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Search results 1 to 100 out of 271 for Tafazzin

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Type Details Score
Protein Domain
IPR000872 | Tafazzin
Type: Family
Description: This entry includes tafazzin and its homologues, such as Taz1 from yeasts and N-acylphosphatidylethanolamine synthase from plants. Tafazzin is an enzyme involved in the cardiolipin remodelling pathway [, ]. The phospholipid cardiolipin is an important component of the inner mitochondrial membrane that is involved in mitochondrial energy production and apoptosis []. In humans tafazzin is expressed at high levels in cardiac and skeletal muscle. As many as 10 isoforms can be present in different amounts in different tissues. Isoforms with hydrophobic N-termini are thought to be membrane anchored, while shorter forms, lacking the hydrophobic stretch, may be cytoplasmic (these latter are found in leukocytes and fibroblasts, but not in heart and skeletal muscle). A central hydrophilic domain may serve as an exposed loop that interacts with other proteins. Defects in the taz gene are the cause of Barth syndrome, a severe inherited disorder, often fatal in childhood. The disease is characterised by cardiac and skeletal myopathy, short stature and neutropenia [].In flies tafazzin is a CoA-independent, acyl-specific phospholipid transacylase with substrate preference for cardiolipin and phosphatidylcholine [].Budding yeast Taz1 is a lyso-phosphatidylcholine acyltransferase that is required for normal phospholipid content of mitochondrial membranes, whose acyl specificity in the reaction relies on lipid chemical composition [, ]. Arabidopsis N-acylphosphatidylethanolamine synthase (NAPE synthase, At1g78690) is an acyltransferase that catalyses the N-acylation of phosphatidylethanolamine to form N-acylphosphatidylethanolamine (N-acyl-PE) [].
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Gene
107049523 | TAZ
Type: gene
Organism: chicken
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Gene
6901 | TAFAZZIN
Type: gene
Organism: human
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Gene
549220 | tafazzin
Type: gene
Organism: frog, western clawed
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Gene
119868552 | TAFAZZIN
Type: gene
Organism: dog, domestic
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Protein
Q91WF0
Organism: Mus musculus/domesticus
Length: 262  
Fragment?: false
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Gene
363521 | Tafazzin
Type: gene
Organism: rat
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Gene
449590 | TAFAZZIN
Type: gene
Organism: chimpanzee
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Gene
515177 | TAFAZZIN
Type: gene
Organism: cattle
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Gene
321965 | tafazzin
Type: gene
Organism: zebrafish
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Gene
574297 | TAFAZZIN
Type: gene
Organism: macaque, rhesus
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Protein Coding Gene
MGI:109626 | Tafazzin
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein
Q91WF0-2
Organism: Mus musculus/domesticus
Length:  
Fragment?: false
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Protein
F6V7B7
Organism: Mus musculus/domesticus
Length: 21  
Fragment?: true
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Publication
28202545 | -
First Author: Schlame M
Year: 2017
Journal: J Biol Chem
Title: The Basis for Acyl Specificity in the Tafazzin Reaction.
Volume: 292
Issue: 13
Pages: 5499-5506
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Publication
19619503 | -
First Author: Houtkooper RH
Year: 2009
Journal: Biochim Biophys Acta
Title: The enigmatic role of tafazzin in cardiolipin metabolism.
Volume: 1788
Issue: 10
Pages: 2003-14
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Publication
8630491 | J:44131
First Author: Bione S
Year: 1996
Journal: Nat Genet
Title: A novel X-linked gene, G4.5. is responsible for Barth syndrome.
Volume: 12
Issue: 4
Pages: 385-9
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Publication
15588229 | -
First Author: Testet E
Year: 2005
Journal: Biochem J
Title: Ypr140wp, 'the yeast tafazzin', displays a mitochondrial lysophosphatidylcholine (lyso-PC) acyltransferase activity related to triacylglycerol and mitochondrial lipid synthesis.
Volume: 387
Issue: Pt 3
Pages: 617-26
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Publication
21803774 | -
First Author: Bulat E
Year: 2011
Journal: J Biol Chem
Title: Putative N-acylphosphatidylethanolamine synthase from Arabidopsis thaliana is a lysoglycerophospholipid acyltransferase.
Volume: 286
Issue: 39
Pages: 33819-31
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Publication
19164547 | -
First Author: Malhotra A
Year: 2009
Journal: Proc Natl Acad Sci U S A
Title: Role of calcium-independent phospholipase A2 in the pathogenesis of Barth syndrome.
Volume: 106
Issue: 7
Pages: 2337-41
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Publication
17082194 | -
First Author: Xu Y
Year: 2006
Journal: J Biol Chem
Title: The enzymatic function of tafazzin.
Volume: 281
Issue: 51
Pages: 39217-24
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Protein
J3JS92
Organism: Mus musculus/domesticus
Length: 248  
Fragment?: false
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Protein
H3BK99
Organism: Mus musculus/domesticus
Length: 175  
Fragment?: false
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Protein
Q810E6
Organism: Mus musculus/domesticus
Length: 238  
Fragment?: false
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Protein
Q810E7
Organism: Mus musculus/domesticus
Length: 177  
Fragment?: false
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Protein
Q8BMZ3
Organism: Mus musculus/domesticus
Length: 189  
Fragment?: false
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Protein
F6TQ32
Organism: Mus musculus/domesticus
Length: 64  
Fragment?: true
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Protein
H3BKZ8
Organism: Mus musculus/domesticus
Length: 178  
Fragment?: true
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Protein
B7FAU2
Organism: Mus musculus/domesticus
Length: 134  
Fragment?: true
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Protein
I7HJS2
Organism: Mus musculus/domesticus
Length: 263  
Fragment?: false
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Protein
B2KKU5
Organism: Mus musculus/domesticus
Length: 150  
Fragment?: true
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Protein
H3BJJ8
Organism: Mus musculus/domesticus
Length: 148  
Fragment?: true
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Publication
19114128 | J:192156
First Author: Acehan D
Year: 2009
Journal: Mitochondrion
Title: Distinct effects of tafazzin deletion in differentiated and undifferentiated mitochondria.
Volume: 9
Issue: 2
Pages: 86-95
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Publication
21091282 | J:176041
First Author: Soustek MS
Year: 2011
Journal: Hum Gene Ther
Title: Characterization of a transgenic short hairpin RNA-induced murine model of Tafazzin deficiency.
Volume: 22
Issue: 7
Pages: 865-71
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Publication
23130124 | J:187733
 
First Author: Phoon CK
Year: 2012
Journal: J Am Heart Assoc
Title: Tafazzin knockdown in mice leads to a developmental cardiomyopathy with early diastolic dysfunction preceding myocardial noncompaction.
Volume: 1
Issue: 2
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Publication
30055293 | J:270716
First Author: Cole LK
Year: 2018
Journal: Biochim Biophys Acta Mol Basis Dis
Title: Aberrant cardiolipin metabolism is associated with cognitive deficiency and hippocampal alteration in tafazzin knockdown mice.
Volume: 1864
Issue: 10
Pages: 3353-3367
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Publication
26114544 | J:238324
First Author: Cadalbert LC
Year: 2015
Journal: PLoS One
Title: Mouse Tafazzin Is Required for Male Germ Cell Meiosis and Spermatogenesis.
Volume: 10
Issue: 6
Pages: e0131066
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Publication
30389594 | J:289466
 
First Author: Kim J
Year: 2018
Journal: Mitochondrion
Title: Cardiac mitochondrial structure and function in tafazzin-knockdown mice.
Volume: 43
Pages: 53-62
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Publication
25919711 | J:292961
First Author: Hsu P
Year: 2015
Journal: Autophagy
Title: Cardiolipin remodeling by TAZ/tafazzin is selectively required for the initiation of mitophagy.
Volume: 11
Issue: 4
Pages: 643-52
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Publication
21068380 | J:167527
First Author: Acehan D
Year: 2011
Journal: J Biol Chem
Title: Cardiac and skeletal muscle defects in a mouse model of human Barth syndrome.
Volume: 286
Issue: 2
Pages: 899-908
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Publication
33895725 | J:334611
First Author: Maguire ARR
Year: 2021
Journal: Immunohorizons
Title: Tafazzin Modulates Allergen-Induced Mast Cell Inflammatory Mediator Secretion.
Volume: 5
Issue: 4
Pages: 182-192
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Publication
32665401 | J:298731
First Author: Le CH
Year: 2020
Journal: J Biol Chem
Title: Tafazzin deficiency impairs CoA-dependent oxidative metabolism in cardiac mitochondria.
Volume: 295
Issue: 35
Pages: 12485-12497
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UniProt Feature
UniProt Feature
Begin: 1
Description: Tafazzin
Type: chain
End: 262
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Publication
23616771 | J:290923
 
First Author: Powers C
Year: 2013
Journal: Front Physiol
Title: Diminished Exercise Capacity and Mitochondrial bc1 Complex Deficiency in Tafazzin-Knockdown Mice.
Volume: 4
Pages: 74
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Publication
29557170 | J:292571
First Author: Kimura T
Year: 2018
Journal: Biochemistry
Title: Substantial Decrease in Plasmalogen in the Heart Associated with Tafazzin Deficiency.
Volume: 57
Issue: 14
Pages: 2162-2175
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Gene
785078 | LOC785078
Type: gene
Organism: cattle
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Publication
34019639 | J:307184
 
First Author: Cole LK
Year: 2021
Journal: Endocrinology
Title: Tafazzin Deficiency Reduces Basal Insulin Secretion and Mitochondrial Function in Pancreatic Islets From Male Mice.
Volume: 162
Issue: 7
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Publication
35816277 | J:334315
First Author: Zegallai HM
Year: 2022
Journal: FASEB J
Title: Tafazzin deficiency in mouse mesenchymal stem cells promote reprogramming of activated B lymphocytes toward immunosuppressive phenotypes.
Volume: 36
Issue: 8
Pages: e22443
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Publication
36917259 | J:338013
First Author: Wang S
Year: 2023
Journal: Hum Mol Genet
Title: Genetic modifiers modulate phenotypic expression of tafazzin deficiency in a mouse model of Barth syndrome.
Volume: 32
Issue: 12
Pages: 2055-2067
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Publication
34767647 | J:334316
First Author: Zegallai HM
Year: 2021
Journal: FASEB J
Title: Tafazzin deficiency impairs mitochondrial metabolism and function of lipopolysaccharide activated B lymphocytes in mice.
Volume: 35
Issue: 12
Pages: e22023
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Publication
34979560 | J:334612
First Author: Sohn J
Year: 2022
Journal: Blood Adv
Title: A new murine model of Barth syndrome neutropenia links TAFAZZIN deficiency to increased ER stress-induced apoptosis.
Volume: 6
Issue: 8
Pages: 2557-2577
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Publication
26692032 | J:250637
First Author: Szczepanek K
Year: 2016
Journal: Biochim Biophys Acta
Title: Acquired deficiency of tafazzin in the adult heart: Impact on mitochondrial function and response to cardiac injury.
Volume: 1861
Issue: 4
Pages: 294-300
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Publication
31603701 | J:282302
First Author: Ren M
Year: 2019
Journal: Am J Physiol Heart Circ Physiol
Title: A critical appraisal of the tafazzin knockdown mouse model of Barth syndrome: what have we learned about pathogenesis and potential treatments?
Volume: 317
Issue: 6
Pages: H1183-H1193
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Publication
36154620 | J:335524
First Author: Zhu S
Year: 2022
Journal: Circulation
Title: Mitochondrial Stress Induces an HRI-eIF2α Pathway Protective for Cardiomyopathy.
Volume: 146
Issue: 13
Pages: 1028-1031
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Publication
30930145 | J:284785
First Author: Seneviratne AK
Year: 2019
Journal: Cell Stem Cell
Title: The Mitochondrial Transacylase, Tafazzin, Regulates for AML Stemness by Modulating Intracellular Levels of Phospholipids.
Volume: 24
Issue: 4
Pages: 621-636.e16
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Publication
30332638 | J:270756
First Author: Chowdhury A
Year: 2018
Journal: Cell Rep
Title: Defective Mitochondrial Cardiolipin Remodeling Dampens HIF-1α Expression in Hypoxia.
Volume: 25
Issue: 3
Pages: 561-570.e6
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Publication
33112430 | J:299339
     
First Author: Goncalves RLS
Year: 2020
Journal: FEBS Lett
Title: Cardiolipin deficiency in Barth syndrome is not associated with increased superoxide/H2 O2 production in heart and skeletal muscle mitochondria.
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Publication
29336355 | J:307224
First Author: Ikon N
Year: 2018
Journal: J Biomed Res
Title: Evaluation of cardiolipin nanodisks as lipid replacement therapy for Barth syndrome
Volume: 32
Issue: 2
Pages: 107-112
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Publication
32146862 | J:307561
First Author: Wang S
Year: 2020
Journal: Circ Res
Title: AAV Gene Therapy Prevents and Reverses Heart Failure in a Murine Knockout Model of Barth Syndrome.
Volume: 126
Issue: 8
Pages: 1024-1039
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Publication
31444868 | J:289464
First Author: Braun JL
Year: 2019
Journal: Physiol Rep
Title: SERCA2a tyrosine nitration coincides with impairments in maximal SERCA activity in left ventricles from tafazzin-deficient mice.
Volume: 7
Issue: 16
Pages: e14215
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Publication
30008435 | J:263791
 
First Author: Johnson JM
Year: 2018
Journal: J Mol Cell Cardiol
Title: Targeted overexpression of catalase to mitochondria does not prevent cardioskeletal myopathy in Barth syndrome.
Volume: 121
Pages: 94-102
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Publication
30788385 | J:307562
 
First Author: Suzuki-Hatano S
Year: 2019
Journal: Mol Ther Methods Clin Dev
Title: AAV9-TAZ Gene Replacement Ameliorates Cardiac TMT Proteomic Profiles in a Mouse Model of Barth Syndrome.
Volume: 13
Pages: 167-179
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Publication
31434794 | J:284797
 
First Author: Kimura T
Year: 2019
Journal: Life Sci Alliance
Title: Plasmalogen loss caused by remodeling deficiency in mitochondria.
Volume: 2
Issue: 4
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Publication
23410936 | J:292572
First Author: Kiebish MA
Year: 2013
Journal: J Lipid Res
Title: Dysfunctional cardiac mitochondrial bioenergetic, lipidomic, and signaling in a murine model of Barth syndrome.
Volume: 54
Issue: 5
Pages: 1312-25
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Publication
25860817 | J:292573
First Author: Soustek MS
Year: 2015
Journal: J Inherit Metab Dis
Title: Endurance training ameliorates complex 3 deficiency in a mouse model of Barth syndrome.
Volume: 38
Issue: 5
Pages: 915-22
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Publication
31186346 | J:280735
First Author: Li Y
Year: 2019
Journal: J Biol Chem
Title: Cardiolipin-induced activation of pyruvate dehydrogenase links mitochondrial lipid biosynthesis to TCA cycle function.
Volume: 294
Issue: 30
Pages: 11568-11578
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Publication
34129362 | J:339058
First Author: Zhu S
Year: 2021
Journal: Circ Heart Fail
Title: Cardiolipin Remodeling Defects Impair Mitochondrial Architecture and Function in a Murine Model of Barth Syndrome Cardiomyopathy.
Volume: 14
Issue: 6
Pages: e008289
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Publication
30070157 | J:289465
First Author: Suzuki-Hatano S
Year: 2019
Journal: Hum Gene Ther
Title: AAV-Mediated TAZ Gene Replacement Restores Mitochondrial and Cardioskeletal Function in Barth Syndrome.
Volume: 30
Issue: 2
Pages: 139-154
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Publication
33264603 | J:300251
First Author: Corrado M
Year: 2020
Journal: Cell Metab
Title: Dynamic Cardiolipin Synthesis Is Required for CD8+ T Cell Immunity.
Volume: 32
Issue: 6
Pages: 981-995.e7
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Publication
32418915 | J:289468
 
First Author: Cole LK
Year: 2020
Journal: J Mol Cell Cardiol
Title: Cardiolipin deficiency elevates susceptibility to a lipotoxic hypertrophic cardiomyopathy.
Volume: 144
Pages: 24-34
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Publication
34648376 | J:321012
First Author: Bertero E
Year: 2021
Journal: Circulation
Title: Loss of Mitochondrial Ca2+ Uniporter Limits Inotropic Reserve and Provides Trigger and Substrate for Arrhythmias in Barth Syndrome Cardiomyopathy.
Volume: 144
Issue: 21
Pages: 1694-1713
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Publication
15499385 | -
First Author: Lu B
Year: 2004
Journal: Biochem Cell Biol
Title: Complex expression pattern of the Barth syndrome gene product tafazzin in human cell lines and murine tissues.
Volume: 82
Issue: 5
Pages: 569-76
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Publication
23221956 | J:292830
First Author: Ostojic O
Year: 2013
Journal: J Appl Physiol (1985)
Title: The effects of chronic muscle use and disuse on cardiolipin metabolism.
Volume: 114
Issue: 4
Pages: 444-52
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Protein Coding Gene
MGP_CAROLIEiJ_G0033178 | -
Type: protein_coding_gene
Organism: Mus caroli
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Protein Coding Gene
MGP_129S1SvImJ_G0035838 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AJ_G0035819 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AKRJ_G0035744 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_BALBcJ_G0035804 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C3HHeJ_G0035509 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGI_C57BL6J_109626 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C57BL6NJ_G0036334 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CASTEiJ_G0034800 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CBAJ_G0035484 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_DBA2J_G0035641 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_FVBNJ_G0035585 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_LPJ_G0035726 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NODShiLtJ_G0035623 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NZOHlLtJ_G0036356 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PWKPhJ_G0034499 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_WSBEiJ_G0034941 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PahariEiJ_G0031721 | -
Type: protein_coding_gene
Organism: Mus pahari
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Protein Coding Gene
MGP_SPRETEiJ_G0034333 | -
Type: protein_coding_gene
Organism: Mus spretus
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GXD Expression
GXD Expression
     
Probe: MGI:7620338
Assay Type: RT-PCR
Annotation Date: 2024-04-12
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1610528
Stage: TS28
Assay Id: MGI:7620353
Age: postnatal day 10
Specimen Label: Ctrl
Detected: true
Specimen Num: 1
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GXD Expression
GXD Expression
     
Probe: MGI:7620338
Assay Type: RT-PCR
Annotation Date: 2024-04-12
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1610528
Stage: TS28
Assay Id: MGI:7620353
Age: postnatal day 10
Specimen Label: cKO
Detected: true
Specimen Num: 2
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GXD Expression
GXD Expression
     
Probe: MGI:7620338
Assay Type: RT-PCR
Annotation Date: 2024-04-12
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:1610528
Stage: TS28
Assay Id: MGI:7620353
Age: postnatal day 10
Specimen Label: TKO
Detected: false
Specimen Num: 3
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GXD Expression
GXD Expression
     
Probe: MGI:7620338
Assay Type: RT-PCR
Annotation Date: 2024-04-12
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:1610528
Stage: TS28
Assay Id: MGI:7620353
Age: postnatal day 10
Specimen Label: dcKO
Detected: false
Specimen Num: 4
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GXD Expression
GXD Expression
     
Probe: MGI:5309817
Assay Type: RNA in situ
Annotation Date: 2012-06-12
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:3516422
Stage: TS22
Assay Id: MGI:5423143
Age: embryonic day 14.5
Specimen Label: EB28; Specimen B152
Detected: false
Specimen Num: 1
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GXD Expression
GXD Expression
     
Probe: MGI:5309817
Assay Type: RNA in situ
Annotation Date: 2012-06-12
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:1716122
Stage: TS22
Assay Id: MGI:5423143
Age: embryonic day 14.5
Specimen Label: EB28; Specimen B152
Detected: false
Specimen Num: 1
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GXD Expression
GXD Expression
     
Probe: MGI:5309817
Assay Type: RNA in situ
Annotation Date: 2012-06-12
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:1691622
Stage: TS22
Assay Id: MGI:5423143
Age: embryonic day 14.5
Specimen Label: EB28; Specimen B152
Detected: false
Specimen Num: 1
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GXD Expression
GXD Expression
     
Probe: MGI:5309817
Assay Type: RNA in situ
Annotation Date: 2012-06-12
Strength: Absent
Sex: Not Specified
Emaps: EMAPS:1760622
Stage: TS22
Assay Id: MGI:5423143
Age: embryonic day 14.5
Specimen Label: EB28; Specimen B152
Detected: false
Specimen Num: 1
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