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Mechanism of the diletion of plastid DNA in pollen-derived albino and its application as a vector.

Research Project

Project/Area Number 03660001
Research Category

Grant-in-Aid for General Scientific Research (C)

Allocation TypeSingle-year Grants
Research Field Breeding science
Research InstitutionHirosaki University

Principal Investigator

HARADA Takeo  Hirosaki University, Faculty of Agriculture Associate Professor, 農学部, 助教授 (10228645)

Project Period (FY) 1991 – 1992
Project Status Completed (Fiscal Year 1992)
Budget Amount *help
¥2,200,000 (Direct Cost: ¥2,200,000)
Fiscal Year 1992: ¥700,000 (Direct Cost: ¥700,000)
Fiscal Year 1991: ¥1,500,000 (Direct Cost: ¥1,500,000)
KeywordsRice / Anther culture / Albino / Chloroplast DNA / Plastid DNA / Linear DNA / Hairpin telomere / Vector / ベクター
Research Abstract

Albino rice plants derived from pollen contain plastid genomes that have suffered large-scale deletions. From the roots of albino plants, we obtained several calli containing homogeneous plastid DNA differing in the size and position of the deletion. Southern blotting and pulsed field gel electrophoresis experiments revealed that the DNAs were linear molecules having a hairpin structure at both termini, existing as monomers (19 kb) or dimers, trimers and tetramers liked to form head-to-head and tail-to-tail multimers. This characteristic form is similar to that of the vaccinia virus, in which the replication origin is thought to lie at or near the hairpin termini. Farthermore, polymerase chain reaction experiments revealed complete loss of the ribosomal RNA genes of the plastid DNA. The results suggest that plant cells can grow without translation occurring in plastids. All of the deleted plastid DNAs commonly retained the region containing the tRNA^<Glu> gene(trnE), which is essential for biosynthesis of porphyrin. As porphyrin is the precursor of heme for mitochondria and other organelles, it is considered that trnE on the remnant plastid genome may be transcribed by an RNA polymerase encoded on nuclear DNA.

Report

(3 results)
  • 1992 Annual Research Report   Final Research Report Summary
  • 1991 Annual Research Report
  • Research Products

    (8 results)

All Other

All Publications (8 results)

  • [Publications] 原田 竹雄: "Large-scale deletions of plastid DNAin rice anther culture." Theor.Appl.Genet. 81. 157-161 (1991)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] 原田 竹雄: "Pollen-derived rice calli that have large deletions in plastid DNA do not require protein synthesis in plastids for growth." Mol.Gen.Genet.233. 145-150 (1992)

    • Description
      「研究成果報告書概要(和文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] Harada T, Sato T, Asaka D, Matsukawa I.: "Large-scale deletions of plastid DNA in rice anther culture." Theor. Appl. Genet.81. 157-161 (1991)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] Harada T. Ishikawa R, Niizeki M, Saito K.: "Pollen-derived rice calli that have large deletions in plastid DNA do not require protein synthesis in plastids for growth." Mol. Gen. Genet.233. 145-150 (1992)

    • Description
      「研究成果報告書概要(欧文)」より
    • Related Report
      1992 Final Research Report Summary
  • [Publications] 原田 竹雄: "Large-scale deletions of plastid DNA in rice anther culture." Theor.Appl.Genet.81. 157-161 (1991)

    • Related Report
      1992 Annual Research Report
  • [Publications] 原田 竹雄: "Pollen-derived rice calli that have large deletions in plastid DNA do not require protein synthesis in plastids for growth." Mol.Gen.Genet.233. 145-150 (1992)

    • Related Report
      1992 Annual Research Report
  • [Publications] 原田 竹雄: "Largeーscale deletions of rice plastid DNA in anther culture" Theor.Appl.Genet.80. 157-161 (1991)

    • Related Report
      1991 Annual Research Report
  • [Publications] 原田 竹雄: "The conformation of largeーscale deleted plastid DNA in rice calli derived from pollen show no requirement for translation in plastid for plant cell growth to occur." Mol.Gen.Genet.

    • Related Report
      1991 Annual Research Report

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Published: 1991-04-01   Modified: 2016-04-21  

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