Department of Zoology, University of Texas at Austin, Austin, Texas 78712.
Genetics. 1979 Jun;92(2):485-502. doi: 10.1093/genetics/92.2.485.
Mutants of the cut (ct) locus can be divided into two classes: viable and lethal. Most of the viable alleles are characterized by varying degrees of scalloping and notching of the wings. One mutant, kinked femur, exhibits kinking of the femurs and failure of wing expansion, but no other changes in wing structure. In heterozygous combination with the other viable alleles, it exhibits complete complementation, but it fails to complement with lethal ct alleles with respect to its viable phenotype. Similarly, all of the other viable ct alleles express a mutant wing phenotype when heterozygous with lethal ct alleles.-Mapping experiments indicate that the lethal alleles, which comprise the majority of all ct mutations recovered, are confined to a small region at the right end of the locus. That this restriction is real and not an artifact imposed by the limited number of lethal mutations mapped in the locus is supported by an examination of the mutant ct(JC20), a presumptive deficiency for the left-most third of the locus. Despite its behavior as a deletion, ct(JC20) is viable, though mutant, in combination with the lethal alleles. The restriction of the noncomplementary lethals to a small part of the locus, distinct from the other ct mutants, suggests a polarity that may define a segment that functions only in cis within the complex.-Based on the comparison of the data with the prediction of several models, we suggest that the left portion of the locus, which contains the viable alleles, defines a regulatory region controlling the expression of the locus, while the segment encoding a polypeptide product is at the right end and only it is capable of mutating to a lethal state.
ct 位点的突变可分为两类:存活和致死。大多数存活等位基因的特征是翅膀的不同程度的扇形和缺口。一种名为“弯曲股骨”的突变体表现为股骨弯曲和翅膀无法展开,但翅膀结构没有其他变化。在与其他存活等位基因的杂合组合中,它表现出完全互补,但与致死 ct 等位基因在其存活表型上不互补。同样,所有其他存活 ct 等位基因在与致死 ct 等位基因杂合时都表现出突变翅膀表型。-定位实验表明,大多数回收的 ct 突变都是致死等位基因,它们局限于位点右端的一个小区域。这种限制是真实的,而不是由定位到的致死突变数量有限所造成的假象,这一点得到了对突变 ct(JC20)的检查的支持,ct(JC20)是一个假定的位点最左边三分之一的缺失。尽管它表现为缺失,但 ct(JC20)与致死等位基因结合时是存活的,尽管是突变的。非互补致死等位基因限制在位点的一小部分,与其他 ct 突变体不同,这表明存在极性,可能定义了一个仅在复杂的顺式中发挥作用的片段。-基于对数据的比较和对几个模型的预测,我们提出,包含存活等位基因的位点的左部分定义了一个调控区域,控制着位点的表达,而编码多肽产物的片段位于右端,只有它能够突变为致死状态。