Ubiquitylation by Trim32 causes coupled loss of desmin, Z-bands, and thin filaments in muscle atrophy (Q36444247)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22908310%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

title

Ubiquitylation by Trim32 causes coupled loss of desmin, Z-bands, and thin filaments in muscle atrophy (English)

1 reference

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11 February 2020

1 reference

1

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11 February 2020

3

Steven P Gygi

1 reference

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11 February 2020

author name string

Bo Zhai

series ordinal

2

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11 February 2020

Alfred L Goldberg

series ordinal

4

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11 February 2020

language of work or name

English

0 references

publication date

1 August 2012

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11 February 2020

published in

Journal of Cell Biology

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11 February 2020

volume

198

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11 February 2020

issue

4

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11 February 2020

page(s)

575-589

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Myostatin induces degradation of sarcomeric proteins through a Smad3 signaling mechanism during skeletal muscle wasting

11 February 2020

cites work

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The common missense mutation D489N in TRIM32 causing limb girdle muscular dystrophy 2H leads to loss of the mutated protein in knock-in mice resulting in a Trim32-null phenotype

30 September 2017

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Peroxisome proliferator-activated receptor gamma coactivator 1alpha or 1beta overexpression inhibits muscle protein degradation, induction of ubiquitin ligases, and disuse atrophy

30 September 2017

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Regulation of the psoriatic chemokine CCL20 by E3 ligases Trim32 and Piasy in keratinocytes

30 September 2017

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During muscle atrophy, thick, but not thin, filament components are degraded by MuRF1-dependent ubiquitylation

30 September 2017

1 reference

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TRIM32 is an E3 ubiquitin ligase for dysbindin

30 September 2017

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Properties of easily releasable myofilaments: are they the first step in myofibrillar protein turnover?

30 September 2017

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Deficiency of the E3 ubiquitin ligase TRIM32 in mice leads to a myopathy with a neurogenic component

30 September 2017

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A myopathy-linked desmin mutation perturbs striated muscle actin filament architecture

30 September 2017

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Tripartite motif protein 32 facilitates cell growth and migration via degradation of Abl-interactor 2

30 September 2017

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FoxO3 coordinately activates protein degradation by the autophagic/lysosomal and proteasomal pathways in atrophying muscle cells

30 September 2017

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FoxO3 controls autophagy in skeletal muscle in vivo

30 September 2017

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The E3 Ligase MuRF1 degrades myosin heavy chain protein in dexamethasone-treated skeletal muscle

30 September 2017

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Myosin accumulation and striated muscle myopathy result from the loss of muscle RING finger 1 and 3

30 September 2017

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30 September 2017

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Protein degradation by the ubiquitin-proteasome pathway in normal and disease states

30 September 2017

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Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11)

30 September 2017

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Trim32 is a ubiquitin ligase mutated in limb girdle muscular dystrophy type 2H that binds to skeletal muscle myosin and ubiquitinates actin

30 September 2017

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The molecular basis of skeletal muscle atrophy

30 September 2017

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Foxo transcription factors induce the atrophy-related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy

30 September 2017

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Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression

30 September 2017

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Activation of caspase-3 is an initial step triggering accelerated muscle proteolysis in catabolic conditions

30 September 2017

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Functional significance of the specific sites phosphorylated in desmin at cleavage furrow: Aurora-B may phosphorylate and regulate type III intermediate filaments during cytokinesis coordinatedly with Rho-kinase

30 September 2017

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Caspase proteolysis of desmin produces a dominant-negative inhibitor of intermediate filaments and promotes apoptosis

30 September 2017

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Limb-girdle muscular dystrophy type 2H associated with mutation in TRIM32, a putative E3-ubiquitin-ligase gene

30 September 2017

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AAA-ATPase p97/Cdc48p, a cytosolic chaperone required for endoplasmic reticulum-associated protein degradation

30 September 2017

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Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy

30 September 2017

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Identification of ubiquitin ligases required for skeletal muscle atrophy

30 September 2017

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The tyrosine kinase negative regulator c-Cbl as a RING-type, E2-dependent ubiquitin-protein ligase

30 September 2017

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A novel repeat domain that is often associated with RING finger and B-box motifs.

30 September 2017

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Desmin is essential for the tensile strength and integrity of myofibrils but not for myogenic commitment, differentiation, and fusion of skeletal muscle

30 September 2017

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Disruption of muscle architecture and myocardial degeneration in mice lacking desmin

30 September 2017

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The amino acid sequence of chicken muscle desmin provides a common structural model for intermediate filament proteins.

30 September 2017

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Phosphorylation of desmin in vitro inhibits formation of intermediate filaments; identification of three kinase A sites in the aminoterminal head domain

30 September 2017

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Immunological characterization of the subunit of the 100 A filaments from muscle cells

30 September 2017

1 reference

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The distribution of desmin (100 Å) filaments in primary cultures of embryonic chick cardiac cells

30 September 2017

1 reference

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Visualization of protein kinase activities in single cells by antibodies against phosphorylated vimentin and GFAP.

30 September 2017

1 reference

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Rapid disuse and denervation atrophy involve transcriptional changes similar to those of muscle wasting during systemic diseases

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514026

Protein kinase C-mediated desmin phosphorylation is related to myofibril disarray in cardiomyopathic hamster heart

28 June 2018

1 reference

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Effects of food deprivation on protein synthesis and degradation in rat skeletal muscles

28 June 2018

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Absence of caspase-3 protects against denervation-induced skeletal muscle atrophy.

28 June 2018

1 reference

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Coordinate activation of autophagy and the proteasome pathway by FoxO transcription factor.

21 September 2018

1 reference

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Induction of protein degradation in skeletal muscle by a phorbol ester involves upregulation of the ubiquitin-proteasome proteolytic pathway

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514026

RING protein Trim32 associated with skin carcinogenesis has anti-apoptotic and E3-ubiquitin ligase properties

21 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3514026

Expression of a calpastatin transgene slows muscle wasting and obviates changes in myosin isoform expression during murine muscle disuse

21 September 2018

1 reference

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Desmin mutations as a cause of right ventricular heart failure affect the intercalated disks

21 September 2018

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12 December 2020

Lectin binding and desmin expression during necrosis, regeneration, and neurogenic atrophy of human skeletal muscle

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12 December 2020

Remodeling of the cytoskeletal lattice in denervated skeletal muscle

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12 December 2020

Importance of the ATP-ubiquitin-proteasome pathway in the degradation of soluble and myofibrillar proteins in rabbit muscle extracts

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12 December 2020

The association of desmin with the developing myofibrils of cultured embryonic rat heart myocytes

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12 December 2020

Intermediate filament forming ability of desmin derivatives lacking either the amino-terminal 67 or the carboxy-terminal 27 residues

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12 December 2020

Site-specific phosphorylation induces disassembly of vimentin filaments in vitro

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12 December 2020

Identifiers

DOI

10.1083/JCB.201110067

1 reference

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