Wilson Ryan C, Pata Janice D
Division of Molecular Medicine, Wadsworth Center, New York State Department of Health, The State University of New York at Albany, Albany, NY 12201-0509, USA.
Mol Cell. 2008 Mar 28;29(6):767-79. doi: 10.1016/j.molcel.2008.01.014.
Dbh is a Y family translesion DNA polymerase that accurately bypasses some damaged forms of deoxyguanosine, but also generates single-base deletion errors at frequencies of up to 50%, in specific hot spot sequences. We describe preinsertion binary, insertion ternary, and postinsertion binary crystal structures of Dbh synthesizing DNA after making a single-base deletion. The skipped template base adopts an extrahelical conformation stabilized by interactions with the C-terminal domain of the enzyme. DNA translocation and positioning of the next templating base at the active site, with space opposite to accommodate incoming nucleotide, occur independently of nucleotide binding, incorporation, and pyrophosphate release. We also show that Dbh creates single-base deletions more rapidly when the skipped base is located two or three bases upstream of the nascent base pair than when it is directly adjacent to the templating base, indicating that Dbh predominantly creates single-base deletions by template slippage rather than by dNTP-stabilized misalignment.
Dbh是一种Y家族跨损伤DNA聚合酶,它能准确绕过某些受损形式的脱氧鸟苷,但在特定热点序列中也会以高达50%的频率产生单碱基缺失错误。我们描述了Dbh在产生单碱基缺失后合成DNA时的插入前二元、插入三元和插入后二元晶体结构。跳过的模板碱基采用一种通过与酶的C末端结构域相互作用而稳定的螺旋外构象。DNA转位以及下一个模板碱基在活性位点的定位,同时在对面留出空间以容纳进入的核苷酸,这一过程独立于核苷酸结合、掺入和焦磷酸释放。我们还表明,当跳过的碱基位于新生碱基对上游两三个碱基处时,Dbh产生单碱基缺失的速度比其直接与模板碱基相邻时更快,这表明Dbh主要通过模板滑动而非dNTP稳定的错配来产生单碱基缺失。