Literature DB >> 22987008

Tafazzin senses curvature.

Klaus Gawrisch1.   

Abstract

The phospholipid-lysophospholipid transacylase tafazzin is responsible for enrichment of the cardiolipin fraction of mitochondria with tetralinoleoyl-cardiolipin. The specificity for linoleoyl hydrocarbon chains is now explained by the specific action of tafazzin on negatively curved lipid monolayers.

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Year:  2012        PMID： 22987008      PMCID： PMC3478944          DOI： 10.1038/nchembio.1068

Source DB:  PubMed          Journal:  Nat Chem Biol        ISSN： 1552-4450            Impact factor:   15.040


  9 in total

1.  Barth syndrome may be due to an acyltransferase deficiency.

Authors:  A F Neuwald
Journal:  Curr Biol       Date:  1997-08-01       Impact factor: 10.834

2.  Cardiolipin microdomains localize to negatively curved regions of Escherichia coli membranes.

Authors:  Lars D Renner; Douglas B Weibel
Journal:  Proc Natl Acad Sci U S A       Date:  2011-03-28       Impact factor: 11.205

3.  The enzymatic function of tafazzin.

Authors:  Yang Xu; Ashim Malhotra; Mindong Ren; Michael Schlame
Journal:  J Biol Chem       Date:  2006-11-02       Impact factor: 5.157

4.  An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes.

Authors:  P G Barth; H R Scholte; J A Berden; J M Van der Klei-Van Moorsel; I E Luyt-Houwen; E T Van 't Veer-Korthof; J J Van der Harten; M A Sobotka-Plojhar
Journal:  J Neurol Sci       Date:  1983-12       Impact factor: 3.181

5.  Deficiency of tetralinoleoyl-cardiolipin in Barth syndrome.

Authors:  Michael Schlame; Jeffrey A Towbin; Paul M Heerdt; Roswitha Jehle; Salvatore DiMauro; Thomas J J Blanck
Journal:  Ann Neurol       Date:  2002-05       Impact factor: 10.422

6.  Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria.

Authors:  Devrim Acehan; Zaza Khuchua; Riekelt H Houtkooper; Ashim Malhotra; Johanna Kaufman; Frédéric M Vaz; Mindong Ren; Howard A Rockman; David L Stokes; Michael Schlame
Journal:  Mitochondrion       Date:  2008-12-11       Impact factor: 4.160

7.  Formation of molecular species of mitochondrial cardiolipin. 1. A novel transacylation mechanism to shuttle fatty acids between sn-1 and sn-2 positions of multiple phospholipid species.

Authors:  Ashim Malhotra; Yang Xu; Mindong Ren; Michael Schlame
Journal:  Biochim Biophys Acta       Date:  2009-01-21

8.  Mitochondrial mislocalization and altered assembly of a cluster of Barth syndrome mutant tafazzins.

Authors:  Steven M Claypool; J Michael McCaffery; Carla M Koehler
Journal:  J Cell Biol       Date:  2006-07-31       Impact factor: 10.539

9.  A novel X-linked gene, G4.5. is responsible for Barth syndrome.

Authors:  S Bione; P D'Adamo; E Maestrini; A K Gedeon; P A Bolhuis; D Toniolo
Journal:  Nat Genet       Date:  1996-04       Impact factor: 38.330
  9 in total
  7 in total

Review 1.  TAZ encodes tafazzin, a transacylase essential for cardiolipin formation and central to the etiology of Barth syndrome.

Authors:  Anders O Garlid; Calvin T Schaffer; Jaewoo Kim; Hirsh Bhatt; Vladimir Guevara-Gonzalez; Peipei Ping
Journal:  Gene       Date:  2019-10-21       Impact factor: 3.688

Review 2.  Cholesterol-induced suppression of membrane elastic fluctuations at the atomistic level.

Authors:  Trivikram R Molugu; Michael F Brown
Journal:  Chem Phys Lipids       Date:  2016-05-03       Impact factor: 3.329

3.  An overview of inborn errors of complex lipid biosynthesis and remodelling.

Authors:  Foudil Lamari; Fanny Mochel; Jean-Marie Saudubray
Journal:  J Inherit Metab Dis       Date:  2014-09-20       Impact factor: 4.982

Review 4.  Cardiolipin remodeling: a regulatory hub for modulating cardiolipin metabolism and function.

Authors:  Cunqi Ye; Zheni Shen; Miriam L Greenberg
Journal:  J Bioenerg Biomembr       Date:  2014-11-29       Impact factor: 2.945

Review 5.  Cardiolipin and its different properties in mitophagy and apoptosis.

Authors:  Xiao-Xiao Li; Bun Tsoi; Yi-Fang Li; Hiroshi Kurihara; Rong-Rong He
Journal:  J Histochem Cytochem       Date:  2015-02-11       Impact factor: 2.479

Review 6.  Barth Syndrome: From Mitochondrial Dysfunctions Associated with Aberrant Production of Reactive Oxygen Species to Pluripotent Stem Cell Studies.

Authors:  Ana Saric; Karine Andreau; Anne-Sophie Armand; Ian M Møller; Patrice X Petit
Journal:  Front Genet       Date:  2016-01-20       Impact factor: 4.599

Review 7.  Barth syndrome cardiomyopathy: targeting the mitochondria with elamipretide.

Authors:  Hani N Sabbah
Journal:  Heart Fail Rev       Date:  2020-10-01       Impact factor: 4.214
  7 in total

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