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DOI 10.1016/j.meegid.2016.04.029

Медицинская библиотека · Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases · 2016

Lack of specific alleles for the bovine chemokine (C-X-C) receptor type 4 (CXCR4) gene in West African cattle questions its role as a candidate for trypanotolerance.

Álvarez Isabel, Pérez-Pardal Lucía, Traoré Amadou, Fernández Iván, Goyache Félix

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

A panel of 81 Asian, African and European cattle (Bos taurus and B. indicus) was analysed for the whole sequence of the CXCR4 gene (3844bp), a strong candidate for cattle trypanotolerance. Thirty-one polymorphic sites identified gave 31 different haplotypes. Neutrality tests rejected the hypothesis of either positive or purifying selection. Bayesian phylogenetic tree showed differentiation of haplotypes into two clades gathering genetic variability predating domestication. Related with clades definition, linkage disequilibrium analyses suggested the existence of one only linkage block on the CXCR4 gene. Two tag SNPs identified on exon 2 captured 50% of variability. Whatever the analysis carried out, no clear separation between cattle groups was identified. Most haplotypes identified in West African taurine cattle were also found in European cattle and in Asian and West African zebu. West African taurine samples did not carry unique variants on the CXCR4 gene sequence. The current analysis failed in identifying a causal mutation on the CXCR4 gene underlying a previously reported QTL for cattle trypanotolerance on BTA2.

Для цитирования: Álvarez Isabel, Pérez-Pardal Lucía, Traoré Amadou, Fernández Iván, Goyache Félix. Lack of specific alleles for the bovine chemokine (C-X-C) receptor type 4 (CXCR4) gene in West African cattle questions its role as a candidate for trypanotolerance.. Infection, genetics and evolution : journal of molecular epidemiology and evolutionary genetics in infectious diseases. 2016. DOI: 10.1016/j.meegid.2016.04.029.

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