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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

HLA-G variability and haplotypes detected by massively parallel sequencing procedures in the geographicaly distinct population samples of Brazil and Cyprus

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Castelli, Erick C. ; Gerasimou, Petroula ; Paz, Michelle A. ; Ramalho, Jaqueline ; Porto, Iane O. P. ; Lima, Thalitta H. A. ; Souza, Andreia S. ; Veiga-Castelli, Luciana C. ; Collares, Cristhianna V. A. ; Donadi, Eduardo A. ; Mendes-Junior, Celso T. ; Costeas, Paul
Total Authors: 12
Document type: Journal article
Source: Molecular Immunology; v. 83, p. 115-126, MAR 2017.
Web of Science Citations: 18
Abstract

The HLA-G molecule presents immunomodulatory properties that might inhibit immune responses when interacting with specific Natural Killer and T cell receptors, such as KIR2DL4, ILT2 and ILT4. Thus, HLA-G might influence the outcome of situations in which fine immune system modulation is required, such as autoimmune diseases, transplants, cancer and pregnancy. The majority of the studies regarding the HLA-G gene variability so far was restricted to a specific gene segment (i.e., promoter, coding or 3' untranslated region), and was performed by using Sanger sequencing and probabilistic models to infer haplotypes. Here we propose a massively parallel sequencing (NGS) with a bioinformatics strategy to evaluate the entire HLA-G regulatory and coding segments, with haplotypes inferred relying more on the straightforward haplotyping capabilities of NGS, and less on probabilistic models. Then, HLA-G variability was surveyed in two admixed population samples of distinct geographical regions and demographic backgrounds, Cyprus and Brazil. Most haplotypes (promoters, coding, 3'UTR and extended ones) were detected both in Brazil and Cyprus and were identical to the ones already described by probabilistic models, indicating that these haplotypes are quite old and may be present worldwide. (C) 2017 Elsevier Ltd. All rights reserved. (AU)

FAPESP's process: 13/17084-2 - Evaluation of MHC Class I genes variability, regulation and evolutive history
Grantee:Erick da Cruz Castelli
Support Opportunities: Regular Research Grants
FAPESP's process: 14/18730-8 - Immunogenetic markers for gestational Diabetes mellitus
Grantee:Eduardo Antônio Donadi
Support Opportunities: Regular Research Grants