The why and how of DNA unlinking

被引:73
作者
Liu, Zhirong [3 ,4 ]
Deibler, Richard W. [5 ]
Chan, Hue Sun [6 ,7 ]
Zechiedrich, Lynn [1 ,2 ]
机构
[1] Baylor Coll Med, Dept Mol Virol & Microbiol, Verna & Marrs McLean Dept Biochem & Mol Biol, Houston, TX 77030 USA
[2] Baylor Coll Med, Dept Pharmacol, Houston, TX 77030 USA
[3] Peking Univ, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
[4] Peking Univ, Ctr Theoret Biol, Beijing 100871, Peoples R China
[5] Harvard Univ, Sch Med, Dept Syst Biol, Boston, MA 02115 USA
[6] Univ Toronto, Fac Med, Dept Mol Genet, Toronto, ON M5S 1A8, Canada
[7] Univ Toronto, Fac Med, Dept Biochem, Toronto, ON M5S 1A8, Canada
关键词
LOCAL JUXTAPOSITION GEOMETRY; SITE-SPECIFIC RECOMBINATION; TOPOISOMERASE-II; ESCHERICHIA-COLI; CYCLE CHECKPOINT; DOUBLE HELIX; TOPOLOGY; GYRASE; MECHANISM; IV;
D O I
10.1093/nar/gkp041
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The nucleotide sequence of DNA is the repository of hereditary information. Yet, it is now clear that the DNA itself plays an active role in regulating the ability of the cell to extract its information. Basic biological processes, including control of gene transcription, faithful DNA replication and segregation, maintenance of the genome and cellular differentiation are subject to the conformational and topological properties of DNA in addition to the regulation imparted by the sequence itself. How do these DNA features manifest such striking effects and how does the cell regulate them? In this review, we describe how misregulation of DNA topology can lead to cellular dysfunction. We then address how cells prevent these topological problems. We close with a discussion on recent theoretical advances indicating that the topological problems, themselves, can provide the cues necessary for their resolution by type-2 topoisomerases.
引用
收藏
页码:661 / 671
页数:11
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