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巴尔比亚尼环1基因中的转录终止与3'端形成以及3'端内含子的切除紧密相关。

Transcriptional termination in the Balbiani ring 1 gene is closely coupled to 3'-end formation and excision of the 3'-terminal intron.

作者信息

Baurén G, Belikov S, Wieslander L

机构信息

Department of Molecular Genome Research, Stockholm University, S-106 91 Stockholm, Sweden.

出版信息

Genes Dev. 1998 Sep 1;12(17):2759-69. doi: 10.1101/gad.12.17.2759.

Abstract

We have analyzed transcription termination, 3'-end formation, and excision of the 3'-terminal intron in vivo in the Balbiani ring 1 (BR1) gene and its pre-mRNA. We show that full-length RNA transcripts are evenly spaced on the gene from a position 300 bp upstream to a region 500-700 bp downstream of the polyadenylation sequence. Very few full-length transcripts and no short, cleaved, nascent transcripts could be observed downstream of this region. Pre-mRNA with 10-20 adenylate residues accumulates at the active gene and then rapidly leaves from the gene locus. Only polyadenylated pre-mRNAs could be detected in the nucleoplasm. Our results are consistent with the hypothesis that transcription termination occurs in a narrow region for the majority of transcripts, simultaneous with 3'-end formation. Excision of the 3'-terminal intron occurs before 3'-end formation in about 5% of the nascent transcripts. When transcription terminates, 3' cleavage takes place and 10-20 adenylate residues are added, the 3'-terminal intron is excised from additionally about 75% of the pre-mRNA at the gene locus. Our data support a close temporal and spatial coupling of transcription termination and the cleavage and initial polyadenylation of 3'-end formation. Excision of the 3'-terminal intron is highly stimulated as the cleavage/polyadenylation complex assembles and 3'-end formation is initiated.

摘要

我们分析了巴尔比亚尼环1(BR1)基因及其前体mRNA在体内的转录终止、3'端形成以及3'末端内含子的切除情况。我们发现,全长RNA转录本在基因上从聚腺苷酸化序列上游300 bp处到下游500 - 700 bp区域均匀分布。在该区域下游几乎观察不到全长转录本,也没有短的、切割后的新生转录本。带有10 - 20个腺苷酸残基的前体mRNA在活跃基因处积累,然后迅速从基因位点离开。仅在核质中能检测到聚腺苷酸化的前体mRNA。我们的结果与以下假设一致:大多数转录本的转录终止发生在一个狭窄区域,与3'端形成同时进行。约5%的新生转录本在3'端形成之前切除3'末端内含子。当转录终止时,进行3'切割并添加10 - 20个腺苷酸残基,在基因位点另外约75%的前体mRNA上切除3'末端内含子。我们的数据支持转录终止与3'端形成的切割和初始聚腺苷酸化在时间和空间上紧密耦合。随着切割/聚腺苷酸化复合体组装并启动3'端形成,3'末端内含子的切除受到高度刺激。

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