TRANSCRIPTION INITIATION IN THE 2 LEADER EXONS OF THE RAT IGF-I GENE OCCURS FROM DISPERSE VERSUS LOCALIZED SITES

被引:95
作者
ADAMO, ML
BENHUR, H
LEROITH, D
ROBERTS, CT
机构
[1] Diabetes Branch, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda
关键词
D O I
10.1016/S0006-291X(05)80269-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Rat IGF-I mRNAs contain two different 5′-UTR sequences as a result of alternate splicing of leader exons. Using a combination of solution hybridization/RNase protection and primer extension assays, we have mapped the transcriptional start sites in these leader exons. There appear to be three putative transcription start sites in exon I spread over a 140-bp region, the most upstream of which defines a 381 bp-long exon 1. There appear to be three distinct start sites in exon 2, the most upstream of which defines a greater than 770 bp-long exon 2. The two downstream start sites in exon 1 together account for ∼70% of IGF-I gene expression in adult rat liver. Essentially all of the remaining IGF-I gene expression comes from the second start site in exon 2. Rat IGF-I gene transcription may therefore be regulated by two distinct promoter regions, a disperse promoter for exon 1, with several transcription initiation sites, and a more typical promoter region for exon 2, which controls transcription initiation from a discrete region. © 1991 Academic Press, Inc.
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页码:887 / 893
页数:7
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