Protein-protein interactions in the core nucleotide excision repair pathway

被引:0
|
作者
D'Souza, Areetha [1 ,3 ,4 ]
Kim, Mihyun [1 ,2 ]
Chazin, Walter J. [3 ,4 ,5 ]
Scharer, Orlando D. [1 ,2 ,3 ]
机构
[1] Inst Basic Sci, Ctr Genom Integr, Ulsan 44919, South Korea
[2] Ulsan Natl Inst Sci & Technol, Dept Biol Sci, Ulsan 44919, South Korea
[3] Vanderbilt Univ, Dept Biochem, Nashville, TN 37232 USA
[4] Vanderbilt Univ, Ctr Struct Biol, Nashville, TN 37232 USA
[5] Vanderbilt Univ, Dept Chem, Nashville, TN 37232 USA
基金
新加坡国家研究基金会;
关键词
DNA repair; Nucleotide excision repair; Xeroderma pigmentosum; Protein-protein interactions; GROUP-C PROTEIN; DNA-DAMAGE RECOGNITION; XERODERMA-PIGMENTOSUM; COCKAYNE-SYNDROME; XPC PROTEIN; MOLECULAR-MECHANISMS; STRUCTURAL BASIS; BINDING DOMAIN; DUAL INCISION; TFIIH;
D O I
10.1016/j.dnarep.2024.103728
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Nucleotide excision repair (NER) clears genomes of DNA adducts formed by UV light, environmental agents, and antitumor drugs. Gene mutations that lead to defects in the core NER reaction cause the skin cancer-prone disease xeroderma pigmentosum. . In NER, DNA lesions are excised within an oligonucleotide of 25-30 residues via a complex, multi-step reaction that is regulated by protein-protein interactions. These interactions were first characterized in the 1990s using pull-down, co-IP and yeast two-hybrid assays. More recently, high-resolution structures and detailed functional studies have started to yield detailed pictures of the progression along the NER reaction coordinate. In this review, we highlight how the study of interactions among proteins by structural and/or functional studies have provided insights into the mechanisms by which the NER machinery recognizes and excises DNA lesions. Furthermore, we identify reported, but poorly characterized or unsubstantiated interactions in need of further validation.
引用
收藏
页数:9
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