SPG20 protein spartin is recruited to midbodies by ESCRT-III protein Ist1 and participates in cytokinesis (Q24296616)

22 June 2017

SPG20 protein spartin is recruited to midbodies by ESCRT-III protein Ist1 and participates in cytokinesis (English)

1 reference

IST1 factor associated with ESCRT-III

22 June 2017

0 references

0 references

1 reference

GOA release 2020-03-11

1 reference

GOA release 2020-03-11

cell division

1 reference

GOA release 2020-03-11

author name string

Benoît Renvoisé

1

1 reference

22 June 2017

Rell L Parker

2

1 reference

22 June 2017

Dong Yang

3

1 reference

22 June 2017

Joanna C Bakowska

4

1 reference

22 June 2017

James H Hurley

5

1 reference

22 June 2017

Craig Blackstone

6

1 reference

22 June 2017

language of work or name

English

0 references

publication date

18 August 2010

1 reference

Molecular Biology of the Cell

22 June 2017

1 reference

22 June 2017

21

1 reference

22 June 2017

3293-3303

1 reference

22 June 2017

19

1 reference

describes a project that uses

22 June 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC2947466/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

Membrane budding and scission by the ESCRT machinery: it's all in the neck

1 reference

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PtdIns(3)P controls cytokinesis through KIF13A-mediated recruitment of FYVE-CENT to the midbody

19 March 2017

1 reference

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Endogenous spartin (SPG20) is recruited to endosomes and lipid droplets and interacts with the ubiquitin E3 ligases AIP4 and AIP5

19 March 2017

1 reference

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No strings attached: the ESCRT machinery in viral budding and cytokinesis

19 March 2017

1 reference

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Structural basis for ESCRT-III protein autoinhibition

19 March 2017

1 reference

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Ab initio protein modelling reveals novel human MIT domains

19 March 2017

1 reference

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Essential role of hIST1 in cytokinesis

19 March 2017

1 reference

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Biochemical analyses of human IST1 and its function in cytokinesis

19 March 2017

1 reference

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Spastin couples microtubule severing to membrane traffic in completion of cytokinesis and secretion

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

Structural basis for midbody targeting of spastin by the ESCRT-III protein CHMP1B

19 March 2017

1 reference

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Two distinct modes of ESCRT-III recognition are required for VPS4 functions in lysosomal protein targeting and HIV-1 budding

19 March 2017

1 reference

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Final stages of cytokinesis and midbody ring formation are controlled by BRUCE

19 March 2017

1 reference

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Plasma membrane deformation by circular arrays of ESCRT-III protein filaments

19 March 2017

1 reference

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ESCRT-III recognition by VPS4 ATPases

19 March 2017

1 reference

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Troyer syndrome protein spartin is mono-ubiquitinated and functions in EGF receptor trafficking

19 March 2017

1 reference

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Cellular Localization, Oligomerization, and Membrane Association of the Hereditary Spastic Paraplegia 3A (SPG3A) Protein Atlastin

19 March 2017

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Structural Basis of Ist1 Function and Ist1-Did2 Interaction in the Multivesicular Body Pathway and Cytokinesis

19 March 2017

1 reference

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Structural basis for selective recognition of ESCRT-III by the AAA ATPase Vps4

19 March 2017

1 reference

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Membrane scission by the ESCRT-III complex

19 March 2017

1 reference

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Novel Ist1-Did2 complex functions at a late step in multivesicular body sorting

19 March 2017

1 reference

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ESCRT-III dysfunction causes autophagosome accumulation and neurodegeneration

19 March 2017

1 reference

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Spartin activates atrophin-1-interacting protein 4 (AIP4) E3 ubiquitin ligase and promotes ubiquitination of adipophilin on lipid droplets

19 March 2017

1 reference

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Developmental and degenerative features in a complicated spastic paraplegia.

27 September 2017

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The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signalling

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

A role for ubiquitin ligases and Spartin/SPG20 in lipid droplet turnover

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms

27 September 2017

1 reference

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Lack of spartin protein in Troyer syndrome: a loss-of-function disease mechanism?

27 September 2017

1 reference

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Ist1 regulates Vps4 localization and assembly

27 September 2017

1 reference

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The hereditary spastic paraplegia protein spartin localises to mitochondria

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

Endogenous spartin, mutated in hereditary spastic paraplegia, has a complex subcellular localization suggesting diverse roles in neurons.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

The Troyer syndrome (SPG20) protein spartin interacts with Eps15.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

Traffic accidents: molecular genetic insights into the pathogenesis of the hereditary spastic paraplegias

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

The hereditary spastic paraplegia protein spastin interacts with the ESCRT-III complex-associated endosomal protein CHMP1B.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

The identification of a conserved domain in both spartin and spastin, mutated in hereditary spastic paraplegia

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

SPG20 is mutated in Troyer syndrome, an hereditary spastic paraplegia.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

Classification of the hereditary ataxias and paraplegias

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

The Troyer syndrome. A recessive form of spastic paraplegia with distal muscle wasting

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

Troyer syndrome revisited. A clinical and radiological study of a complicated hereditary spastic paraplegia.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2947466

29 November 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/20719964

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Genetic testing for the spastic paraplegias: drowning by numbers

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20719964

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1091/MBC.E09-10-0879

1 reference

22 June 2017

0 references

1 reference