Ashley T
Chromosoma. 1983;88(3):178-83. doi: 10.1007/BF00285617.
Electron microscopy of pachytene nuclei of mice heterozygous for either of two reciprocal X-7 translocations (R5 or R6) revealed a high frequency of heteromorphic bivalents involving the translocated chromosomes. In both translocations the break was in the proximal third of the 7 and the distal third of the X, but the R5 breaks were closer to the 7 centromere and X telomere than the R6 breaks. In both translocations the 7 frequently synapsed nonhomologously with the X7. In R5 the part of the X to which the 7 synapsed may include a region that synapses with the Y in normal mice. However, in R6 the 7 synapsed with a portion of the X that never synapses with the Y (Synapsis was clearly in the "differentiated" region). In both translocations the Y synapsed maximally with the X portion of the 7X in those nuclei in which there was nonhomologous synapsis of the 7 with the X7. The Y occasionally synapsed nonhomologously with the 7 portion of the 7X. The behavior of the bivalents suggests that the autosomal portions of the 7X and X7 may alter the behavior of the sex-chromosome portions. Both the nonhomologous synapsis of the Y with the 7X and the timing of events during pachytene have led us to question the "homology" between the X and Y in this species.
对两种相互易位(R5或R6)中的任何一种杂合的小鼠粗线期细胞核进行电子显微镜观察,发现涉及易位染色体的异形二价体频率很高。在这两种易位中,断裂都发生在7号染色体近端的三分之一处和X染色体远端的三分之一处,但R5的断裂比R6的断裂更靠近7号染色体着丝粒和X染色体端粒。在这两种易位中,7号染色体经常与X7非同源配对。在R5中,与7号染色体配对的X染色体部分可能包括在正常小鼠中与Y染色体配对的区域。然而,在R6中,7号染色体与X染色体的一部分配对,而这部分在正常情况下从不与Y染色体配对(配对明显发生在“分化”区域)。在这两种易位中,在7号染色体与X7非同源配对的细胞核中,Y染色体与7X的X染色体部分最大程度地配对。Y染色体偶尔也会与7X的7号染色体部分非同源配对。二价体的行为表明,7X和X7的常染色体部分可能会改变性染色体部分的行为。Y染色体与7X的非同源配对以及粗线期事件的时间安排,使我们对该物种中X和Y之间的“同源性”产生了质疑。