Adverts

Open Access Articles- Top Results for PKD1

PKD1

Template:Infobox3cols/rowTemplate:Infobox3cols/rowTemplate:Infobox3cols/rowTemplate:Infobox3cols/rowTemplate:Infobox3cols/row
Identifiers
SymbolsPKD1 ; PBP; Pc-1; TRPP1
External IDsOMIM601313 MGI97603 HomoloGene250 ChEMBL: 5772 GeneCards: PKD1 Gene
RNA expression pattern
File:PBB GE PKD1 202328 s at tn.png
File:PBB GE PKD1 202327 s at tn.png
File:PBB GE PKD1 216949 s at tn.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez531018763
EnsemblENSG00000008710ENSMUSG00000032855
UniProtP98161O08852
RefSeq (mRNA)NM_000296NM_013630
RefSeq (protein)NP_000287NP_038658
Location (UCSC)Chr 16:
2.14 – 2.19 Mb
Chr 17:
24.55 – 24.6 Mb
PubMed search[1][2]

Polycystin-1 is a protein that in humans is encoded by the PKD1 gene.[1][2]

Gene

Splice variants encoding different isoforms have been noted for PKD1. The gene is closely linked to six pseudogenes in a known duplicated region on chromosome 16p.[3]

File:PKD1PKD2 en.png
Illustration of PKD1 and PKD2 proteins at the cell membrane

Function

Polycystin-1 is a glycoprotein which contains a large N-terminal extracellular region, multiple transmembrane domains and a cytoplasmic C-tail. It may function as an integral membrane protein involved in cell-cell/matrix interactions, and may modulate intracellular calcium homoeostasis and other signal-transduction pathways. It plays a role in renal tubular development, and mutations in this gene have been associated with autosomal dominant polycystic kidney disease.

Interactions

Polycystin-1 has been shown to interact with polycystin-2[4][5] and RGS7.[6]

See also

References

  1. ^ Hughes J, Ward CJ, Peral B, Aspinwall R, Clark K, San Millán JL et al. (June 1995). "The polycystic kidney disease 1 (PKD1) gene encodes a novel protein with multiple cell recognition domains". Nat. Genet. 10 (2): 151–160. PMID 7663510. doi:10.1038/ng0695-151. 
  2. ^ "Polycystic kidney disease: the complete structure of the PKD1 gene and its protein. The International Polycystic Kidney Disease Consortium". Cell 81 (2): 289–98. April 1995. PMID 7736581. doi:10.1016/0092-8674(95)90339-9. 
  3. ^ "Entrez Gene: PKD1 polycystic kidney disease 1 (autosomal dominant)". 
  4. ^ Tsiokas L, Kim E, Arnould T, Sukhatme VP, Walz G (June 1997). "Homo- and heterodimeric interactions between the gene products of PKD1 and PKD2". Proc. Natl. Acad. Sci. U.S.A. 94 (13): 6965–6970. PMC 21268. PMID 9192675. doi:10.1073/pnas.94.13.6965. 
  5. ^ Tsiokas L, Arnould T, Zhu C, Kim E, Walz G, Sukhatme VP (March 1999). "Specific association of the gene product of PKD2 with the TRPC1 channel". Proc. Natl. Acad. Sci. U.S.A. 96 (7): 3934–3939. PMC 22398. PMID 10097141. doi:10.1073/pnas.96.7.3934. 
  6. ^ Kim E, Arnould T, Sellin L, Benzing T, Comella N, Kocher O et al. (May 1999). "Interaction between RGS7 and polycystin". Proc. Natl. Acad. Sci. U.S.A. 96 (11): 6371–6376. PMC 26888. PMID 10339594. doi:10.1073/pnas.96.11.6371. 

Further reading

  • Islam, Md. Shahidul (January 2011). Transient Receptor Potential Channels. Advances in Experimental Medicine and Biology 704. Berlin: Springer. p. 700. ISBN 978-94-007-0264-6. 
  • Wilson PD (2001). "Polycystin: new aspects of structure, function, and regulation". J. Am. Soc. Nephrol. 12 (4): 834–45. PMID 11274246. 
  • Boletta A, Germino GG (2004). "Role of polycystins in renal tubulogenesis". Trends Cell Biol. 13 (9): 484–492. PMID 12946628. doi:10.1016/S0962-8924(03)00169-7. 
  • Everson GT, Taylor MR, Doctor RB (2004). "Polycystic disease of the liver". Hepatology 40 (4): 774–782. PMID 15382167. doi:10.1002/hep.20431. 
  • Weimbs T (2007). "Regulation of mTOR by polycystin-1: is polycystic kidney disease a case of futile repair?". Cell Cycle 5 (21): 2425–2429. PMID 17102641. doi:10.4161/cc.5.21.3408. 
</dl>

External links

This article incorporates text from the United States National Library of Medicine, which is in the public domain.

Lua error in package.lua at line 80: module 'Module:Buffer' not found.