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猪NOD1配体识别受损的多态性及其在猪群体中的分布

Porcine NOD1 polymorphisms with impaired ligand recognition and their distribution in pig populations.

作者信息

Shinkai Hiroki, Matsumoto Toshimi, Toki Daisuke, Okumura Naohiko, Terada Kei, Uenishi Hirohide

机构信息

Animal Immune and Cell Biology Research Unit, Division of Animal Sciences, National Institute of Agrobiological Sciences, 1-2 Owashi, Tsukuba, Ibaraki 305-8634, Japan.

Advanced Genomics Laboratory, Agrogenomics Research Center, National Institute of Agrobiological Sciences, 1-2 Owashi, Tsukuba, Ibaraki 305-8634, Japan.

出版信息

Mol Immunol. 2015 Feb;63(2):305-11. doi: 10.1016/j.molimm.2014.07.020. Epub 2014 Aug 13.

Abstract

Nucleotide-binding oligomerization domain 1 (NOD1) is a cytosolic pattern recognition receptor that recognizes γ-d-glutamyl-meso-diaminopimelic acid (iE-DAP), a component of bacterial peptidoglycan. NOD1 is thought to be involved in the immune homeostasis mediated by intestinal microbiota as well as the host defense against infection. In this study, we identified 12 synonymous and nine nonsynonymous single nucleotide polymorphisms (SNPs) in the coding sequence of porcine NOD1 within major commercial breeds in the swine industry. Among the nonsynonymous SNPs, two amino-acid alterations located in the leucine-rich repeats region, glycine to glutamic acid at position 641 (G641E) and aspartic acid to asparagine at position 918 (D918N), impaired iE-DAP-induced activation of nuclear factor-κB. These alleles showed the recessive mode of inheritance and therefore are likely to be maintained in pig populations at high frequencies. These results suggest the possibility for improvement in disease resistance by eliminating the G641E and D918N alleles of NOD1 from commercial pig populations.

摘要

核苷酸结合寡聚化结构域1(NOD1)是一种胞质模式识别受体,可识别细菌肽聚糖的成分γ-d-谷氨酰-间二氨基庚二酸(iE-DAP)。NOD1被认为参与了由肠道微生物群介导的免疫稳态以及宿主对感染的防御。在本研究中,我们在养猪业主要商业品种的猪NOD1编码序列中鉴定出12个同义单核苷酸多态性(SNP)和9个非同义SNP。在非同义SNP中,位于富含亮氨酸重复序列区域的两个氨基酸改变,第641位的甘氨酸变为谷氨酸(G641E)和第918位的天冬氨酸变为天冬酰胺(D918N),损害了iE-DAP诱导的核因子κB的激活。这些等位基因表现出隐性遗传模式,因此可能在猪群中以高频率维持。这些结果表明,通过从商业猪群中消除NOD1的G641E和D918N等位基因来提高抗病性是有可能的。

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