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3' processing of histone H4 precursor mRNA requires the presence of a small nuclear RNP particle.

作者信息

Pironcheva G, Russev G

机构信息

Institute of Molecular Biology, Bulgarian Academy of Science, Sofia.

出版信息

Int J Biochem. 1991;23(10):1043-7. doi: 10.1016/0020-711x(91)90143-b.

DOI:10.1016/0020-711x(91)90143-b
PMID:1838526
Abstract
  1. Incubation of in vitro synthesized mouse histone H4 mRNA precursors in nuclear extracts of mouse 3T6 fibroblasts, rat L6-5 myoblasts and myotubes yields processed mRNA species. A processing activity was identified in all three kinds of extracts that cleaves the precursor transcripts, generating mRNA species with mature 3' termini. 2. The processing activity is present both in proliferating (mouse 3T6 fibroblast, rat L6-5 myoblast) and terminally differentiated (rat L6 myotube) cells. 3. The efficiency of the endonucleolytic cleavage reactions was higher in a homologous system, i.e. in the presence of nuclear extracts from mouse 3T6 fibroblasts, than in a heterologous system, i.e. in the presence of rat myoblast or myotube extracts. 4. The in vitro processing activity is specifically inhibited by anti-Sm antibodies, which suggests the requirement of an snRNP particle for H4 pre-mRNA maturation.
摘要

相似文献

1
3' processing of histone H4 precursor mRNA requires the presence of a small nuclear RNP particle.
Int J Biochem. 1991;23(10):1043-7. doi: 10.1016/0020-711x(91)90143-b.
2
Histone H4 mRNA levels are down-regulated by 3' RNA processing during terminal differentiation of myoblasts.在成肌细胞终末分化过程中,组蛋白H4信使核糖核酸水平通过3'核糖核酸加工而被下调。
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Generation of histone mRNA 3' ends by endonucleolytic cleavage of the pre-mRNA in a snRNP-dependent in vitro reaction.通过在体外依赖于小核核糖核蛋白(snRNP)的反应中对前体信使核糖核酸(pre-mRNA)进行核酸内切酶切割来生成组蛋白信使核糖核酸(mRNA)的3'末端。
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Both conserved signals on mammalian histone pre-mRNAs associate with small nuclear ribonucleoproteins during 3' end formation in vitro.在体外3' 端形成过程中,哺乳动物组蛋白前体mRNA上的两个保守信号均与小核核糖核蛋白相关联。
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Cell cycle-dependent regulation of histone precursor mRNA processing by modulation of U7 snRNA accessibility.通过调节U7小核仁RNA的可及性实现细胞周期依赖性组蛋白前体mRNA加工的调控。
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