The enigmatic role of tafazzin in cardiolipin metabolism

被引:123
作者
Houtkooper, Riekelt H. [1 ]
Turkenburg, Marjolein [1 ]
Poll-The, Bwee Tien [2 ]
Karall, Daniela [3 ]
Perez-Cerda, Celia [4 ]
Morrone, Amelia [5 ]
Malvagia, Sabrina [5 ]
Wanders, Ronald J. [1 ]
Kulik, Willem [1 ]
Vaz, Frederic M. [1 ]
机构
[1] Univ Amsterdam, Acad Med Ctr, Lab Genet Metab Dis, NL-1100 DE Amsterdam, Netherlands
[2] Univ Amsterdam, Acad Med Ctr, Dept Paediat Neurol, NL-1100 DE Amsterdam, Netherlands
[3] Innsbruck Med Univ, Innsbruck, Austria
[4] Univ Autonoma Madrid, Ctr Diagnost Enfermedades Mol, Dept Biol Mol, Fac Ciencias,CIBERER, E-28049 Madrid, Spain
[5] Meyer Childrens Hosp, Clin Pediat Neurol, Metab & Muscular Unit, Florence, Italy
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 2009年 / 1788卷 / 10期
关键词
Tafazzin; Cardiolipin; Barth syndrome; Splice variant; Tissue distribution; Quantitative PCR; IONIZATION MASS-SPECTROMETRY; RAT-LIVER MITOCHONDRIA; BARTH-SYNDROME; ELECTROSPRAY-IONIZATION; SHOTGUN LIPIDOMICS; RESPIRATORY-CHAIN; INNER MEMBRANE; YEAST; MONOLYSOCARDIOLIPIN; PURIFICATION;
D O I
10.1016/j.bbamem.2009.07.009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mitochondrial phospholipid cardiolipin plays an important role in cellular metabolism as exemplified by its involvement in mitochondrial energy production and apoptosis. Following its biosynthesis, cardiolipin is actively remodeled to achieve its final acyl composition. An important cardiolipin remodeling enzyme is tafazzin, of which several mRNA splice variants exist. Mutations in the tafazzin gene cause the X-linked recessive disorder Barth syndrome. In addition to providing an overview of the current knowledge in literature about tafazzin, we present novel experimental data and use this to discuss the functional role of the different tafazzin variants in cardiolipin metabolism in relation to Barth syndrome. We developed and performed specific quantitative PCR analyses of different tafazzin mRNA splice variants in 16 human tissues and correlated this with the tissue cardiolipin profile. In BTHS fibroblasts we showed that mutations in the tafazzin gene affected both the level and distribution of tafazzin mRNA variants. Transient expression of selected human tafazzin variants in BTHS fibroblasts showed for the first time in a human cell system that tafazzin lacking exon5 indeed functions in cardiolipin remodeling. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:2003 / 2014
页数:12
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