Diversity of mouse proton-translocating ATPase:: presence of multiple isoforms of the C, d and G subunits

被引:78
作者
Sun-Wada, GH
Yoshimizu, T
Imai-Senga, Y
Wada, Y
Futai, M
机构
[1] Osaka Univ, Inst Sci & Ind Res, Div Biol Sci, Ibaraki, Osaka 5670047, Japan
[2] Japan Sci & Technol Corp, CREST, Ibaraki, Osaka 5670047, Japan
关键词
acidic organelle; endosome; lysosome; vacuolar-type proton-translocating ATPase; kidney; lung; tissue-specific isoform;
D O I
10.1016/S0378-1119(02)01099-5
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Vacuolar-type proton-translocating ATPases (V-ATPases), multimeric proton pumps, are involved in a wide variety of physiological processes. For their diverse functions, V-ATPases utilize a specific subunit isoform(s). Here, we reported the molecular cloning and characterization of three novel subunit isoforms, C2, d2 and G3, of mouse V-ATPase. These isoforms were expressed in a tissue-specific manner, in contrast to the ubiquitously expressed C1, d1 and G1 isoforms. C2 was expressed predominantly in lung and kidney, and d2 and G3 specifically in kidney. We introduced these isoforms into yeasts lacking the corresponding genes. Although the G3 and d2 did not rescue the vmaDelta phenotype, d1 and the two C isoforms functionally complemented the Deltavma6 and Deltavma5, respectively, indicating that they are bona fide subunits of V-ATPase. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:147 / +
页数:8
相关论文
共 30 条
[1]  
BAUERLE C, 1993, J BIOL CHEM, V268, P12749
[2]   Normalization and subtraction of cap-trapper-selected cDNAs to prepare full-length cDNA libraries for rapid discovery of new genes [J].
Carninci, P ;
Shibata, Y ;
Hayatsu, N ;
Sugahara, Y ;
Shibata, K ;
Itoh, M ;
Konno, H ;
Okazaki, Y ;
Muramatsu, M ;
Hayashizaki, Y .
GENOME RESEARCH, 2000, 10 (10) :1617-1630
[3]   Mutational analysis of the subunit C (Vma5p) of the yeast vacuolar H+-ATPase [J].
Curtis, KK ;
Francis, SA ;
Oluwatosin, Y ;
Kane, PM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (11) :8979-8988
[4]  
Futai M, 2000, J EXP BIOL, V203, P107
[5]   Diverse roles of single membrane organelles: Factors establishing the acid lumenal pH [J].
Futai, M ;
Oka, T ;
Moriyama, Y ;
Wada, Y .
JOURNAL OF BIOCHEMISTRY, 1998, 124 (02) :259-267
[6]   Physiology and biochemistry of the kidney vacuolar H+-ATPase [J].
Gluck, SL ;
Underhill, DM ;
Iyori, M ;
Holliday, LS ;
Kostrominova, TY ;
Lee, BS .
ANNUAL REVIEW OF PHYSIOLOGY, 1996, 58 :427-445
[7]   MOLECULAR-CLONING OF CDNA-ENCODING THE 16KDA SUBUNIT OF VACUOLAR H+-ATPASE FROM MOUSE CEREBELLUM [J].
HANADA, H ;
HASEBE, M ;
MORIYAMA, Y ;
MAEDA, M ;
FUTAI, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 176 (03) :1062-1067
[8]   The murine genome contains one functional gene and two pseudogenes coding for the 16 kDa proteolipid subunit of vacuolar H+-ATPase [J].
Hayami, K ;
Noumi, T ;
Inoue, H ;
Sun-Wada, GH ;
Yoshimizu, T ;
Kanazawa, H .
GENE, 2001, 273 (02) :199-206
[9]  
HO MN, 1993, J BIOL CHEM, V268, P221
[10]   A human gene, ATP6E1, encoding a testis-specific isoform of H+-ATPase subunit E [J].
Imai-Senga, Y ;
Sun-Wada, GH ;
Wada, Y ;
Futai, M .
GENE, 2002, 289 (1-2) :7-12