Mitochondrial morphological and functional defects in yeast caused by yme1 are suppressed by mutation of a 26S protease subunit homologue.
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YME1L controls the accumulation of respiratory chain subunits and is required for apoptotic resistance, cristae morphogenesis, and cell proliferationBiochemical and functional analysis of the YME1 gene product, an ATP and zinc-dependent mitochondrial protease from S. cerevisiae.Genetic basis of mitochondrial function and morphology in Saccharomyces cerevisiae.Mdm30 is an F-box protein required for maintenance of fusion-competent mitochondria in yeast.Prohibitins regulate membrane protein degradation by the m-AAA protease in mitochondria.Inactivation of YME2/RNA12, which encodes an integral inner mitochondrial membrane protein, causes increased escape of DNA from mitochondria to the nucleus in Saccharomyces cerevisiae.Complementary whole-genome technologies reveal the cellular response to proteasome inhibition by PS-341The regulatory particle of the Saccharomyces cerevisiae proteasome.Active site mutants in the six regulatory particle ATPases reveal multiple roles for ATP in the proteasome.Mitochondrial inheritance is delayed in Saccharomyces cerevisiae cells lacking the serine/threonine phosphatase PTC1.Homozygous YME1L1 mutation causes mitochondriopathy with optic atrophy and mitochondrial network fragmentationA 200-amino acid ATPase module in search of a basic functionYeast models of human mitochondrial diseases: from molecular mechanisms to drug screening.Maintenance and integrity of the mitochondrial genome: a plethora of nuclear genes in the budding yeastMultifunctional Mitochondrial AAA ProteasesMitochondrial-nuclear DNA interactions contribute to the regulation of nuclear transcript levels as part of the inter-organelle communication system.Msp1/ATAD1 maintains mitochondrial function by facilitating the degradation of mislocalized tail-anchored proteinsOrganelle-cytoskeletal interactions: actin mutations inhibit meiosis-dependent mitochondrial rearrangement in the budding yeast Saccharomyces cerevisiae.Assembly of mitochondrial cytochrome c-oxidase, a complicated and highly regulated cellular process.Proteasome mutants, pre4-2 and ump1-2, suppress the essential function but not the mitochondrial RNase P function of the Saccharomyces cerevisiae gene RPM2.Maintenance of mitochondrial morphology is linked to maintenance of the mitochondrial genome in Saccharomyces cerevisiae.Protein degradation within mitochondria: versatile activities of AAA proteases and other peptidases.Hsp90 and mitochondrial proteases Yme1 and Yta10/12 participate in ATP synthase assembly in Saccharomyces cerevisiae.Unmasking a temperature-dependent effect of the P. anserina i-AAA protease on aging and development.A mutation in a novel yeast proteasomal gene, RPN11/MPR1, produces a cell cycle arrest, overreplication of nuclear and mitochondrial DNA, and an altered mitochondrial morphologyMAP-1 and IAP-1, two novel AAA proteases with catalytic sites on opposite membrane surfaces in mitochondrial inner membrane of Neurospora crassa.Numtogenesis as a mechanism for development of cancer.Multiple genes, including a member of the AAA family, are essential for degradation of unassembled subunit 2 of cytochrome c oxidase in yeast mitochondria.The mitochondrial quality control protein Yme1 is necessary to prevent defective mitophagy in a yeast model of Barth syndrome.The ATP-dependent PIM1 protease is required for the expression of intron-containing genes in mitochondriaAAA proteases with catalytic sites on opposite membrane surfaces comprise a proteolytic system for the ATP-dependent degradation of inner membrane proteins in mitochondriaRegulated protein degradation in mitochondria.Mitochondrial distribution and inheritance.Genetic and biochemical basis for viability of yeast lacking mitochondrial genomes.Expression of the Saccharomyces cerevisiae gene YME1 in the petite-negative yeast Schizosaccharomyces pombe converts it to petite-positiveSubstrate recognition by AAA+ ATPases: distinct substrate binding modes in ATP-dependent protease Yme1 of the mitochondrial intermembrane spaceParticipation of the proteasomal lid subunit Rpn11 in mitochondrial morphology and function is mapped to a distinct C-terminal domain.Mutations in the mitochondrial ATP synthase gamma subunit suppress a slow-growth phenotype of yme1 yeast lacking mitochondrial DNA.Combined chemical and genetic approach to inhibit proteolysis by the proteasome.The ZbYME2 gene from the food spoilage yeast Zygosaccharomyces bailii confers not only YME2 functions in Saccharomyces cerevisiae, but also the capacity for catabolism of sorbate and benzoate, two major weak organic acid preservatives.
P2860
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P2860
Mitochondrial morphological and functional defects in yeast caused by yme1 are suppressed by mutation of a 26S protease subunit homologue.
description
1994 nî lūn-bûn
@nan
1994年の論文
@ja
1994年論文
@yue
1994年論文
@zh-hant
1994年論文
@zh-hk
1994年論文
@zh-mo
1994年論文
@zh-tw
1994年论文
@wuu
1994年论文
@zh
1994年论文
@zh-cn
name
Mitochondrial morphological an ...... 6S protease subunit homologue.
@en
type
label
Mitochondrial morphological an ...... 6S protease subunit homologue.
@en
prefLabel
Mitochondrial morphological an ...... 6S protease subunit homologue.
@en
P2093
P2860
P356
P1476
Mitochondrial morphological an ...... 6S protease subunit homologue.
@en
P2093
C L Campbell
P E Thorsness
P2860
P304
P356
10.1091/MBC.5.8.899
P577
1994-08-01T00:00:00Z