<?xml version="1.0"?>
<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:title>HLA-E coding and 3 ' untranslated region variability determined by next-generation sequencing in two West-African population samples</dc:title>
  <dc:creator>Castelli, E. C.</dc:creator>
  <dc:creator>Mendes, C. T.</dc:creator>
  <dc:creator>Sabbagh, A.</dc:creator>
  <dc:creator>Porto, I. O. P.</dc:creator>
  <dc:creator>/Garcia, Andr&#xE9;</dc:creator>
  <dc:creator>Ramalho, J.</dc:creator>
  <dc:creator>Lima, T. H. A.</dc:creator>
  <dc:creator>Massaro, J. D.</dc:creator>
  <dc:creator>Dias, F. C.</dc:creator>
  <dc:creator>Collares, C. V. A.</dc:creator>
  <dc:creator>/Jamonneau, Vincent</dc:creator>
  <dc:creator>/Bucheton, Bruno</dc:creator>
  <dc:creator>Camara, M.</dc:creator>
  <dc:creator>Donadi, E. A.</dc:creator>
  <dc:subject>West-African populations</dc:subject>
  <dc:subject>HLA-E</dc:subject>
  <dc:subject>Next-generation sequencing (NGS)</dc:subject>
  <dc:subject>Polymorphisms</dc:subject>
  <dc:subject>Haplotypes</dc:subject>
  <dc:subject>Non-classical HLA</dc:subject>
  <dc:subject>Africa</dc:subject>
  <dc:description>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.</dc:description>
  <dc:date>2015</dc:date>
  <dc:type>text</dc:type>
  <dc:identifier>https://www.documentation.ird.fr/hor/fdi:010066010</dc:identifier>
  <dc:identifier>fdi:010066010</dc:identifier>
  <dc:identifier>Castelli E. C., Mendes C. T., Sabbagh A., Porto I. O. P., Garcia Andr&#xE9;, Ramalho J., Lima T. H. A., Massaro J. D., Dias F. C., Collares C. V. A., Jamonneau Vincent, Bucheton Bruno, Camara M., Donadi E. A.. HLA-E coding and 3 ' untranslated region variability determined by next-generation sequencing in two West-African population samples. 2015, 76 (12),  945-953</dc:identifier>
  <dc:language>EN</dc:language>
  <dc:coverage>GUINEE</dc:coverage>
  <dc:coverage>BURKINA FASO</dc:coverage>
</oai_dc:dc>
