1999 Fiscal Year Final Research Report Summary
Structure and function of mRNA capping enzyme
| Project/Area Number |
10680587
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| Research Category |
Grant-in-Aid for Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Structural biochemistry
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| Research Institution | Kitasato University |
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Principal Investigator |
TSUKAMOTO Toshihiko Kitasato University, Department of pharmacology, Associate Professor, 薬学部, 助教授 (10236862)
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| Co-Investigator(Kenkyū-buntansha) |
MIZUMOTO Kiyohisa Kitasato University, Department of pharmacology, Professor, 薬学部, 教授 (80092344)
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| Project Period (FY) |
1998 – 1999
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| Keywords | mRNA capping enzyme / mRNA cap methyltransferase / mRNA cap structure / RNA processing / RNA polymerase II / Transcription |
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| Research Abstract |
The mRNA cap structure is synthesized by a series of reactions catalyzed by mRNA capping enzyme (RNA 5'-triphosphatase and mRNA guanylyltransferase) and mRNA (guanine-7-)methytransferase (mRNA cap methyltransferase). Here we isolated Saccharomyces cerevisiae RNA 5'-triphosphatase (capping enzyme beta subunit) gene (CET1), two human capping enzeme cDNAs (hCAP1a, b), and three human mRNA (guanine-7-)methyltransferase cDNAs (hCMT1a, b, c). CET1 encodes 549 amino acids with a calculated MィイD2rィエD2 of 61,849 and bears no significant sequence similarities to RNA 5'-triphosphatase of human capping enzyme (hCAP1) including the tyrosine specific protein phosphatase (PTP) active site motif. Gene disruption experiment showed that CET1 is essential for yeast cell growth. hCAP1a and hCAP1b encode 597 and 541 amino acids, respectively, and are different only at the region coding for the C-terminal portion of the enzyme. The regions conserved among mRNA guanylytransferases are observed in hCAP1 except that one conserved region was absent in the hCAP1b protein. Deletion mutant analysis of hCAP1a showed that the N-terminal 213 amino acid fragment containing PTP motif catalyzed the RNA 5'-trihosphatase activity and the C-terminal 369 amino acid fragment contained the mRNA guanylyltransferase activity. hCAP1b showed RNA 5'-triphosphatase activity, but neither enzyme-GMP covalent complex formation or cap structure formation was detected. HCMT1a and hCMT1b encode 476 and 504 amino acids, respectively, and differ only at the region coding for the C-terminal portion of the enzyme after amino acid residue 465.
3. RT-PCR showed that all 3 types of mRNAs were expressed in every tissue examined. Comparison of the deduced amino acid sequences with those of other viral and cellular enzymes showed the regions which are highly conserved among mRNA (guanine-7)methyltransferases.
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Research Products
(7 results)
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[Publications] Tsukamoto, T., Shibagaki, Y., Murakoshi, T., Suzuki, M., Nakamura, A., Gotoh. H., and Mizumoto,K.: "Cloning and characterizaqtion of two human cDNAs encoding mRNA capping enzyme."Biochem. Biophys. Res. Commun.. 243. 101-108 (1998)
Description
「研究成果報告書概要(欧文)」より
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[Publications] Tsukamoto, T., Shibagaki, Y., Imajoh-Ohmi, S., Murakoshi, T., Suzuki, M., Nakamura, A., Gotoh. H., and Mizumoto, K.: "Isolation and characterization of the yeast mRNA capping enzyme βsubunit gene encoding RNA 5ィイD1,ィエD1-triphosphatase, which is essential for cell viability."Biochem. Biophys. Res. Commun.. 239. 116-122 (1997)
Description
「研究成果報告書概要(欧文)」より
