Analysis of the albino-locus region of the mouse. I. Origin and viability

Abstract

Numerous specific-locus experiments designed to test the mutagenic effect of external radiation have yielded, in over 3,600,000 animals observed, altogether 119 presumed mutations involving the c locus. Of these, 55 were viable and albino (c(av)), 13 were viable and of various intermediate pigment types (c(xv)), four were subvital (c(as) and c(xs)), seven were neonatally lethal albinos (c(al)), 28 prenatally lethal albinos (c(al)); 12 died untested. All of the prenatally lethal and at least one of the neonatally lethal c-locus mutations ((al) classes) are probably deficiencies that the authors have analyzed extensively in other experiments. Since absence of the locus mimics albino in phenotype, the intermediates (c(xv) and c(xs) groups) probably resulted from intragenic changes. The class of viable albino mutants (c(av)) might include, in addition to intragenic changes, some extremely small deficiencies. - The effects on viability of c-locus lethals (c(al)'s) in heterozygous condition are not drastic enough to be perceived in stocks of mixed genetic background except in the case of the longest known deficiencies and a few others. - Analysis of the relation between radiation treatment and type of c-locus mutants obtained shows that the relative frequency of viable mutations, for each germ-cell type, is greater for low-LET than for neutron irradiation; however, the difference for any individual cell type is not significant. The majority (66.7%) of mutations derived from X- or γ-ray irradiated spermatogonia are viable, and the proportion of 'intermediates' among these viables is similar to that among presumed spontaneous c-locus mutations. No significant dose-rate effect on the proportion of lethals could be demonstrated within the set of mutants induced by low-LET irradiation of spermatogonia. Although sets from other germ-cell stages are too small for statistical tests, the results for oocytes are similar, as far as they go. Furthermore, most of the c-locus mutations induced in spermatogonia, even by high-dose-rate X-ray or γ irradiation, are of a type most likely to result from single-track events (62% c(xv), c(xs), and c(av); plus 16% presumed deficiencies not involving the closest marker). These results support the view that most of the reduction in mutation frequency at low dose rates is not due to a change in relative proportion of two-track and one-track ionizing events.