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通过对猪进行生物学候选基因分析评估HOXA10、ZFPM2和MMP2基因与阴囊疝的关联。

Association of HOXA10, ZFPM2, and MMP2 genes with scrotal hernias evaluated via biological candidate gene analyses in pigs.

作者信息

Zhao Xia, Du Zhi-Qiang, Vukasinovic Natascha, Rodriguez Fernanda, Clutter Archie C, Rothschild Max F

机构信息

Department of Animal Science and Center for Integrated Animal Genomics, College of Agriculture and Life Sciences, Iowa State University, Ames, IA 50011, USA.

出版信息

Am J Vet Res. 2009 Aug;70(8):1006-12. doi: 10.2460/ajvr.70.8.1006.

Abstract

OBJECTIVE

To evaluate the associations between 14 biological candidate genes and scrotal hernias in pigs.

ANIMALS

1,534 Pietrain-based pigs, including 692 individuals from 298 pig families and 842 male pigs without family information.

PROCEDURES

Pigs were classified as affected or unaffected for scrotal hernias. Single nucleotide polymorphisms of candidate genes were analyzed via PCR assays and genotyped. Statistical analyses were performed on the family-trio and the case-control data.

RESULTS

2 genes involved in collagen metabolism (homeobox A10 [HOXA10] and matrix metalloproteinases 2 [MMP2]) and 1 gene encoding zinc finger protein multitype 2 (ZFPM2, important in the development of diaphragmatic hernia) were significantly associated with hernias. Pigs with these genotypes had high odds of developing scrotal hernias in the case and control groups (2 ZFPM2 variants: odds ratio, 4.3 [95% confidence interval, 2.78 to 6.64] and 4.45[95%confidenceinterval,2.88to6.88]). Anothergene, collagentypeII A 1(COL2A1),was potentially involved in hernia development.

CONCLUSIONS AND CLINICAL RELEVANCE

HOXA10, ZFPM2, MMP2, and COL2A1 could have important roles in pig hernia development and potentially be useful for marker-assisted selection in the pig industry.

IMPACT FOR HUMAN MEDICINE

Pigs are used for the study of many human diseases because of their physiologic similarities. Genes associated with scrotal hernias in this study may be directly used in understanding the molecular mechanisms underlying this defect in humans.

摘要

目的

评估14个生物学候选基因与猪阴囊疝之间的关联。

动物

1534头皮特兰猪,包括来自298个猪家族的692头个体以及842头无家族信息的雄性猪。

方法

猪被分类为阴囊疝患病或未患病。通过聚合酶链反应(PCR)分析候选基因的单核苷酸多态性并进行基因分型。对家系三联体数据和病例对照数据进行统计分析。

结果

2个参与胶原蛋白代谢的基因(同源框A10 [HOXA10] 和基质金属蛋白酶2 [MMP2])以及1个编码多类型锌指蛋白2(ZFPM2,在膈疝发育中起重要作用)的基因与疝显著相关。具有这些基因型的猪在病例组和对照组中发生阴囊疝的几率较高(2个ZFPM2变体:优势比分别为4.3 [95%置信区间,2.78至6.64] 和4.45 [95%置信区间,2.88至6.88])。另一个基因,II型胶原蛋白A1(COL2A1),可能参与疝的发育。

结论及临床意义

HOXA10、ZFPM2、MMP2和COL2A1可能在猪疝的发育中起重要作用,并且可能对养猪业的标记辅助选择有用。

对人类医学的影响

由于猪与人类在生理上的相似性,猪被用于许多人类疾病的研究。本研究中与阴囊疝相关的基因可能直接用于理解人类这种缺陷的分子机制。

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