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c-MYC DNA结合位点的测定。

Determination of the c-MYC DNA-binding site.

作者信息

Halazonetis T D, Kandil A N

机构信息

Department of Cancer Research, Merck Sharp & Dohme Research Laboratories, West Point, PA 19486.

出版信息

Proc Natl Acad Sci U S A. 1991 Jul 15;88(14):6162-6. doi: 10.1073/pnas.88.14.6162.

Abstract

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.

摘要

c-MYC原癌基因编码的蛋白质的羧基末端与DNA结合蛋白的螺旋-环-螺旋家族相似,并识别一个六核苷酸长的DNA序列。我们使用体外翻译的c-MYC蛋白来进一步确定其DNA结合特异性。最初鉴定出的六核苷酸对于c-MYC与DNA结合是必需的,但并不充分;c-MYC的靶位点是一个12核苷酸长的回文序列。该位点存在于细胞生长过程中表达的基因的调控区域内。c-MYC螺旋-环-螺旋基序内的点突变会消除DNA结合和转化活性,表明c-MYC作为一种DNA结合蛋白来转化细胞。c-MYC可能通过激活细胞分裂所需基因的转录来转化细胞。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f13/52042/08f0584f7d68/pnas01064-0234-a.jpg

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