Literature DB >> 9753630

The subcellular location of the yeast Saccharomyces cerevisiae homologue of the protein defective in the juvenile form of Batten disease.

J B Croopnick1, H C Choi, D M Mueller.   

Abstract

The mutation responsible for the juvenile form of Batten disease was mapped to a single gene, Cln3 (T. J. Lerner et al. (1995) Cell 82:949-957). Yeast Saccharomyces cerevisiae has an open reading frame, BTN1 (YHC3), that encodes the putative homologue of Cln3p. Primary structure comparison indicates that the human Cln3p and yeast Btn1p are 59% similar and 39% identical and they have similar hydropathy profiles. Gene disruption of BTN1 in yeast has no apparent effect on growth or viability of the cells under a variety of conditions. Gene fusion protein constructs of green fluorescent protein (GFP) and Btn1p, with GFP at the amino and carboxyl ends of Btn1p, localize to the vacuole in yeast. These data indicate that BTN1 is a nonessential gene under most growth conditions which functions in the vacuole in yeast Saccharomyces cerevisiae.

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Year:  1998        PMID: 9753630     DOI: 10.1006/bbrc.1998.9272

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN: 0006-291X            Impact factor:   3.575


  14 in total

1.  Phenotypic reversal of the btn1 defects in yeast by chloroquine: a yeast model for Batten disease.

Authors:  D A Pearce; C J Carr; B Das; F Sherman
Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-28       Impact factor: 11.205

2.  The yeast model for batten disease: mutations in BTN1, BTN2, and HSP30 alter pH homeostasis.

Authors:  S Chattopadhyay; N E Muzaffar; F Sherman; D A Pearce
Journal:  J Bacteriol       Date:  2000-11       Impact factor: 3.490

3.  Interaction with Btn2p is required for localization of Rsglp: Btn2p-mediated changes in arginine uptake in Saccharomyces cerevisiae.

Authors:  Subrata Chattopadhyay; David A Pearce
Journal:  Eukaryot Cell       Date:  2002-08

4.  Btn2, a Hook1 ortholog and potential Batten disease-related protein, mediates late endosome-Golgi protein sorting in yeast.

Authors:  Rachel Kama; Micah Robinson; Jeffrey E Gerst
Journal:  Mol Cell Biol       Date:  2006-11-13       Impact factor: 4.272

5.  Interaction among Btn1p, Btn2p, and Ist2p reveals potential interplay among the vacuole, amino acid levels, and ion homeostasis in the yeast Saccharomyces cerevisiae.

Authors:  Yoojin Kim; Subrata Chattopadhyay; Sarahjane Locke; David A Pearce
Journal:  Eukaryot Cell       Date:  2005-02

6.  Nitric oxide signaling is disrupted in the yeast model for Batten disease.

Authors:  Nuno S Osório; Agostinho Carvalho; Agostinho J Almeida; Sérgio Padilla-Lopez; Cecília Leão; João Laranjinha; Paula Ludovico; David A Pearce; Fernando Rodrigues
Journal:  Mol Biol Cell       Date:  2007-05-02       Impact factor: 4.138

7.  Interaction between Sdo1p and Btn1p in the Saccharomyces cerevisiae model for Batten disease.

Authors:  Seasson Phillips Vitiello; Jared W Benedict; Sergio Padilla-Lopez; David A Pearce
Journal:  Hum Mol Genet       Date:  2009-12-16       Impact factor: 6.150

8.  A role in vacuolar arginine transport for yeast Btn1p and for human CLN3, the protein defective in Batten disease.

Authors:  Yoojin Kim; Denia Ramirez-Montealegre; David A Pearce
Journal:  Proc Natl Acad Sci U S A       Date:  2003-12-05       Impact factor: 11.205

9.  Btn3 is a negative regulator of Btn2-mediated endosomal protein trafficking and prion curing in yeast.

Authors:  Vydehi Kanneganti; Rachel Kama; Jeffrey E Gerst
Journal:  Mol Biol Cell       Date:  2011-03-25       Impact factor: 4.138

10.  pH-dependent localization of Btn1p in the yeast model for Batten disease.

Authors:  Devin M Wolfe; Sergio Padilla-Lopez; Seasson Phillips Vitiello; David A Pearce
Journal:  Dis Model Mech       Date:  2010-10-19       Impact factor: 5.758

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