G-quadruplex Structures Contribute to Differential Radiosensitivity of the Human Genome

被引:33
作者
Kumari, Nitu [1 ]
Vartak, Supriya V. [1 ]
Dahal, Sumedha [1 ]
Kumari, Susmita [1 ]
Desai, Sagar S. [2 ,3 ]
Gopalakrishnan, Vidya [1 ,4 ]
Choudhary, Bibha [2 ]
Raghavan, Sathees C. [1 ]
机构
[1] Indian Inst Sci, Dept Biochem, Bangalore 560012, Karnataka, India
[2] Inst Bioinformat & Appl Biotechnol, Electronics City 560100, Bangalore, India
[3] Manipal Acad Higher Educ, Manipal 576104, Karnataka, India
[4] St Josephs Coll, Dept Zool, Irinjalakkuda 680121, Kerala, India
关键词
DOUBLE-STRAND BREAKS; MAJOR BREAKPOINT REGION; DNA-DAMAGE RESPONSE; WERNER-SYNDROME PROTEIN; HOMOLOGOUS RECOMBINATION; RECQ HELICASES; RADIATION; REPAIR; PROMOTER; INSTABILITY;
D O I
10.1016/j.isci.2019.10.033
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
DNA, the fundamental unit of human cell, generally exists in Watson-Crick base-paired B-DNA form. Often, DNA folds into non-B forms, such as four-stranded G-quadruplexes. It is generally believed that ionizing radiation (IR) induces DNA strand-breaks in a random manner. Here, we show that regions of DNA enriched in G-quadruplex structures are less sensitive to IR compared with B-DNA in vitro and inside cells. Planar G-quartet of G4-DNA is shielded from IR-induced free radicals, unlike single- and double-stranded DNA. Whole-genome sequence analysis and real-time PCR reveal that genomic regions abundant in G4-DNA are protected from radiation-induced breaks and can be modulated by G4 stabilizers. Thus, our results reveal that formation of G4 structures contribute toward differential radiosensitivity of the human genome.
引用
收藏
页码:288 / +
页数:49
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