Attenuated function of a variant form of the helix-loop-helix protein, Id-3, generated by an alternative splicing mechanism

被引:22
作者
Deed, RW
Jasiok, M
Norton, JD
机构
[1] CRC Department of Gene Regulation, Paterson Inst. for Cancer Research, Christie Hospital NHS Trust, Manchester M20 9BX, Wilmslow Road
基金
英国医学研究理事会;
关键词
gene expression; transcription factor; helix-loop-helix; RNA splicing;
D O I
10.1016/0014-5793(96)00868-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
The Id family of helix-loop-helix proteins function as negative regulators of DNA binding, basic helix-loop-helix proteins in the regulation of cell growth and differentiation. We report here on the identification of a 17 kDa variant off the 14 kDa Id-3 protein termed Id-3L (long version) which possesses a unique 60 amino acid carboxy-terminus generated by readthrough of a 'coding intron' and alternative splicing, Northern analysis revealed expression of a minor 1.1 kb Id-3L transcript together with the predominant 0.95 kb Id-3 transcript in the majority of adult human tissues analysed, The variant Id-3L protein is functionally distinguishable from conventional Id-3 since in in vitro DNA mobility shift assays, it was greatly impaired in its ability to abrogate binding of the basic helix-loop-helix protein, E47, to an E box recognition sequence.
引用
收藏
页码:113 / 116
页数:4
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