IFT88
Intraflagellar transport protein 88 homolog is a protein that in humans is encoded by the IFT88 gene.[1][2]
This gene encodes a member of the tetratrico peptide repeat (TPR) family. Mutations of a similar gene in mouse can cause polycystic kidney disease. Two transcript variants encoding distinct isoforms have been identified for this gene.[2]
Interactions
IFT88 has been shown to interact with BAT2.[3]
References
- ^ Schrick JJ, Onuchic LF, Reeders ST, Korenberg J, Chen XN, Moyer JH, Wilkinson JE, Woychik RP (Sep 1995). "Characterization of the human homologue of the mouse Tg737 candidate polycystic kidney disease gene". Hum Mol Genet 4 (4): 559–567. doi:10.1093/hmg/4.4.559. PMID 7633404.
- ^ a b "Entrez Gene: IFT88 intraflagellar transport 88 homolog (Chlamydomonas)". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8100.
- ^ Lehner, Ben; Semple Jennifer I, Brown Stephanie E, Counsell Damian, Campbell R Duncan, Sanderson Christopher M (Jan. 2004). "Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region". Genomics (United States) 83 (1): 153–167. doi:10.1016/S0888-7543(03)00235-0. ISSN 0888-7543. PMID 14667819.
Further reading
- Murcia NS, Sweeney WE, Avner ED; Sweeney (1999). "New insights into the molecular pathophysiology of polycystic kidney disease". Kidney Int. 55 (4): 1187–1197. doi:10.1046/j.1523-1755.1999.00370.x. PMID 10200981.
- Moyer JH, Lee-Tischler MJ, Kwon HY et al. (1994). "Candidate gene associated with a mutation causing recessive polycystic kidney disease in mice". Science 264 (5163): 1329–1333. doi:10.1126/science.8191288. PMID 8191288.
- Onuchic LF, Schrick JJ, Ma J et al. (1996). "Sequence analysis of the human hTg737 gene and its polymorphic sites in patients with autosomal recessive polycystic kidney disease". Mamm. Genome 6 (11): 805–808. doi:10.1007/BF00539009. PMID 8597639.
- Isfort RJ, Cody DB, Doersen CJ et al. (1997). "The tetratricopeptide repeat containing Tg737 gene is a liver neoplasia tumor suppressor gene". Oncogene 15 (15): 1797–1803. doi:10.1038/sj.onc.1201535. PMID 9362446.
- Bonura C, Paterlini-Brechot P, Brechot C (1999). "Structure and expression of Tg737, a putative tumor suppressor gene, in human hepatocellular carcinomas". Hepatology 30 (3): 677–681. doi:10.1002/hep.510300325. PMID 10462374.
- Taulman PD, Haycraft CJ, Balkovetz DF, Yoder BK (2001). "Polaris, a protein involved in left-right axis patterning, localizes to basal bodies and cilia". Mol. Biol. Cell 12 (3): 589–99. PMC 30966. PMID 11251073. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=30966.
- Harrington JJ, Sherf B, Rundlett S et al. (2001). "Creation of genome-wide protein expression libraries using random activation of gene expression". Nat. Biotechnol. 19 (5): 440–445. doi:10.1038/88107. PMID 11329013.
- Strausberg RL, Feingold EA, Grouse LH et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–16903. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=139241.
- Lehner B, Semple JI, Brown SE et al. (2004). "Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region". Genomics 83 (1): 153–167. doi:10.1016/S0888-7543(03)00235-0. PMID 14667819.
- Khanna H, Hurd TW, Lillo C et al. (2005). "RPGR-ORF15, which is mutated in retinitis pigmentosa, associates with SMC1, SMC3, and microtubule transport proteins". J. Biol. Chem. 280 (39): 33580–33587. doi:10.1074/jbc.M505827200. PMC 1249479. PMID 16043481. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1249479.
- Robert A, Margall-Ducos G, Guidotti JE et al. (2007). "The intraflagellar transport component IFT88/polaris is a centrosomal protein regulating G1-S transition in non-ciliated cells". J. Cell. Sci. 120 (Pt 4): 628–637. doi:10.1242/jcs.03366. PMID 17264151.