Biology:Trefoil factor 1
 Generic protein structure example |
Trefoil factor 1 is a protein that in humans is encoded by the TFF1 gene[1][2] (also called pS2 gene[3]).
Function
Members of the trefoil family are characterized by having at least one copy of the trefoil motif, a 40-amino acid domain that contains three conserved disulfides. They are stable secretory proteins expressed in gastrointestinal mucosa. Their functions are not defined, but they may protect the mucosa from insults, stabilize the mucus layer, and affect healing of the epithelium. This gene, which is expressed in the gastric mucosa, has also been studied because of its expression in human tumors. This gene and two other related trefoil family member genes are found in a cluster on chromosome 21.[2]
Glycan binding
All three human trefoil factors are lectins that interact specifically with the disaccharide GlcNAc-α-1,4-Gal.[4] This disaccharide is an unusual glycotope that is only known to exist on the large, heavily glycosylated, mucins in the mucosa. By cross-linking mucins through the bivalent binding of this glycotope, the trefoil factors are then able to reversibly modulate the thickness and viscosity of the mucus.[4]
In gastric carcinoma
TFF1 expression is frequently lost in gastric carcinoma, probably through mechanism of DNA methylation, and it is therefore considered as a tumor suppressor gene.[5]
References
- ↑ "Human trefoil peptides: genomic structure in 21q22.3 and coordinated expression". Eur J Hum Genet 4 (6): 308–15. May 1997. doi:10.1159/000472224. PMID 9043862.
- ↑ 2.0 2.1 "Entrez Gene: TFF1 trefoil factor 1". https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=7031.
- ↑ "A Role for Methyl-CpG Binding Domain Protein 2 in the Modulation of the Estrogen Response of pS2/TFF1 Gene". PLOS ONE 5 (3). 2010. doi:10.1371/journal.pone.0009665. PMID 20300195. Bibcode: 2010PLoSO...5.9665C.
- ↑ 4.0 4.1 "Trefoil factors share a lectin activity that defines their role in mucus". Nature Communications 11 (1). May 2020. doi:10.1038/s41467-020-16223-7. PMID 32404934. Bibcode: 2020NatCo..11.2265J.
- ↑ "DNA methylation of trefoil factor 1 (TFF1) is associated with the tumorigenesis of gastric carcinoma.". Mol Med Rep 9 (1): 109–117. Jan 2014. doi:10.3892/mmr.2013.1772. PMID 24190027. http://www.spandidos-publications.com/mmr/9/1/109.
Further reading
- "Ocular TFF-Peptides: New Mucus-Associated Secretory Products of Conjunctival Goblet Cells". Lacrimal Gland, Tear Film, and Dry Eye Syndromes 3. Advances in Experimental Medicine and Biology. 506. 2003. pp. 313–6. doi:10.1007/978-1-4615-0717-8_44. ISBN 978-1-4613-5208-2.
- "Antipeptide antibodies against the pNR-2 oestrogen-regulated protein of human breast cancer cells and detection of pNR-2 expression in normal tissues by immunohistochemistry.". J. Pathol. 163 (2): 95–104. 1991. doi:10.1002/path.1711630204. PMID 1707960.
- "Complete primary structure of the human estrogen-responsive gene (pS2) product.". J. Biochem. 107 (1): 73–6. 1990. doi:10.1093/oxfordjournals.jbchem.a123014. PMID 2185238.
- "hSP, the domain-duplicated homolog of pS2 protein, is co-expressed with pS2 in stomach but not in breast carcinoma.". EMBO J. 9 (2): 407–14. 1990. doi:10.1002/j.1460-2075.1990.tb08125.x. PMID 2303034.
- "Expression of the pS2 gene in human gastric cancer cells derived from poorly differentiated adenocarcinoma.". FEBS Lett. 261 (2): 283–6. 1990. doi:10.1016/0014-5793(90)80572-Z. PMID 2311759. Bibcode: 1990FEBSL.261..283T.
- "Breast cancer-associated pS2 protein: synthesis and secretion by normal stomach mucosa.". Science 241 (4866): 705–8. 1988. doi:10.1126/science.3041593. PMID 3041593. Bibcode: 1988Sci...241..705R.
- "[Primary structure of human protein pS2]". Comptes Rendus de l'Académie des Sciences, Série III 307 (19): 825–31. 1989. PMID 3146413.
- "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. 1988. doi:10.1016/S0006-291X(88)81094-5. PMID 3261981. Bibcode: 1988BBRC..155..366M.
- "Structure of the human oestrogen-responsive gene pS2.". Nucleic Acids Res. 15 (4): 1401–14. 1987. doi:10.1093/nar/15.4.1401. PMID 3822834.
- "Cloning of a gene expressed in human breast cancer and regulated by estrogen in MCF-7 cells.". DNA 4 (1): 11–21. 1985. doi:10.1089/dna.1985.4.11. PMID 3838275.
- "Sequence of the pS2 mRNA induced by estrogen in the human breast cancer cell line MCF-7.". Nucleic Acids Res. 12 (6): 2861–78. 1984. doi:10.1093/nar/12.6.2861. PMID 6324130.
- "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. 1993. doi:10.1016/0016-5085(93)90956-d. PMID 8405856.
- "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. 1996. doi:10.1111/j.1432-1033.1995.847_3.x. PMID 8521850.
- "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. 1997. doi:10.1006/geno.1996.4511. PMID 9070946.
- "High-resolution solution structure of human pNR-2/pS2: a single trefoil motif protein.". J. Mol. Biol. 267 (2): 418–32. 1997. doi:10.1006/jmbi.1997.0896. PMID 9096235.
- "Homodimerization and hetero-oligomerization of the single-domain trefoil protein pNR-2/pS2 through cysteine 58.". Biochem. J. 327 (1): 117–23. 1997. doi:10.1042/bj3270117. PMID 9355742.
- "Regulation of hormone-induced histone hyperacetylation and gene activation via acetylation of an acetylase.". Cell 98 (5): 675–86. 1999. doi:10.1016/S0092-8674(00)80054-9. PMID 10490106.
- "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. 2000. doi:10.1136/gut.46.3.312. PMID 10673290.
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