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Delagoutte E Goellner GM Guo J Baldacci G McMurray CT 《The Journal of biological chemistry》2008,283(19):13341-13356
Small insertions and deletions of trinucleotide repeats (TNRs) can occur by polymerase slippage and hairpin formation on either template or newly synthesized strands during replication. Although not predicted by a slippage model, deletions occur preferentially when 5'-CTG is in the lagging strand template and are highly favored over insertion events in rapidly replicating cells. The mechanism for the deletion bias and the orientation dependence of TNR instability is poorly understood. We report here that there is an orientation-dependent impediment to polymerase progression on 5'-CAG and 5'-CTG repeats that can be relieved by the binding of single-stranded DNA-binding protein. The block depends on the primary sequence of the TNR but does not correlate with the thermodynamic stability of hairpins. The orientation-dependent block of polymerase passage is the strongest when 5'-CAG is the template. We propose a "template-push" model in which the slow speed of DNA polymerase across the 5'-CAG leading strand template creates a threat to helicase-polymerase coupling. To prevent uncoupling, the TNR template is pushed out and by-passed. Hairpins do not cause the block, but appear to occur as a consequence of polymerase pass-over. 相似文献
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Assembly and disassembly of the Drosophila RNA polymerase II complex during transcription. 总被引:11,自引:0,他引:11
J T Kadonaga 《The Journal of biological chemistry》1990,265(5):2624-2631
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Activation of transcription factor IIIC by the adenovirus E1A protein 总被引:56,自引:0,他引:56
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