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On the Components of Segregation Distortion in DROSOPHILA MELANOGASTER. III. Nature of Enhancer of Sd

机译:关于果蝇的分离畸变的组成。三 Sd增强剂的性质

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摘要

Analysis of X-ray-induced deletions in the Segregation Distorter (SD) chromosome, SD-5, revealed that this chromosome had a gene proximal to lt in the centric heterochromatin of 2L that strongly enhanced the meiotic drive caused by the SD chromosome. This Enhancer of Segregation Distortion [E(SD)] locus had not been characterized in earlier studies of SD chromosomes because it cannot be readily separated by recombination from the Responder (Rsp) locus in the proximal heterochromatin of 2R.—To determine whether E(SD) is a general component of all SD chromosomes and to examine further its effects on distortion, we produced deletions of E(SD) in three additional SD chromosomes. Analysis of these deletions leads to the following conclusions: (1) along with Sd and Rsp, E(SD) is common to all SD chromosomes; (2) the E(SD) allele on each SD chromosome enhances distortion by the same amount, which indicates that allelic variation at the E(SD) locus is not responsible for the different drive strengths seen among SD chromosomes; (3) E(SD) causes very little or no distortion by itself in the absence of Sd; (4) E(SD), like Sd, acts in a dosage-dependent manner; (5) E(SD) exerts its effect in cis or trans to Sd; and (6) if E(SD)+ exists, its function is not related to SD.
机译:X射线诱导的偏析畸变(SD)染色体SD-5的缺失分析表明,该染色体在2L中心异染色质中的lt附近有一个基因,该基因强烈增强了SD染色体导致的减数分裂驱动。这种分离失真增强子[E(SD)]基因座在早期的SD染色体研究中并未得到表征,因为它无法通过重组与2R近端异染色质的响应者(Rsp)基因座轻易地分离。 SD)是所有SD染色体的一般组成部分,为了进一步检查其对畸变的影响,我们在另外三个SD染色体中产生了E(SD)缺失。对这些缺失的分析得出以下结论:(1)与Sd和Rsp一起,E(SD)对所有 SD 染色体都是通用的; (2)每条 SD 染色体上的 E(SD)等位基因会增加相同程度的畸变,这表明 E(SD)处的等位基因变异基因座与 SD 染色体中不同的驱动强度无关。 (3)在没有 Sd 的情况下, E(SD)自身几乎不会或不会引起失真; (4) E(SD) Sd 一样,以剂量依赖性方式起作用; (5) E(SD) cis trans 中对 Sd 发挥作用; (6)如果 E(SD) + 存在,则其功能与 SD 不相关。

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