Lane P W, Davisson M T
Jackson Laboratory, Bar Harbor, Maine 04609.
J Hered. 1990 Jan-Feb;81(1):43-50. doi: 10.1093/oxfordjournals.jhered.a110923.
Several X-linked mutations that have associated sex chromosomal nondisjunction have been identified in the mouse. We describe a new semidominant X-linked mutation called patchy fur (Paf) that produces an abnormal coat. It maps to the distal end of the murine X chromosome very near the XY pseudoautosomal region. The degree of severity in affected mice is hemizygous males greater than homozygous females greater than heterozygous females. An unusual feature of Paf is that either the mutation itself or an inseparable chromosomal abnormality causes delayed disjunction of the X and Y chromosomes at meiotic metaphase I, which in turn results in approximately 19% XO progeny and slightly less than 1% XXY progeny from Paf/Y males. The effect occurs only in male carriers and thus must extend into the proximal end of the XY pairing region.
在小鼠中已鉴定出几种与性染色体不分离相关的X连锁突变。我们描述了一种新的半显性X连锁突变,称为斑驳毛(Paf),它会产生异常的被毛。它定位于小鼠X染色体的远端,非常靠近XY假常染色体区域。受影响小鼠的严重程度为半合子雄性大于纯合子雌性大于杂合子雌性。Paf的一个不寻常特征是,要么突变本身,要么不可分离的染色体异常导致减数分裂中期I时X和Y染色体的分离延迟,这反过来又导致Paf/Y雄性产生约19%的XO后代和略少于1%的XXY后代。这种效应仅发生在雄性携带者中,因此一定延伸到XY配对区域的近端。