Winsor E J, Ferguson-Smith M A, Shire J G
Cytogenet Cell Genet. 1978;21(1-2):11-8. doi: 10.1159/000130874.
A sex reversal factor (Sxr) that causes mice having apparently normal X chromosomes to become phenotypically male is transmitted in an autosomal pattern. The origin of the Sxr factor is still unknown. It seems most likely that it has originated from an autosomal gene mutation or is the result of a translocation of part of the Y chromosome to one of the autosomes. Chromosomes from four XY and six XO mice carrying this sex reversal factor were examined in the diakinesis stage of meiosis. The following unusual observations were noted: (1) in XY males carrying the Sxr factor, the X and Y chromosomes were separated more often than in controls. (2) The Y chromosome tends to be closer to an autosome when the X and Y are separate than when the X and Y are attached. (3) A chromosome fragment was present in 4/226 cells from two XO males and a single cell from an XY, Sxr carrier. Although there is no direct evidence, these observations seem to favor the possibility that the Sxr factor involves a chromosomal rearrangement rather than a single gene mutation.
一种导致具有明显正常X染色体的小鼠表现为雄性表型的性反转因子(Sxr)以常染色体模式遗传。Sxr因子的起源仍然未知。它似乎最有可能源自常染色体基因突变,或者是Y染色体的一部分易位到某一条常染色体的结果。在减数分裂的终变期检查了携带这种性反转因子的4只XY小鼠和6只XO小鼠的染色体。记录到以下异常观察结果:(1)在携带Sxr因子的XY雄性小鼠中,X和Y染色体分离的频率比对照组更高。(2)当X和Y分离时,Y染色体比X和Y相连时更倾向于靠近一条常染色体。(3)在来自两只XO雄性小鼠的226个细胞中有4个以及来自一只XY Sxr携带者的单个细胞中存在一个染色体片段。尽管没有直接证据,但这些观察结果似乎支持Sxr因子涉及染色体重排而非单个基因突变的可能性。