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黑腹果蝇中Dras3 - 粗糙 - 无蜕皮激素染色体区域(62B3 - 4至62D3 - 4)的遗传学:隐性致死突变分析

The genetics of the Dras3-Roughened-ecdysoneless chromosomal region (62B3-4 to 62D3-4) in Drosophila melanogaster: analysis of recessive lethal mutations.

作者信息

Sliter T J, Henrich V C, Tucker R L, Gilbert L I

机构信息

Department of Biology, University of North Carolina, Chapel Hill 27599-3280.

出版信息

Genetics. 1989 Oct;123(2):327-36. doi: 10.1093/genetics/123.2.327.

Abstract

The genetic organization of interval 62B3-4 to 62D3-4 on the Drosophila third chromosome was investigated. The region (designated DRE) includes four known loci: Roughened (R; 3-1.4), defined by a dominant mutation disrupting eye morphology; the nonvital locus Aprt, structural gene for adenine phosphoribosyltransferase; Dras3, a homolog of the vertebrate ras oncogene; and 1(3)ecdysoneless (1(3)ecd), a gene that has been implicated in the regulation of larval molting hormone (ecdysteroid) synthesis. Overlapping chromosomal deletions of the region were generated by gamma-ray-induced reversion of the R mutation. Recessive lethal mutations were isolated based upon failure to complement the recessive lethality of Df(3L)RR2, a deletion of the DRE region that removes 16-18 polytene chromosome bands. A total of 117 mutations were isolated following ethyl methanesulfonate and gamma-ray mutagenesis. These and two additional define 13 lethal complementation groups. Mutations at two loci were recovered at disproportionately high rates. One of these loci is preferentially sensitive to radiation-induced mutational alterations. Additionally, an unusually low recovery rate for cytologically detectable rearrangement breakpoints within the gamma-ray-sensitive locus suggests that an interval of the DRE region closely linked to the R locus may be dominantly sensitive to position effects. Lethal phase analysis of mutant hemizygotes indicates that a high proportion of DRE-region loci (11 of 13) are necessary for larval development. Mutations in five loci cause predominantly first-instar larval lethality, while mutations in four other loci cause predominantly second-instar lethality. Mutations in two loci cause late-larval lethality associated with abnormal imaginal disc development. A temperature-sensitive allele of one newly identified complementation group blocks ecdysteroid-induced pupariation. This developmental block is overcome by dietary 20-hydroxyecdysone, suggesting that a second locus in the region in addition to l(3)ecd may play a role in the regulation of late larval ecdysteroid levels.

摘要

对果蝇第三染色体上62B3 - 4至62D3 - 4区间的基因组织进行了研究。该区域(命名为DRE)包括四个已知基因座:粗糙(R;3 - 1.4),由一个破坏眼睛形态的显性突变所定义;非必需基因座Aprt,腺嘌呤磷酸核糖转移酶的结构基因;Dras3,脊椎动物ras癌基因的同源物;以及1(3)无蜕皮激素(1(3)ecd),一个与幼虫蜕皮激素(蜕皮甾类)合成调控有关的基因。通过γ射线诱导R突变的回复产生了该区域的重叠染色体缺失。基于不能互补Df(3L)RR2的隐性致死性分离出隐性致死突变,Df(3L)RR2是DRE区域的一个缺失,它去除了16 - 18条多线染色体带。在甲磺酸乙酯和γ射线诱变后共分离出117个突变。这些突变以及另外两个突变定义了13个致死互补群。在两个基因座上的突变以不成比例的高频率被回收。其中一个基因座对辐射诱导的突变改变特别敏感。此外,在γ射线敏感基因座内细胞学可检测的重排断点的回收率异常低,这表明与R基因座紧密连锁的DRE区域的一个区间可能对位置效应具有显性敏感性。突变半合子的致死期分析表明,DRE区域的大部分基因座(13个中的11个)对幼虫发育是必需的。五个基因座中的突变主要导致一龄幼虫致死,而其他四个基因座中的突变主要导致二龄幼虫致死。两个基因座中的突变导致与异常成虫盘发育相关的晚期幼虫致死。一个新鉴定的互补群的温度敏感等位基因阻断蜕皮甾类诱导的化蛹。这种发育阻断可通过添加20 - 羟基蜕皮酮的饮食克服,这表明该区域除了1(3)ecd之外的第二个基因座可能在晚期幼虫蜕皮甾类水平的调控中起作用。

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