The effect of the TRF2 N-terminal and TRFH regions on telomeric G-quadruplex structures

被引:41
作者
Pedroso, Ilene M. [1 ]
Hayward, William [1 ]
Fletcher, Terace M. [1 ]
机构
[1] Univ Miami, Miller Sch Med, Dept Biochem & Mol Biol, Miami, FL 33101 USA
关键词
IN-VITRO; MAMMALIAN TELOMERES; CRYSTAL-STRUCTURES; BINDING PROTEIN; TTAGGG REPEATS; DNA JUNCTIONS; K+ SOLUTION; SEQUENCE; LOOP; STRAND;
D O I
10.1093/nar/gkn1081
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 sequence of human telomeric DNA consists of tandem repeats of 5-d(TTAGGG)-3. This guanine-rich DNA can form G-quadruplex secondary structures which may affect telomere maintenance. A current model for telomere protection by the telomere-binding protein, TRF2, involves the formation of a t-loop which is stabilized by a strand invasion-like reaction. This type of reaction may be affected by G-quadruplex structures. We analyzed the influence of the arginine-rich, TRF2 N-terminus (TRF2(B)), as well as this region plus the TRFH domain of TRF2 (TRF2(BH)), on the structure of G-quadruplexes. Circular dichroism results suggest that oligonucleotides with 4, 7 and 8 5-d(TTAGGG)-3 repeats form hybrid structures, a mix of parallel/antiparallel strand orientation, in K. TRF2(B) stimulated the formation of parallel-stranded structures and, in some cases, intermolecular structures. TRF2(BH) also stimulated intermolecular but not parallel-stranded structures. Only full-length TRF2 and TRF2(BH) stimulated uptake of a telomeric single-stranded oligonucleotide into a plasmid containing telomeric DNA in the presence of K. The results in this study suggest that G-quadruplex formation inhibits oligonucleotide uptake into the plasmid, but the inhibition can be overcome by TRF2. This study is the first analysis of the effects of TRF2 domains on G-quadruplex structures and has implications for the role of G-quadruplexes and TRF2 in the formation of t-loops.
引用
收藏
页码:1541 / 1554
页数:14
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