Postel Edith H
Department of Molecular Biology, Princeton University, Princeton, New Jersey 08546-5414, USA.
J Bioenerg Biomembr. 2003 Feb;35(1):31-40. doi: 10.1023/a:1023485505621.
NM23/NDPk proteins play critical roles in cancer and development; however, our understanding of the underlying biochemical mechanisms is still limited. This large family of highly conserved proteins are known to participate in many events related to DNA metabolism, including nucleotide binding and nucleoside triphosphate synthesis, DNA binding and transcription, and cleavage of DNA strands via covalent protein-DNA complexes. The chemistry of the DNA-cleavage reaction of NM23-H2/NDPk is characteristic of DNA repair enzymes. Both the DNA cleavage and the NDPk reactions are conserved between E. coli and the human enzymes, and several conserved amino acid side chains involved in catalysis are shared by these reactions. It is proposed here that NM23/NDP kinases are important regulators of gene expression during development and cancer via previously unrecognized roles in DNA repair and recombination, and via previously unrecognized pathways and mechanisms of genetic control.
NM23/NDPk蛋白在癌症和发育过程中发挥着关键作用;然而,我们对其潜在生化机制的了解仍然有限。已知这一高度保守的蛋白大家族参与许多与DNA代谢相关的事件,包括核苷酸结合和三磷酸核苷合成、DNA结合和转录,以及通过共价蛋白-DNA复合物切割DNA链。NM23-H2/NDPk的DNA切割反应化学性质具有DNA修复酶的特征。DNA切割反应和NDPk反应在大肠杆菌和人类酶之间是保守的,并且这些反应共享几个参与催化的保守氨基酸侧链。本文提出,NM23/NDP激酶通过在DNA修复和重组中以前未被认识的作用,以及通过以前未被认识的遗传控制途径和机制,在发育和癌症过程中是基因表达的重要调节因子。