Karthikeyan G, Chary K V, Rao B J
Department of Biological Sciences, Tata Institute of Fundamental Research, Bombay, India.
Nucleic Acids Res. 1999 Oct 1;27(19):3851-8. doi: 10.1093/nar/27.19.3851.
Polymerase slippage during DNA synthesis by the Klenow fragment of DNA polymerase across A, C, G and T repeats (30 bases) has been studied. Within minutes, duplexes that contain only repeats (30 bp) expand dramatically to several hundred base pairs long. Rate comparisons in a repeat duplex when one strand was expanded as against that when both strands were expanded suggest a model of migrating hairpin loops which in the latter case coalesce into a duplex. Moreover, slippage (at the proximal or 3'-end) is subject to positive and negative effects from the 5'-end (distal) of the same strand. Growing T and G strands generate T.A:T and G-G:C motif fold-back structures at the distal end that hamper slippage at the proximal end. On the other hand, growing tails at the distal end upon annealing with excess complementary template accentuates proximal slippage several-fold.
对DNA聚合酶的Klenow片段在DNA合成过程中跨越A、C、G和T重复序列(30个碱基)时的聚合酶滑动现象进行了研究。在几分钟内,仅包含重复序列(30 bp)的双链会急剧扩展至数百个碱基对长。当一条链扩展时与两条链都扩展时的重复双链速率比较表明,存在一种迁移发夹环模型,在后一种情况下,这些环会合并成一个双链。此外,(在近端或3'端的)滑动会受到同一条链5'端(远端)的正向和负向影响。正在延伸的T链和G链在远端产生T.A:T和G-G:C基序的回折结构,这会阻碍近端的滑动。另一方面,与过量互补模板退火时,远端不断增长的尾巴会使近端滑动增强数倍。