Worm Breeder's Gazette 9(3): 30
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.
We have continued to isolate and characterize mec mutants in TR679 [mut- 2(r459)]. Our progress to date is: {Figure 1} Thus, nine of the 16 genes for which we've obtained touch insensitive mutants are represented in this set. (In addition, we have isolated two unc-55 mutants and several unc-31 mutants in these TR679 screens.) The outcrossing and analysis of these mutations is in various degrees of completion. We have used these mutations to isolate the mec-3 gene (WBG 9 #1 p. 31) and the mec-14 gene (see this issue). In addition, a single Tc1-containing fragment cosegregates with the one mec-2 mutation so far studied. As indicated in the table, we have obtained spontaneous revertants in a number of the TR679-derived mec strains. Four of these were found by screening the original mec isolates before outcrossing. This was usually difficult as the strains were often unhealthy and had low brood sizes. Recently, however, we have taken advantage of the mut-2 mutator activity mapped near unc-13 by Mike Finney. By eliminating a unc-13(e51) chromosome, we made mut-2:mec doubles using outcrossed strains with spontaneous mutations in mec-2, lting strains were quite healthy and had reasonable brood sizes. All three strains have reverted to wild type will relative ease (i.e. a single afternoon's worth of screening). One advantage of this method is that Mec and nonMec siblings are often healthy enough to grow up to generate DNA for comparison.