Promoter analysis of the human mismatch repair gene hMSH2

Gene

Volumn 213, Issue 1-2, 1998, Pages 141-147

  Iwahashi, Yuki ^a   Ito, Emi ^b   Yanagisawa, Yuka ^b   Akiyama, Yoshimitsu ^b   Yuasa, Yasuhito ^b   Onodera, Takashi ^a   Maruyama, Kazuo ^b  

^a UNIVERSITY OF TOKYO   (Japan)

^b TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

Author keywords

Alu sequences; CpG island; HNPCC; Housekeeping genes

Indexed keywords

DNA;

ALU SEQUENCE; ANIMAL CELL; ARTICLE; CONTROLLED STUDY; CPG ISLAND; DNA POLYMORPHISM; DNA REPAIR; DNA SEQUENCE; GENE CLUSTER; GENE DELETION; GENE EXPRESSION; HETEROZYGOTE; HOUSEKEEPING GENE; HUMAN; MOUSE; NONHUMAN; NUCLEOTIDE SEQUENCE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; PROMOTER REGION; RESTRICTION FRAGMENT LENGTH POLYMORPHISM; TATA BOX; TRANSCRIPTION INITIATION;

ALLELES; BASE SEQUENCE; COLORECTAL NEOPLASMS, HEREDITARY NONPOLYPOSIS; CPG ISLANDS; DNA MUTATIONAL ANALYSIS; DNA REPAIR; DNA-BINDING PROTEINS; GENE EXPRESSION REGULATION; GENES; GENETIC MARKERS; HUMANS; LOSS OF HETEROZYGOSITY; MOLECULAR SEQUENCE DATA; MUTS HOMOLOG 2 PROTEIN; POLYMERASE CHAIN REACTION; POLYMORPHISM, RESTRICTION FRAGMENT LENGTH; PROMOTER REGIONS (GENETICS); PROTO-ONCOGENE PROTEINS; SEQUENCE DELETION; TRANSCRIPTION, GENETIC;

ANIMALIA;

EID: 0032525830     PISSN: 03781119     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0378-1119(98)00187-5     Document Type: Article

References (26)

1. Aaltonen L.A., Peltomaki P., Leach F.S., Sistonen P., Pylkkanen L., Mecklin J.P., Jarvinen H., Powell S.M., Jen J., Hamilton S.R., Petersen G.M., Kinzer K.W., Vogelstein B. Clues to the pathogenesis of familial colorectal cancer. Science. 260:1993;812-816.
2. Brini A.T., Lee G.M., Kinet J.P. Involvement of Alu sequences in the cell-specific regulation of transcription of the gamma chain of Fc and T cell receptors. J. Biol. Chem. 268:1993;1355-1361.
3. Bronner C.E., Baker S.M., Morrison P.T., Warren G., Smith L.G., Lescoe M.K., Kane M., Earabino C., Lipford J., Lindblom A., Tannergard P., Bollag R.J., Godwin A.R., Ward D.C., Nordenskjoid M. Mutation in the DNA mismatch repair gene homologue hMLH1 is associated with hereditary non-polyposis colon cancer. Nature. 368:1994;258-261.
4. Cedar H. DNA methylation and gene activity. Cell. 53:1988;3-4.
5. Fishel R., Ewel A., Lescoe M.K. Purified human MSH2 protein binds to DNA containing mismatched nucleotides. Cancer Res. 54:1994;5539-5542.
6. Fishel R., Lescoe M.K., Rao M.R., Copeland N.G., Jenkins N.A., Garber J., Kane M., Kolodner R. The human mutator gene homolog MSH2 and its association with hereditary nonpolyposis colon. Cell. 75:1993;1027-1038.
7. Kane M., Loda M., Gaida G.M., Lipman J., Mishra R., Goldman H., Jessup J.M., Kolodner R. Methylation of the hMLH1 promoter correlates with lack of expression of hMLH1 in sporadic colon tumors and mismatch repair-defective human tumor cell lines. Cancer Res. 57:1997;808-811.
8. Leach F.S., Nicolaides N.C., Papadopoulos N., Liu B., Jen J., Parsons R., Peltomaki P., Sistonen P., Aaltonen L.A., Nystrom-Lahti M., Guan X.-L., Zhang J., Meltzer P.S., Yu J.-W., Kao F.-T., Chen D.J., Cerosaletti K.M., Fournier R.E.K., Todd S., Lewis T., Leach R.J., Naylor S.L., Weissenbach J., Mecklin J.-P., Jarvinen H., Petersen G.M., Hamilton S.R., Green J., Jass J., Watson P., Lynch H.T., Trent J.M., Chapelle A., Kinzler K.W., Vogelstein B. Mutations of a mutS homolog in hereditary nonpolyposis colorectal cancer. Cell. 75:1993;1215-1225.
9. Lynch H.T., Smyrk T. Hereditary nonpolyposis colorectal cancer (Lynch syndrome). An updated review. Cancer. 78:1996;1149-1167.
10. Maruyama K., Sugano S. Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides. Gene. 138:1994;171-174.
11. Muta H., Noguchi M., Perucho M., Ushio K., Sugihara K., Ochiai A., Nawata H., Hirohashi S. Clinical implications of microsatellite instability in colorectal cancers. Cancer. 77:1996;265-270.
12. Nicolaides N.C., Papadopoulos N., Liu B., Wei Y.F., Carter K.C., Ruben S.M., Rosen C.A., Haseltine W.A., Fleischmann R.D., Fraser C.M., Adams M.D., Venter J.C., Dunlop M.G., Hamilton S.R., Petersen G.M., Chapelle A., Vogelstein B., Kinzler K.W. Mutations of two PMS homologues in hereditary nonpolyposis colon cancer. Nature. 371:1994;75-80.
13. Nystrom-Lahti M., Kristo P., Nicolaides N.C., Chang S.Y., Aaltonen L.A., Moisio A.L., Jarvinen H.J., Mecklin J.P., Kinzler K.W., Vogelstein B., Chapelle A., Peltomaki P. Founding mutations and Alu-mediated recombination in hereditary colon cancer. Nat. Med. 1:1995;1203-1206.
14. Oto M., Miyake S., Yuasa Y. Optimization of nonradioisotopic single strand conformation polymorphism analysis with a conventional minislab gel electrophoresis apparatus. Anal. Biochem. 213:1993;19-22.
15. Palombo F., Hughes M., Jiricny J., Truong O., Hsuan J. Mismatch repair and cancer. Nature. 367:1994;417.
16. Papadopoulos N., Nicolaides N.C., Wei Y.F., Ruben S.M., Carter K.C., Rosen C.A., Haseltine W.A., Fleischmann R.D., Fraser C.M., Adams M.D., Venter J.C., Hamilton S.R., Petersen G.M., Watson P., Lynch H.T., Peltomaki P., Mecklin J.P., Chapelle A., Kinzler K.W., Vogelstein B. Mutation of a mutL homolog in hereditary colon. Science. 263:1994;1625-1629.
17. Peltomaki P., Lothe R.A., Aaltonen L.A., Pylkkanen L., Nystrom-Lahti M., Seruca R., David L., Holm R., Ryberg D., Haugen A., Brogger A., Borresen A.-L., de la Chapelle A. Microsatellite instability is associated with tumors that characterize the hereditary non-polyposis colorectal carcinoma syndrome. Cancer Res. 53:1993;5853-5855.
18. Prowse A.H., Webster A.R., Richards F.M., Richard S., Olschwang S., Resche F., Affara N.A., Maher E.R. Somatic inactivation of the VHL gene in von-Hippel-Lindau disease tumors. Am. J. Hum. Genet. 60:1997;765-771.
19. Rydberg B. Bromouracil mutagenesis and mismatch repair in mutator strains of Escherichia coli. Mutat. Res. 52:1978;11-24.
20. Sakai T., Ohtani N., McGee T.L., Robbins P.D., Dryja T.P. Oncogenic germ-line mutations in Sp1 and ATF sites in the human retinoblastoma gene. Nature. 353:1991;83-86.
21. Scherer S.J., Seib T., Seitz G., Dooley S., Welter C. Isolation and characterization of the human mismatch repair gene hMSH2 promoter region. Hum. Genet. 97:1996;114-116.
22. Scherer S.J., Welter C., Zang K.D., Dooley S. Specific in vitro binding of p53 to the promoter region of the human mismatch repair gene hMSH2. Biochem. Biophys. Res. Commun. 221:1996;722-728.
23. Siebert P.D., Chenchik A., Kellogg D.E., Lukyanov K.A., Lukyanov S.A. An improved PCR method for walking in uncloned genomic DNA. Nucleic Acids Res. 23:1995;1087-1088.
24. Vasen H.F., Mecklin J.P., Khan P.M., Lynch H.T. The International Collaborative Group on Hereditary Non-Polyposis Colorectal Cancer (ICG-HNPCC). Dis. Colon Rectum. 34:1991;424-425.
25. Wijnen J., Khan P.M., Vasen H., van der Klift H., Mulder A., van Leeuwen-Cornelisse I., Bakker B., Losekoot M., Moller P., Fodde R. Hereditary nonpolyposis colorectal cancer families not complying with the Amsterdam criteria show extremely low frequency of mismatch-repair-gene mutations. Am. J. Hum. Genet. 61:1997;329-335.
26. Yanagisawa Y., Ito E., Iwahashi Y., Akiyama Y., Yuasa Y., Maruyama K. Isolation and characterization of the 5′ region of the human mismatch repair gene hPMS1. Biochem. Biophys. Res. Commun. 243:1998;738-743.