Pioneer translation products as an alternative source for MHC-I antigenic peptides

被引:11
作者
Apcher, Sebastien [1 ]
Daskalogianni, Chrysoula [2 ]
Fahraeus, Robin [2 ,3 ]
机构
[1] Univ Paris 11, Inst Gustave Roussy, U1015, Dept Immunol, F-94805 Villejuif, France
[2] Univ Paris 07, Inst Genet Mol, INSERM, Equipe Labellisee Ligue Canc,UMR1162, F-75010 Paris, France
[3] Masaryk Mem Canc Inst, RECAMO, Brno 65653, Czech Republic
关键词
MHC class I antigen presentation; Alternative mRNA translation products; SYNTHETIC LONG PEPTIDES; CYTOLYTIC T-LYMPHOCYTES; DENDRITIC CELLS; INTRON SEQUENCE; MAJOR SOURCE; VIRUS; INHIBITION; DISPLAY; PROTEIN;
D O I
10.1016/j.molimm.2015.04.019
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
The notion that alternative peptide substrates can be processed and presented to the MHC class I pathway has opened for new aspects on how the immune system detects infected or damaged cells. Recent works show that antigenic peptides are derived from intron sequences in pre-mRNAs target for the nonsensemediated degradation pathway. Introns are spliced out co-transcriptionally suggesting that such pioneer translation products (PTPs) are synthesized on the nascent RNAs in the nuclear compartment to ensure that the first peptides to emerge from an mRNA are destined for the class I pathway. This illustrates an independent translation event during mRNA maturation that give rise to specific peptide products with a specific function in the immune system. The characterization of the translation apparatus responsible for PTP synthesis will pave the way for understanding how PTP production is regulated in different tissues under different conditions and will help designing new vaccine strategies. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:68 / 71
页数:4
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