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

被引:77
作者
Baurén, G
Belikov, S
Wieslander, L [1 ]
机构
[1] Stockholm Univ, Dept Mol Genome Res, S-10691 Stockholm, Sweden
[2] Karolinska Inst, Dept Cell & Mol Biol, S-17177 Stockholm, Sweden
[3] VA Engelhardt Mol Biol Inst, Moscow 117984, Russia
关键词
splicing; pre-mRNA processing; gene expression;
D O I
10.1101/gad.12.17.2759
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页码:2759 / 2769
页数:11
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