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鸡主要组织相容性复合体经典 I 类和 II B 类基因杂交技术的开发与优化。

Development and optimization of a hybridization technique to type the classical class I and class II B genes of the chicken MHC.

机构信息

Department of Pathology, University of Cambridge, Tennis Court Road, Cambridge, CB2 1QP, UK.

LGC Ltd., Newmarket Road, Fordham, Ely, CB7 5WW, UK.

出版信息

Immunogenetics. 2019 Nov;71(10):647-663. doi: 10.1007/s00251-019-01149-2. Epub 2019 Nov 25.

Abstract

The classical class I and class II molecules of the major histocompatibility complex (MHC) play crucial roles in immune responses to infectious pathogens and vaccines as well as being important for autoimmunity, allergy, cancer and reproduction. These classical MHC genes are the most polymorphic known, with roughly 10,000 alleles in humans. In chickens, the MHC (also known as the BF-BL region) determines decisive resistance and susceptibility to infectious pathogens, but relatively few MHC alleles and haplotypes have been described in any detail. We describe a typing protocol for classical chicken class I (BF) and class II B (BLB) genes based on a hybridization method called reference strand-mediated conformational analysis (RSCA). We optimize the various steps, validate the analysis using well-characterized chicken MHC haplotypes, apply the system to type some experimental lines and discover a new chicken class I allele. This work establishes a basis for typing the MHC genes of chickens worldwide and provides an opportunity to correlate with microsatellite and with single nucleotide polymorphism (SNP) typing for approaches involving imputation.

摘要

主要组织相容性复合体(MHC)的经典 I 类和 II 类分子在免疫反应中对感染病原体和疫苗起着至关重要的作用,并且对自身免疫、过敏、癌症和生殖也很重要。这些经典的 MHC 基因是已知的最具多态性的,人类约有 10000 个等位基因。在鸡中,MHC(也称为 BF-BL 区域)决定了对感染病原体的决定性抗性和易感性,但在任何详细程度上都只描述了相对较少的 MHC 等位基因和单倍型。我们描述了一种基于称为参考链介导构象分析(RSCA)的杂交方法的经典鸡类 I(BF)和类 II B(BLB)基因的分型方案。我们优化了各个步骤,使用特征明确的鸡 MHC 单倍型验证了分析,将该系统应用于一些实验品系的分型,并发现了一个新的鸡类 I 等位基因。这项工作为全世界鸡的 MHC 基因分型奠定了基础,并为与微卫星和单核苷酸多态性(SNP)分型相关的方法提供了关联的机会,包括推断。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2104/6900278/81ecccdaa999/251_2019_1149_Fig1_HTML.jpg

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