Baurén G, Jiang W Q, Bernholm K, Gu F, Wieslander L
Department of Cell and Molecular Biology, Medical Nobel Institute, Karolinska Institutet, Stockholm, Sweden.
J Cell Biol. 1996 Jun;133(5):929-41. doi: 10.1083/jcb.133.5.929.
We describe the dynamic organization of pre-mRNA splicing factors in the intact polytene nuclei of the dipteran Chironomus tentans. The snRNPs and an SR non-snRNP splicing factor are present in excess, mainly distributed throughout the interchromatin. Approximately 10% of the U2 snRNP and an SR non-snRNP splicing factor are associated with the chromosomes, highly enriched in active gene loci where they are bound to RNA. We demonstrate that the splicing factors are specifically recruited to a defined gene upon induction of transcription during physiological conditions. Concomitantly, the splicing factors leave gene loci in which transcription is turned off. We also demonstrated that upon general transcription inhibition, the splicing factors redistribute from active gene loci to the interchromatin. Our findings demonstrate the dynamic intranuclear organization of splicing factors and a tight linkage between transcription and the intranuclear organization of the splicing machinery.
我们描述了双翅目昆虫摇蚊完整多线核中前体mRNA剪接因子的动态组织。小核核糖核蛋白颗粒(snRNPs)和一种SR非snRNP剪接因子过量存在,主要分布在整个染色质间区域。大约10%的U2 snRNP和一种SR非snRNP剪接因子与染色体相关,在活跃基因位点高度富集,它们在这些位点与RNA结合。我们证明,在生理条件下转录诱导时,剪接因子会被特异性招募到特定基因。与此同时,剪接因子会离开转录被关闭的基因位点。我们还证明,在一般转录抑制时,剪接因子会从活跃基因位点重新分布到染色质间区域。我们的研究结果证明了剪接因子在细胞核内的动态组织以及转录与剪接机制在细胞核内组织之间的紧密联系。