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导致异常剪接变体的α-2-巨球蛋白基因外显子 29 c.3535A>T 与奶牛乳腺炎有关。

The exon 29 c.3535A>T in the alpha-2-macroglobulin gene causing aberrant splice variants is associated with mastitis in dairy cattle.

机构信息

Laboratory of Molecular Genetics and Breeding, Center of Dairy Cattle Research, Shandong Academy of Agricultural Sciences, Industry North Road 159, Jinan 250131, Shandong, People's Republic of China.

出版信息

Immunogenetics. 2012 Nov;64(11):807-16. doi: 10.1007/s00251-012-0639-8. Epub 2012 Aug 26.

Abstract

Alpha-2-macroglobulin (A2M) binds proteases, thereby acting as defense barriers against pathogens in the plasma and tissues of vertebrates and invertebrates. Quantitative real-time polymerase chain reaction (PCR) and the isobaric tags for relative and absolute quantitation method were used to determine the expression levels of A2M mRNA and proteins in mastitis-infected mammary tissues. A2M mRNA and protein expression were significantly higher in mastitis-infected mammary tissues than those in healthy tissues. We also identified 23 novel A2M splice variants in the bovine mammary tissues using reverse transcription PCR combined with clone sequencing. These splice variants predominantly affected the bait region, the inhibitory region, and the thioester region of the protein, which have the functional key roles in inhibiting the proteases of pathogens. Genomic sequencing analysis revealed a nonsynonymous c.3535A>T single-nucleotide polymorphism (SNP) in exon 29, which is located within a putative exonic splice enhancer and may be the reason why the A2M gene produces the aberrant splice variant A2M-AS4. Our findings suggest that the A2M gene can play its role by alternative splicing mechanism and it may be of significance against mastitis. This study provides clues to better understand the function of the bovine A2M gene and the effects of the exonic SNP on the production of aberrant splice variants.

摘要

α-2-巨球蛋白(A2M)可结合蛋白酶,从而在脊椎动物和无脊椎动物的血浆和组织中充当防御病原体的屏障。采用实时定量聚合酶链反应(PCR)和相对和绝对定量同位素标记技术(iTRAQ)方法来确定乳腺炎感染的乳腺组织中 A2M mRNA 和蛋白的表达水平。乳腺炎感染的乳腺组织中 A2M mRNA 和蛋白的表达水平明显高于健康组织。我们还通过逆转录 PCR 结合克隆测序在牛乳腺组织中鉴定出 23 种新的 A2M 剪接变体。这些剪接变体主要影响蛋白的诱饵区、抑制区和硫酯区,这些区域在抑制病原体蛋白酶方面具有关键功能。基因组测序分析显示,29 号外显子内存在非同义 c.3535A>T 单核苷酸多态性(SNP),该 SNP 位于推定的外显子剪接增强子内,可能是 A2M 基因产生异常剪接变体 A2M-AS4 的原因。我们的研究结果表明,A2M 基因可以通过选择性剪接机制发挥作用,这可能对抗乳腺炎具有重要意义。本研究为更好地理解牛 A2M 基因的功能以及外显子 SNP 对异常剪接变体产生的影响提供了线索。

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