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Host factors required for internal initiation of translation on poliovirus RNA

Research Project

Project/Area Number 07457081
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Research Field Virology
Research InstitutionThe University of Tokyo

Principal Investigator

TOYODA Haruka  The University of Tokyo, The Institute of Medical Science, Lecturer, 医科学研究所, 講師 (10197973)

Project Period (FY) 1995 – 1996
Project Status Completed (Fiscal Year 1996)
Budget Amount *help
¥6,400,000 (Direct Cost: ¥6,400,000)
Fiscal Year 1996: ¥2,800,000 (Direct Cost: ¥2,800,000)
Fiscal Year 1995: ¥3,600,000 (Direct Cost: ¥3,600,000)
KeywordsPoliovirus / IRES / Host factor / in vitro translation / UV-corosslinking / PTB
Research Abstract

Translation of poliovirus (PV) RNA is initiated by entry of ribosomes into the nucleotide sequence (internal ribosomal entry site ; IRES) with in the 5'-untranslated region (5'-UTR) and contains 5 stem loop (SL) structures. Efficiency of this translation initiation in rabbit reticulocyte lysates (RRL) was very poor and was greatly enhanced by the addition of the ribosomal salt-wash fraction (RSW) prepared from HeLa cells. This stimulation activity in the RSW was partially purified and its molecular weight was estimated to be more than 240,000. Several proteins that bind spoecifically to these SL structures in this poliovirus IRES were detected. Among those, a 57 kDa protein, recognized by antibodies against polypyrimidide tract-binding protein (PTB), and a 40 kDa protein (p40) which is identified as PCBP2 (polyC binding protein) bound to SLIV.In addition, 36 kDa (p36) and 80kDa (p80) proteins bind to SLV spesifically. The purification of p36 and p80 are now on progress.

Report

(3 results)
  • 1996 Annual Research Report   Final Research Report Summary
  • 1995 Annual Research Report

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Published: 1995-04-01   Modified: 2016-04-21  

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