Translation of pre-spliced RNAs in the nuclear compartment generates peptides for the MHC class I pathway

被引:93
作者
Apcher, Sebastien [1 ]
Millot, Guy [1 ]
Daskalogianni, Chrysoula [1 ]
Scherl, Alexander [2 ]
Manoury, Benedicte [3 ]
Fahraeus, Robin [1 ]
机构
[1] Univ Paris 07, Inst Natl Sante & Rech Med, Equipe Labellise Ligue Canc, Inst Genet Mol,Hop St Louis,Unite Mixte Rech 940, F-75010 Paris, France
[2] Ctr Med Univ Geneva, Biomed Prote Res Grp, CH-1211 Geneva 4, Switzerland
[3] Univ Paris 05, Hop Necker, Inst Natl Sante & Rech Med, Unite Mixte Rech S 1013, F-75743 Paris, France
关键词
MHC class; restricted antigen presentation; mRNA maturation; nuclear translation; CYTOLYTIC T-LYMPHOCYTES; MYELIN BASIC-PROTEIN; ANTIGENIC PEPTIDES; MAMMALIAN-CELLS; INTRON SEQUENCE; VIRAL PROTEIN; MESSENGER-RNA; CUTTING EDGE; MAJOR SOURCE; REV PROTEIN;
D O I
10.1073/pnas.1309956110
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
The scanning of maturing mRNAs by ribosomes plays a key role in the mRNA quality control process. When ribosomes first engage with the newly synthesized mRNA, and if peptides are produced, is unclear, however. Here we show that ribosomal scanning of prespliced mRNAs occurs in the nuclear compartment, and that this event produces peptide substrates for the MHC class I pathway. Inserting antigenic peptide sequences in introns that are spliced out before the mRNAs exit the nuclear compartment results in an equal amount of antigenic peptide products as when the peptides are encoded from the main open reading frame (ORF). Taken together with the detection of intron-encoded nascent peptides and RPS6/RPL7-carrying complexes in the perinucleolar compartment, these results show that peptides are produced by a translation event occurring before mRNA splicing. This suggests that ribosomes occupy and scan mRNAs early in the mRNA maturation process, and suggests a physiological role for nuclear mRNA translation, and also helps explain how the immune system tolerates peptides derived from tissue-specific mRNA splice variants.
引用
收藏
页码:17951 / 17956
页数:6
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