Matsuda Y, Chapman V M
Department of Molecular and Cellular Biology, Roswell Park Cancer Institute, Buffalo, NY 14263.
Cytogenet Cell Genet. 1992;60(1):74-8. doi: 10.1159/000133299.
Sex-chromosomal aneuploidy was identified in four female progeny of 200 interspecific backcrosses between laboratory mice (C57BL/6Ros) and Mus spretus. The progeny included two 39,XO monosomy mice resulting from a backcross with M. spretus, as well as a 41,XXX trisomic mouse and a 40,XX/41,XXX mosaic mouse resulting from two separate backcrosses with C57BL/6 mice. The parental origin and meiotic stage of the aneuploidies was determined for each of the mice using a series of markers that identified allelic differences in the parental X-chromosome genes present in the hybrid female. Two of the probes identified differences in repeated elements between the M. spretus and laboratory mouse X chromosomes, whereas the remaining sites involved restriction fragment length differences of single-copy genes detectable by Southern analysis. These markers indicated that the aneuploidies were most likely of maternal origin and that the trisomy resulted from a nondisjunction at the second meiotic division. In contrast, the mosaic female could have originated either from a trisomic embryo that had lost a single X in a portion of its cells or from a mitotic nondisjunction during early embryogenesis that resulted in XXX and XO daughter cells, with subsequent loss of the XO cells.
在实验室小鼠(C57BL/6Ros)与西班牙小鼠(Mus spretus)的200次种间回交产生的雌性后代中,鉴定出了性染色体非整倍体。这些后代包括两只与西班牙小鼠回交产生的39,XO单体小鼠,以及两只分别与C57BL/6小鼠回交产生的41,XXX三体小鼠和40,XX/41,XXX嵌合体小鼠。使用一系列标记物确定了每只小鼠非整倍体的亲本来源和减数分裂阶段,这些标记物可识别杂种雌性中亲本X染色体基因的等位基因差异。其中两个探针识别出西班牙小鼠和实验室小鼠X染色体之间重复元件的差异,而其余位点涉及通过Southern分析可检测到的单拷贝基因的限制性片段长度差异。这些标记物表明,非整倍体很可能起源于母本,三体性是由第二次减数分裂时的不分离导致的。相比之下,嵌合体雌性可能起源于一个三体胚胎,该胚胎在其部分细胞中丢失了一条X染色体,或者起源于早期胚胎发育过程中的有丝分裂不分离,导致产生XXX和XO子细胞,随后XO细胞丢失。