DETERMINATION OF THE C-MYC DNA-BINDING SITE

被引:180
作者
HALAZONETIS, TD
KANDIL, AN
机构
[1] Department of Cancer Research, Merck Sharp and Dohme Res. Labs., West Point
关键词
ONCOGENE; TRANSCRIPTION FACTOR TFEB; HELIX-LOOP-HELIX MOTIF;
D O I
10.1073/pnas.88.14.6162
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The carboxyl terminus of the protein encoded by the c-MYC protooncogene has similarity to the helix-loop-helix family of DNA-binding proteins and recognizes a six-nucleotide-long DNA sequence. We have used in vitro-translated c-MYC protein to further define its DNA-binding specificity. The hexanucleotide originally identified is necessary for DNA binding by c-MYC, but not sufficient; the c-MYC target site is a 12-nucleotide-long palindrome. This site is present within regulatory regions of genes that are expressed during cell growth. Point mutations within the helix-loop-helix motif of c-MYC abolish DNA-binding and transforming activities, indicating that c-MYC acts as a DNA-binding protein to transform cells. c-MYC may transform cells by activating transcription of genes required for cell division.
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页码:6162 / 6166
页数:5
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