HLA-G, -E and -F regulatory and coding region variability and haplotypes in the Beninese Toffin population sample. (December 2018)
- Record Type:
- Journal Article
- Title:
- HLA-G, -E and -F regulatory and coding region variability and haplotypes in the Beninese Toffin population sample. (December 2018)
- Main Title:
- HLA-G, -E and -F regulatory and coding region variability and haplotypes in the Beninese Toffin population sample
- Authors:
- Sonon, Paulin
Sadissou, Ibrahim
Tokplonou, Léonidas
M'po, Kuumaaté K.G.
Glitho, Sonya S.C.
Agniwo, Privat
Ibikounlé, Moudachirou
Massaro, Juliana Doblas
Massougbodji, Achille
Moreau, Philippe
Sabbagh, Audrey
Mendes-Junior, Celso T.
Moutairou, Kabirou A.
Castelli, Erick C.
Courtin, David
Donadi, Eduardo A. - Abstract:
- Highlights: HLA-G/E/F are the most conserved HLA class I genes even in Africans. Despite population diversity selection pressures maintained low HLA-E/F/G diversity. Conserved protein diversity supports the immunomodulatory role of HLA-E/F/G. Toffin ethnic group could be considered as a rich repository for genetic variation. Abstract: HLA-G/E/F genes exhibit immunomodulatory properties and are expressed in placenta. Little attention has been devoted to the study of these genes in sub-Saharan African populations, which are yet the most diverse. To fill this gap, we evaluated the complete gene variability, approximately 5.1 kb for HLA-G (n = 149), 7.7 kb for HLA-E (n = 150) and 6.2 kb for HLA-F (n = 152) in the remote Beninese Toffin population, using massive parallel sequencing. Overall, 96, 37 and 68 variable sites were detected along the entire HLA-G, -E and -F, respectively, arranged into region-specific haplotypes; i.e., promoter haplotypes (16, 19, and 15 respectively), coding haplotypes (19, 15, and 29 respectively), 3' untranslated region (3′UTR) haplotypes (12, 7 and 2, respectively) and extended haplotypes (33, 31 and 32 respectively). All promoter/coding/3'UTR haplotypes followed the patterns already described in worldwide populations. HLA-E was the most conserved, exhibiting mainly two full-length encoded-molecules (E*01:01 and E*01:03), followed by HLA-F, three full-length proteins (F*01:01, F*01:02 and F*01:03) and HLA-G, four proteins: three full-lengthHighlights: HLA-G/E/F are the most conserved HLA class I genes even in Africans. Despite population diversity selection pressures maintained low HLA-E/F/G diversity. Conserved protein diversity supports the immunomodulatory role of HLA-E/F/G. Toffin ethnic group could be considered as a rich repository for genetic variation. Abstract: HLA-G/E/F genes exhibit immunomodulatory properties and are expressed in placenta. Little attention has been devoted to the study of these genes in sub-Saharan African populations, which are yet the most diverse. To fill this gap, we evaluated the complete gene variability, approximately 5.1 kb for HLA-G (n = 149), 7.7 kb for HLA-E (n = 150) and 6.2 kb for HLA-F (n = 152) in the remote Beninese Toffin population, using massive parallel sequencing. Overall, 96, 37 and 68 variable sites were detected along the entire HLA-G, -E and -F, respectively, arranged into region-specific haplotypes; i.e., promoter haplotypes (16, 19, and 15 respectively), coding haplotypes (19, 15, and 29 respectively), 3' untranslated region (3′UTR) haplotypes (12, 7 and 2, respectively) and extended haplotypes (33, 31 and 32 respectively). All promoter/coding/3'UTR haplotypes followed the patterns already described in worldwide populations. HLA-E was the most conserved, exhibiting mainly two full-length encoded-molecules (E*01:01 and E*01:03), followed by HLA-F, three full-length proteins (F*01:01, F*01:02 and F*01:03) and HLA-G, four proteins: three full-length (G*01:01, G*01:03 and G*01:04) and one truncated (G*01:05N). Although HLA-G/E/F alleles in the Toffin population were the most frequently observed worldwide, the frequencies of the coding haplotypes were closely similar to those described for other African populations (Guinea-Conakry and Burkina-Faso), when compared to non-African ones (Brazilian), indicating that variable sites along these genes were present in Africa before human dispersion. … (more)
- Is Part Of:
- Molecular immunology. Volume 104(2018:Dec.)
- Journal:
- Molecular immunology
- Issue:
- Volume 104(2018:Dec.)
- Issue Display:
- Volume 104 (2018)
- Year:
- 2018
- Volume:
- 104
- Issue Sort Value:
- 2018-0104-0000-0000
- Page Start:
- 108
- Page End:
- 127
- Publication Date:
- 2018-12
- Subjects:
- HLA-G/E/F human leukocyte antigen G, E, F -- UTR untranslated region -- MHC human major histocompatibility complex -- DCs dendritic cells -- NK natural killer cells -- ILT-(2, 4) Ig-like transcript receptor 2 and 4 -- DNA deoxyribonucleic acid -- PCR polymerase chain reaction -- qPCR quantitative real-time PCR -- BAM binary alignment map -- IGV integrative genomics viewer -- VCF variant call format -- GATK genome analysis toolkit -- LD linkage disequilibrium -- MAF minor allele frequency -- SNP single nucleotide polymorphism -- STR short tandem repeat -- P. f Plasmodium falciparum -- Kb kilobases (103 bases) -- mRNA messenger RNA (ribonucleic acid) -- SINE short interspersed nuclear element
HLA-E -- HLA-F -- HLA-G -- Haplotypes -- Massive parallel sequencing -- African
Immunochemistry -- Periodicals
Molecular biology -- Periodicals
Immunochemistry -- Periodicals
Allergy and Immunology -- Periodicals
Molecular Biology -- Periodicals
Immunochimie -- Périodiques
Biologie moléculaire -- Périodiques
Immunochemistry
Molecular biology
Periodicals
Electronic journals
571.96 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01615890 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.molimm.2018.08.016 ↗
- Languages:
- English
- ISSNs:
- 0161-5890
- Deposit Type:
- Legaldeposit
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