مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Verion

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

video

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

sound

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Persian Version

مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

View:

702
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Download:

0
مرکز اطلاعات علمی Scientific Information Database (SID) - Trusted Source for Research and Academic Resources

Cites:

Information Journal Paper

Title

STUDY ON POPULATION STRUCTURE OF PYRICULARIA GRISEA ISOLATED FROM RICE, BASED ON REP-PCR DNA FINGERPRINTING AND IDENTIFICATION OF VCGS

Pages

  227-239

Abstract

 Thirty five monoconidial isolates of the fungal culture collection Pyricularia grisea were examined, to identify the vegetative compatibility groups and characterize the genetic diversity of isolates as through rep-PCR genomic fingerprinting. The isolates were collected from ricefields during 1997-1999. Genetic diversity of P. grisea isolates was studied as based on DNA fingerprinting through rep-PCR using two primers previously designed based on the nucleotidal sequence in ERIC and BOX regions. They generated variable length fragments ranging from 400 to 2500 bp. Phenetic analysis let to differentiation of four distinct CLONAL LINEAGEs designated as A to D. CLONAL LINEAGE A with 74.28% frequency, constituted the largest fingerprinting group. For VCG analyses NIT MUTANTs were obtained from fast growing sectors on Minimal Medium (MM) containing 5% potassium chlorate. Complementation between NIT MUTANTs of isolates was tested on MM. Four vegetative compatibility groups were determined including VCG1, VCG2, VCG3 and VCG4. Group VCG3 comprised of 14 isolates was the dominant VC group among others. This study revealed that isolates obtained from rice were designated in the four VC groups forming heterokaryon with each other; however these isolates were separated with more than 80% similarity from each other using rep-PCR marker with most of isolates being VCG3 were determined in A CLONAL LINEAGE. Both VCGs and rep-PCR analyses determined low genetic diversity in P. grisea population from rice.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    MOTALEBI, P., JAVAN NIKKHAH, M., OKHOVAT, S.M., & BERDI FOTOUHIFAR, KH.. (2011). STUDY ON POPULATION STRUCTURE OF PYRICULARIA GRISEA ISOLATED FROM RICE, BASED ON REP-PCR DNA FINGERPRINTING AND IDENTIFICATION OF VCGS. IRANIAN JOURNAL OF PLANT PROTECTION SCIENCE (IRANIAN JOURNAL OF AGRICULTURAL SCIENCES), 42(2), 227-239. SID. https://sid.ir/paper/171641/en

    Vancouver: Copy

    MOTALEBI P., JAVAN NIKKHAH M., OKHOVAT S.M., BERDI FOTOUHIFAR KH.. STUDY ON POPULATION STRUCTURE OF PYRICULARIA GRISEA ISOLATED FROM RICE, BASED ON REP-PCR DNA FINGERPRINTING AND IDENTIFICATION OF VCGS. IRANIAN JOURNAL OF PLANT PROTECTION SCIENCE (IRANIAN JOURNAL OF AGRICULTURAL SCIENCES)[Internet]. 2011;42(2):227-239. Available from: https://sid.ir/paper/171641/en

    IEEE: Copy

    P. MOTALEBI, M. JAVAN NIKKHAH, S.M. OKHOVAT, and KH. BERDI FOTOUHIFAR, “STUDY ON POPULATION STRUCTURE OF PYRICULARIA GRISEA ISOLATED FROM RICE, BASED ON REP-PCR DNA FINGERPRINTING AND IDENTIFICATION OF VCGS,” IRANIAN JOURNAL OF PLANT PROTECTION SCIENCE (IRANIAN JOURNAL OF AGRICULTURAL SCIENCES), vol. 42, no. 2, pp. 227–239, 2011, [Online]. Available: https://sid.ir/paper/171641/en

    Related Journal Papers

    Related Seminar Papers

  • No record.
  • Related Plans

  • No record.
  • Recommended Workshops






    Move to top
    telegram sharing button
    whatsapp sharing button
    linkedin sharing button
    twitter sharing button
    email sharing button
    email sharing button
    email sharing button
    sharethis sharing button