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10.1186/s12864-017-3760-0

http://scihub22266oqcxt.onion/10.1186/s12864-017-3760-0
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suck abstract from ncbi


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pmid28521747      BMC+Genomics 2017 ; 18 (ä): ä
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  • Insights into the ancestral organisation of the mammalian MHC class II region from the genome of the pteropid bat, Pteropus alecto #MMPMID28521747
  • Ng JHJ; Tachedjian M; Wang LF; Baker ML
  • BMC Genomics 2017[]; 18 (ä): ä PMID28521747show ga
  • Background: Bats are an extremely successful group of mammals and possess a variety of unique characteristics, including their ability to co-exist with a diverse range of pathogens. The major histocompatibility complex (MHC) is the most gene dense and polymorphic region of the genome and MHC class II (MHC-II) molecules play a vital role in the presentation of antigens derived from extracellular pathogens and activation of the adaptive immune response. Characterisation of the MHC-II region of bats is crucial for understanding the evolution of the MHC and of the role of pathogens in shaping the immune system. Results: Here we describe the relatively contracted MHC-II region of the Australian black flying-fox (Pteropus alecto), providing the first detailed insight into the MHC-II region of any species of bat. Twelve MHC-II genes, including one locus (DRB2) located outside the class II region, were identified on a single scaffold in the bat genome. The presence of a class II locus outside the MHC-II region is atypical and provides evidence for an ancient class II duplication block. Two non-classical loci, DO and DM and two classical, DQ and DR loci, were identified in P. alecto. A putative classical, DPB pseudogene was also identified. The bat?s antigen processing cluster, though contracted, remains highly conserved, thus supporting its importance in antigen presentation and disease resistance. Conclusions: This detailed characterisation of the bat MHC-II region helps to fill a phylogenetic gap in the evolution of the mammalian class II region and is a stepping stone towards better understanding of the immune responses in bats to viral, bacterial, fungal and parasitic infections. Electronic supplementary material: The online version of this article (doi:10.1186/s12864-017-3760-0) contains supplementary material, which is available to authorized users.
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