Tetraplex DNA and its interacting proteins

被引:133
作者
Fry, Michael [1 ]
机构
[1] Technion Israel Inst Technol, Bruce Rappaport Fac Med, Dept Biochem, IL-31096 Haifa, Israel
来源
FRONTIERS IN BIOSCIENCE-LANDMARK | 2007年 / 12卷
关键词
tetraplex DNA; quadruplex DNA; tetrahelical DNA; guanine quartets; telomere DNA; DNA recombination; transcriptional regulation; nucleotide expansion disorders; review;
D O I
10.2741/2391
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
Mounting evidence indicates that certain nucleotide sequences impose non-canonical secondary structures on DNA. The resulting variable conformations are thought to bestow on the DNA informational content additional to that encoded by its linear arrangement of bases. DNA sequences that include clusters of contiguous guanine residues readily form in vitro diverse types of four-stranded structures collectively named tetraplex or quadruplex DNA. Data suggest that tetraplex DNA structures are likely to be formed in vivo and to have roles in key biological processes such as regulation of gene transcription, maintenance of telomeres, DNA recombination and the packaging of retroviral genome. A credible argument for the existence of quadruplex DNA in vivo is the prevalence of numerous viral and cellular proteins that interact physically and functionally with tetrahelical DNA. Some such proteins bind selectively and tightly to tetraplex DNA, others promote the formation of DNA tetrahelices or act to unwind them, and several nucleases cleave tetraplex DNA preferentially. The protein-mediated structural transformations of quadruplex DNA and its selective nucleolytic cleavage argue strongly for transient formation of tetrahelical DNA in the cell. This review surveys tetraplex structures of DNA and their interacting proteins and appraises the evidence for their biological roles.
引用
收藏
页码:4336 / 4351
页数:16
相关论文
共 171 条
[1]   Meiosis-specific yeast Hop1 protein promotes synapsis of double-stranded DNA helices via the formation of guanine quartets [J].
Anuradha, S ;
Muniyappa, K .
NUCLEIC ACIDS RESEARCH, 2004, 32 (08) :2378-2385
[2]   Molecular aspects of meiotic chromosome synapsis and recombination [J].
Anuradha, S ;
Muniyappa, K .
PROGRESS IN NUCLEIC ACID RESEARCH AND MOLECULAR BIOLOGY, VOL 79, 2005, 79 :49-132
[3]   Interaction of human DNA topoisomerase I with G-quartet structures [J].
Arimondo, PB ;
Riou, JF ;
Mergny, JL ;
Tazi, J ;
Sun, JS ;
Garestier, T ;
Hélène, C .
NUCLEIC ACIDS RESEARCH, 2000, 28 (24) :4832-4838
[4]   Ability of thrombin to act as molecular chaperone, inducing formation of quadruplex structure of thrombin-binding aptamer [J].
Baldrich, E ;
O'Sullivan, CK .
ANALYTICAL BIOCHEMISTRY, 2005, 341 (01) :194-197
[5]   The SV40 large T-antigen helicase can unwind four stranded DNA structures linked by G-quartets [J].
Baran, N ;
Pucshansky, L ;
Marco, Y ;
Benjamin, S ;
Manor, H .
NUCLEIC ACIDS RESEARCH, 1997, 25 (02) :297-303
[6]   A mouse cytoplasmic exoribonuclease (mXRN1p) with preference for G4 tetraplex substrates [J].
Bashkirov, VI ;
Scherthan, H ;
Solinger, JA ;
Buerstedde, JM ;
Heyer, WD .
JOURNAL OF CELL BIOLOGY, 1997, 136 (04) :761-773
[7]   Following aptamer-thrombin binding by force measurements [J].
Basnar, Bernhard ;
Elnathan, Roey ;
Willner, Itamar .
ANALYTICAL CHEMISTRY, 2006, 78 (11) :3638-3642
[8]   SELECTION OF SINGLE-STRANDED-DNA MOLECULES THAT BIND AND INHIBIT HUMAN THROMBIN [J].
BOCK, LC ;
GRIFFIN, LC ;
LATHAM, JA ;
VERMAAS, EH ;
TOOLE, JJ .
NATURE, 1992, 355 (6360) :564-566
[9]   Isolation and characterization of a monoclonal anti-quadruplex DNA antibody from autoimmune "viable motheaten" mice [J].
Brown, BA ;
Li, YQ ;
Brown, JC ;
Hardin, CC ;
Roberts, JF ;
Pelsue, SC ;
Shultz, LD .
BIOCHEMISTRY, 1998, 37 (46) :16325-16337
[10]   Construction and characterization of a quadruplex DNA selective single-chain autoantibody from a viable motheaten mouse hybridoma with homology to telomeric DNA binding proteins [J].
Brown, JC ;
Brown, BA ;
Li, YQ ;
Hardin, CC .
BIOCHEMISTRY, 1998, 37 (46) :16338-16348