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豌豆(Psium sativum L.)根尖中编码H1组蛋白和类H1组蛋白序列的mRNA的分子克隆与表达

Molecular cloning and expression of mRNAs encoding H1 histone and an H1 histone-like sequences in root tips of pea (Psium sativum L.).

作者信息

Woo H H, Brigham L A, Hawes M C

机构信息

Department of Plant Pathology, University of Arizona, Tucson 85721, USA.

出版信息

Plant Mol Biol. 1995 Sep;28(6):1143-7. doi: 10.1007/BF00032675.

Abstract

Two cDNA clones representing mRNAs, highly expressed in pea root tips, were isolated by mRNA differential display. Ribonuclease protection analyses showed different patterns of expression of these two messages in several pea tissues. Sequence analysis showed that the first clone, PsH1b-40, has 100% homology with a previously isolated H1 histone cDNA, PsH1b. However, it has an additional 30 nt at the 3' end which is absent in PsH1b, suggesting possible multiple polyadenylation sites in the same mRNA. The second clone, PsH1b-41, encodes a deduced 19.5 kDa protein of 185 amino acids with an isoelectric point of 11.5. The putative globular domain of the encoded protein showed 67-71% residue identity with globular domains of 28 kDa pea PsH1b H1 histone and Arabidopsis thaliana H1-1 H1 histone. It has 9 repeating motifs of (T/S)XXK. In the C-terminal domain, there are four lysine-rich repeating motifs of SXK(T/S)PXKKXK which may be involved in chromatin condensation and decondensation. Southern blot analysis of nuclear DNA shows that PsH1-41 belongs to a multigene family.

摘要

通过mRNA差异显示技术分离出了两个代表在豌豆根尖中高表达的mRNA的cDNA克隆。核糖核酸酶保护分析表明,这两条信息在几种豌豆组织中的表达模式不同。序列分析表明,第一个克隆PsH1b - 40与先前分离的H1组蛋白cDNA PsH1b具有100%的同源性。然而,它在3'端有额外的30个核苷酸,而PsH1b中没有,这表明同一mRNA中可能存在多个聚腺苷酸化位点。第二个克隆PsH1b - 41编码一个推导的19.5 kDa的蛋白质,由185个氨基酸组成,等电点为11.5。编码蛋白的假定球状结构域与28 kDa豌豆PsH1b H1组蛋白和拟南芥H1 - 1 H1组蛋白的球状结构域具有67 - 71%的残基同一性。它有9个(T/S)XXK重复基序。在C末端结构域,有四个富含赖氨酸的SXK(T/S)PXKKXK重复基序,可能参与染色质的凝聚和去凝聚。核DNA的Southern印迹分析表明,PsH1 - 41属于一个多基因家族。

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