G-quadruplex formation in human telomeric (TTAGGG)4 sequence with complementary strand in close vicinity under molecularly crowded condition

被引:73
作者
Kan, Zhong-Yuan
Lin, Yi
Wang, Feng
Zhuang, Xin-Ying
Zhao, Yong
Pang, Dai-Wen
Hao, Yu-Hua
Tan, Zheng [1 ]
机构
[1] Wuhan Univ, Coll Life Sci, Lab Biochem & Biophys, Wuhan 430072, Peoples R China
[2] Wuhan Univ, Coll Chem & Mol Sci, Wuhan 430072, Peoples R China
[3] Chinese Acad Sci, Inst Zool, State Key Lab Biomembrane & Membrane Biotechnol, Beijing 100080, Peoples R China
关键词
D O I
10.1093/nar/gkm203
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
Chromosomes in vertebrates are protected at both ends by telomere DNA composed of tandem (TTAGGG)(n) repeats. DNA replication produces a blunt-ended leading strand telomere and a lagging strand telomere carrying a single-stranded G-rich overhang at its end. The G-rich strand can form G-quadruplex structure in the presence of K+ or Na+. At present, it is not clear whether quadruplex can form in the double-stranded telomere region where the two complementary strands are constrained in close vicinity and quadruplex formation, if possible, has to compete with the formation of the conventional Watson-Crick duplex. In this work, we studied quadruplex formation in oligonucleotides and double- stranded DNA containing both the G- and C- rich sequences to better mimic the in vivo situation. Under such competitive condition only duplex was observed in dilute solution containing physiological concentration of K+. However, quadruplex could preferentially form and dominate over duplex structure under molecular crowding condition created by PEG as a result of significant quadruplex stabilization and duplex destabilization. This observation suggests quadruplex may potentially form or be induced at the blunt end of a telomere, which may present a possible alternative form of structures at telomere ends.
引用
收藏
页码:3646 / 3653
页数:8
相关论文
共 51 条
[1]   HAIRPIN AND PARALLEL QUARTET STRUCTURES FOR TELOMERIC SEQUENCES [J].
BALAGURUMOORTHY, P ;
BRAHMACHARI, SK ;
MOHANTY, D ;
BANSAL, M ;
SASISEKHARAN, V .
NUCLEIC ACIDS RESEARCH, 1992, 20 (15) :4061-4067
[2]   Switching and signaling at the telomere [J].
Blackburn, EH .
CELL, 2001, 106 (06) :661-673
[3]   Verification of antiparallel G-quadruplex structure in human telomeres by using two-photon excitation fluorescence lifetime imaging microscopy of the 3,6-bis(1-methyl-4-vinylpyridinium)carbazole diiodide molecule [J].
Chang, CC ;
Chu, JF ;
Kao, FJ ;
Chiu, YC ;
Lou, PJ ;
Chen, HC ;
Chang, TC .
ANALYTICAL CHEMISTRY, 2006, 78 (08) :2810-2815
[4]   Detection of quadruplex DNA structures in human telomeres by a fluorescent carbazole derivative [J].
Chang, CC ;
Kuo, IC ;
Ling, IF ;
Chen, CT ;
Chen, HC ;
Lou, PJ ;
Lin, JJ ;
Chang, TC .
ANALYTICAL CHEMISTRY, 2004, 76 (15) :4490-4494
[5]   A fluorescent carbazole derivative: High sensitivity for quadruplex DNA [J].
Chang, CC ;
Wu, JY ;
Chien, CW ;
Wu, WS ;
Liu, H ;
Kang, CC ;
Yu, LJ ;
Chang, TC .
ANALYTICAL CHEMISTRY, 2003, 75 (22) :6177-6183
[6]   Biochemical effects of molecular crowding [J].
Chebotareva, NA ;
Kurganov, BI ;
Livanova, NB .
BIOCHEMISTRY-MOSCOW, 2004, 69 (11) :1239-+
[7]   ACID-FACILITATED SUPRAMOLECULAR ASSEMBLY OF G-QUADRUPLEXES IN D(CGG)(4) [J].
CHEN, FM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (39) :23090-23096
[8]   G-quadruplex formation within the promoter of the KRAS proto-oncogene and its effect on transcription [J].
Cogoi, Susanna ;
Xodo, Luigi E. .
NUCLEIC ACIDS RESEARCH, 2006, 34 (09) :2536-2549
[9]   Biophysical and biological properties of quadruplex oligodeoxyribonucleotides [J].
Dapic, V ;
Abdomerovic, V ;
Marrington, R ;
Peberdy, J ;
Rodger, A ;
Trent, JO ;
Bates, PJ .
NUCLEIC ACIDS RESEARCH, 2003, 31 (08) :2097-2107
[10]   Antiproliferative activity of G-quartet-forming oligonucleotides with backbone and sugar modifications [J].
Dapic, V ;
Bates, PJ ;
Trent, JO ;
Rodger, A ;
Thomas, SD ;
Miller, DM .
BIOCHEMISTRY, 2002, 41 (11) :3676-3685