DCTN1

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Dynactin subunit 1 is a protein that in humans is encoded by the DCTN1 gene.[5]

PDBOrtholog search: PDBe RCSB
AliasesDCTN1, DAP-150, DP-150, P135, dynactin subunit 1
Quick facts Available structures, PDB ...
DCTN1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesDCTN1, DAP-150, DP-150, P135, dynactin subunit 1
External IDsOMIM: 601143; MGI: 107745; HomoloGene: 3011; GeneCards: DCTN1; OMA:DCTN1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001198866
NM_001198867
NM_007835
NM_001347310

RefSeq (protein)

NP_001185795
NP_001185796
NP_001334239
NP_031861

Location (UCSC)Chr 2: 74.36 – 74.39 MbChr 6: 83.14 – 83.18 Mb
PubMed search[3][4]
Wikidata
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Function

This gene encodes the largest subunit of dynactin, a macromolecular complex consisting of 23 subunits (11 individual proteins ranging in size from 22 to 150 kD).[6] Dynactin binds to cytoplasmic dynein, dynein cargo adaptors, and microtubules.[7] It is involved in a diverse array of cellular functions, including ER-to-Golgi transport, the centripetal movement of lysosomes and endosomes, spindle formation, chromosome movement, nuclear positioning, and axonogenesis.

This subunit is commonly referred to p150-glued.[5] It is present in two copies per dynactin complex and forms an ≈75 nm long flexible arm that extends from the main body of dynactin.[6] The p150-glued arm contains binding sites for microtubules,[8] the microtubule plus tip binding protein EB1,[9] and the N-terminus of the dynein intermediate chain.[10][11]

Alternative splicing of this gene results in at least 2 functionally distinct isoforms: a ubiquitously expressed one and a brain-specific one. Based on its cytogenetic location, this gene is considered as a candidate gene for limb-girdle muscular dystrophy.[12]

Interactions

DCTN1 has been shown to interact with:

References

Further reading

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