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Originally published In Press as doi:10.1074/jbc.M106488200 on August 9, 2001

J. Biol. Chem., Vol. 276, Issue 43, 40050-40054, October 26, 2001
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a4, a Unique Kidney-specific Isoform of Mouse Vacuolar H+-ATPase Subunit a*

Toshihiko OkaDagger , Yoshiko MurataDagger , Miwako NambaDagger , Takao YoshimizuDagger , Takao ToyomuraDagger , Akitsugu Yamamoto§, Ge-Hong Sun-WadaDagger , Naotaka Hamasaki, Yoh WadaDagger , and Masamitsu FutaiDagger ||

From the Dagger  Division of Biological Sciences, Institute of Scientific and Industrial Research, Osaka University, Core Research for Evolutional Science and Technology (CREST) of the Japan Science and Technology Corporation, Osaka 567-0047, Japan, the § Department of Physiology, Kansai Medical University, Moriguchi, Osaka 570-8506, Japan, and the  Department of Clinical Chemistry and Laboratory Medicine, Kyushu University, Fukuoka 812-8582, Japan

The vacuolar-type H+-ATPase (V-ATPase) translocates protons across membranes. Here, we have identified a mouse cDNA coding for a fourth isoform (a4) of the membrane sector subunit a of V-ATPase. This isoform was specifically expressed in kidney, but not in the heart, brain, spleen, lung, liver, muscle, or testis. Immunoprecipitation experiments, together with sequence similarities for other isoforms (a1, a2, and a3), indicate that the a4 isoform is a component of V-ATPase. Moreover, histochemical studies show that a4 is localized in the apical and basolateral plasma membranes of cortical alpha - and beta -intercalated cells, respectively. These results suggest that the V-ATPase, with the a4 isoform, is important for renal acid/base homeostasis.


* The costs of publication of this article were defrayed in part by the payment of page charges. The article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

The nucleotide sequence(s) reported in this paper has been submitted to the GenBankTM/EMBL Data Bank with accession number(s) AB050903.

|| To whom correspondence should be addressed. Tel.: 81-6-6879-8480; Fax: 81-6-6875-5724; E-mail: m-futai@sanken.osaka-u.ac.jp.


Copyright © 2001 by The American Society for Biochemistry and Molecular Biology, Inc.
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