Perkins Thomas T, Dalal Ravindra V, Mitsis Paul G, Block Steven M
Department of Biological Sciences, Stanford University, Stanford, CA 94305, USA.
Science. 2003 Sep 26;301(5641):1914-8. doi: 10.1126/science.1088047. Epub 2003 Aug 28.
Lambda exonuclease processively degrades one strand of duplex DNA, moving 5'-to-3' in an ATP-independent fashion. When examined at the single-molecule level, the speeds of digestion were nearly constant at 4 nanometers per second (12 nucleotides per second), interspersed with pauses of variable duration. Long pauses, occurring at stereotypical locations, were strand-specific and sequence-dependent. Pause duration and probability varied widely. The strongest pause, GGCGAT TCT, was identified by gel electrophoresis. Correlating single-molecule dwell positions with sequence independently identified the motif GGCGA. This sequence is found in the left lambda cohesive end, where exonuclease inhibition may contribute to the reduced recombination efficiency at that end.
λ外切核酸酶以不依赖ATP的方式沿5'至3'方向连续降解双链DNA的一条链。在单分子水平上进行检测时,消化速度几乎恒定为每秒4纳米(每秒12个核苷酸),其间穿插着持续时间可变的停顿。在固定位置出现的长时间停顿具有链特异性且依赖于序列。停顿持续时间和概率差异很大。通过凝胶电泳确定了最强的停顿序列GGCGATTCT。将单分子停留位置与序列相关联,独立鉴定出基序GGCGA。该序列存在于λ噬菌体左侧粘性末端,外切核酸酶抑制可能导致该末端重组效率降低。