Thierry-Mieg D
Genetics. 1982 Feb;100(2):209-37. doi: 10.1093/genetics/100.2.209.
The genetic properties of a pleiotropic mutant mapping at 1.4 +/- 0.1 in band 3B3 or its adjacent interbands on the X chromosome are described. The mutation is expressed autonomously in germ line cells, where it is recessive and has antimorphic properties. At 29 degrees, the mutation blocks oocyte differentiation, causing female sterility. At lower temperatures, it disturbs the maternal information in the egg; as a result, the progeny lack germ line cells (grandchildless phenotype) and exhibit defects of the cuticular pattern. The mutation is also expressed in somatic cells through zygotic interactions with neighboring regions, including 3A2, 3A3 (zeste), 3C1-2, 3C4 and 3C6-8 (Notch). We interpret the data by postulating that the expression of sets of dispersed genes might be controlled by the local topology of the chromosome, itself constrained by pairing of dispersed repeated elements. We call the mutation paralog.
本文描述了一个多效性突变体的遗传特性,该突变体位于X染色体3B3带或其相邻间带,位置为1.4 +/- 0.1。该突变在生殖系细胞中自主表达,在生殖系细胞中它是隐性的,并具有反形态特性。在29摄氏度时,该突变会阻断卵母细胞分化,导致雌性不育。在较低温度下,它会干扰卵中的母体信息;结果,后代缺乏生殖系细胞(孙代无后代表型),并表现出表皮图案缺陷。该突变还通过与包括3A2、3A3(小体)、3C1 - 2、3C4和3C6 - 8(Notch)在内的相邻区域的合子相互作用在体细胞中表达。我们通过假设分散基因集的表达可能受染色体局部拓扑结构控制来解释这些数据,而染色体局部拓扑结构本身又受分散重复元件配对的限制。我们将该突变称为旁系同源突变。