Department of Biology, Princeton University, Princeton, New Jersey 08544.
Genetics. 1983 Apr;103(4):617-31. doi: 10.1093/genetics/103.4.617.
The X-chromosome:autosome balance in D. melanogaster appears to control both sex determination and dosage compensation through effects on a maternally influenced sex-linked gene called Sex-lethal (Sxl; 1-19.2). To facilitate molecular and genetic analysis of Sxl, we attempted to determine the locations of all ethyl methanesulfonate (EMS)-mutable genes vital to both sexes in the region between 6E1 and 7B1. This area includes approximately 1 cM of the genetic map on each side of Sxl and was reported by C. B. Bridges to contain 26 salivary gland polytene chromosome bands. The region appears rather sparsely populated with genes vital to both sexes, since the 122 recessive lethal mutations we recovered fell into only nine complementation groups. From one to 38 alleles of each gene were recovered. There was a preponderance of embryonic lethals in this area, although the lethal periods of loss-of-function mutations included larval, pupal and adult stages as well. Since the screen required that mutations be recessive and lethal to males, our failure to recover new Sxl alleles was the result expected for a gene with a female-specific function. An attempt was made to identify recessive male-specific lethals in this region, but none were found. Precise map positions were determined for eight of the nine vital genes. An interesting feature of the map is the location of Sxl in the middle of a 0.6- to 0.7-cM interval that appears to be devoid of genes vital to both sexes. The genetic location was determined of breakpoints near Sxl for all available chromosome rearrangements. Sxl is most likely located just to the left of band 7A1. We determined the relationship of our EMS-induced mutations in these nine genes to alleles induced by others. From this we conclude that the various genes appear to differ significantly from each other in their relative sensitivity to mutation by EMS vs. X rays.
X 染色体:在 D. melanogaster 中,常染色体与 X 染色体的平衡似乎通过影响一个母源性的性连锁基因(称为 Sex-lethal,Sxl;1-19.2)来控制性别决定和剂量补偿。为了促进 Sxl 的分子和遗传分析,我们试图确定位于 Sxl 两侧的 6E1 和 7B1 之间的区域中对两性都至关重要的所有乙基甲磺酸乙酯(EMS)可突变基因的位置。该区域大约包含 Sxl 两侧遗传图谱的 1cM,据 C. B. Bridges 报道,该区域包含 26 个唾腺多线染色体带。由于我们回收的 122 个隐性致死突变仅分为九个互补群,因此该区域对于两性都至关重要的基因似乎相对稀少。每个基因都有 1 到 38 个等位基因。该区域以胚胎致死为主,尽管功能丧失突变的致死期也包括幼虫、蛹和成虫阶段。由于该筛选要求突变是隐性的并且对雄性致死,因此我们未能回收新的 Sxl 等位基因是该基因具有雌性特异性功能的预期结果。该区域也尝试鉴定隐性雄性特异性致死,但未发现。九个关键基因中的八个确定了精确的图谱位置。图谱的一个有趣特征是 Sxl 位于一个 0.6-0.7cM 间隔的中间,该间隔似乎没有对两性都至关重要的基因。确定了 Sxl 附近所有现有染色体重排的断裂点的遗传位置。Sxl 最有可能位于 7A1 带的左侧。我们确定了这九个基因中 EMS 诱导突变与其他诱导突变的等位基因之间的关系。由此我们得出结论,与 X 射线相比,各种基因在对 EMS 突变的相对敏感性方面似乎差异很大。