Inhibitory effect of a short Z-DNA forming sequence on transcription elongation by T7 RNA polymerase

被引:49
|
作者
Ditlevson, Jennifer V. [1 ]
Tornaletti, Silvia [1 ]
Belotserkovskii, Boris P. [1 ]
Teijeiro, Virginia [1 ]
Wang, Guliang [2 ]
Vasquez, Karen M. [2 ]
Hanawalt, Philip C. [1 ]
机构
[1] Stanford Univ, Dept Biol Sci, Stanford, CA 94305 USA
[2] Univ Texas MD Anderson Canc Ctr, Div Sci Pk Res, Dept Carcinogenesis, Smithville, TX 78957 USA
关键词
D O I
10.1093/nar/gkn136
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
DNA sequences capable of forming unusual secondary structures can be a source of genomic instability. In some cases that instability might be affected by transcription, as recently shown for the Z-DNA forming sequence (CG)(14), which causes genomic instability both in mammalian cells and in bacteria, and this effect increases with its transcription. We have investigated the effect of this (CG)(14) sequence on transcription with T7 RNA polymerase in vitro. We detected partial transcription blockage within the sequence; the blockage increased with negative supercoiling of the template DNA. This effect was not observed in a control self-complementary sequence of identical length and base composition as the (CG)(14) sequence, when the purinepyrimidine alternation required for Z-DNA formation was disrupted. These findings suggest that the inhibitory effect on T7 transcription results from Z-DNA formation in the (CG)(14) sequence rather than from an effect of the sequence composition or from hairpin formation in either the DNA or the RNA product.
引用
收藏
页码:3163 / 3170
页数:8
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