Fujii T, Yokoyama T, Ninagi O, Kakehashi K, Obara Y, Nenoi M, Ishikawa T, Mita K, Shimada T, Abe H
Department of Biological Production, Faculty of Agriculture, Tokyo University of Agriculture and Technology, Saiwai-cho 3-5-8, Fuchu, Tokyo 183-8509, Japan.
Genetica. 2007 Jul;130(3):267-80. doi: 10.1007/s10709-006-9104-7. Epub 2006 Oct 10.
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.
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。