Lack of mitochondrial anionic phospholipids causes an inhibition of translation of protein components of the electron transport chain. A yeast genetic model system for the study of anionic phospholipid function in mitochondria (Q43596677)

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English	Lack of mitochondrial anionic phospholipids causes an inhibition of translation of protein components of the electron transport chain. A yeast genetic model system for the study of anionic phospholipid function in mitochondria	scientific article

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Europe PubMed Central

PubMed publication ID

25 November 2017

Lack of mitochondrial anionic phospholipids causes an inhibition of translation of protein components of the electron transport chain. A yeast genetic model system for the study of anionic phospholipid function in mitochondria (English)

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Europe PubMed Central

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25 November 2017

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Ostrander DB

1

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Europe PubMed Central

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25 November 2017

Zhang M

2

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25 November 2017

Mileykovskaya E

3

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25 November 2017

Rho M

4

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25 November 2017

Dowhan W

5

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25 November 2017

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publication date

2 May 2001

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25 November 2017

Journal of Biological Chemistry

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25 November 2017

276

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25 November 2017

27

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25 November 2017

25262-25272

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Europe PubMed Central

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25 November 2017

Eukaryotic phospholipid biosynthesis

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Cardiolipins and biomembrane function

1 reference

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Mitochondrial involvement in Parkinson's disease, Huntington's disease, hereditary spastic paraplegia and Friedreich's ataxia

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Oxidative damage and mitochondrial decay in aging

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Mitochondrial involvement in Alzheimer's disease

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Anionic phospholipids are determinants of membrane protein topology

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Membrane fusion and the lamellar-to-inverted-hexagonal phase transition in cardiolipin vesicle systems induced by divalent cations

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In vivo evidence for the involvement of anionic phospholipids in initiation of DNA replication in Escherichia coli

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The ATPase activity of SecA is regulated by acidic phospholipids, SecY, and the leader and mature domains of precursor proteins

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Activation of beef-heart cytochrome c oxidase by cardiolipin and analogues of cardiolipin

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Cardiolipin synthesis during the cell cycle of the yeastSaccharomyces cerevisiae

1 reference

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Absence of cardiolipin in the crd1 null mutant results in decreased mitochondrial membrane potential and reduced mitochondrial function

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Isolation of a chinese hamster ovary (CHO) cDNA encoding phosphatidylglycerophosphate (PGP) synthase, expression of which corrects the mitochondrial abnormalities of a PGP synthase-defective mutant of CHO-K1 cells

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Cardiolipin is not essential for the growth of Saccharomyces cerevisiae on fermentable or non-fermentable carbon sources

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Isolation and characterization of the gene (CLS1) encoding cardiolipin synthase in Saccharomyces cerevisiae

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The PEL1 gene (renamed PGS1) encodes the phosphatidylglycero-phosphate synthase of Saccharomyces cerevisiae

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Phosphatidylglycerolphosphate synthase encoded by the PEL1/PGS1 gene in Saccharomyces cerevisiae is localized in mitochondria and its expression is regulated by phospholipid precursors

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Molecular cloning of the PEL1 gene of Saccharomyces cerevisiae that is essential for the viability of petite mutants

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Regulation of Profilin Localization in Saccharomyces cerevisiae by Phosphoinositide Metabolism

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A ten-minute DNA preparation from yeast efficiently releases autonomous plasmids for transformation of Escherichia coli

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A Set of Vectors with a Tetracycline-Regulatable Promoter System for Modulated Gene Expression inSaccharomyces cerevisiae

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Dimethylaminostyrylmethylpyridiniumiodine (daspmi) as a fluorescent probe for mitochondria in situ

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Characterization of a microsomal subfraction associated with mitochondria of the yeast, Saccharomyces cerevisiae. Involvement in synthesis and import of phospholipids into mitochondria

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Molecular characterization of the PEL1 gene encoding a putative phosphatidylserine synthase.

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Isolation and biochemical characterization of organelles from the yeast, Saccharomyces cerevisiae

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The complete sequence of the mitochondrial genome of Saccharomyces cerevisiae

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The role of subunit 4, a nuclear-encoded protein of the F0 sector of yeast mitochondrial ATP synthase, in the assembly of the whole complex.

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21 January 2018

Translational control of endogenous and recoded nuclear genes in yeast mitochondria: regulation and membrane targeting.

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Degradation of Cytochrome Oxidase Subunits in Mutants of Yeast Lacking Cytochrome c and Suppression of the Degradation by Mutation of yme1

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Accumulation of mitochondrially synthesized Saccharomyces cerevisiae Cox2p and Cox3p depends on targeting information in untranslated portions of their mRNAs.

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Oxa1p mediates the export of the N- and C-termini of pCoxII from the mitochondrial matrix to the intermembrane space

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21 January 2018

Oxa1p, an essential component of the N-tail protein export machinery in mitochondria

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Glucose repression of yeast mitochondrial transcription: kinetics of derepression and role of nuclear genes

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Genetic determination of the mitochondrial adenine nucleotide translocation system and ITS role in the eukaryotic cell

1 reference

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Identification of a nuclear gene (FMC1) required for the assembly/stability of yeast mitochondrial F(1)-ATPase in heat stress conditions

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Association between the endoplasmic reticulum and mitochondria of yeast facilitates interorganelle transport of phospholipids through membrane contact

1 reference

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21 January 2018

Identifiers

10.1074/JBC.M103689200

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 November 2017

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