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在大鼠大脑中特异性表达的H1(0) RNA结合蛋白。

H1(0) RNA-binding proteins specifically expressed in the rat brain.

作者信息

Scaturro M, Nastasi T, Raimondi L, Bellafiore M, Cestelli A, Di Liegro I

机构信息

Dipartimento di Biologia Cellulare e dello Sviluppo "Alberto Monroy, " viale delle Scienze, Parco d'Orleans, 90128 Palermo, Italy.

出版信息

J Biol Chem. 1998 Aug 28;273(35):22788-91. doi: 10.1074/jbc.273.35.22788.

Abstract

During brain maturation, histone H1(0) accumulates in both nerve and glial cells. The expression of this "linker" histone, the role of which still remains unclear, is a complex process, having both transcriptional and post-transcriptional regulatory components. In particular, the expression of H1(0) in rat cortical neurons is regulated mainly at the post-transcriptional level, and unknown cellular proteins are likely to affect H1(0) mRNA stability and/or translation. In looking for such factors, we tested the ability of rat brain extracts to protect H1(0) RNA probe from degradation by T1 RNase. The results reported here demonstrate that rat brain contains at least one major (p40) and two minor (p110 and p70) binding factors, specific for H1(0) RNA, all of which are much more or exclusively expressed in adult rat brain, when compared with other tissues. The binding of the factors is confined to a portion of the 3'-untranslated region (3'-UTR), which is highly conserved among murine and human H1(0) mRNAs. These findings suggest that the proteins identified play a critical role in regulating the expression of H1(0) histone in the brain of mammals.

摘要

在大脑成熟过程中,组蛋白H1(0)在神经细胞和胶质细胞中均有积累。这种“连接”组蛋白的作用仍不清楚,其表达是一个复杂的过程,具有转录和转录后调控成分。特别是,大鼠皮质神经元中H1(0)的表达主要在转录后水平受到调控,未知的细胞蛋白可能会影响H1(0) mRNA的稳定性和/或翻译。在寻找此类因子的过程中,我们测试了大鼠脑提取物保护H1(0) RNA探针不被T1核糖核酸酶降解的能力。此处报道的结果表明,大鼠脑含有至少一种主要的(p40)和两种次要的(p110和p70)与H1(0) RNA特异性结合的因子,与其他组织相比,所有这些因子在成年大鼠脑中表达量更高或仅在成年大鼠脑中表达。这些因子的结合局限于3'-非翻译区(3'-UTR)的一部分,该区域在小鼠和人类H1(0) mRNA中高度保守。这些发现表明,所鉴定的蛋白质在调节哺乳动物脑中H1(0)组蛋白的表达中起关键作用。

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