A Review of the Genetic Studies and the Pathogenic Mechanism of Feline Polycystic Kidney Disease

Jae Yeon Lee, Jeong‐In Baek
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Abstract

Autosomal-dominant polycystic kidney disease (ADPKD) is a progressive genetic disease in which multiple small and large fluid-filled sacs (cysts or cysts) are formed in one or both kidneys. Polycystic kidney disease in cats is classified as an autosomal dominant genetic disease and has been found to be caused by mutations in the PKD1 gene that is coding a unit of mechanosensitive calcium channel, polycystin 1. It shows that humans and cats share a genetic cause for polycystic kidney disease. In this paper, we try to understand the pathogenesis of polycystic kidney disease through the genetic mutations and protein functions of feline polycystic kidney syndrome reported so far, and discuss the direction of genetic research that needs to be performed in the future.
猫多囊肾病的遗传研究及致病机制综述
常染色体显性多囊肾病(ADPKD)是一种进行性遗传病,在一个或两个肾脏形成多个大小的充满液体的囊(囊肿或囊肿)。猫的多囊肾病被归类为常染色体显性遗传病,已发现是由PKD1基因突变引起的,该基因编码机械敏感钙通道多囊蛋白1。这表明人类和猫都有多囊肾病的遗传原因。本文试图通过目前报道的猫多囊肾综合征的基因突变和蛋白功能来了解多囊肾病的发病机制,并探讨未来需要开展的遗传学研究方向。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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