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人类组织金属蛋白酶抑制剂基因的X染色体失活

X chromosome inactivation of the human TIMP gene.

作者信息

Brown C J, Flenniken A M, Williams B R, Willard H F

机构信息

Department of Genetics, Stanford University, CA 94305.

出版信息

Nucleic Acids Res. 1990 Jul 25;18(14):4191-5. doi: 10.1093/nar/18.14.4191.

Abstract

X chromosome inactivation results in the cis-limited inactivation of most, but not all, genes on one of the two X chromosomes in mammalian females. The molecular basis for inactivation is unknown. In order to examine the transcriptional activity of human X-linked genes, a series of mouse-human somatic cell hybrids under positive selection for the active or inactive human X chromosome has been created. Northern blot analysis of RNA from these hybrids showed that the human MIC2 gene, which is known to escape X inactivation, was transcribed in hybrids with either the active or inactive X chromosome. In contrast, the human TIMP gene was only transcribed in hybrids with an active human X chromosome. Further analysis using the polymerase chain reaction showed that there was at least one-hundred fold less transcription of the TIMP gene from the inactive X than from the active X chromosome. These findings demonstrate that the human TIMP gene is subject to X inactivation at the level of transcription, and illustrate the usefulness of the polymerase chain reaction to study the extent of X-linked gene repression by the process of X inactivation.

摘要

X染色体失活导致哺乳动物雌性两条X染色体之一上的大多数(但不是全部)基因发生顺式受限失活。失活的分子基础尚不清楚。为了检测人类X连锁基因的转录活性,已构建了一系列在活性或非活性人类X染色体正选择下的小鼠-人类体细胞杂种。对这些杂种RNA的Northern印迹分析表明,已知逃避X染色体失活的人类MIC2基因在具有活性或非活性X染色体的杂种中均有转录。相比之下,人类TIMP基因仅在具有活性人类X染色体的杂种中转录。使用聚合酶链反应的进一步分析表明,来自非活性X染色体的TIMP基因转录比来自活性X染色体的转录至少少一百倍。这些发现表明,人类TIMP基因在转录水平上受到X染色体失活的影响,并说明了聚合酶链反应在研究X染色体失活过程中X连锁基因抑制程度方面的有用性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eb07/331178/b694f6d96eee/nar00198-0147-a.jpg

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