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在家蚕中导致雄性肌肉萎缩和雌性异常卵子发生的性染色体重排的分离与鉴定

Isolation and characterization of sex chromosome rearrangements generating male muscle dystrophy and female abnormal oogenesis in the silkworm, Bombyx mori.

作者信息

Fujii T, Yokoyama T, Ninagi O, Kakehashi K, Obara Y, Nenoi M, Ishikawa T, Mita K, Shimada T, Abe H

机构信息

Department of Biological Production, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Saiwai-cho 3-5-8, Fuchu, Tokyo 183-8509, Japan.

出版信息

Genetica. 2007 Jul;130(3):267-80. doi: 10.1007/s10709-006-9104-7. Epub 2006 Oct 10.

Abstract

In deletion-mapping of W-specific RAPD (W-RAPD) markers and putative female determinant gene (Fem), we used X-ray irradiation to break the translocation-carrying W chromosome (W( Ze )). We succeeded in obtaining a fragment of the W( Ze ) chromosome designated as Ze (W), having 3 of 12 W-RAPD markers (W-Bonsai, W-Yukemuri-S, W-Yukemuri-L). Inheritance of the Ze (W) fragment by males indicates that it does not include the Fem gene. On the basis of these results, we determined the relative positions of W-Yukemuri-S and W-Yukemuri-L, and we narrowed down the region where Fem gene is located. In addition to the Ze (W) fragment, the Z chromosome was also broken into a large fragment (Z(1)) having the +( sch ) (1-21.5) and a small fragment (Z(2)) having the +( od ) (1-49.6). Moreover, a new chromosomal fragment (Ze (W)Z(2)) was generated by a fusion event between the Ze (W) and the Z(2) fragments. We analyzed the genetic behavior of the Z(1) fragment and the Ze (W)Z(2) fragment during male (Z/Z(1) Ze (W)Z(2)) and female (Z(1) Ze (W)Z(2)/W) meiosis using phenotypic markers. It was observed that the Z(1) fragment and the Z or the W chromosomes separate without fail. On the other hand, non-disjunction between the Ze (W)Z(2) fragment and the Z chromosome and also between the Ze (W)Z(2) fragment and the W chromosome occurred. Furthermore, the females (2A: Z/Ze (W)Z(2)/W) and males (2A: Z/Z(1)) resulting from non-disjunction between the Ze (W)Z(2) fragment and the W chromosome had phenotypic defects: namely, females exhibited abnormal oogenesis and males were flapless due to abnormal indirect flight muscle structure. These results suggest that Z(2) region of the Z chromosome contains dose-sensitive gene(s), which are involved in oogenesis and indirect flight muscle development.

摘要

在对W特异性随机扩增多态性DNA(W-RAPD)标记和假定的雌性决定基因(Fem)进行缺失作图时,我们使用X射线照射来断裂携带易位的W染色体(W(Ze))。我们成功获得了W(Ze)染色体的一个片段,命名为Ze(W),它含有12个W-RAPD标记中的3个(W-盆景、W-雪村-S、W-雪村-L)。雄性对Ze(W)片段的遗传表明它不包含Fem基因。基于这些结果,我们确定了W-雪村-S和W-雪村-L的相对位置,并缩小了Fem基因所在的区域。除了Ze(W)片段外,Z染色体也断裂成一个大的片段(Z(1)),其携带+(sch)(1-21.5),以及一个小的片段(Z(2)),其携带+(od)(1-49.6)。此外,通过Ze(W)片段和Z(2)片段之间的融合事件产生了一个新的染色体片段(Ze(W)Z(2))。我们使用表型标记分析了Z(1)片段和Ze(W)Z(2)片段在雄性(Z/Z(1) Ze(W)Z(2))和雌性(Z(1) Ze(W)Z(2)/W)减数分裂过程中的遗传行为。观察到Z(1)片段与Z或W染色体必然分离。另一方面,Ze(W)Z(2)片段与Z染色体之间以及Ze(W)Z(2)片段与W染色体之间发生了不分离现象。此外,由于Ze(W)Z(2)片段与W染色体之间不分离而产生的雌性(2A: Z/Ze(W)Z(2)/W)和雄性(2A: Z/Z(1))有表型缺陷:即雌性表现出异常的卵子发生,雄性由于间接飞行肌结构异常而无翅。这些结果表明,Z染色体的Z(2)区域含有剂量敏感基因,这些基因参与卵子发生和间接飞行肌发育。

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