Skip to main content
Japanese Journal of Cancer Research : Gann logoLink to Japanese Journal of Cancer Research : Gann
. 2002 Apr;93(4):369–373. doi: 10.1111/j.1349-7006.2002.tb01266.x

Deletion of Dinucleotide Repeat (Δ14 Allele) in the Methylthioadenosine Phosphorylase (MTAP) Promoter and the Allelotype of MTAP Promoter in the Japanese Population

Yuwaraj Kadariya 1, Junji Nishioka 1, Kaname Nakatani 1, Kunio Nakashima 2, Tsutomu Nobori 1,
PMCID: PMC5927014  PMID: 11985785

Abstract

5′‐Deoxy‐5′‐methylthioadenosine phosphorylase (MTAP) is an enzyme involved in purine and polyamine metabolism and is ubiquitously expressed in normal human tissues and cells. However, this enzyme has been found to be deficient in a variety of human cancers. Although the enzyme deficiency is known to be caused by MTAP gene deletion, human diffuse histiocytic lymphoma cell line DHL‐9 without any detectable MTAP activity has been found to possess the intact MTAP gene. These lines of evidence suggested that promoter abnormality might cause the MTAP deficiency in DHL‐9. Therefore, we analyzed the MTAP promoter region of DHL‐9 and found the deletion of 14 bases in its sequence. We designated the allele lacking (GT)6GC as dinucleotide repeat deletion (Δ14 allele) and determined the effect of the Δ14 allele on the MTAP promoter activity by a luciferase reporter assay. We have also analyzed the distribution of the Δ14 allele and wild‐type (WT) allele in the Japanese population by PCR assay. A reporter plasmid harboring the Δ14 allele exhibited luciferase activity comparable to that of a plasmid containing the WT allele. Forty‐six (22%) out of 210 people were homozygous for WT allele in the MTAP promoter, whereas 43 (20.5%) were homozygous for Δ14 allele. The remaining 121 people (57.5%) possessed Δ14/WT alleles in the MTAP promoter region. These results indicated that the Δ14 allele has nothing to do with MTAP deficiency in DHL‐9. The Δ14 allele is distributed among the general population irrespective of gender.

Keywords: MTAP, DHL‐9, Promoter activity, Δ14 allele

Full Text

The Full Text of this article is available as a PDF (176.2 KB).

REFERENCES

  • 1.Yu , J. , Batova , A. , Shao , L. , Carrera , C. J. and Yu , A. L.Presence of methylthioadenosine phosphorylase (MTAP) in haematopoietic stem/progenitor cells: its therapeutic implications for MTAP (‐) malignancies . Clin. Cancer Res. , 3 , 433 – 438 ( 1997. ). [PubMed] [Google Scholar]
  • 2.Kamatani , N. , Nelson‐Rees , W. A. and Carson , D. A.Selective killing of human malignant cell lines deficient in methylthioadenosine phosphorylase, a purine metabolic enzyme . Proc. Natl. Acad. Sci. USA , 78 , 1219 – 1223 ( 1981. ). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Nobori , T. , Takabayashi , K. , Tran , P. , Orvis , L. , Batova , A. , Yu , A. L. and Carson , D. A.Genomic cloning of methylthioadenosine phosphorylase: a purine metabolic enzyme deficient in multiple different cancers . Proc. Natl. Acad. Sci. USA , 93 , 6203 – 6208 ( 1996. ). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 4.Kamb , A. , Gruis , N. A. , Weaver‐Feldhaus , J. , Liu , Q. , Harshman , K. , Tavtigian , S. V. , Stockert , E. , Day , R. S.III , Johnson , B. E. and Skolnick , M. H.A cell cycle regulator potentially involved in genesis of many tumor types . Science , 264 , 436 – 440 ( 1994. ). [DOI] [PubMed] [Google Scholar]
  • 5.Nobori , T. , Miura , K. , Wu , D. J. , Lois , A. , Takabayashi , K. and Carson , D. A.Deletions of the cyclin‐dependent kinase‐4 inhibitor gene in multiple human cancers . Nature , 368 , 753 – 756 ( 1994. ). [DOI] [PubMed] [Google Scholar]
  • 6.Carrera , C. J. , Eddy , K. L. , Shows , T. B. and Carson , D. A.Assignment of the gene for methylthioadenosine phosphorylase to human chromosome 9 by mouse‐human somatic cell hybridization . Proc. Natl. Acad. Sci. USA , 81 , 2665 – 2668 ( 1984. ). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7.Kamatani , N. and Carson , D. A.Dependence of adenine production upon polyamine synthesis in cultured human lymphoblasts . Biochim. Biophys. Acta , 675 , 344 – 350 ( 1981. ). [DOI] [PubMed] [Google Scholar]
  • 8.Zhi‐Hao , C. , Zhang , H. and Savarese , T. M.Gene deletion selectivity: codeletion of the gene for p16INK4, methylthioadenosine phophorylase, and the α‐ and β‐interferons in human pancreatic cell carcinoma lines and its implications for chemotherapy . Cancer Res. , 56 , 1083 – 1090 ( 1996. ). [PubMed] [Google Scholar]
  • 9.Olopade , O. I. , Jenkins , R. B. , Ransom , T. D. , Malik , K. , Pomykala , H. , Nobori , T. , Cowan , J. M. , Rowley , J. D. and Diaz , M. O.Molecular analysis of deletions of the short arm of chromosome 9 in human gliomas . Cancer Res. , 52 , 2523 – 2529 ( 1992. ). [PubMed] [Google Scholar]
  • 10.M'soka , T. J. , Nishioka , J. , Taga , A. , Kato , K. , Hawasaki , H. , Yamada , Y. , Yu , A. , Komada , Y. and Nobori , T.Detection of methylthioadenosine phosphorylase (MTAP) and p16 gene deletion in T cell acute lymphoblastic leukemia by real time quantitative PCR assay . Leukemia , 14 , 935 – 940 ( 2000. ). [DOI] [PubMed] [Google Scholar]
  • 11.Batova , A. , Diccianni , M. B. , Nobori , T. , Vu , T. , Yu , J. , Bridgeman , L. and Yu , A. L.Frequent deletion in the methylthioadenosine phosphorylase gene in T‐cell acute lymphoblastic leukemia: strategies for enzyme targeted therapy . Blood , 88 , 3083 – 3090 ( 1996. ). [PubMed] [Google Scholar]
  • 12.Hori , Y. , Hori , H. , Yamada , Y. , Carrera , C. J. , Tomonaga , M. , Kamihira , S. , Carson , D. S. and Nobori , T.The methylthioadenosine phosphorylase gene is frequently co‐deleted with the p16INK4a gene in acute type adult T‐cell leukemia . Int. J. Cancer , 75 , 51 – 56 ( 1998. ). [DOI] [PubMed] [Google Scholar]
  • 13.Fountain , J. W. , Karayiorgou , M. , Ernstoff , M. S. , Kirkwood , J. M. , Vlock , D. R. , Titus‐Ernstoff , L. , Bouchard , B. , Vijayasaradhi , S. , Houghton , A. N. , Lahti , J. , Kidd , V. J. , Housman , D. E. and Dracopoli , N. C.Homozygous deletions within human chromosome band 9p21 in melanoma . Proc. Natl. Acad. Sci. USA , 89 , 10557 – 10561 ( 1992. ). [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Schmid , M. , Malicki , D. , Nobori , T. , Rosenbach , M. D. , Campbell , K. , Carson , D. A. and Carrera , C. J.Homozygous deletion of methylthioadenosine phosphorylase (MTAP) are more frequent than p16INK4A (CDKN2) homozygous deletions in primary non‐small cell lung cancers (NSCLC) . Oncogene , 17 , 2669 – 2675 ( 1998. ). [DOI] [PubMed] [Google Scholar]
  • 15.Olopade , O. I. , Buchhagen , D. L. , Malik , K. , Sherman , J. , Nobori , T. , Bader , S. , Nau , M. M. , Gazdar , A. F. , Minna , J. D. and Diaz , M. O.Homozygous loss of the interferon genes defines the critical region on 9p that is deleted in lung cancers . Cancer Res. , 53 , 2410 – 2415 ( 1993. ). [PubMed] [Google Scholar]
  • 16.Kaneko , S. , Nishioka , J. , Tanaka , M. , Nakashima , K. and Nobori , T.Transcriptional regulation of the CDK inhibitor p16INK4a gene by a novel pRB‐associated repressor, RBAR1 . Biochem. Mol. Biol. Int. , 47 , 205 – 215 ( 1999. ). [DOI] [PubMed] [Google Scholar]
  • 17.Ohkubo , T. , Tanaka , M. and Nakashima , K.Molecular cloning of the chicken prolactin gene and activation by pit‐1 and cAMP‐induced factor in GH3 cells . Gen. Comp. Endocrinol. , 119 , 208 – 216 ( 2000. ). [DOI] [PubMed] [Google Scholar]
  • 18.Efstratiadis , A. , Posakony , J. W. , Maniatis , T. , Lawn , R. M. , O'Connell , C. , Spritz , R. A. , DeRiel , J. K. , Forget , B. G. , Weissman , S. M. , Slightom , J. L. , Blechl , A. E. , Smithies , O. , Baralle , F. E. , Shoulders , C. C. and Proudfoot , N. J.The structure and evolution of the human β‐globin gene family . Cell , 21 , 653 – 668 ( 1980. ). [DOI] [PubMed] [Google Scholar]
  • 19.Oron‐Karni , V. , Filon , D. , Rund , D. and Oppenheim , A.A novel mechanism generating short deletion/insertions following slippage is suggested by mutation in the human α2‐globin gene . Hum. Mol. Genet. , 6 , 881 – 885 ( 1997. ). [DOI] [PubMed] [Google Scholar]

Articles from Japanese Journal of Cancer Research : Gann are provided here courtesy of Wiley

RESOURCES