A role for sequestosome 1/p62 in mitochondrial dynamics, import and genome integrity. - Wikidata - wikimedia - TriplyDB

A role for sequestosome 1/p62 in mitochondrial dynamics, import and genome integrity.

A role for sequestosome 1/p62 in mitochondrial dynamics, import and genome integrity.

http://www.wikidata.org/entity/Q42024119

about

Emerging functional cross-talk between the Keap1-Nrf2 system and mitochondria Mitochondrial dysfunction in amyotrophic lateral sclerosis - a valid pharmacological target?Quantitative proteomics of synaptic and nonsynaptic mitochondria: insights for synaptic mitochondrial vulnerability.Aging synaptic mitochondria exhibit dynamic proteomic changes while maintaining bioenergetic function Pathogenic p62/SQSTM1 mutations impair energy metabolism through limitation of mitochondrial substrates.Mitochondrial stress and activation of PI3K and Akt survival pathway in bladder ischemia.Interaction of SQSTM1 with the motor protein dynein--SQSTM1 is required for normal dynein function and trafficking.Myeloid malignancies with chromosome 5q deletions acquire a dependency on an intrachromosomal NF-κB gene network SQSTM1/p62 interacts with HDAC6 and regulates deacetylase activity.Beclin 1 and p62 expression in non-small cell lung cancer: relation with malignant behaviors and clinical outcome.Elimination of paternal mitochondria in mouse embryos occurs through autophagic degradation dependent on PARKIN and MUL1.Regulation of autophagy and mitophagy by nutrient availability and acetylation.Inhibition of stress-inducible HSP70 impairs mitochondrial proteostasis and function.Mitochondrial and lysosomal biogenesis are activated following PINK1/parkin-mediated mitophagy.Behavioral effects of SQSTM1/p62 overexpression in mice: support for a mitochondrial role in depression and anxiety Implications of mitochondrial network organization in mitochondrial stress signalling in NARP cybrid and Rho0 cells.From autophagy to mitophagy: the roles of P62 in neurodegenerative diseases.Roles of p62 in BDNF-dependent autophagy suppression and neuroprotection against mitochondrial dysfunction in rat cortical neurons.Overexpression of PGC-1α in aging muscle enhances a subset of young-like molecular patterns.Role of Optineurin in the Mitochondrial Dysfunction: Potential Implications in Neurodegenerative Diseases and Cancer.

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A role for sequestosome 1/p62 in mitochondrial dynamics, import and genome integrity.

http://www.wikidata.org/entity/Q42024119

description

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name

A role for sequestosome 1/p62 in mitochondrial dynamics, import and genome integrity.

@en

A role for sequestosome 1/p62 in mitochondrial dynamics, import and genome integrity.

@nl

type

label

A role for sequestosome 1/p62 in mitochondrial dynamics, import and genome integrity.

@en

A role for sequestosome 1/p62 in mitochondrial dynamics, import and genome integrity.

@nl

prefLabel

A role for sequestosome 1/p62 in mitochondrial dynamics, import and genome integrity.

@en

A role for sequestosome 1/p62 in mitochondrial dynamics, import and genome integrity.

@nl

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J.BBAMCR.2012.11.004

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Biochimica et Biophysica Acta

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A role for sequestosome 1/p62 in mitochondrial dynamics, import and genome integrity.

@en

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Jorge Moscat

http://www.w3.org/2001/XMLSchema#string

M Lamar Seibenhener

http://www.w3.org/2001/XMLSchema#string

Maria-Theresa Diaz-Meco

http://www.w3.org/2001/XMLSchema#string

Marie W Wooten

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Michael C Wooten

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Yifeng Du

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P2860

PINK1/Parkin-mediated mitophagy is dependent on VDAC1 and p62/SQSTM1

p62/SQSTM1 is required for Parkin-induced mitochondrial clustering but not mitophagy; VDAC1 is dispensable for both

Homeostatic levels of p62 control cytoplasmic inclusion body formation in autophagy-deficient mice

Disease-causing mutations in parkin impair mitochondrial ubiquitination, aggregation, and HDAC6-dependent mitophagy

p62, a phosphotyrosine-independent ligand of the SH2 domain of p56lck, belongs to a new class of ubiquitin-binding proteins

p62/SQSTM1 binds directly to Atg8/LC3 to facilitate degradation of ubiquitinated protein aggregates by autophagy

Autophagy suppresses tumorigenesis through elimination of p62

Molecular and functional characterization of the p62 complex, an assembly of nuclear pore complex glycoproteins

Quantitative colocalization analysis of multicolor confocal immunofluorescence microscopy images: pushing pixels to explore biological phenomena

Structural basis for sorting mechanism of p62 in selective autophagy

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10.1016/J.BBAMCR.2012.11.004

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