首页> 外文期刊>Genetics: A Periodical Record of Investigations Bearing on Heredity and Variation >Molecular Genetic Analysis of Two Loci (Ity2 and Ity3) Involved in the Host Response to Infection With Salmonella Typhimurium Using Congenic Mice and Expression Profiling
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Molecular Genetic Analysis of Two Loci (Ity2 and Ity3) Involved in the Host Response to Infection With Salmonella Typhimurium Using Congenic Mice and Expression Profiling

机译:利用同源小鼠和表达谱分析两个涉及鼠伤寒沙门氏菌感染宿主应答的基因座(Ity2和Ity3)的分子遗传学分析

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Numerous genes have been identified to date that contribute to the host response to systemic Salmonella Typhimurium infection in mice. We have previously identified two loci, Ity2 and Ity3 , that control survival to Salmonella infection in the wild-derived inbred MOLF/Ei mouse using a (C57BL/6J × MOLF/Ei)F2cross. We validated the existence of these two loci by creating congenic mice carrying each quantitative trait locus (QTL) in isolation. Subcongenic mice generated for each locus allowed us to define the critical intervals underlying Ity2 and Ity3 . Furthermore, expression profiling was carried out with the aim of identifying differentially expressed genes within the critical intervals as potential candidate genes. Genomewide expression arrays were used to interrogate expression differences in the Ity2 congenics, leading to the identification of a new candidate gene ( Havcr2 , hepatitis A virus cellular receptor 2). Interval-specific oligonucleotide arrays were created for Ity3 , identifying one potential candidate gene ( Chi3l1 , chitinase 3-like 1) to be pursued further. The combination of the use of congenics in QTL confirmation and fine mapping and in the identification of candidate genes by expression profiling has been successful and represents a step toward quantitative gene(s) identification.
机译:迄今为止,已经鉴定出许多基因,这些基因有助于宿主对小鼠系统性鼠伤寒沙门氏菌感染的反应。我们以前已经确定了两个基因座Ity2和Ity3,它们使用(C57BL / 6J×MOLF / Ei)F2cross控制野生来源的近交MOLF / Ei小鼠沙门氏菌感染的存活。我们通过创建分离携带每个定量性状基因座(QTL)的同类小鼠来验证这两个基因座的存在。为每个基因座生成的亚基因小鼠允许我们定义Ity2和Ity3的关键区间。此外,进行表达谱分析的目的是鉴定关键间隔内差异表达的基因作为潜在候选基因。全基因组表达阵列用于询问Ity2同系基因的表达差异,从而鉴定出新的候选基因(Havcr2,甲型肝炎病毒细胞受体2)。为Ity3创建了间隔特异的寡核苷酸阵列,确定了一个可能的候选基因(Chi3l1,几丁质酶3样1),以进一步进行研究。在QTL确认和精细作图以及通过表达谱分析鉴定候选基因中使用同系基因的组合已经成功,代表了向定量基因鉴定的一步。

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