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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。

Histone H4 mRNA levels are down-regulated by 3' RNA processing during terminal differentiation of myoblasts.

作者信息

Larson D E, Hoffmann I, Zahradka P, Birnstiel M L, Sells B H

机构信息

Department of Molecular Biology and Genetics, College of Biological Science, University of Guelph, Canada.

出版信息

Biochim Biophys Acta. 1992 Jun 15;1131(2):139-44. doi: 10.1016/0167-4781(92)90068-b.

DOI:10.1016/0167-4781(92)90068-b
PMID:1610893
Abstract

The capacity for 3' processing of the histone H4 pre-mRNA is lost following differentiation of rat L6 myoblasts to myotubes. Nuclear extracts prepared from proliferating myoblasts, but not differentiated myotubes, actively process histone H4 pre-mRNA in vitro. The activity of two factors required for 3' processing, the heat-labile factor and U7 snRNP, also changes during the differentiation period, concurrent with the loss of 3' processing activity. During myotube formation, the activity of the heat-labile factor decreases significantly while the 5' sequences of the U7 snRNA become progressively resistant to micrococcal nuclease digestion. Thus, the dramatic down-shift in histone H4 mRNA levels which occurs during myoblast differentiation is controlled at both the transcriptional and posttranscriptional level.

摘要

大鼠L6成肌细胞分化为肌管后,组蛋白H4前体mRNA的3'加工能力丧失。从增殖的成肌细胞而非分化的肌管中制备的核提取物,能够在体外积极加工组蛋白H4前体mRNA。3'加工所需的两种因子——热不稳定因子和U7 snRNP的活性,在分化期间也会发生变化,这与3'加工活性的丧失同时出现。在肌管形成过程中,热不稳定因子的活性显著降低,而U7 snRNA的5'序列对微球菌核酸酶消化的抗性逐渐增强。因此,成肌细胞分化过程中组蛋白H4 mRNA水平的显著下调在转录和转录后水平均受到调控。

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1
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。
Biochim Biophys Acta. 1992 Jun 15;1131(2):139-44. doi: 10.1016/0167-4781(92)90068-b.
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3' processing of histone H4 precursor mRNA requires the presence of a small nuclear RNP particle.
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Down-regulation of histone H3 and H4 gene transcription in differentiated L6 myotubes.
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The steady state levels and structure of the U7 snRNP are constant during the human cell cycle: lack of cell cycle regulation of histone mRNA 3' end formation.U7小核核糖核蛋白颗粒(U7 snRNP)的稳态水平和结构在人类细胞周期中保持恒定:组蛋白mRNA 3'末端形成缺乏细胞周期调控。
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ZFP100, a component of the active U7 snRNP limiting for histone pre-mRNA processing, is required for entry into S phase.ZFP100是活性U7 snRNP的一个组成部分,对组蛋白前体mRNA加工具有限制作用,进入S期需要该蛋白。
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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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U7 snRNP particles bind H4 pre-mRNA in vitro.
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A unique subspecies of histone H4 mRNA from rat myoblasts contains poly(A).来自大鼠成肌细胞的一种独特的组蛋白H4 mRNA亚种含有多聚腺苷酸。
Proc Natl Acad Sci U S A. 1985 Oct;82(20):6760-4. doi: 10.1073/pnas.82.20.6760.

引用本文的文献

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Novel function of U7 snRNA in the repression of HERV1/LTR12s and lincRNAs in human cells.U7 snRNA 在抑制人细胞中的 HERV1/LTR12s 和 lincRNAs 中的新功能。
Nucleic Acids Res. 2024 Sep 23;52(17):10504-10519. doi: 10.1093/nar/gkae738.
2
Length suppression in histone messenger RNA 3'-end maturation: processing defects of insertion mutant premessenger RNAs can be compensated by insertions into the U7 small nuclear RNA.组蛋白信使核糖核酸3'-末端成熟过程中的长度抑制:插入突变前体信使核糖核酸的加工缺陷可通过插入U7小核核糖核酸得到补偿。
Proc Natl Acad Sci U S A. 1996 Dec 10;93(25):14659-64. doi: 10.1073/pnas.93.25.14659.