the present time.
The male-specific Unc screen was suggested to us by the observation 
that, in addition to loss of T rays, mab-19(bx38) males coiled 
transiently at a higher frequency and for a longer duration than him-5(
e1490) males (for a description of mab-19(bx38), see the accompanying 
article).  We observed what may be anomalous mating behavior: mab-19(
bx38) males are unable to efficiently flip around the ends of moving 
hermaphrodites during the backward search for the vulva and end up 
coiling upon themselves, starting from the tail.  mab-19(bx38) males 
are almost infertile, possibly due to a mating defect.  We wanted to 
correlate the infertility and coiling phenotype with the loss of the T-
derived rays.  We tried ablating T.a in him-5(e1490) males, but found 
no difference in the frequency with which wild-type or surgically 
altered males coiled on mating plates.  Surgically altered males 
produced cross progeny (but fewer than wild-type males), whereas mab-
19(bx38) males did not.  Therefore, loss of T-rays alone did not 
account for the infertility.
We then attempted to isolate Mab mutants on the basis of male-
specific coiling in clonal populations from mutagenized hermaphrodites.
F1 hermaphrodite progeny of EMS-mutagenized animals [him-5(e1490)] 
were picked separately to 35mm seeded plates.  F1 populations were 
scored at 12x for male-specific coiling.  15 plates out of 
approximately 750 contained males that were coiling more than control 
him-5(e1490) plates.  Males from each of these plates were scored at 
400x on agar pads.  Of the 15, two plates contained severely Mab males 
(blunt, rounded tail phenotypes).  Another plate contained males that 
had lumpy rays (Ram phenotype).  A single plate contained males that 
were missing T-derived rays (bx59).  The other 11 plates did not 
contain males with any obvious Mab phenotype.
Since we were able to find only a few plates that seemed to contain 
male-specific coilers, and of these, almost 25% contained animals that 
exhibited an obvious Mab phenotype, it appears that the premise of the 
male-specific Unc screen may have been correct.  Since one of the 
mutations isolated resulted in loss of the T-derived rays, it is 
possible that the T rays may be necessary for flipping around the end 
of the hermaphrodite during the search for the vulva.  However, bx59 
males are more fertile than mab-19(bx38) males, although we have not 
performed any mating efficiency tests to date.