AN UNUSUAL STRUCTURE OF A PUTATIVE T-CELL ONCOGENE WHICH ALLOWS PRODUCTION OF SIMILAR PROTEINS FROM DISTINCT MESSENGER-RNAS

被引:86
作者
BOEHM, T
GREENBERG, JM
BULUWELA, L
LAVENIR, I
FORSTER, A
RABBITTS, TH
机构
关键词
alternative initiation codon; chromosome translocation; dual promoter; exon structure; T cell receptor;
D O I
10.1002/j.1460-2075.1990.tb08183.x
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
We previously identified a putative T cell oncogene on chromosome 11 near a translocation t(11;14)(p15;q11) in a human T cell tumour. The gene is transcribed from distinct promoters which have unrelated sequences, which occur within close but distinct methylation-free islands and which allow cell specific production of mRNA. The alternative first exons each contain a protein initiation codon from which two species of protein can be made, differing by only a single amino acid. The protein sequence is highly conserved between man and mouse (98%) and the same single codon difference between alternative first exons is also conserved. This is, therefore, a new form of eukaryotic gene organization from which similar proteins can be made from distinct mRNA species.
引用
收藏
页码:857 / 868
页数:12
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