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人类组蛋白H1.1编码基因的表达与染色体定位

Expression and chromosomal mapping of the gene encoding the human histone H1.1.

作者信息

Burfeind P, Hoyer-Fender S, Doenecke D, Hochhuth C, Engel W

机构信息

Institut für Humangenetik der Universität, Göttingen, Germany.

出版信息

Hum Genet. 1994 Dec;94(6):633-9. doi: 10.1007/BF00206957.

Abstract

The expression of a human histone H1 isoform (H1.1) was studied in several human tissues. Northern blot analysis has revealed that this gene is expressed in testis and thymus, but not in other human tissues. In this report, we demonstrate that the expression of the histone H1.1 gene in human testis is restricted to early round spermatids that belong to the fraction of postmeiotic sperm cells. Transcripts hybridizing with the human H1.1 gene could not be detected in testis of mouse, rat, bull or boar. Southern blot analysis with human genomic DNA, DNA from different Old World monkeys (chimpanzee, orangutan, gorilla and rhesus monkey) and DNA from several mammalian species has revealed that the histone H1.1 gene is highly conserved in higher primates, whereas no cross-hybridization can be detected with DNA from other mammalian species such as mouse, rat, hamster or bull. In a previous report, the human histone H1.1 gene and other H1 genes (H1.2-H1.5, H1t) were assigned to chromosome 6 by polymerase chain reaction analysis using human-rodent cell hybrid DNA; fluorescence in situ hybridization indicated that these genes form part of a major gene cluster on the short arm of chromosome 6. We have confirmed the localization of histone H1.1 to chromosome 6 and have regionally assigned the locus to 6p21.3 by radioactive in situ hybridization.

摘要

在多种人体组织中研究了一种人类组蛋白H1亚型(H1.1)的表达。Northern印迹分析表明,该基因在睾丸和胸腺中表达,但在其他人体组织中不表达。在本报告中,我们证明人类睾丸中组蛋白H1.1基因的表达仅限于属于减数分裂后精子细胞部分的早期圆形精子细胞。在小鼠、大鼠、公牛或公猪的睾丸中未检测到与人类H1.1基因杂交的转录本。用人基因组DNA、来自不同旧世界猴(黑猩猩、猩猩、大猩猩和恒河猴)的DNA以及来自几种哺乳动物物种的DNA进行Southern印迹分析表明,组蛋白H1.1基因在高等灵长类动物中高度保守,而与来自其他哺乳动物物种(如小鼠、大鼠、仓鼠或公牛)的DNA未检测到交叉杂交。在之前的一份报告中,通过使用人-啮齿动物细胞杂交DNA的聚合酶链反应分析,将人类组蛋白H1.1基因和其他H1基因(H1.2 - H1.5、H1t)定位到6号染色体;荧光原位杂交表明这些基因构成了6号染色体短臂上一个主要基因簇的一部分。我们已经证实了组蛋白H1.1在6号染色体上的定位,并通过放射性原位杂交将该基因座定位到6p21.3区域。

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