Reflections on the state of play in somatic hypermutation

被引:5
|
作者
Steele, Edward J. [1 ,2 ]
机构
[1] Australian Natl Univ, Inst Adv Studies, Res Sch Biol Sci, Genom Interact Grp, Canberra, ACT 2601, Australia
[2] Australian Natl Univ, Inst Adv Studies, Res Sch Biol Sci, CILR, Canberra, ACT 2601, Australia
关键词
mechanism somatic hypermutation; reverse transcriptase model; A : T targeted phase IISHM; DNA polymerase eta; A-to-I RNA editing;
D O I
10.1016/j.molimm.2008.02.002
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
Somatic hypermutation (SHM) of rearranged variable genes proceeds in two phases. Phase I which is well understood is triggered by activation-induced cytidine deaminase (AID) and targets mutations at C:G base pairs equally on both DNA strands. Phase II, is less well understood, and targets A:T base pairs by coopting DNA polymerase-eta and acts in a strand biased fashion such that mutations off A exceed mutations of T by two- to threefold. Current molecular models attempting to explain A:T targeted Phase 11 are critically reviewed. It is the author's viewpoint that the 'RT-model', which invokes both transcription-coupled DNA and RNA deamination together with error-prone reverse transcription via Pol-eta, is the best explanation of current somatic hypermutation data. (c) 2008 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2723 / 2726
页数:4
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