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关于信使前体RNA与转录。一篇综述。

On pre-messenger RNA and transcriptions. A review.

作者信息

Scherrer K, Imaizumi-Scherrer M T, Reynaud C A, Therwath A

出版信息

Mol Biol Rep. 1979 May 31;5(1-2):5-28. doi: 10.1007/BF00777484.

Abstract

From the present review integrating old and new data emerge a few principles of gene expression in eukaryotes, and an infinite variety of possible mechanistic details generating the overal pattern. The few principles, most of which are not fundamentally new, may thus be summarized. 1) The eukaryotic genome is subdivided into transcriptional units: into transcriptons which are subject to individual activation controlled at DNA level. 2) Viral genomes may contain one or a few transcriptons, while cells of multicellular organisms contain from 3 x 10(3) in diptera up to an estimated 2 x 10(5) in birds and mammals. 3) Transcriptons may include one or several coding sequences. 4) Transcriptons vary considerably in size: in mammals and birds their size spectrum falls into the 2,000 to 20,000 bp range. 5) Units of coding information constituting one message (genes) and, possibly, units of regulative information are frequently broken up and stored within the transcripton in sub-genic blocks (of so far unknown significance) in general located at a certain distance from the 5' and 3' transcript terminals which are determined by the promotor and terminator signals. 6) The gene, in its specific definition as the functional unit underlying the phenotype, is in general constituted posttranscriptionally by the processing mechanisms from the mosaic of its genomic subunits in the transcripton; segments of coding, service and regulative sequences are recombined within themselves and with each other, polygenic transcripts separate into their unit messages. 7) Activated transcriptons produce pre-mRNA; these primary transcripts are colinear with the DNA of the transcriptional unit. 8) Primary pre-mRNA is processed into secondary pre-mRNA's by extragenic cleavage and intragenic ("splicing") processing, giving rise stepwise to functional mRNA. During this process chemical modifications as methylation, 5'-terminal capping and 3'-terminal polyadenylation take place. 9) Translation yields either potentially functional polypeptides or polycistronic polyproteins subject to further processing. 10) Processing is a regulated process; it involves many of the possible phases and mechanisms of post-transcriptional regulation (cf. 39, 40).

摘要

通过整合新旧数据的当前综述,真核生物基因表达的一些原则浮现出来,以及产生整体模式的无限多种可能的机制细节。因此,可以总结出这些为数不多的原则,其中大多数并非根本性的新内容。1)真核生物基因组被细分为转录单位:即转录子,其受到在DNA水平上控制的个体激活。2)病毒基因组可能包含一个或几个转录子,而多细胞生物的细胞包含从双翅目的3×10³个到鸟类和哺乳动物估计的2×10⁵个。3)转录子可能包括一个或几个编码序列。4)转录子的大小差异很大:在哺乳动物和鸟类中,其大小范围在2000至20000碱基对之间。5)构成一条信息(基因)的编码信息单位以及可能的调控信息单位经常被分解并存储在转录子内的亚基因块中(其意义至今未知),这些亚基因块通常位于由启动子和终止子信号确定的5'和3'转录末端一定距离处。6)基因,就其作为表型基础的功能单位的特定定义而言,通常在转录后由转录子中其基因组亚基的镶嵌体通过加工机制构成;编码、服务和调控序列的片段在自身内部以及相互之间进行重组,多基因转录本分离成其单位信息。7)激活的转录子产生前体mRNA;这些初级转录本与转录单位的DNA共线性。8)初级前体mRNA通过基因外切割和基因内(“剪接”)加工被加工成二级前体mRNA,逐步产生功能性mRNA。在此过程中会发生甲基化、5'末端加帽和3'末端聚腺苷酸化等化学修饰。9)翻译产生潜在功能性多肽或需要进一步加工的多顺反子多蛋白。10)加工是一个受调控的过程;它涉及转录后调控的许多可能阶段和机制(参见39、40)。

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