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      <ref-type name="Journal Article">17</ref-type>
      <work-type>ACL : Articles dans des revues avec comité de lecture répertoriées par l'AERES</work-type>
      <contributors>
        <authors>
          <author>
            <style face="normal" font="default" size="100%">Castelli, E. C.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Mendes, C. T.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Sabbagh, A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Porto, I. O. P.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Garcia, André</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Ramalho, J.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Lima, T. H. A.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Massaro, J. D.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Dias, F. C.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Collares, C. V. A.</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Jamonneau, Vincent</style>
          </author>
          <author>
            <style face="bold" font="default" size="100%">Bucheton, Bruno</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Camara, M.</style>
          </author>
          <author>
            <style face="normal" font="default" size="100%">Donadi, E. A.</style>
          </author>
        </authors>
      </contributors>
      <titles>
        <title>HLA-E coding and 3 ' untranslated region variability determined by next-generation sequencing in two West-African population samples</title>
        <secondary-title>Human Immunology</secondary-title>
      </titles>
      <pages>945-953</pages>
      <keywords>
        <keyword>West-African populations</keyword>
        <keyword>HLA-E</keyword>
        <keyword>Next-generation sequencing (NGS)</keyword>
        <keyword>Polymorphisms</keyword>
        <keyword>Haplotypes</keyword>
        <keyword>Non-classical HLA</keyword>
        <keyword>Africa</keyword>
        <keyword>GUINEE</keyword>
        <keyword>BURKINA FASO</keyword>
      </keywords>
      <dates>
        <year>2015</year>
      </dates>
      <call-num>fdi:010066010</call-num>
      <language>ENG</language>
      <periodical>
        <full-title>Human Immunology</full-title>
      </periodical>
      <isbn>0198-8859</isbn>
      <accession-num>ISI:000366437900011</accession-num>
      <number>12</number>
      <electronic-resource-num>10.1016/j.humimm.2015.06.016</electronic-resource-num>
      <urls>
        <related-urls>
          <url>https://www.documentation.ird.fr/hor/fdi:010066010</url>
        </related-urls>
        <pdf-urls>
          <url>https://www.documentation.ird.fr/intranet/publi/2016/01/010066010.pdf</url>
        </pdf-urls>
      </urls>
      <volume>76</volume>
      <remote-database-provider>Horizon (IRD)</remote-database-provider>
      <abstract>HLA-E is a non-classical Human Leucocyte Antigen class I gene with immunomodulatory properties. Whereas HLA-E expression usually occurs at low levels, it is widely distributed amongst human tissues, has the ability to bind self and non-self antigens and to interact with NK cells and T lymphocytes, being important for immunosurveillance and also for fighting against infections. HLA-E is usually the most conserved locus among all class I genes. However, most of the previous studies evaluating HLA-E variability sequenced only a few exons or genotyped known polymorphisms. Here we report a strategy to evaluate HLA-E variability by next-generation sequencing (NGS) that might be used to other HLA loci and present the HLA-E haplotype diversity considering the segment encoding the entire HLA-E mRNA (including 5'UTR, introns and the 3'UTR) in two African population samples, Susu from Guinea-Conakry and Lobi from Burkina Faso. Our results indicate that (a) the HLA-E gene is indeed conserved, encoding mainly two different protein molecules; (b) Africans do present several unknown HLA-E alleles presenting synonymous mutations; (c) the HLA-E 3'UTR is quite polymorphic and (d) haplotypes in the HLA-E 3'UTR are in close association with HLA-E coding alleles. NGS has proved to be an important tool on data generation for future studies evaluating variability in non-classical MHC genes.</abstract>
      <custom6>050 ; 106</custom6>
      <custom1>UR216 / UR177</custom1>
      <custom7>Brésil / Guinée</custom7>
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