Tautomerization-dependent recognition and excision of oxidation damage in base-excision DNA repair. Academic Article uri icon

Overview

abstract

  • NEIL1 (Nei-like 1) is a DNA repair glycosylase guarding the mammalian genome against oxidized DNA bases. As the first enzymes in the base-excision repair pathway, glycosylases must recognize the cognate substrates and catalyze their excision. Here we present crystal structures of human NEIL1 bound to a range of duplex DNA. Together with computational and biochemical analyses, our results suggest that NEIL1 promotes tautomerization of thymine glycol (Tg)-a preferred substrate-for optimal binding in its active site. Moreover, this tautomerization event also facilitates NEIL1-catalyzed Tg excision. To our knowledge, the present example represents the first documented case of enzyme-promoted tautomerization for efficient substrate recognition and catalysis in an enzyme-catalyzed reaction.

authors

  • Zhu, Chenxu
  • Lu, Lining
  • Zhang, Jun
  • Yue, Zongwei
  • Song, Jinghui
  • Zong, Shuai
  • Liu, Menghao
  • Stovicek, Olivia
  • Gao, Yi Qin
  • Yi, Chengqi

publication date

  • June 27, 2016

Research

keywords

  • DNA
  • DNA Glycosylases
  • DNA Repair

Identity

PubMed Central ID

  • PMC4948311

Scopus Document Identifier

  • 84978141978

Digital Object Identifier (DOI)

  • 10.1073/pnas.1604591113

PubMed ID

  • 27354518

Additional Document Info

volume

  • 113

issue

  • 28