Unit of Structural Dynamics of Biological Macromolecules and UMR 3528 du CNRS, Institut Pasteur, 75015 Paris, France.
Unit of Structural Dynamics of Biological Macromolecules and UMR 3528 du CNRS, Institut Pasteur, 75015 Paris, France.
Curr Opin Struct Biol. 2018 Dec;53:22-31. doi: 10.1016/j.sbi.2018.03.019. Epub 2018 Apr 12.
Terminal deoxynucleotidyltransferase (TdT) is a member of the polX family which is involved in DNA repair. It has been known for years as an untemplated DNA polymerase used during V(D)J recombination to generate diversity at the CDR3 region of immunoglobulins and T-cell receptors. Recently, however, TdT was crystallized in the presence of a complete DNA synapsis made of two double-stranded DNA (dsDNA), each with a 3' protruding end, and overlapping with only one micro-homology base-pair, thus giving structural insight for the first time into DNA synthesis across strands. It was subsequently shown that TdT indeed has an in trans template-dependent activity in the presence of an excess of the downstream DNA duplex. A possible biological role of this dual activity is discussed.
末端脱氧核苷酸转移酶(TdT)是 polX 家族的成员,参与 DNA 修复。多年来,它一直被认为是一种无模板 DNA 聚合酶,在 V(D)J 重组过程中用于在免疫球蛋白和 T 细胞受体的 CDR3 区域产生多样性。然而,最近 TdT 在存在由两条双链 DNA(dsDNA)组成的完整 DNA 联会的情况下被结晶,每条 dsDNA 都有一个 3'突出端,并且只有一个微同源碱基对重叠,从而首次提供了跨链 DNA 合成的结构见解。随后表明,在过量下游 DNA 双链体的存在下,TdT 确实具有反式模板依赖性活性。讨论了这种双重活性的可能生物学作用。