Dock8

Dock8
Dedicator of cytokinesis 8
Identifiers
Symbols DOCK8; FLJ00026; FLJ00152; FLJ00346; MRD2; ZIR8
External IDs OMIM611432 MGI1921396 HomoloGene52414 GeneCards: DOCK8 Gene
Orthologs
Species Human Mouse
Entrez 81704 76088
Ensembl ENSG00000107099 ENSMUSG00000052085
UniProt Q8NF50 Q6KAM7
RefSeq (mRNA) NM_001190458.1 NM_028785.3
RefSeq (protein) NP_001177387.1 NP_083061.2
Location (UCSC) Chr 9:
0.21 – 0.47 Mb
Chr 19:
25.07 – 25.28 Mb
PubMed search [1] [2]

Dock8 (Dedicator of cytokinesis 8), also known as Zir3, is a large (~190 kDa) protein involved in intracellular signalling networks.[1] It is a member of the DOCK-C subfamily of the DOCK family of guanine nucleotide exchange factors (GEFs) which function as activators of small G proteins.

Contents

Discovery

Dock8 was identified during a yeast two hybrid (YTH) screen for proteins that interact with the Rho family small G protein Cdc42.[2] Subsequent northern blot analysis revealed high levels of Dock8 expression in the placenta, lung, kidney and pancreas as well as lower levels in the heart, brain and skeletal muscle.

Function

Dock8 shares the same core domain arrangement as all other DOCK proteins, with a DHR2 domain which, in other proteins, contains GEF activity and a DHR1 domain known, in other proteins, to interact with phospholipids. In the YTH system Dock8 was reported to interact with both Rac1 and Cdc42. However, no stable interaction between Dock8 and these small G proteins was observed in a GST-pulldown assay. This may be due to the fact many DOCK-G protein interactions require the presence of adaptor proteins to stabilise the complex and thus facilitate nucleotide exchange.[3]

Dock8 in disease

Despite the fact that little is known about the cellular role of Dock8 its importance has been highlighted in several studies which have identified distruption of the DOCK8 gene in disease. Deletion and reduced expression of Dock8 have been reported in a human lung cancer cell line[4] and Dock8 was also identified as a putative candidate gene associated with progression of gliomas.[5] Interestingly, Dock8 has been reported to be disrupted in two unrelated patients with mental retardation.[6]

Autosomal recessive DOCK8 deficiency is associated with a variant of combined immunodeficiency. This variant of Hyperimmunoglobulin E syndrome (HIES) was first described in 2004 [7] and was now found to have a genetic mutation in the DOCK8 gene.[8]

References

  1. ^ "Entrez Gene: DOCK8 dedicator of cytokinesis 8". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=81704. 
  2. ^ Ruusala A, Aspenström P (August 2004). "Isolation and characterisation of DOCK8, a member of the DOCK180-related regulators of cell morphology". FEBS Letters 572 (1-3): 159–66. doi:10.1016/j.febslet.2004.06.095. PMID 15304341. 
  3. ^ Lu M, Ravichandran KS (2006). "Dock180-ELMO cooperation in Rac activation". Methods Enzymol. 406: 388–402. doi:10.1016/S0076-6879(06)06028-9. PMID 16472672. 
  4. ^ Takahashi K, Kohno T, Ajima R, et al. (February 2006). "Homozygous deletion and reduced expression of the DOCK8 gene in human lung cancer". Int. J. Oncol. 28 (2): 321–28. PMID 16391785. 
  5. ^ Idbaih A, Carvalho Silva R, Crinière E, et al. (July 2008). "Genomic changes in progression of low-grade gliomas". J. Neurooncol. Article in press (2): 133–40. doi:10.1007/s11060-008-9644-z. PMID 18618226. 
  6. ^ Griggs BL, Ladd S, Saul RA, et al. (February 2008). "Dedicator of cytokinesis 8 is disrupted in two patients with mental retardation and developmental disabilities". Genomics 91 (2): 195. doi:10.1016/j.ygeno.2007.10.011. PMC 2245991. PMID 18060736. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2245991. 
  7. ^ Renner ED, Puck JM, Holland SM, Schmitt M, Weiss M, Frosch M, Bergmann M, Davis J, Belohradsky BH, Grimbacher B (2004). "Autosomal recessive hyperimmunoglobulin E syndrome: a distinct disease entity". J Pediatr. 144 (1): 93–9. doi:10.1016/S0022-3476(03)00449-9. PMID 14722525. 
  8. ^ Zhang Q, Davis JC, Lamborn IT, Freeman AF, Jing H, Favreau AJ, Matthews HF, Davis J, Turner ML, Uzel G, Holland SM, Su HC (September 2009). "Combined Immunodeficiency Associated with DOCK8 Mutations". N. Engl. J. Med. 361 (21): 2046–55. doi:10.1056/NEJMoa0905506. PMC 2965730. PMID 19776401. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=2965730. Lay summary – nih.gov/news. 

Further reading




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  • DOCK8 — (англ. сокр. от Dedicator of cytokinesis 8  букв. «обеспечитель цитокинеза 8»), также известный как Zir3,  высокомолекулярный ( 190 кДа[1]) белок, участвующий в сетях межклеточного обмена сигналами. Он входит в подсемейство DOCK C… …   Википедия

  • RHOQ — Ras homolog gene family, member Q, also known as RHOQ, is a human gene.cite web | title = Entrez Gene: RHOQ ras homolog gene family, member Q| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=23433|… …   Wikipedia

  • Dock7 — Dedicator of cytokinesis 7 Identifiers Symbols DOCK7; KIAA1771; ZIR2 External IDs …   Wikipedia

  • RHOJ — Ras homolog gene family, member J, also known as RHOJ, is a human gene.cite web | title = Entrez Gene: RHOJ ras homolog gene family, member J| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene Cmd=ShowDetailView TermToSearch=57381|… …   Wikipedia

  • DOCK (protein) — Zir redirects here. For other uses, see Zir (disambiguation) Dedicator of cytokinesis Identifiers Symbol Ded cyto Pfam PF06920 InterPro …   Wikipedia

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