Fanconi anemia, complementation group C
Fanconi anemia group C protein is a protein that in humans is encoded by the FANCC gene.[1][2]
The protein encoded by this gene delays the onset of apoptosis and promotes homologous recombination repair of damaged DNA. Mutations in this gene result in Fanconi anemia.[2]
Interactions
Fanconi anemia, complementation group C has been shown to interact with STAT1,[3][4][5] ZBTB32,[4][6] GSTP1,[7][4] Cdk1,[4][8] SPTAN1,[9][10] HSPA1A,[11][4] FANCF,[12][13] FANCA[14][13][10][15][16][17][18][19] and FANCE.[20][12][18][21][22]
References
- ^ Strathdee CA, Duncan AM, Buchwald M (Jun 1993). "Evidence for at least four Fanconi anaemia genes including FACC on chromosome 9". Nat Genet 1 (3): 196–8. doi:10.1038/ng0692-196. PMID 1303234.
- ^ a b "Entrez Gene: FANCC Fanconi anemia, complementation group C". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2176.
- ^ Pang, Q; Fagerlie S, Christianson T A, Keeble W, Faulkner G, Diaz J, Rathbun R K, Bagby G C (Jul. 2000). "The Fanconi Anemia Protein FANCC Binds to and Facilitates the Activation of STAT1 by Gamma Interferon and Hematopoietic Growth Factors". Mol. Cell. Biol. (UNITED STATES) 20 (13): 4724–35. doi:10.1128/MCB.20.13.4724-4735.2000. ISSN 0270-7306. PMC 85895. PMID 10848598. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=85895.
- ^ a b c d e Reuter, Tanja Y; Medhurst Annette L, Waisfisz Quinten, Zhi Yu, Herterich Sabine, Hoehn Holger, Gross Hans J, Joenje Hans, Hoatlin Maureen E, Mathew Christopher G, Huber Pia A J (Oct. 2003). "Yeast two-hybrid screens imply involvement of Fanconi anemia proteins in transcription regulation, cell signaling, oxidative metabolism, and cellular transport". Exp. Cell Res. (United States) 289 (2): 211–21. doi:10.1016/S0014-4827(03)00261-1. ISSN 0014-4827. PMID 14499622.
- ^ Pang, Q; Christianson T A, Keeble W, Diaz J, Faulkner G R, Reifsteck C, Olson S, Bagby G C (Sep. 2001). "The Fanconi anemia complementation group C gene product: structural evidence of multifunctionality". Blood (United States) 98 (5): 1392–401. doi:10.1182/blood.V98.5.1392. ISSN 0006-4971. PMID 11520787.
- ^ Hoatlin, M E; Zhi Y, Ball H, Silvey K, Melnick A, Stone S, Arai S, Hawe N, Owen G, Zelent A, Licht J D (Dec. 1999). "A novel BTB/POZ transcriptional repressor protein interacts with the Fanconi anemia group C protein and PLZF". Blood (UNITED STATES) 94 (11): 3737–47. ISSN 0006-4971. PMID 10572087.
- ^ Cumming, R C; Lightfoot J, Beard K, Youssoufian H, O'Brien P J, Buchwald M (Jul. 2001). "Fanconi anemia group C protein prevents apoptosis in hematopoietic cells through redox regulation of GSTP1". Nat. Med. (United States) 7 (7): 814–20. doi:10.1038/89937. ISSN 1078-8956. PMID 11433346.
- ^ Kupfer, G M; Yamashita T, Naf D, Suliman A, Asano S, D'Andrea A D (Aug. 1997). "The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2". Blood (UNITED STATES) 90 (3): 1047–54. ISSN 0006-4971. PMID 9242535.
- ^ McMahon, L W; Sangerman J, Goodman S R, Kumaresan K, Lambert M W (Jun. 2001). "Human alpha spectrin II and the FANCA, FANCC, and FANCG proteins bind to DNA containing psoralen interstrand cross-links". Biochemistry (United States) 40 (24): 7025–34. doi:10.1021/bi002917g. ISSN 0006-2960. PMID 11401546.
- ^ a b McMahon, L W; Walsh C E, Lambert M W (Nov. 1999). "Human alpha spectrin II and the Fanconi anemia proteins FANCA and FANCC interact to form a nuclear complex". J. Biol. Chem. (UNITED STATES) 274 (46): 32904–8. doi:10.1074/jbc.274.46.32904. ISSN 0021-9258. PMID 10551855.
- ^ Pang, Qishen; Christianson Tracy A, Keeble Winifred, Koretsky Tara, Bagby Grover C (Dec. 2002). "The anti-apoptotic function of Hsp70 in the interferon-inducible double-stranded RNA-dependent protein kinase-mediated death signaling pathway requires the Fanconi anemia protein, FANCC". J. Biol. Chem. (United States) 277 (51): 49638–43. doi:10.1074/jbc.M209386200. ISSN 0021-9258. PMID 12397061.
- ^ a b Léveillé, France; Blom Eric, Medhurst Annette L, Bier Patrick, Laghmani El Houari, Johnson Mark, Rooimans Martin A, Sobeck Alexandra, Waisfisz Quinten, Arwert Fré, Patel K J, Hoatlin Maureen E, Joenje Hans, de Winter Johan P (Sep. 2004). "The Fanconi anemia gene product FANCF is a flexible adaptor protein". J. Biol. Chem. (United States) 279 (38): 39421–30. doi:10.1074/jbc.M407034200. ISSN 0021-9258. PMID 15262960.
- ^ a b de Winter, J P; van der Weel L, de Groot J, Stone S, Waisfisz Q, Arwert F, Scheper R J, Kruyt F A, Hoatlin M E, Joenje H (Nov. 2000). "The Fanconi anemia protein FANCF forms a nuclear complex with FANCA, FANCC and FANCG". Hum. Mol. Genet. (ENGLAND) 9 (18): 2665–74. doi:10.1093/hmg/9.18.2665. ISSN 0964-6906. PMID 11063725.
- ^ Garcia-Higuera, I; Kuang Y, Näf D, Wasik J, D'Andrea A D (Jul. 1999). "Fanconi Anemia Proteins FANCA, FANCC, and FANCG/XRCC9 Interact in a Functional Nuclear Complex". Mol. Cell. Biol. (UNITED STATES) 19 (7): 4866–73. ISSN 0270-7306. PMC 84285. PMID 10373536. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=84285.
- ^ Reuter, T; Herterich S, Bernhard O, Hoehn H, Gross H J (Jan. 2000). "Strong FANCA/FANCG but weak FANCA/FANCC interaction in the yeast 2-hybrid system". Blood (UNITED STATES) 95 (2): 719–20. ISSN 0006-4971. PMID 10627486.
- ^ Thomashevski, Andrei; High Anthony A, Drozd Mary, Shabanowitz Jeffrey, Hunt Donald F, Grant Patrick A, Kupfer Gary M (Jun. 2004). "The Fanconi anemia core complex forms four complexes of different sizes in different subcellular compartments". J. Biol. Chem. (United States) 279 (25): 26201–9. doi:10.1074/jbc.M400091200. ISSN 0021-9258. PMID 15082718.
- ^ Meetei, Amom Ruhikanta; de Winter Johan P, Medhurst Annette L, Wallisch Michael, Waisfisz Quinten, van de Vrugt Henri J, Oostra Anneke B, Yan Zhijiang, Ling Chen, Bishop Colin E, Hoatlin Maureen E, Joenje Hans, Wang Weidong (Oct. 2003). "A novel ubiquitin ligase is deficient in Fanconi anemia". Nat. Genet. (United States) 35 (2): 165–70. doi:10.1038/ng1241. ISSN 1061-4036. PMID 12973351.
- ^ a b Taniguchi, Toshiyasu; D'Andrea Alan D (Oct. 2002). "The Fanconi anemia protein, FANCE, promotes the nuclear accumulation of FANCC". Blood (United States) 100 (7): 2457–62. doi:10.1182/blood-2002-03-0860. ISSN 0006-4971. PMID 12239156.
- ^ Otsuki, Tetsuya; Young David B, Sasaki Dennis T, Pando Matthew P, Li Jianwu, Manning Anthony, Hoekstra Merl, Hoatlin Maureen E, Mercurio Frank, Liu Johnson M (2002). "Fanconi anemia protein complex is a novel target of the IKK signalsome". J. Cell. Biochem. (United States) 86 (4): 613–23. doi:10.1002/jcb.10270. ISSN 0730-2312. PMID 12210728.
- ^ Gordon, Susan M; Buchwald Manuel (Jul. 2003). "Fanconi anemia protein complex: mapping protein interactions in the yeast 2- and 3-hybrid systems". Blood (United States) 102 (1): 136–41. doi:10.1182/blood-2002-11-3517. ISSN 0006-4971. PMID 12649160.
- ^ Medhurst, A L; Huber P A, Waisfisz Q, de Winter J P, Mathew C G (Feb. 2001). "Direct interactions of the five known Fanconi anaemia proteins suggest a common functional pathway". Hum. Mol. Genet. (England) 10 (4): 423–9. doi:10.1093/hmg/10.4.423. ISSN 0964-6906. PMID 11157805.
- ^ Pace, Paul; Johnson Mark, Tan Wu Meng, Mosedale Georgina, Sng Chelvin, Hoatlin Maureen, de Winter Johan, Joenje Hans, Gergely Fanni, Patel K J (Jul. 2002). "FANCE: the link between Fanconi anaemia complex assembly and activity". EMBO J. (England) 21 (13): 3414–23. doi:10.1093/emboj/cdf355. ISSN 0261-4189. PMC 125396. PMID 12093742. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=125396.
Further reading
- Strathdee CA, Gavish H, Shannon WR, Buchwald M (1992). "Cloning of cDNAs for Fanconi's anaemia by functional complementation". Nature 356 (6372): 763–7. doi:10.1038/356763a0. PMID 1574115.
- Strathdee CA, Gavish H, Shannon WR, Buchwald M (1992). "Cloning of cDNAs for Fanconi's anaemia by functional complementation". Nature 358 (6385): 434. doi:10.1038/358434a0. PMID 1641028.
- Verlander PC, Kaporis A, Liu Q et al. (1996). "Carrier frequency of the IVS4 + 4 A-->T mutation of the Fanconi anemia gene FAC in the Ashkenazi Jewish population". Blood 86 (11): 4034–8. PMID 7492758.
- Yamashita T, Barber DL, Zhu Y et al. (1994). "The Fanconi anemia polypeptide FACC is localized to the cytoplasm". Proc. Natl. Acad. Sci. U.S.A. 91 (14): 6712–6. doi:10.1073/pnas.91.14.6712. PMC 44273. PMID 7517562. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=44273.
- Segal GM, Magenis RE, Brown M et al. (1994). "Repression of Fanconi anemia gene (FACC) expression inhibits growth of hematopoietic progenitor cells". J. Clin. Invest. 94 (2): 846–52. doi:10.1172/JCI117405. PMC 296166. PMID 7518843. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=296166.
- Youssoufian H (1994). "Localization of Fanconi anemia C protein to the cytoplasm of mammalian cells". Proc. Natl. Acad. Sci. U.S.A. 91 (17): 7975–9. doi:10.1073/pnas.91.17.7975. PMC 44527. PMID 8058745. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=44527.
- Whitney MA, Jakobs P, Kaback M et al. (1994). "The Ashkenazi Jewish Fanconi anemia mutation: incidence among patients and carrier frequency in the at-risk population". Hum. Mutat. 3 (4): 339–41. doi:10.1002/humu.1380030402. PMID 8081385.
- Murer-Orlando M, Llerena JC, Birjandi F et al. (1993). "FACC gene mutations and early prenatal diagnosis of Fanconi's anaemia". Lancet 342 (8872): 686. doi:10.1016/0140-6736(93)91800-2. PMID 8103176.
- Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
- Verlander PC, Lin JD, Udono MU et al. (1994). "Mutation analysis of the Fanconi anemia gene FACC". Am. J. Hum. Genet. 54 (4): 595–601. PMC 1918103. PMID 8128956. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=1918103.
- Whitney MA, Saito H, Jakobs PM et al. (1993). "A common mutation in the FACC gene causes Fanconi anaemia in Ashkenazi Jews". Nat. Genet. 4 (2): 202–5. doi:10.1038/ng0693-202. PMID 8348157.
- Gibson RA, Buchwald M, Roberts RG, Mathew CG (1993). "Characterisation of the exon structure of the Fanconi anaemia group C gene by vectorette PCR". Hum. Mol. Genet. 2 (1): 35–8. doi:10.1093/hmg/2.1.35. PMID 8490620.
- Gavish H, dos Santos CC, Buchwald M (1993). "A Leu554-to-Pro substitution completely abolishes the functional complementing activity of the Fanconi anemia (FACC) protein". Hum. Mol. Genet. 2 (2): 123–6. doi:10.1093/hmg/2.2.123. PMID 8499901.
- Youssoufian H, Li Y, Martin ME, Buchwald M (1996). "Induction of Fanconi anemia cellular phenotype in human 293 cells by overexpression of a mutant FAC allele". J. Clin. Invest. 97 (4): 957–62. doi:10.1172/JCI118519. PMC 507141. PMID 8613549. http://www.pubmedcentral.nih.gov/articlerender.fcgi?tool=pmcentrez&artid=507141.
- Yamashita T, Wu N, Kupfer G et al. (1996). "Clinical variability of Fanconi anemia (type C) results from expression of an amino terminal truncated Fanconi anemia complementation group C polypeptide with partial activity". Blood 87 (10): 4424–32. PMID 8639804.
- Lo Ten Foe JR, Rooimans MA, Joenje H, Arwert F (1996). "Novel frameshift mutation (1806insA) in exon 14 of the Fanconi anemia C gene, FAC". Hum. Mutat. 7 (3): 264–5. doi:10.1002/(SICI)1098-1004(1996)7:3<264::AID-HUMU11>3.0.CO;2-0. PMID 8829660.
- Gibson RA, Morgan NV, Goldstein LH et al. (1996). "Novel mutations and polymorphisms in the Fanconi anemia group C gene". Hum. Mutat. 8 (2): 140–8. doi:10.1002/(SICI)1098-1004(1996)8:2<140::AID-HUMU6>3.0.CO;2-F. PMID 8844212.
- Kupfer GM, Yamashita T, Naf D et al. (1997). "The Fanconi anemia polypeptide, FAC, binds to the cyclin-dependent kinase, cdc2". Blood 90 (3): 1047–54. PMID 9242535.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
External Links