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哺乳动物细胞核中前体mRNA剪接的定位

Localization of pre-mRNA splicing in mammalian nuclei.

作者信息

Zhang G, Taneja K L, Singer R H, Green M R

机构信息

Howard Hughes Medical Institute, University of Massachusetts Medical Center, Worcester 01605.

出版信息

Nature. 1994;372(6508):809-12. doi: 10.1038/372809a0.

Abstract

In mammalian nuclei, precursor messenger RNA splicing factors are distributed non-uniformly. Antibodies directed against structural polypeptides of small nuclear ribonucleoprotein particles (snRNPs) and some non-snRNP splicing factors have shown that these components are concentrated in about 20-50 nuclear 'speckles'. These and other non-homogeneous distributions have been proposed to indicate nuclear 'compartments' that are distinct from the sites of transcription and in which RNA processing occurs. We have tested this idea using a new approach. Previous structural and biochemical data have shown that splicing can occur in association with transcription. Nascent RNA of specific genes can be detected by in situ hybridization as intense spots of nuclear stain which map to the sites of transcription. Here we identify active pre-mRNA splicing sites by localizing the nascent spliced mRNA of specific genes. We find that splicing occurs at the sites of transcription, which are not coincident with intranuclear speckles. We conclude that the nucleus is not compartmentalized with respect to transcription and pre-mRNA splicing.

摘要

在哺乳动物细胞核中,前体信使核糖核酸剪接因子分布并不均匀。针对小核核糖核蛋白颗粒(snRNP)的结构多肽以及一些非snRNP剪接因子的抗体显示,这些成分集中在约20至50个核“斑点”中。有人提出,这些及其他非均匀分布表明存在与转录位点不同的核“区室”,RNA加工在其中进行。我们使用一种新方法对这一观点进行了验证。先前的结构和生化数据表明,剪接可与转录同时发生。特定基因的新生RNA可通过原位杂交检测为核染色的密集斑点,这些斑点对应于转录位点。在此,我们通过定位特定基因的新生剪接mRNA来确定活跃的前体mRNA剪接位点。我们发现剪接发生在转录位点,这些位点与核内斑点并不重合。我们得出结论,就转录和前体mRNA剪接而言,细胞核并非是分隔的。

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