TFF1
Trefoil faktor 1 jest protein koji je kod ljudi kodiran genom TFF1 sa hromosoma 21.[5][6] (također zvani pS2 gen[7]).
Aminokiselinska sekvenca
[uredi | uredi izvor]Dužina polipeptidnog lanca je 84 aminokiseline, a molekulska težina 9.150 Da.[6]
10 | 20 | 30 | 40 | 50 | ||||
---|---|---|---|---|---|---|---|---|
MATMENKVIC | ALVLVSMLAL | GTLAEAQTET | CTVAPRERQN | CGFPGVTPSQ | ||||
CANKGCCFDD | TVRGVPWCFY | PNTIDVPPEE | ECEF |
Funkcija
[uredi | uredi izvor]Članovi porodice Trefoil odlikuju se po tome što imaju najmanje jednu kopiju trefoilski motiv, domena od 40 aminokiselina koji sadrži tri konzervirana disulfida. To su stabilni sekretorni proteini eksprimirani u gastrointestinalno sluzokoži. Njihove funkcije nisu definirane, ali mogu zaštititi sluznicu od ozljeda, stabilizirati sloj sluzi i uticati na zacjeljivanje epitela. Ovaj gen, koji je eksprimiran u sluznici želuca, također je proučavan zbog njegove ekspresije u ljudskim tumorima. Sa dva druga srodna gena člana porodice trefiola nalaze se u klasteru na hromosomu 21.[6]
Vezivanje glikana
[uredi | uredi izvor]Sva tri ljudska trefoilska faktora su lektini koji su u specifičnoj interakciji sa disaharidom GlcNAc-α-1,4-Gal.[8] Ovaj disaharid je neobičan glikotop za koji se zna da postoji samo na velikim, jako glikozilovanim, mucinima u sluznici. Unakrsnim povezivanjem mucina putem dvovalentno vezivanje ovog glikotopa, trefiolni faktori su tada u stanju da reverzibilno moduliraju debljinu i viskoznost sluzi.[8]
Kod karcinoma želuca
[uredi | uredi izvor]Ekspresija TFF1 se često gubi u karcinomu želuca, vjerovatno preko mehanizma metilacija DNK, te se stoga smatra genom za supresiju tumora.[9]
Reference
[uredi | uredi izvor]- ^ a b c GRCh38: Ensembl release 89: ENSG00000160182 - Ensembl, maj 2017
- ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000024032 - Ensembl, maj 2017
- ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
- ^ Gött P, Beck S, Machado JC, Carneiro F, Schmitt H, Blin N (May 1997). "Human trefoil peptides: genomic structure in 21q22.3 and coordinated expression". Eur J Hum Genet. 4 (6): 308–15. doi:10.1159/000472224. PMID 9043862. S2CID 25235589.
- ^ a b c "Entrez Gene: TFF1 trefoil factor 1".
- ^ Chatagnon A, Ballestar E, Esteller M, Dante R (2010). "A Role for Methyl-CpG Binding Domain Protein 2 in the Modulation of the Estrogen Response of pS2/TFF1 Gene". PLOS ONE. 5 (3): e9665. Bibcode:2010PLoSO...5.9665C. doi:10.1371/journal.pone.0009665. PMC 2837351. PMID 20300195.
- ^ a b Järvå MA, Lingford JP, John A, Soler NM, Scott NE, Goddard-Borger ED (May 2020). "Trefoil factors share a lectin activity that defines their role in mucus". Nature Communications. 11 (1): 2265. Bibcode:2020NatCo..11.2265J. doi:10.1038/s41467-020-16223-7. PMC 7221086. PMID 32404934.
- ^ Feng G, Zhang Y, Yuan H, Bai R, Zheng J, Zhang J, Song M (Jan 2014). "DNA methylation of trefoil factor 1 (TFF1) is associated with the tumorigenesis of gastric carcinoma". Mol Med Rep. 9 (1): 109–117. doi:10.3892/mmr.2013.1772. PMID 24190027.
Dopunska literatuea
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- Mori K, Fujii R, Kida N, Ohta M, Hayashi K (1988). "Identification of a polypeptide secreted by human breast cancer cells (MCF-7) as the human estrogen-responsive gene (pS2) product". Biochem. Biophys. Res. Commun. 155 (1): 366–72. doi:10.1016/S0006-291X(88)81094-5. PMID 3261981.
- Jeltsch JM, Roberts M, Schatz C, Garnier JM, Brown AM, Chambon P (1987). "Structure of the human oestrogen-responsive gene pS2". Nucleic Acids Res. 15 (4): 1401–14. doi:10.1093/nar/15.4.1401. PMC 340557. PMID 3822834.
- Prud'homme JF, Fridlansky F, Le Cunff M, Atger M, Mercier-Bodart C, Pichon MF, Milgrom E (1985). "Cloning of a gene expressed in human breast cancer and regulated by estrogen in MCF-7 cells". DNA. 4 (1): 11–21. doi:10.1089/dna.1985.4.11. PMID 3838275.
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- Hanby AM, Poulsom R, Singh S, Elia G, Jeffery RE, Wright NA (1993). "Spasmolytic polypeptide is a major antral peptide: distribution of the trefoil peptides human spasmolytic polypeptide and pS2 in the stomach". Gastroenterology. 105 (4): 1110–6. doi:10.1016/0016-5085(93)90956-d. PMID 8405856.
- Polshakov VI, Frenkiel TA, Westley B, Chadwick M, May F, Carr MD, Feeney J (1996). "NMR-based structural studies of the pNR-2/pS2 single domain trefoil peptide. Similarities to porcine spasmolytic peptide and evidence for a monomeric structure". Eur. J. Biochem. 233 (3): 847–55. doi:10.1111/j.1432-1033.1995.847_3.x. PMID 8521850.
- Seib T, Blin N, Hilgert K, Seifert M, Theisinger B, Engel M, Dooley S, Zang KD, Welter C (1997). "The three human trefoil genes TFF1, TFF2, and TFF3 are located within a region of 55 kb on chromosome 21q22.3". Genomics. 40 (1): 200–2. doi:10.1006/geno.1996.4511. PMID 9070946.
- Polshakov VI, Williams MA, Gargaro AR, Frenkiel TA, Westley BR, Chadwick MP, May FE, Feeney J (1997). "High-resolution solution structure of human pNR-2/pS2: a single trefoil motif protein". J. Mol. Biol. 267 (2): 418–32. doi:10.1006/jmbi.1997.0896. PMID 9096235.
- Chadwick MP, Westley BR, May FE (1997). "Homodimerization and hetero-oligomerization of the single-domain trefoil protein pNR-2/pS2 through cysteine 58". Biochem. J. 327 (1): 117–23. doi:10.1042/bj3270117. PMC 1218770. PMID 9355742.
- Chen H, Lin RJ, Xie W, Wilpitz D, Evans RM (1999). "Regulation of hormone-induced histone hyperacetylation and gene activation via acetylation of an acetylase". Cell. 98 (5): 675–86. doi:10.1016/S0092-8674(00)80054-9. PMID 10490106. S2CID 14697597.
- Newton JL, Allen A, Westley BR, May FE (2000). "The human trefoil peptide, TFF1, is present in different molecular forms that are intimately associated with mucus in normal stomach". Gut. 46 (3): 312–20. doi:10.1136/gut.46.3.312. PMC 1727855. PMID 10673290.