Structural Basis for the Persistence of Homing Endonucleases in Transcription Factor IIB Inteins

被引:16
作者
Iwai, Hideo [1 ]
Mikula, Kornelia M. [1 ]
Oeemig, Jesper S. [1 ,4 ]
Zhou, Dongwen [2 ,5 ]
Li, Mi [2 ,3 ]
Wlodawer, Alexander [2 ]
机构
[1] Univ Helsinki, Inst Biotechnol, Res Program Struct Biol & Biophys, POB 65, FIN-00014 Helsinki, Finland
[2] NCI, Macromol Crystall Lab, Frederick, MD 21702 USA
[3] Frederick Natl Lab Canc Res, Leidos Biomed Res, Basic Sci Program, Frederick, MD 21702 USA
[4] Vrije Univ Brussel VIB, VIB Ctr Struct Biol, Brussels, Belgium
[5] Blood Ctr Wisconsin, Blood Res Inst, Milwaukee, WI 53226 USA
基金
芬兰科学院;
关键词
inteins; protein splicing; homing endonuclease; horizontal gene transfer; FUNCTIONAL MINI-INTEINS; YEAST VMA1 PROTOZYME; CRYSTAL-STRUCTURE; MOLECULAR-REPLACEMENT; PROTEIN LIGATION; EVOLUTION; GENE; DOMAIN; CRYSTALLOGRAPHY; DEGENERATION;
D O I
10.1016/j.jmb.2017.10.016
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
Inteins are mobile genetic elements that are spliced out of proteins after translation. Some inteins contain a homing endonuclease (HEN) responsible for their propagation. Hedgehog/INTein (HINT) domains catalyzing protein splicing and their nested HEN domains are thought to be functionally independent because of the existence of functional mini-inteins without HEN domains. Despite the lack of obvious mutualism between HEN and HINT domains, HEN domains are persistently found at one specific site in inteins, indicating their potential functional role in protein splicing. Here we report crystal structures of inactive and active mini-inteins derived from inteins residing in the transcription factor IIB of Methanococcus jannaschii and Methanocaldococcus vulcanius, revealing a novel modified HINT fold that might provide new insights into the mutualism between the HEN and HINT domains. We propose an evolutionary model of inteins and a functional role of HEN domains in inteins. (c) 2017 Published by Elsevier Ltd.
引用
收藏
页码:3942 / 3956
页数:15
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