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人脾组蛋白H4。分离及氨基酸序列。

Human spleen histone H4. Isolation and amino acid sequence.

作者信息

Hayashi T, Ohe Y, Hayashi H, Iwai K

出版信息

J Biochem. 1982 Dec;92(6):1995-2000. doi: 10.1093/oxfordjournals.jbchem.a134131.

Abstract

The amino acid sequence of human spleen histone H4 was investigated as part of a study on histone evolution, following previous investigations of human spleen histones H2B (J. Biochem. 85, 615-624), H2A (J. Biochem. 88, 27-34), and H3 (J. Biochem. 90, 1205-1211). The H4 fraction was obtained as described previously and further purified by Bio-Gel P-60 chromatography. The purified H4 was digested with trypsin and the peptides were fractionated by repeated column chromatographies with reasonable recoveries. Certain peptides were sequenced, and three modified residues (alpha-N-Ac-Ser-1, epsilon-N-Ac-Lys-16, and epsilon-N-Me-Lys-20) and one heterogeneous residue (Asn/Asp-25), which is probably a result of postsynthetic deamidation, were found. Thus, the human H4 was deduced to have a sequence of 102 amino acid residues completely identical with that of calf thymus H4, including the presence of three modified residues and the absence of any variant sequence. It is concluded that the animal H4 sequences and their postsynthetic modifications have been strongly conserved during the evolutionary process leading to man, as strongly as or more strongly than the H3 sequence, and much more strongly than the H2A and H2B sequences.

摘要

作为组蛋白进化研究的一部分,在先前对人脾组蛋白H2B(《生物化学杂志》85卷,615 - 624页)、H2A(《生物化学杂志》88卷,27 - 34页)和H3(《生物化学杂志》90卷,1205 - 1211页)进行研究之后,对人脾组蛋白H4的氨基酸序列进行了研究。H4组分如前所述获得,并通过Bio - Gel P - 60柱色谱进一步纯化。将纯化的H4用胰蛋白酶消化,肽段通过反复柱色谱分离,回收率合理。对某些肽段进行了测序,发现了三个修饰残基(α - N - 乙酰 - 丝氨酸 - 1、ε - N - 乙酰 - 赖氨酸 - 16和ε - N - 甲基 - 赖氨酸 - 20)和一个异质性残基(天冬酰胺/天冬氨酸 - 25),后者可能是合成后脱酰胺作用的结果。因此,推断人H4具有102个氨基酸残基的序列,与小牛胸腺H4的序列完全相同,包括存在三个修饰残基且不存在任何变异序列。得出的结论是,在导致人类的进化过程中,动物H4序列及其合成后修饰与H3序列一样强烈或更强烈地得到了保守,比H2A和H2B序列保守得多。

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