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前体信使核糖核酸剪接因子在RNA聚合酶II转录位点的分布。

Distribution of pre-mRNA splicing factors at sites of RNA polymerase II transcription.

作者信息

Neugebauer K M, Roth M B

机构信息

Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.

出版信息

Genes Dev. 1997 May 1;11(9):1148-59. doi: 10.1101/gad.11.9.1148.

Abstract

If pre-mRNA splicing begins during RNA synthesis, then transcriptionally active genes may be expected to contain high concentrations of pre-mRNA splicing factors. However, previous studies have localized splicing factors to a network of "speckles," which is distinct from individual sites of gene transcription where pre-mRNA is spliced. Speckles have been detected with antibodies specific for splicing snRNPs and members of the SR family of splicing factors. Here we report that dilution of these probes results in the visualization of hundreds of sites throughout the HeLa cell nucleus, the size and distribution of which are consistent with transcription units viewed with light microscopy. Importantly, these sites of highest SR protein concentration frequently coincide in three-dimensional space with active sites of RNA polymerase II transcription. A newly developed reagent specific for a single member of the SR family, SRp20, detects a subset (approximately 20%) of these sites, suggesting the gene-specific accumulation of these splicing regulators, which have distinct functions in pre-mRNA splicing. These observations question the view that the nucleus and its functions are highly compartmentalized; instead, they support a model in which the localization of these and possibly other gene regulators is determined primarily by their function.

摘要

如果前体mRNA剪接在RNA合成期间开始,那么转录活跃的基因可能会含有高浓度的前体mRNA剪接因子。然而,先前的研究已将剪接因子定位到一个“斑点”网络,该网络与前体mRNA进行剪接的基因转录的各个位点不同。已使用针对剪接核小核糖核蛋白颗粒(snRNP)和SR剪接因子家族成员的特异性抗体检测到斑点。在此我们报告,这些探针的稀释导致在整个HeLa细胞核中可视化数百个位点,其大小和分布与光学显微镜下观察到的转录单位一致。重要的是,这些SR蛋白浓度最高的位点在三维空间中经常与RNA聚合酶II转录的活性位点重合。一种新开发的针对SR家族单个成员SRp20的试剂检测到这些位点的一个子集(约20%),表明这些剪接调节因子在基因特异性上的积累,它们在前体mRNA剪接中具有不同的功能。这些观察结果对细胞核及其功能高度分隔的观点提出了质疑;相反,它们支持一种模型,即这些以及可能其他基因调节因子的定位主要由其功能决定。

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