Aziz N, Maxwell M M, St Jacques B, Brenner B M
Department of Medicine, Brigham and Women's Hospital, Boston, Massachusetts.
Mol Cell Biol. 1993 Mar;13(3):1847-53. doi: 10.1128/mcb.13.3.1847-1853.1993.
Polycystic kidney disease (PKD) is characterized by progressive enlargement of the kidneys due to numerous expanding cysts ultimately leading to renal failure. We have identified a gene, Ke 6, located within the H-2K/tw5 region on mouse chromosome 17, which is downregulated in two distinct murine models of heritable PKD. Ke 6 is a member of the short-chain alcohol dehydrogenase family and possess remarkable amino acid sequence conservation with several bacterial proteins with oxidoreductase function. The Ke 6 gene gives rise to two transcripts--a 1-kb Ke 6a mRNA which is abundant in kidney and liver tissue and a 1.4-kb Ke 6b mRNA which is found at a moderate level in spleen tissue. We report here the complete nucleotide sequence of Ke 6a cDNA and the expression of the Ke 6 gene in murine models of PKD. The Ke 6 gene may be intimately involved in the manifestation of these cystic kidney diseases.
多囊肾病(PKD)的特征是由于大量不断增大的囊肿导致肾脏逐渐肿大,最终导致肾衰竭。我们已经鉴定出一个基因Ke 6,它位于小鼠17号染色体的H-2K/tw5区域内,在两种不同的遗传性PKD小鼠模型中表达下调。Ke 6是短链醇脱氢酶家族的成员,与几种具有氧化还原酶功能的细菌蛋白具有显著的氨基酸序列保守性。Ke 6基因产生两种转录本——一种1 kb的Ke 6a mRNA,在肾脏和肝脏组织中丰富,另一种1.4 kb的Ke 6b mRNA,在脾脏组织中以中等水平存在。我们在此报告Ke 6a cDNA的完整核苷酸序列以及Ke 6基因在PKD小鼠模型中的表达。Ke 6基因可能与这些多囊肾病的表现密切相关。