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This article is part of the supplement: Proceedings of the International Symposium on Animal Genomics for Animal Health (AGAH 2010)

Open Access Proceedings

Transcription variants of SLA-7, a swine non classical MHC class I gene

Rui Hu123, Gaëtan Lemonnier123, Emmanuelle Bourneuf123, Silvia Vincent-Naulleau123 and Claire Rogel-Gaillard123*

Author affiliations

1 INRA, UMR de Génétique Animale et Biologie Intégrative, Jouy-en-Josas, France

2 CEA, DSV, iRCM, Laboratoire de Radiobiologie et Etude du Génome, Jouy-en-Josas, France

3 AgroParisTech, UMR de Génétique Animale et Biologie Intégrative, Jouy-en-Josas, France

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Citation and License

BMC Proceedings 2011, 5(Suppl 4):S10  doi:10.1186/1753-6561-5-S4-S10

Published: 3 June 2011

Abstract

In pig, very little information is available on the non classical class I (Ib) genes of the Major Histocompatibility Complex (MHC) i.e. SLA-6, -7 and -8. Our aim was to focus on the transcription pattern of the SLA-7 gene. RT-PCR experiments were carried out with SLA-7 specific primers targeting either the full coding sequence (CDS) from exon 1 to the 3 prime untranslated region (3UTR) or a partial CDS from exon 4 to the 3UTR. We show that the SLA-7 gene expresses a full length transcript not yet identified that refines annotation of the gene with eight exons instead of seven as initially described from the existing RefSeq RNA. These two RNAs encode molecules that differ in cytoplasmic tail length. In this study, another SLA-7 transcript variant was characterized, which encodes a protein with a shorter alpha 3 domain, as a consequence of a splicing site within exon 4. Surprisingly, a cryptic non canonical GA-AG splicing site is used to generate this transcript variant. An additional SLA-7 variant was also identified in the 3UTR with a splicing site occurring 31 nucleotides downstream to the stop codon. In conclusion, the pig SLA-7 MHC class Ib gene presents a complex transcription pattern with two transcripts encoding various molecules and transcripts that do not alter the CDS and may be subject to post-transcriptional regulation.