Primase-polymerases: how to make a primer from scratch

被引:1
|
作者
Bainbridge, Lewis J. [1 ]
Zabrady, Katerina [1 ]
Doherty, Aidan J. [1 ]
机构
[1] Univ Sussex, Genome Damage & Stabil Ctr, Sch Life Sci, Brighton BN1 9RQ, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
DNA PRIMASE; REPLICATION FORKS; CRYSTAL-STRUCTURE; PLASMID RSF1010; MOLECULAR-BASIS; HUMAN PRIMPOL; INITIATION; DOMAIN; MECHANISM; RNA;
D O I
10.1042/BSR20221986
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To pass on genetic information to the next generation, cells must faithfully replicate their genomes to provide copies for each daughter cell. To synthesise these duplicates, cells employ specialised enzymes called DNA polymerases, which rapidly and accurately replicate nucleic acid polymers. However, most polymerases lack the ability to directly initiate DNA synthesis and required specialised replicases called primases to make short polynucleotide primers, from which they then extend. Replicative primases (eukaryotes and archaea) belong to a functionally diverse enzyme superfamily known as Primase-Polymerases (Prim-Pols), with orthologues present throughout all domains of life. Characterised by a conserved catalytic Prim-Pol domain, these enzymes have evolved various roles in DNA metabolism, including DNA replication, repair, and damage tolerance. Many of these biological roles are fundamentally underpinned by the ability of Prim-Pols to generate primers de novo. This review examines our current understanding of the catalytic mechanisms utilised by Prim-Pols to initiate primer synthesis.
引用
收藏
页数:13
相关论文
共 50 条