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果蝇中磷酸化H1组蛋白与卫星DNA之间的相关性

Correlation between phosphorylated H1 histones and satellite DNAs in Drosophila virilis.

作者信息

Blumenfeld M, Orf J W, Sina B J, Kreber R A, Callahan M A, Mullins J I, Snyder L A

出版信息

Proc Natl Acad Sci U S A. 1978 Feb;75(2):866-70. doi: 10.1073/pnas.75.2.866.

Abstract

Drosophila virilis DNA contains satellites I, II, and III. D. novamexicana DNA contains satellite I. D. virilis H1 histone contains subfractions a, b, c, d, and e; D. novamexicana H1 contains subfractions a, b, and c. Therefore, satellites II and III might be correlated with H1d and H1e. To test the validity of this correlation, the H1 histones of polytene nuclei, which contain less than 1% satellite DNA, were analyzed. Polytene nuclei of D. virilis contain substantially decreased levels of H1c and H1e and marginally decreased levels of H1d. Polytene nuclei of D. novamexicana contain decreased levels of H1c.H1c is correlated with satellite I (common to D. virilis and D. novamexicana); H1e is correlated with satellites II and III; H1d is not correlated with any satellite DNA, because its level is virtually unchanged in polytene cells lacking detectable amounts of satellite DNA. Alkaline phosphatase digestion of the H1 histones reveals that H1c is the phosphorylated form of H1b and H1e is the phosphorylated form of H1d. Therefore, the under-replication of satellite DNAs is correlated with the decreased phosphorylation of H1 histones. In vitro, D. virilis H1 histones preferentially bind D. virilis DNAs in the progression III greater than II greater than I greater than main band, whereas D. virilis core histones do not preferentially bind any D. virilis DNA. As an extension of these results, we suggest that phosphorylated H1 histones bind D. virilis satellite DNAs in vivo and are involved in the compaction of heterochromatin.

摘要

果蝇(Drosophila virilis)的DNA含有卫星序列I、II和III。新墨西哥果蝇(D. novamexicana)的DNA含有卫星序列I。果蝇H1组蛋白含有亚组分a、b、c、d和e;新墨西哥果蝇H1含有亚组分a、b和c。因此,卫星序列II和III可能与H1d和H1e相关。为了检验这种相关性的有效性,对含有不到1%卫星DNA的多线核中的H1组蛋白进行了分析。果蝇的多线核中H1c和H1e的水平大幅下降,H1d的水平略有下降。新墨西哥果蝇的多线核中H1c的水平下降。H1c与卫星序列I相关(果蝇和新墨西哥果蝇共有);H1e与卫星序列II和III相关;H1d与任何卫星DNA均无相关性,因为在缺乏可检测量卫星DNA的多线细胞中其水平基本不变。对H1组蛋白进行碱性磷酸酶消化后发现,H1c是H1b的磷酸化形式,H1e是H1d的磷酸化形式。因此,卫星DNA的复制不足与H1组蛋白磷酸化的减少相关。在体外,果蝇H1组蛋白在进展过程中优先结合果蝇DNA,结合能力顺序为III大于II大于I大于主带,而果蝇核心组蛋白不优先结合任何果蝇DNA。作为这些结果的延伸,我们认为磷酸化的H1组蛋白在体内结合果蝇卫星DNA,并参与异染色质的压缩。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/835d/411358/15085375a698/pnas00014-0340-a.jpg

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