The Functional Consequences of Eukaryotic Topoisomerase 1 Interaction with G-Quadruplex DNA

被引:14
作者
Berroyer, Alexandra [1 ,2 ]
Kim, Nayun [1 ,2 ]
机构
[1] Univ Texas Hlth Sci Ctr Houston, Dept Microbiol & Mol Genet, Houston, TX 77030 USA
[2] Univ Texas MD Anderson Canc Ctr, UT Hlth, Grad Sch Biomed Sci, Houston, TX 77030 USA
基金
美国国家卫生研究院;
关键词
topoisomerase I; G-quadruplex; genome instability; SUPPRESS GENOME INSTABILITY; I GENE; MUTATIONAL LANDSCAPE; PREFERENTIAL BINDING; ESCHERICHIA-COLI; REPLICATION; PROTEIN; CANCER; TRANSCRIPTION; SEQUENCE;
D O I
10.3390/genes11020193
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Topoisomerase I in eukaryotic cells is an important regulator of DNA topology. Its catalytic function is to remove positive or negative superhelical tension by binding to duplex DNA, creating a reversible single-strand break, and finally religating the broken strand. Proper maintenance of DNA topological homeostasis, in turn, is critically important in the regulation of replication, transcription, DNA repair, and other processes of DNA metabolism. One of the cellular processes regulated by the DNA topology and thus by Topoisomerase I is the formation of non-canonical DNA structures. Non-canonical or non-B DNA structures, including the four-stranded G-quadruplex or G4 DNA, are potentially pathological in that they interfere with replication or transcription, forming hotspots of genome instability. In this review, we first describe the role of Topoisomerase I in reducing the formation of non-canonical nucleic acid structures in the genome. We further discuss the interesting recent discovery that Top1 and Top1 mutants bind to G4 DNA structures in vivo and in vitro and speculate on the possible consequences of these interactions.
引用
收藏
页数:15
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