Russell P J, Srb A M
Genetics. 1972 Jun;71(2):233-45. doi: 10.1093/genetics/71.2.233.
When homozygous in zygotes, mutant alleles at the peak locus in linkage group V of Neurospora crassa initiate aberrant asci that are nonlinear, in contrast to the linear asci characteristic of wild type. Most mutant alleles are recessive, inasmuch as crosses of the mutant strains with wild type give linear asci. However, five different mutant alleles, when heterozygous with the wild-type allele, act in varying degrees as zygote dominants, initiating both linear and nonlinear asci, the relative proportions depending on the allele. Five modifiers that act on the dominance relationships of at least one of the five possible heterozygotes of a dominant peak and its wild-type allele have been characterized, four of them having been obtained by selection directed against a phenocopy of these mutants induced by treatment of wild type with l-sorbose. The pattern of modifier specificity observed among the various dominant peak heterozygotes indicates that the phenotypic effects are produced by a complex relationship between the modifiers and the dominant peak alleles in relation to their wild-type allele. In all but two cases the direction of modification, where present, is towards decreasing the dominance of the mutant allele in the heterozygote, evidenced by an increase in the percentage of linear asci when compared with control data. The modifiers exert their maximum modification when they themselves are heterozygous with their wild-type alleles and when the dominant peak allele is heterozygous with its wild-type allele. No modification occurs when heterozygous modifiers are included in zygotes homozygous for a dominant peak allele, reinforcing the notion that the modifiers act on the dominance relationship existent between a dominant peak allele and its wild-type allele, rather than influencing some activity of the mutant allele itself. The modifiers have no detectable effect of their own on ascus morphology, since homozygous modifier zygotes initiate entirely linear asci when only wild-type alleles of peak are present in the zygotes. Their only detectable effect, other than dominance modification, appears to be in conferring sorbose resistance to the mycelium. The modifiers are unlinked to the peak locus, and, except for two of them, they are nonallelic.
在粗糙脉孢菌的V连锁群中,当合子为纯合子时,位于峰值位点的突变等位基因会引发异常的子囊,这些子囊是非线性的,这与野生型的线性子囊特征形成对比。大多数突变等位基因是隐性的,因为突变菌株与野生型杂交会产生线性子囊。然而,五个不同的突变等位基因与野生型等位基因杂合时,在不同程度上表现为合子显性,会引发线性和非线性子囊,其相对比例取决于等位基因。已经鉴定出五个修饰基因,它们作用于一个显性峰值及其野生型等位基因的五个可能杂合子中至少一个的显性关系,其中四个是通过针对用L -山梨糖处理野生型诱导的这些突变体的拟表型进行选择而获得的。在各种显性峰值杂合子中观察到的修饰基因特异性模式表明,表型效应是由修饰基因与显性峰值等位基因相对于其野生型等位基因之间的复杂关系产生的。除了两个案例外,在所有存在修饰的情况下,修饰的方向都是降低杂合子中突变等位基因的显性,与对照数据相比,线性子囊的百分比增加证明了这一点。当修饰基因自身与其野生型等位基因杂合且显性峰值等位基因与其野生型等位基因杂合时,修饰基因发挥最大修饰作用。当杂合修饰基因包含在显性峰值等位基因纯合的合子中时,不会发生修饰,这强化了修饰基因作用于显性峰值等位基因与其野生型等位基因之间存在的显性关系,而不是影响突变等位基因本身某些活性的观点。修饰基因自身对子囊形态没有可检测到的影响,因为当合子中仅存在峰值的野生型等位基因时,纯合修饰基因合子会引发完全线性化的子囊。除了显性修饰外,它们唯一可检测到的影响似乎是赋予菌丝体山梨糖抗性。修饰基因与峰值位点不连锁,并且除了其中两个外,它们是非等位的。