Koenig M, Camerino G, Heilig R, Mandel J L
Nucleic Acids Res. 1984 May 25;12(10):4097-109. doi: 10.1093/nar/12.10.4097.
An X linked human DNA fragment (named DXS31 ) which detects partially homologous sequences on the Y chromosome has been isolated. Regional localisation of the two sex linked sequences was determined using a panel of rodent-human somatic cell hybrids. The X specific sequence is located at the tip of the short arm ( Xp22 .3-pter), i.e. within or close to the region which pairs with the Y chromosome short arm at meiosis. However the Y specific sequence is located in the heterochromatic region of the long arm ( Yq11 -qter) and lies outside from the pairing region. DNAs from several XX male subjects were probed with DXS31 and in all cases a double dose of the X linked fragment was found, and the Y specific fragment was absent. DXS31 detects in chimpanzee a male-female differential pattern identical to that found in man. However results obtained in a more distantly related species, the brown lemur, suggest that the sequences detected by DXS31 in this species might be autosomally coded. The features observed with these X-Y related sequences do not fit with that expected from current hypotheses of homology between the pairing regions of the two sex chromosomes, nor with the pattern observed with other X-Y homologous sequences recently characterized. Our results suggest also that the rule of conservation of X linkage in mammals might not apply to sequences present on the tip of the X chromosome short arm, in bearing with the controversial issue of steroid sulfatase localisation in mouse.
已分离出一个可检测Y染色体上部分同源序列的X连锁人类DNA片段(命名为DXS31)。利用一组啮齿动物-人类体细胞杂种确定了这两个性连锁序列的区域定位。X特异性序列位于短臂末端(Xp22.3-端粒),即在减数分裂时与Y染色体短臂配对的区域内或附近。然而,Y特异性序列位于长臂的异染色质区域(Yq11-端粒),且位于配对区域之外。用DXS31对几名XX男性受试者的DNA进行检测,在所有情况下均发现双倍剂量的X连锁片段,而Y特异性片段缺失。DXS31在黑猩猩中检测到的雌雄差异模式与在人类中发现的相同。然而,在亲缘关系更远的物种——棕色狐猴中获得的结果表明,该物种中DXS31检测到的序列可能由常染色体编码。这些与X-Y相关序列观察到的特征既不符合当前关于两条性染色体配对区域同源性的假设所预期的情况,也不符合最近鉴定的其他X-Y同源序列所观察到的模式。我们的结果还表明,哺乳动物中X连锁的保守规则可能不适用于X染色体短臂末端存在的序列,这与小鼠中类固醇硫酸酯酶定位这一有争议的问题相符。