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A2M基因中的调控突变与奶牛的乳腺炎易感性有关。

Regulatory mutations in the A2M gene are involved in the mastitis susceptibility in dairy cows.

作者信息

Wang X G, Huang J M, Feng M Y, Ju Z H, Wang C F, Yang G W, Yuan J D, Zhong J F

出版信息

Anim Genet. 2014 Feb;45(1):28-37. doi: 10.1111/age.12099.

Abstract

Mutations, such as single nucleotide polymorphisms (SNPs), in the 5′-flanking and microRNA (miRNA) regulatory regions may result in altered gene expression levels and cause diseases. Alpha-2-macroglobulin (A2M) has the function of binding host or foreign peptides and particles, and thereby serves as a defense barrier against pathogens in the plasma and tissues of animals. To investigate the functional markers of the A2M gene associated with mastitis, the promoter was characterized and SNPs that affect promoter activity or binding affinity with the target miRNA were identified using the luciferase reporter assay and real-time quantitative PCR method. Results showed that the core promoter of A2M was found between the bases g.-2641 and g.-2479. Four novel SNPs (g.-724A>G, g.-665G>A, g.-535C>G and g.-520_-519insA) in the promoter region were completely linked. The activity of the mutant haplotype (GAGA) increased by 177% compared with that of the wild haplotype (AGC-). Bta-miR-2898 was upregulated by 6.25-fold in the mammary gland tissues of mastitis-infected cows compared with that of the healthy cows. One SNP (c.4659_4661delC) located in the 3′-untranslated region of the A2M gene may affect the binding affinity with the target bta-miR-2898. Five SNPs exhibited tight linkage. Association analysis showed that the milk somatic cell score for cows with the mutant haplotype (GAGA-) was lower than that for cows with the wild haplotype. Thus, the mutant type can be used as a potential functional marker for a mastitis resistance breeding program in dairy cows. Our findings provided the molecular basis for A2M transcriptional and post-transcriptional regulations. A close relationship between regulatory mutations and mastitis susceptibility of cows also was established.

摘要

5′侧翼和微小RNA(miRNA)调控区域的突变,如单核苷酸多态性(SNP),可能导致基因表达水平改变并引发疾病。α-2-巨球蛋白(A2M)具有结合宿主或外来肽及颗粒的功能,从而在动物的血浆和组织中作为抵御病原体的防御屏障。为了研究与乳腺炎相关的A2M基因功能标记,对其启动子进行了表征,并使用荧光素酶报告基因检测和实时定量PCR方法鉴定了影响启动子活性或与靶miRNA结合亲和力的SNP。结果表明,A2M的核心启动子位于碱基g.-2641和g.-2479之间。启动子区域的四个新SNP(g.-724A>G、g.-665G>A、g.-535C>G和g.-520_-519insA)完全连锁。与野生单倍型(AGC-)相比,突变单倍型(GAGA)的活性增加了177%。与健康奶牛相比,乳腺炎感染奶牛乳腺组织中的Bta-miR-2898上调了6.25倍。位于A2M基因3′非翻译区的一个SNP(c.4659_4661delC)可能影响与靶Bta-miR-2898的结合亲和力。五个SNP表现出紧密连锁。关联分析表明,具有突变单倍型(GAGA-)的奶牛的乳体细胞评分低于具有野生单倍型的奶牛。因此,突变型可作为奶牛乳腺炎抗性育种计划的潜在功能标记。我们的研究结果为A2M的转录和转录后调控提供了分子基础。还建立了调控突变与奶牛乳腺炎易感性之间的密切关系。

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