Molecular cloning of rat klotho cDNA:: Markedly decreased expression of klotho by acute inflammatory stress

被引:137
作者
Ohyama, Y
Kurabayashi, M
Masuda, H
Nakamura, T
Aihara, Y
Kaname, T
Suga, T
Arai, M
Aizawa, H
Matsumura, Y
Kuro-o, M
Nabeshima, Y
Nagail, R
机构
[1] Gunma Univ, Sch Med, Dept Internal Med 2, Maebashi, Gumma 3718511, Japan
[2] Kumamoto Univ, Ctr Anim Resources & Dev, Div Transgen Technol, Kumamoto 8620976, Japan
[3] Univ Texas, SW Med Ctr, Dept Pathol, Dallas, TX 75235 USA
[4] Osaka Univ, Inst Mol & Cellular Biol, Suita, Osaka 5650871, Japan
关键词
D O I
10.1006/bbrc.1998.9576
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have recently identified a novel gene, termed klotho that is involved in the suppression of several aging phenotypes, The gene encodes a membrane protein that shares sequence similarity with the p-glucosidases of bacteria and plants. In this study, we isolated rat klotho cDNA and examined its tissue distribution in rats. The deduced amino acid sequence of rat Klotho protein was 1014 amino acids in length and 94 and 85% homologous to those of mouse and human Klotho proteins, respectively. Northern blot analysis using the rat klotho cDNA probe identified a single transcript of 5.2 kb in size expressed predominantly in the kidney, while RT-PCR detected low levels of expression also in the brain, lung, intestine, and ovaries. During development, klotho expression in the kidney was markedly augmented after birth. Chromosomal localization of rat klotho was mapped to 12q12, Northern blot analysis showed that expression of klotho was markedly decreased by Lipopolysaccharide (LPS) in vivo suggesting that expression of klotho is affected by acute inflammatory stress. The present study leads to a better understanding of the physiologic and pathophysiologic roles Of Klotho. (C) 1998 Academic Press.
引用
收藏
页码:920 / 925
页数:6
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