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关于黑腹果蝇分离畸变的组成部分。

On the components of segregation distortion in Drosophila melanogaster.

作者信息

Ganetzky B

出版信息

Genetics. 1977 Jun;86(2 Pt. 1):321-55.

Abstract

The segregation distorter (SD) complex is a naturally occurring meiotic drive system with the property that males heterozygous for an SD-bearing chromosome 2 and an SD(+)-bearing homolog transmit the SD-bearing chromosome almost exclusively. This distorted segregation is the consequence of an induced dysfunction of those sperm that receive the SD(+) homolog. From previous studies, two loci have been implicated in this phenomenon: the Sd locus which is required to produce distortion, and the Responder (Rsp) locus that is the site at which Sd acts. There are two allelic alternatives of Rsp-sensitive (Rsp(sens)) and insensitive (Rsp(ins)); a chromosome carrying Rsp(ins) is not distorted by SD. In the present study, the function and location of each of these elements was examined by a genetic and cytological characterization of X-ray-induced mutations at each locus. The results indicate the following: (1) the Rsp locus is located in the proximal heterochromatin of 2R; (2) a deletion for the Rsp locus renders a chromosome insensitive to distortion; (3) the Sd locus is located to the left of pr (2-54.5), in the region from 37D2-D7 to 38A6-B2 of the salivary chromosome map; (4) an SD chromosome deleted for Sd loses its ability to distort; (5) there is another important component of the SD system, E(SD), in or near the proximal heterochromatin of 2L, that behaves as a strong enhancer of distortion. The results of these studies allow a reinterpretation of results from earlier analyses of the SD system and serve to limit the possible mechanisms to account for segregation distortion.

摘要

分离畸变(SD)复合体是一种自然存在的减数分裂驱动系统,其特性是携带SD染色体2的杂合雄性与携带SD(+)同源染色体的雄性几乎只传递携带SD的染色体。这种分离畸变是那些接收SD(+)同源染色体的精子功能异常所致。根据以往的研究,有两个基因座与这一现象有关:产生畸变所需的Sd基因座,以及Sd作用的位点应答者(Rsp)基因座。Rsp有敏感(Rsp(sens))和不敏感(Rsp(ins))两种等位基因变体;携带Rsp(ins)的染色体不会被SD畸变。在本研究中,通过对每个基因座X射线诱导突变的遗传和细胞学特征分析,研究了这些元件各自的功能和位置。结果表明:(1)Rsp基因座位于2R的近端异染色质中;(2)Rsp基因座的缺失使染色体对畸变不敏感;(3)Sd基因座位于pr(2-54.5)左侧,在唾液腺染色体图的37D2-D7至38A6-B2区域;(4)缺失Sd的SD染色体失去了畸变能力;(5)在2L近端异染色质内或附近还有SD系统的另一个重要组成部分E(SD),它表现为畸变的强增强子。这些研究结果有助于重新解释早期对SD系统分析的结果,并有助于限制解释分离畸变的可能机制。

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本文引用的文献

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Mechanisms of meiotic drive.减数分裂驱动机制。
Annu Rev Genet. 1970;4:409-36. doi: 10.1146/annurev.ge.04.120170.002205.
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