TAZ1/YPR140W Literature Guide Help

Other names published for TAZ1: YPR140W

TAZ1 - Mutants/Phenotypes (18)

ReferenceOther Genes Addressed
Angelini R, et al.  (2012) Lipidomics of intact mitochondria by MALDI-TOF/MS. J Lipid Res 53(7):1417-25
Short MK, et al.  (2012) The yeast magmas ortholog pam16 has an essential function in fermentative growth that involves sphingolipid metabolism. PLoS One 7(7):e39428
Claypool SM, et al.  (2011) Barth syndrome mutations that cause tafazzin complex lability. J Cell Biol 192(3):447-62
Osman C, et al.  (2010) A mitochondrial phosphatase required for cardiolipin biosynthesis: the PGP phosphatase Gep4. EMBO J 29(12):1976-87
van Gestel RA, et al.  (2010) The influence of the acyl chain composition of cardiolipin on the stability of mitochondrial complexes; an unexpected effect of cardiolipin in alpha-ketoglutarate dehydrogenase and prohibitin complexes. J Proteomics 73(4):806-14
Beranek A, et al.  (2009) Identification of a Cardiolipin-specific Phospholipase Encoded by the Gene CLD1 (YGR110W) in Yeast. J Biol Chem 284(17):11572-8
Gebert N, et al.  (2009) Mitochondrial cardiolipin involved in outer-membrane protein biogenesis: implications for Barth syndrome. Curr Biol 19(24):2133-9
Rijken PJ, et al.  (2009) Cardiolipin molecular species with shorter acyl chains accumulate in Saccharomyces cerevisiae mutants lacking the acyl coenzyme A-binding protein Acb1p: new insights into acyl chain remodeling of cardiolipin. J Biol Chem 284(40):27609-19
Chen S, et al.  (2008) Loss of tafazzin in yeast leads to increased oxidative stress during respiratory growth. Mol Microbiol 68(4):1061-72
Claypool SM, et al.  (2008) Cardiolipin defines the interactome of the major ADP/ATP carrier protein of the mitochondrial inner membrane. J Cell Biol 182(5):937-50
Claypool SM, et al.  (2008) The cardiolipin transacylase, tafazzin, associates with two distinct respiratory components providing insight into Barth syndrome. Mol Biol Cell 19(12):5143-55
Kutik S, et al.  (2008) The translocator maintenance protein Tam41 is required for mitochondrial cardiolipin biosynthesis. J Cell Biol 183(7):1213-21
Stalberg K, et al.  (2008) Identification of a novel GPCAT activity and a new pathway for phosphatidylcholine biosynthesis in S. cerevisiae. J Lipid Res 49(8):1794-806
Claypool SM, et al.  (2006) Mitochondrial mislocalization and altered assembly of a cluster of Barth syndrome mutant tafazzins. J Cell Biol 174(3):379-90
Brandner K, et al.  (2005) Taz1, an outer mitochondrial membrane protein, affects stability and assembly of inner membrane protein complexes: implications for Barth Syndrome. Mol Biol Cell 16(11):5202-14
Testet E, et al.  (2005) Ypr140wp, 'the yeast tafazzin', displays a mitochondrial lysophosphatidylcholine (lyso-PC) acyltransferase activity related to triacylglycerol and mitochondrial lipid synthesis. Biochem J 387(Pt 3):617-26
Gu Z, et al.  (2004) Aberrant cardiolipin metabolism in the yeast taz1 mutant: a model for Barth syndrome. Mol Microbiol 51(1):149-58
Ma L, et al.  (2004) The human TAZ gene complements mitochondrial dysfunction in the yeast taz1Delta mutant. Implications for Barth syndrome. J Biol Chem 279(43):44394-9