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Decapping reaction of mRNA requires Dcp1 in fission yeast: its characterization in different species from yeast to human.

Decapping reaction of mRNA requires Dcp1 in fission yeast: its characterization in different species from yeast to human. Research Abstract Details 

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  • Decapping reaction of mRNA requires Dcp1 in fission yeast: its characterization in different species from yeast to human. Abstract Text:

    takeshi sakunoTakeshi Sakuno,yasuhiro arakiYasuhiro Araki,yuriko ohyaYuriko Ohya,satoshi kofujiSatoshi Kofuji,shinya takahashiShinya Takahashi,shin-ichi hoshinoShin-ichi Hoshino,toshiaki katadaToshiaki Katada,

    Cleavage of the 5'-cap structure is involved in the major 5'-to-3' and nonsense-mediated mRNA decay pathways, and the protein complex consisting of Dcp1 and Dcp2 has been identified as the species responsible for the decapping reaction in Saccharomyces cerevisiae and human. Although in vitro studies indicate that Dcp2 is catalytically an active component, the role of Dcp1 in the decapping reaction remains to be explored in organisms other than budding yeast. To elucidate the Dcp1-dependent decapping mechanisms, we identified the homologues of S. cerevisiae Dcp1 (ScDcp1) in higher eukaryotes and analyzed their functions in the different species. The phenotypes of slow growth and mRNA stabilization induced by Scdcp1-gene disruption in budding yeast could be suppressed by the Shizosaccharomyces pombe SpDcp1 but not by the human homologue hDcp1. In contrast, the same phenotypes caused by Spdcp1-gene disruption in fission yeast were effectively complemented by hDcp1 and its partial sequence comparable to SpDcp1. These results indicate that not only Dcp2 but also Dcp1 plays an indispensable role in mRNA-decay pathway and that the characteristics of Dcp1-dependent decapping reaction in fission yeast hold an intermediate position in the evolution of mRNA-decay machinery from budding yeast to mammals.

    Decapping reaction of mRNA requires Dcp1 in fission yeast: its characterization in different species from yeast to human. Publishing Authors By Initials

    t sakunoT Sakuno,y arakiY Araki,y ohyaY Ohya,s kofujiS Kofuji,s takahashiS Takahashi,s hoshinoS Hoshino,t katadaT Katada,

    For similar proteins: dna-binding proteins: trans-activators research abstracts see: proteins: dna-binding proteins: trans-activators research

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    Decapping reaction of mRNA requires Dcp1 in fission yeast: its characterization in different species from yeast to human. Journal Published:

    PUBLICATION TYPE: Research Support, Non-U.S. Gov

    Journal: Journal of biochemistry

    VOLUME: 136

    Page Numbers: 805-12

    Journal Abbreviation: J. Biochem.

    ISSN: 0021-924X

    DAY: 19

    MONTH: Dec

    YEAR: 2004

    Decapping reaction of mRNA requires Dcp1 in fission yeast: its characterization in different species from yeast to human. Information

    Number of References:

    LANGUAGE: eng

    NlmUniqueID: 376600

    Decapping reaction of mRNA requires Dcp1 in fission yeast: its characterization in different species from yeast to human. Keywords Mesh Terms:

    KEYWORDS: Trans-Activators

    MESH TERMS: metabolism

    Chemical & Substance for Abstract: Decapping reaction of mRNA requires Dcp1 in fission yeast: its characterization in different species from yeast to human. Information

    Substance Name: Dcp1a protein, human

    Registry Number: EC 3.1.27.-

    Grant and Affiliation Information for Decapping reaction of mRNA requires Dcp1 in fission yeast: its characterization in different species from yeast to human.

    AFFILIATION: Department of Physiological Chemistry, Graduate School of Pharmaceutical Sciences, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

    Country: Japan

    Japan Research PublicationJapan Research Publication

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    MEDLINETA: J Biochem

    REFSOURCE: J Biochem (Tokyo). 2005 Mar;137(3):441

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