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鉴定一种在兔肾远曲小管中高表达的新型钾通道基因(KC22)。

Identification of a novel K-channel gene (KC22) that is highly expressed in distal tubule of rabbit kidney.

作者信息

Desir G V, Velázquez H

机构信息

Department of Medicine, Yale University School of Medicine, New Haven, Connecticut 06510.

出版信息

Am J Physiol. 1993 Jan;264(1 Pt 2):F128-33. doi: 10.1152/ajprenal.1993.264.1.F128.

Abstract

The Shaker gene family encodes voltage-gated K channels. Five partial-length Shaker-like cDNAs (KC2, 4, 10, 19, and 22) were previously isolated from rabbit kidney using polymerase chain reaction (PCR) [G. V. Desir, E. Hamlin, A.H. Puente, R.F. Reilly, F. Hiledebrandt, and P. Igarashi. Am. J. Physiol. 262 (Renal Fluid Electrolyte Physiol. 31): F151-F157, 1992]. We now report the cloning of another Shaker-like cDNA (KC6) from rabbit kidney and the identification of one isoform that is highly expressed in rabbit distal tubule cells grown in culture. A partial-length cDNA (859 bp) for KC6 was isolated by PCR amplification of rabbit kidney cDNA using Shaker-specific degenerate primers. KC6 was most similar to the rat brain clone RBK2 (77% amino acid identity) and to the rabbit clone KC19 (78% amino acid identity). Transcript levels for KC2, 4, 6, 10, 19, and 22 were quantified using the ribonuclease protection assay. Transcripts for all six isoforms were detected in renal tissues. KC22 was the most abundant isoform in kidney cortex and medulla (20- to 40-fold greater than the other isoforms). Furthermore, KC22 expression levels were fivefold higher in primary cultures of rabbit distal convoluted tubules and connecting tubules than in whole kidney cortex. Although the partial-length sequence for KC22 represents the most conserved regions in the Shaker gene family it only has 35-88% amino acid identity with other Shaker channels, suggesting that KC22 represents a novel isoform. In contrast, KC4 and KC19 (less abundant in kidney than KC22) are highly homologous to the rat brain clones RBK1 and RBK2, respectively (97% amino acid identity).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

Shaker基因家族编码电压门控钾通道。先前使用聚合酶链反应(PCR)从兔肾中分离出五个部分长度的类Shaker cDNA(KC2、4、10、19和22)[G. V. 德西尔、E. 哈姆林、A. H. 普恩特、R. F. 赖利、F. 希勒德布兰特和P. 五十岚。《美国生理学杂志》262卷(肾流体电解质生理学31):F151 - F157,1992年]。我们现在报告从兔肾中克隆出另一个类Shaker cDNA(KC6),并鉴定出一种在培养的兔远曲小管细胞中高表达的同工型。使用Shaker特异性简并引物通过PCR扩增兔肾cDNA分离出KC6的部分长度cDNA(859 bp)。KC6与大鼠脑克隆RBK2最为相似(氨基酸同一性为77%),与兔克隆KC19也最为相似(氨基酸同一性为78%)。使用核糖核酸酶保护试验对KC2、4、6、10、19和22的转录水平进行定量。在肾组织中检测到所有六种同工型的转录本。KC22是肾皮质和髓质中最丰富的同工型(比其他同工型高20至40倍)。此外,KC22在兔远曲小管和连接小管的原代培养物中的表达水平比整个肾皮质高五倍。尽管KC22的部分长度序列代表了Shaker基因家族中最保守的区域,但它与其他Shaker通道的氨基酸同一性仅为35 - 88%,这表明KC22代表一种新的同工型。相比之下,KC4和KC19(在肾中的丰度低于KC22)分别与大鼠脑克隆RBK1和RBK2高度同源(氨基酸同一性为97%)。(摘要截短于250字)

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