Abstract
A novel matrix metalloproteinase-26 (MMP-26) is known to be specifically expressed in epithelial carcinomas. To facilitate studies of MMP-26 transcriptional regulation, we have cloned and characterized a 1 kb 5'-flanking region of the human MMP-26 gene. Altogether, our findings indicate that the MMP-26 promoter has distinctive structural and functional features among MMP genes. An unusual polyadenylation site proximal to the transcription-factor-binding sites protects transcription of the MMP-26 gene from the upstream promoters and represents a part of the stringent transcriptional regulation of the gene. The MMP-26 gene has a consensus TATA-box and one transcriptional start site located 60 and 35 nucleotides upstream of the translational start site, respectively. The MMP-26 promoter was able to drive luciferase expression in human A549 lung carcinoma, HT1080 fibrosarcoma and HEK293 embryonic kidney cells. The basal transcription efficiency of the MMP-26 promoter is relatively low, thereby explaining the minute expression of the gene in most cells and tissues. When compared with other MMP genes, the MMP-26 promoter contains binding sites for a few transcription factors. Sequential deletion and mutation analysis, and electrophoretic mobility-shift assay have identified the T-cell factor-4 (Tcf-4) motif and the activator protein-1 site as the major regulatory elements of the MMP-26 promoter. Since previous studies have established that the Tcf-4 transcription factor is subjected exclusively to regulation through the beta-catenin/E(epithelial)-cadherin pathway, this implies the specific expression of MMP-26 in cancer cells of epithelial origin.
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- Barker N., Clevers H. Catenins, Wnt signaling and cancer. Bioessays. 2000 Nov;22(11):961–965. doi: 10.1002/1521-1878(200011)22:11<961::AID-BIES1>3.0.CO;2-T. [DOI] [PubMed] [Google Scholar]
- Behre G., Smith L. T., Tenen D. G. Use of a promoterless Renilla luciferase vector as an internal control plasmid for transient co-transfection assays of Ras-mediated transcription activation. Biotechniques. 1999 Jan;26(1):24-6, 28. doi: 10.2144/99261bm03. [DOI] [PubMed] [Google Scholar]
- Belsham D. D., Mellon P. L. Transcription factors Oct-1 and C/EBPbeta (CCAAT/enhancer-binding protein-beta) are involved in the glutamate/nitric oxide/cyclic-guanosine 5'-monophosphate-mediated repression of mediated repression of gonadotropin-releasing hormone gene expression. Mol Endocrinol. 2000 Feb;14(2):212–228. doi: 10.1210/mend.14.2.0418. [DOI] [PubMed] [Google Scholar]
- Brabletz T., Jung A., Dag S., Hlubek F., Kirchner T. beta-catenin regulates the expression of the matrix metalloproteinase-7 in human colorectal cancer. Am J Pathol. 1999 Oct;155(4):1033–1038. doi: 10.1016/s0002-9440(10)65204-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Brew K., Dinakarpandian D., Nagase H. Tissue inhibitors of metalloproteinases: evolution, structure and function. Biochim Biophys Acta. 2000 Mar 7;1477(1-2):267–283. doi: 10.1016/s0167-4838(99)00279-4. [DOI] [PubMed] [Google Scholar]
- Crawford H. C., Fingleton B. M., Rudolph-Owen L. A., Goss K. J., Rubinfeld B., Polakis P., Matrisian L. M. The metalloproteinase matrilysin is a target of beta-catenin transactivation in intestinal tumors. Oncogene. 1999 May 6;18(18):2883–2891. doi: 10.1038/sj.onc.1202627. [DOI] [PubMed] [Google Scholar]
- Crawford H. C., Fingleton B., Gustavson M. D., Kurpios N., Wagenaar R. A., Hassell J. A., Matrisian L. M. The PEA3 subfamily of Ets transcription factors synergizes with beta-catenin-LEF-1 to activate matrilysin transcription in intestinal tumors. Mol Cell Biol. 2001 Feb;21(4):1370–1383. doi: 10.1128/MCB.21.4.1370-1383.2001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Curran S., Murray G. I. Matrix metalloproteinases: molecular aspects of their roles in tumour invasion and metastasis. Eur J Cancer. 2000 Aug;36(13 Spec No):1621–1630. doi: 10.1016/s0959-8049(00)00156-8. [DOI] [PubMed] [Google Scholar]
- Grentzmann G., Ingram J. A., Kelly P. J., Gesteland R. F., Atkins J. F. A dual-luciferase reporter system for studying recoding signals. RNA. 1998 Apr;4(4):479–486. [PMC free article] [PubMed] [Google Scholar]
- He C. Molecular mechanism of transcriptional activation of human gelatinase B by proximal promoter. Cancer Lett. 1996 Sep 10;106(2):185–191. doi: 10.1016/0304-3835(96)04318-2. [DOI] [PubMed] [Google Scholar]
- Huber A. H., Weis W. I. The structure of the beta-catenin/E-cadherin complex and the molecular basis of diverse ligand recognition by beta-catenin. Cell. 2001 May 4;105(3):391–402. doi: 10.1016/s0092-8674(01)00330-0. [DOI] [PubMed] [Google Scholar]
- Illman S. A., Keski-Oja J., Lohi J. Promoter characterization of the human and mouse epilysin (MMP-28) genes. Gene. 2001 Sep 5;275(1):185–194. doi: 10.1016/s0378-1119(01)00664-3. [DOI] [PubMed] [Google Scholar]
- Kolligs F. T., Hu G., Dang C. V., Fearon E. R. Neoplastic transformation of RK3E by mutant beta-catenin requires deregulation of Tcf/Lef transcription but not activation of c-myc expression. Mol Cell Biol. 1999 Aug;19(8):5696–5706. doi: 10.1128/mcb.19.8.5696. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lohi J., Lehti K., Valtanen H., Parks W. C., Keski-Oja J. Structural analysis and promoter characterization of the human membrane-type matrix metalloproteinase-1 (MT1-MMP) gene. Gene. 2000 Jan 25;242(1-2):75–86. doi: 10.1016/s0378-1119(99)00549-1. [DOI] [PubMed] [Google Scholar]
- Lohi J., Wilson C. L., Roby J. D., Parks W. C. Epilysin, a novel human matrix metalloproteinase (MMP-28) expressed in testis and keratinocytes and in response to injury. J Biol Chem. 2000 Dec 19;276(13):10134–10144. doi: 10.1074/jbc.M001599200. [DOI] [PubMed] [Google Scholar]
- Lorenz W. W., Cormier M. J., O'Kane D. J., Hua D., Escher A. A., Szalay A. A. Expression of the Renilla reniformis luciferase gene in mammalian cells. J Biolumin Chemilumin. 1996 Jan-Feb;11(1):31–37. doi: 10.1002/(SICI)1099-1271(199601)11:1<31::AID-BIO398>3.0.CO;2-M. [DOI] [PubMed] [Google Scholar]
- Love J. J., Li X., Case D. A., Giese K., Grosschedl R., Wright P. E. Structural basis for DNA bending by the architectural transcription factor LEF-1. Nature. 1995 Aug 31;376(6543):791–795. doi: 10.1038/376791a0. [DOI] [PubMed] [Google Scholar]
- Marchenko G. N., Ratnikov B. I., Rozanov D. V., Godzik A., Deryugina E. I., Strongin A. Y. Characterization of matrix metalloproteinase-26, a novel metalloproteinase widely expressed in cancer cells of epithelial origin. Biochem J. 2001 Jun 15;356(Pt 3):705–718. doi: 10.1042/0264-6021:3560705. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Marchenko G. N., Strongin A. Y. MMP-28, a new human matrix metalloproteinase with an unusual cysteine-switch sequence is widely expressed in tumors. Gene. 2001 Mar 7;265(1-2):87–93. doi: 10.1016/s0378-1119(01)00360-2. [DOI] [PubMed] [Google Scholar]
- Massova I., Kotra L. P., Fridman R., Mobashery S. Matrix metalloproteinases: structures, evolution, and diversification. FASEB J. 1998 Sep;12(12):1075–1095. [PubMed] [Google Scholar]
- Mattei M. G., Roeckel N., Olsen B. R., Apte S. S. Genes of the membrane-type matrix metalloproteinase (MT-MMP) gene family, MMP14, MMP15, and MMP16, localize to human chromosomes 14, 16, and 8, respectively. Genomics. 1997 Feb 15;40(1):168–169. doi: 10.1006/geno.1996.4559. [DOI] [PubMed] [Google Scholar]
- Mueller M. S., Mauch S., Sedlacek R. Structure of the human MMP-19 gene. Gene. 2000 Jul 11;252(1-2):27–37. doi: 10.1016/s0378-1119(00)00236-5. [DOI] [PubMed] [Google Scholar]
- Nagase H., Woessner J. F., Jr Matrix metalloproteinases. J Biol Chem. 1999 Jul 30;274(31):21491–21494. doi: 10.1074/jbc.274.31.21491. [DOI] [PubMed] [Google Scholar]
- Nelson A. R., Fingleton B., Rothenberg M. L., Matrisian L. M. Matrix metalloproteinases: biologic activity and clinical implications. J Clin Oncol. 2000 Mar;18(5):1135–1149. doi: 10.1200/JCO.2000.18.5.1135. [DOI] [PubMed] [Google Scholar]
- Park H. I., Ni J., Gerkema F. E., Liu D., Belozerov V. E., Sang Q. X. Identification and characterization of human endometase (Matrix metalloproteinase-26) from endometrial tumor. J Biol Chem. 2000 Jul 7;275(27):20540–20544. doi: 10.1074/jbc.M002349200. [DOI] [PubMed] [Google Scholar]
- Pendás A. M., Balbín M., Llano E., Jiménez M. G., López-Otín C. Structural analysis and promoter characterization of the human collagenase-3 gene (MMP13). Genomics. 1997 Mar 1;40(2):222–233. doi: 10.1006/geno.1996.4554. [DOI] [PubMed] [Google Scholar]
- Price S. J., Greaves D. R., Watkins H. Identification of novel, functional genetic variants in the human matrix metalloproteinase-2 gene: role of Sp1 in allele-specific transcriptional regulation. J Biol Chem. 2000 Dec 12;276(10):7549–7558. doi: 10.1074/jbc.M010242200. [DOI] [PubMed] [Google Scholar]
- Rastegar M., Rousseau G. G., Lemaigre F. P. CCAAT/enhancer-binding protein-alpha is a component of the growth hormone-regulated network of liver transcription factors. Endocrinology. 2000 May;141(5):1686–1692. doi: 10.1210/endo.141.5.7478. [DOI] [PubMed] [Google Scholar]
- Roose J., Huls G., van Beest M., Moerer P., van der Horn K., Goldschmeding R., Logtenberg T., Clevers H. Synergy between tumor suppressor APC and the beta-catenin-Tcf4 target Tcf1. Science. 1999 Sep 17;285(5435):1923–1926. doi: 10.1126/science.285.5435.1923. [DOI] [PubMed] [Google Scholar]
- Schreiber E., Matthias P., Müller M. M., Schaffner W. Rapid detection of octamer binding proteins with 'mini-extracts', prepared from a small number of cells. Nucleic Acids Res. 1989 Aug 11;17(15):6419–6419. doi: 10.1093/nar/17.15.6419. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Simcha I., Kirkpatrick C., Sadot E., Shtutman M., Polevoy G., Geiger B., Peifer M., Ben-Ze'ev A. Cadherin sequences that inhibit beta-catenin signaling: a study in yeast and mammalian cells. Mol Biol Cell. 2001 Apr;12(4):1177–1188. doi: 10.1091/mbc.12.4.1177. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Skalnik D. G., Strauss E. C., Orkin S. H. CCAAT displacement protein as a repressor of the myelomonocytic-specific gp91-phox gene promoter. J Biol Chem. 1991 Sep 5;266(25):16736–16744. [PubMed] [Google Scholar]
- Stamenkovic I. Matrix metalloproteinases in tumor invasion and metastasis. Semin Cancer Biol. 2000 Dec;10(6):415–433. doi: 10.1006/scbi.2000.0379. [DOI] [PubMed] [Google Scholar]
- Tetsu O., McCormick F. Beta-catenin regulates expression of cyclin D1 in colon carcinoma cells. Nature. 1999 Apr 1;398(6726):422–426. doi: 10.1038/18884. [DOI] [PubMed] [Google Scholar]
- Valsamakis A., Zeichner S., Carswell S., Alwine J. C. The human immunodeficiency virus type 1 polyadenylylation signal: a 3' long terminal repeat element upstream of the AAUAAA necessary for efficient polyadenylylation. Proc Natl Acad Sci U S A. 1991 Mar 15;88(6):2108–2112. doi: 10.1073/pnas.88.6.2108. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vincenti M. P. The matrix metalloproteinase (MMP) and tissue inhibitor of metalloproteinase (TIMP) genes. Transcriptional and posttranscriptional regulation, signal transduction and cell-type-specific expression. Methods Mol Biol. 2001;151:121–148. doi: 10.1385/1-59259-046-2:121. [DOI] [PubMed] [Google Scholar]
- Westermarck J., Kähäri V. M. Regulation of matrix metalloproteinase expression in tumor invasion. FASEB J. 1999 May;13(8):781–792. [PubMed] [Google Scholar]
- Williamson E. A., Xu H. N., Gombart A. F., Verbeek W., Chumakov A. M., Friedman A. D., Koeffler H. P. Identification of transcriptional activation and repression domains in human CCAAT/enhancer-binding protein epsilon. J Biol Chem. 1998 Jun 12;273(24):14796–14804. doi: 10.1074/jbc.273.24.14796. [DOI] [PubMed] [Google Scholar]
- Ye S. Polymorphism in matrix metalloproteinase gene promoters: implication in regulation of gene expression and susceptibility of various diseases. Matrix Biol. 2000 Dec;19(7):623–629. doi: 10.1016/s0945-053x(00)00102-5. [DOI] [PubMed] [Google Scholar]
- de Coignac A. B., Elson G., Delneste Y., Magistrelli G., Jeannin P., Aubry J. P., Berthier O., Schmitt D., Bonnefoy J. Y., Gauchat J. F. Cloning of MMP-26. A novel matrilysin-like proteinase. Eur J Biochem. 2000 Jun;267(11):3323–3329. doi: 10.1046/j.1432-1327.2000.01363.x. [DOI] [PubMed] [Google Scholar]
