Non-classical HLA-E gene variability in Brazilians: a nearly invariable locus surrounded by the most variable genes in the human genome


Autoria(s): Veiga-Castelli, L. C.; Castelli, E. C.; Junior, Celso Teixeira Mendes; Junior, Wilson Araújo da Silva; Faucher, M. -C.; Beauchemin, K.; Roger, M.; Moreau, P.; Donadi, Eduardo Antonio
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

29/10/2013

29/10/2013

2012

Resumo

The non-classical human leukocyte antigen (HLA) class I genes present a very low rate of variation. So far, only 10 HLA-E alleles encoding three proteins have been described, but only two are frequently found in worldwide populations. Because of its historical background, Brazilians are very suitable for population genetic studies. Therefore, 104 bone marrow donors from Brazil were evaluated for HLA-E exons 14. Seven variation sites were found, including two known single nucleotide polymorphisms (SNPs) at positions +424 and +756 and five new SNPs at positions +170 (intron 1), +1294 (intron 3), +1625, +1645 and +1857 (exon 4). Haplotyping analysis did show eight haplotypes, three of them known as E*01:01:01, E*01:03:01 and E*01:03:02:01 and five HLA-E new alleles that carry the new variation sites. The HLA-E*01:01:01 allele was the predominant haplotype (62.50%), followed by E*01:03:02:01 (24.52%). Selective neutrality tests have disclosed an interesting pattern of selective pressures in which balancing selection is probably shaping allele frequency distributions at an SNP at exon 3 (codon 107), sequence diversity at exon 4 and the non-coding regions is facing significant purifying pressure. Even in an admixed population such as the Brazilian one, the HLA-E locus is very conserved, presenting few polymorphic SNPs in the coding region.

Brazilian National Research Council (CNPq/Brazil) [475670/2007-8, 558476/2008-0]

Brazilian National Research Council (CNPq/Brazil)

CAPESCOFECUB

CAPES-COFECUB [653/09]

CNPq/Brazil [150175/2009-4]

CNPq (Brazil)

Fonds de la Recherche en Sante du Quebec (FRSQ)

Fonds de la Recherche en Sante du Quebec (FRSQ)

Identificador

TISSUE ANTIGENS, MALDEN, v. 79, n. 1, supl. 1, Part 3, pp. 15-24, JAN, 2012

0001-2815

http://www.producao.usp.br/handle/BDPI/36373

10.1111/j.1399-0039.2011.01801.x

http://dx.doi.org/10.1111/j.1399-0039.2011.01801.x

Idioma(s)

eng

Publicador

WILEY-BLACKWELL

MALDEN

Relação

TISSUE ANTIGENS

Direitos

closedAccess

Copyright WILEY-BLACKWELL

Palavras-Chave #BRAZILIANS #EVOLUTION #HAPLOTYPES #HLA-E #POLYMORPHISM #MAJOR HISTOCOMPATIBILITY COMPLEX #LINKAGE DISEQUILIBRIUM #SURFACE EXPRESSION #STATISTICAL-METHOD #E POLYMORPHISM #E BINDS #MHC #POPULATION #SELECTION #EVOLUTION #CELL BIOLOGY #IMMUNOLOGY #PATHOLOGY
Tipo

article

original article

publishedVersion