Venolia L, Gartler S M
Somatic Cell Genet. 1983 Sep;9(5):617-27. doi: 10.1007/BF01574262.
Inactivation of the X chromosome during mammalian spermatogenesis has been postulated to occur by the same mechanism that controls female somatic X chromosome inactivation. We have used DNA-mediated transformation of HPRT- cells to test this idea, because it has been shown previously that inactive X chromosome DNA from somatic cells will not transform HPRT- cells. Isolated DNA from the mature sperm of five mammals (human, mouse, horse, bull, rabbit) were all capable of HPRT transformation, and transformants were confirmed electrophoretically. Measures were taken to ensure that the transformation frequencies observed could not be due to somatic contamination. The positive HPRT transformation result indicates that mature sperm X chromosomal DNA is not modified in the same manner as that of female inactive X chromosomal DNA. Since there is evidence for methylation of the somatic inactive X chromosome, it is possible that methylation, at least for the genes studied, is not involved in sperm X chromosome inactivation.
哺乳动物精子发生过程中X染色体的失活被假定是通过控制雌性体细胞X染色体失活的相同机制发生的。我们利用DNA介导的HPRT-细胞转化来验证这一想法,因为先前已经表明,来自体细胞的失活X染色体DNA不会转化HPRT-细胞。从五种哺乳动物(人类、小鼠、马、公牛、兔子)的成熟精子中分离出的DNA都能够进行HPRT转化,并通过电泳确认了转化体。已采取措施确保观察到的转化频率不是由于体细胞污染所致。HPRT转化呈阳性的结果表明,成熟精子的X染色体DNA与雌性失活X染色体DNA的修饰方式不同。由于有证据表明体细胞失活的X染色体存在甲基化,所以至少对于所研究的基因而言,甲基化可能不参与精子X染色体的失活。