Guarné Alba, Zhao Qinghai, Ghirlando Rodolfo, Yang Wei
Laboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, USA.
Nat Struct Biol. 2002 Nov;9(11):839-43. doi: 10.1038/nsb857.
The SeqA protein binds clusters of fully methylated or hemimethylated GATC sequences at oriC and negatively modulates the initiation of DNA replication. We find that SeqA can be proteolytically cleaved into an N-terminal multimerization and a C-terminal DNA-binding domain and have determined the crystal structure of the C-terminal domain in complex with a hemimethylated GATC site. SeqA makes direct hydrogen bonds and van der Waals contacts with the hemimethylated A-T base pair in addition to interactions with the surrounding bases and DNA backbone. The tetrameric protein-DNA complex found in the crystal suggests that SeqA binds multiple GATC sites on separate DNA duplexes, altering the overall DNA topology and sequestering oriC from replication initiation.
SeqA蛋白结合oriC处完全甲基化或半甲基化的GATC序列簇,并对DNA复制的起始进行负调控。我们发现SeqA可被蛋白水解切割成一个N端多聚化结构域和一个C端DNA结合结构域,并已确定C端结构域与半甲基化GATC位点形成复合物的晶体结构。除了与周围碱基和DNA骨架相互作用外,SeqA还与半甲基化的A-T碱基对形成直接氢键和范德华接触。晶体中发现的四聚体蛋白-DNA复合物表明,SeqA结合在不同DNA双链体上的多个GATC位点,改变了整体DNA拓扑结构,并将oriC与复制起始隔离开来。