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Mechanisms and implications of transcription blockage by guanine-rich DNA sequences
被引:115
作者:
Belotserkovskii, Boris P.
[2
]
Liu, Richard
[2
]
Tornaletti, Silvia
[3
]
Krasilnikova, Maria M.
[4
]
Mirkin, Sergei M.
[1
]
Hanawalt, Philip C.
[2
]
机构:
[1] Tufts Univ, Dept Biol, Medford, MA 02155 USA
[2] Stanford Univ, Dept Biol, Stanford, CA 94305 USA
[3] Univ Florida, Dept Anat & Cell Biol, Gainesville, FL 32610 USA
[4] Penn State Univ, Dept Biochem & Mol Biol, University Pk, PA 16802 USA
来源:
关键词:
R-loops;
DNA supercoiling;
Hoogsteen base pairing;
inosine;
7-deazaquanosine;
T7;
RNA-POLYMERASE;
GENOMIC INSTABILITY;
FORMING SEQUENCE;
COUPLED REPAIR;
HUMAN-DISEASE;
G4;
DNA;
C-MYC;
ELONGATION;
STRAND;
HYBRID;
D O I:
10.1073/pnas.1007580107
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:
Various DNA sequences that interfere with transcription due to their unusual structural properties have been implicated in the regulation of gene expression and with genomic instability. An important example is sequences containing G-rich homopurine-homopyrimidine stretches, for which unusual transcriptional behavior is implicated in regulation of immunogenesis and in other processes such as genomic translocations and telomere function. To elucidate the mechanism of the effect of these sequences on transcription we have studied T7 RNA polymerase transcription of G-rich sequences in vitro. We have shown that these sequences produce significant transcription blockage in an orientation-, length- and supercoiling-dependent manner. Based upon the effects of various sequence modifications, solution conditions, and ribonucleotide substitutions, we conclude that transcription blockage is due to formation of unusually stable RNA/DNA hybrids, which could be further exacerbated by triplex formation. These structures are likely responsible for transcription-dependent replication blockage by G-rich sequences in vivo.
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页码:12816 / 12821
页数:6
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