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正常人类细胞中失活X染色体上G6PD基因座表达降低导致去抑制。

Derepression with decreased expression of the G6PD locus on the inactive X chromosome in normal human cells.

作者信息

Migeon B R, Wolf S F, Mareni C, Axelman J

出版信息

Cell. 1982 Jun;29(2):595-600. doi: 10.1016/0092-8674(82)90175-1.

Abstract

Studies of a unique clone of skin fibroblasts from a normal 46 XX female reveal that the G6PD locus on the inactive X chromosome has been derepressed. The reactivation event occurs spontaneously, and is associated with normal karyotype, including the presence of a late-replicating X chromosome. Analysis of mouse-human hybrids with the relevant chromosome provides evidence that the derepressed locus is on the inactive X, and that reactivation is not extensive (the PGK locus is not derepressed). Nor is any general change in DNA methylation of this chromosome detectable with Hpa II and an X-specific DNA probe. Studies of the glucose-6-phosphate dehydrogenase phenotype in these heterozygous cells indicate that the reactivated X produces only half the enzyme subunits as are produced by the active X. Although this dosage difference may be related to the mutational event responsible for derepression of the locus, these observations along with other evidence suggest that loci on the inactive X, when expressed, have less activity than corresponding loci on the active X.

摘要

对一名正常46 XX女性的皮肤成纤维细胞独特克隆进行的研究表明,失活X染色体上的G6PD基因座已被去抑制。这种再激活事件是自发发生的,并且与正常核型相关,包括存在一条晚复制的X染色体。对带有相关染色体的小鼠 - 人杂种进行分析,提供了证据表明去抑制的基因座位于失活的X染色体上,并且再激活并不广泛(PGK基因座未被去抑制)。用Hpa II和X特异性DNA探针也检测不到该染色体DNA甲基化的任何普遍变化。对这些杂合细胞中葡萄糖 - 6 - 磷酸脱氢酶表型的研究表明,再激活的X产生的酶亚基仅为活性X产生的一半。尽管这种剂量差异可能与导致基因座去抑制的突变事件有关,但这些观察结果以及其他证据表明,失活X染色体上的基因座在表达时,其活性低于活性X染色体上的相应基因座。

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