Linking axonal degeneration to microtubule remodeling by Spastin-mediated microtubule severing (Q24295083)

1

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Edgar R Gomes

2

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Steven M Reisenweber

3

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Gregg G Gundersen

4

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Brett P Lauring

5

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language of work or name

English

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publication date

14 February 2005

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number of pages

8

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Drosophila spastin regulates synaptic microtubule networks and is required for normal motor function

inferred from page(s)

published in

Journal of Cell Biology

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volume

168

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issue

4

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page(s)

599-606

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cites work

1 reference

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Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis

19 March 2017

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An essential role for katanin in severing microtubules in the neuron

19 March 2017

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Katanin is responsible for the M-phase microtubule-severing activity in Xenopus eggs

19 March 2017

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The Vps4p AAA ATPase regulates membrane association of a Vps protein complex required for normal endosome function

19 March 2017

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Katanin, a microtubule-severing protein, is a novel AAA ATPase that targets to the centrosome using a WD40-containing subunit

19 March 2017

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The AAA ATPase Cdc48/p97 and its partners transport proteins from the ER into the cytosol

19 March 2017

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Endosomal transport function in yeast requires a novel AAA-type ATPase, Vps4p

19 March 2017

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A ubiquitous beta-tubulin disrupts microtubule assembly and inhibits cell proliferation

19 March 2017

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Spastin, the protein mutated in autosomal dominant hereditary spastic paraplegia, is involved in microtubule dynamics

19 March 2017

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AAA+ superfamily ATPases: common structure--diverse function

19 March 2017

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Spectrum of SPG4 mutations in autosomal dominant spastic paraplegia

19 March 2017

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Spastin, a new AAA protein, is altered in the most frequent form of autosomal dominant spastic paraplegia

19 March 2017

1 reference

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Identification of in vitro phosphorylation sites in the growth cone protein SCG10. Effect Of phosphorylation site mutants on microtubule-destabilizing activity

19 March 2017

1 reference

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Identification of katanin, an ATPase that severs and disassembles stable microtubules

19 March 2017

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Axonal growth is sensitive to the levels of katanin, a protein that severs microtubules

19 March 2017

1 reference

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Mutations of SPG4 are responsible for a loss of function of spastin, an abundant neuronal protein localized in the nucleus

19 March 2017

1 reference

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Neurodegenerative tauopathies

19 March 2017

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

7 April 2017

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Conserved arginine residues implicated in ATP hydrolysis, nucleotide-sensing, and inter-subunit interactions in AAA and AAA+ ATPases.

27 September 2017

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Phylogenetic analysis of AAA proteins

27 September 2017

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Distinct roles for the AAA ATPases NSF and p97 in the secretory pathway

27 September 2017

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

27 September 2017

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Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias

27 September 2017

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Detyrosinated (Glu) microtubules are stabilized by an ATP-sensitive plus-end cap.

27 September 2017

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Tubulin folding cofactor D is a microtubule destabilizing protein

27 September 2017

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Microtubule disassembly by ATP-dependent oligomerization of the AAA enzyme katanin

27 September 2017

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Defining a pathway of communication from the C-terminal peptide binding domain to the N-terminal ATPase domain in a AAA protein

30 May 2018

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Distinct populations of microtubules: tyrosinated and nontyrosinated alpha tubulin are distributed differently in vivo.

21 January 2018

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Motor domain mutation traps kinesin as a microtubule rigor complex

21 January 2018

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Gain‐of‐function screen identifies a role of the Src64 oncogene in Drosophila mushroom body development

21 January 2018

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Mutant dynactin in motor neuron disease.

21 January 2018

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The ATPase activity of Hsp104, effects of environmental conditions and mutations.

21 January 2018

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The hereditary spastic paraplegia gene, spastin, regulates microtubule stability to modulate synaptic structure and function.

21 January 2018

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The cellular and molecular pathology of the motor system in hereditary spastic paraparesis due to mutation of the spastin gene.

21 January 2018

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The effects of SNAP/SNARE complexes on the ATPase of NSF

21 January 2018

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21 January 2018

1 reference

https://pubmed.ncbi.nlm.nih.gov/15716377

12 December 2020

inferred from PubMed ID database lookup

Hereditary spastic paraplegia: the pace quickens

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15716377

12 December 2020

inferred from PubMed ID database lookup

The presence or absence of a vimentin-type intermediate filament network affects the shape of the nucleus in human SW-13 cells

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/15716377

12 December 2020

inferred from PubMed ID database lookup

Identifiers

DOI

10.1083/JCB.200409058

1 reference

5036491

5036491

1 reference

1 reference

1 reference