Department of Anatomy, Cornell University Medical College, New York, New York 10021.
Genetics. 1976 Jun;83(2):361-72. doi: 10.1093/genetics/83.2.361.
Recessive lethal or semilethal alleles at the T/t locus in the mouse generate new t-variants, with characteristics different from the parent allele at a rate of about 10(-3). Almost invariably the variant chromosome carries marker genes derived from the opposite parental chromosome. New t-mutations obtained in this way are sometimes recessive lethals that are indistinguishable from those in already known complementation groups. Most derived t-mutations are viable, however. This paper summarizes data on the rate and types of variants produced by members of each of the six lethal complementation groups, and by semilethal alleles. It appears that particular complementation groups preferentially generate certain types of variants, and that in general, the pattern of variant production runs "uphill," that is, to less abnormal states. The data are compatible with the hypothesis that t-mutations represent some extent of altered chromosome and that variants are produced by loss of abnormal material.
在小鼠的 T/t 基因座上,隐性致死或半致死等位基因以约 10^(-3)的速率产生具有与亲本等位基因不同特征的新 t-变体。几乎无一例外地,变体染色体携带来自相反亲本染色体的标记基因。以这种方式获得的新 t 突变有时是隐性致死的,与已经已知的互补群中的突变无法区分。然而,大多数衍生的 t 突变是可行的。本文总结了来自六个致死互补群中的每个成员以及半致死等位基因产生的变体的速率和类型的数据。似乎特定的互补群优先产生某些类型的变体,并且通常,变体产生的模式“向上”,即向更正常的状态发展。这些数据与 t 突变代表染色体发生某种程度改变的假设以及变体是通过丢失异常物质产生的假设是一致的。