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:

493
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

Identification of Pathways and Candidate Genes Associated with Resistance to Ascochyta Blight in a Mutant Chickpea Variety using RNA-Seq Analysis

Pages

  69-75

Abstract

Chickpea is involved in biotic and abiotic stresses during its growing period. Ascochyta blight is the most significant fungal disease that causes main yield defection in Chickpea. Breeding to obtain resistant cultivars is the most important method for coping with Ascochyta blight. Evaluation of the pattern of gene expression and identification of resistant genes using RNA-Seq technique provides valuable information for breeders. In present research the transcriptome profile of a C-727 as sensitive variety and CM-88 as a resistance variety were investigated. RNA extracted from the leaves of the plants under Ascochyta infection. following by preparation of depleted RNA library from rRNA. Then, sequencing was performed by illumina genome analyzer deep sequencing. An approximately 84653468 (C-727) and 97400784 (CM-88) raw reads were generated. In total, 3106 genes were determined by differential expression. From 3106 genes in CM-88, 1546 genes showed the decrease in expression and 1560 genes showed the increase in expression than C-727. After KEGG analysis, 1285 genes were recognized in 122 biological pathways. from 1285 genes, 627 and 607 genes were down and up regulated in CM-88. The results of the KEGG analysis and the pattern of expression of the genes showed that the N-Glycan biosynthesis pathway and the pathway for the synthesis of amino acid arginine and a transcription factor that induced hormones related to defense signals was enriched with enhanced expression genes consequently they may play a role in resistance to ascochyta in the varieties studied.

Cites

  • No record.
  • References

  • No record.
  • Cite

    APA: Copy

    Sabokbari Abarghan, Masoumeh, Zaynali Nezhad, Khalil, EBRAHIMIE, ESMAEIL, & SOLTANLOO, HASAN. (2020). Identification of Pathways and Candidate Genes Associated with Resistance to Ascochyta Blight in a Mutant Chickpea Variety using RNA-Seq Analysis. JOURNAL OF CROP BREEDING, 12(33 ), 69-75. SID. https://sid.ir/paper/181083/en

    Vancouver: Copy

    Sabokbari Abarghan Masoumeh, Zaynali Nezhad Khalil, EBRAHIMIE ESMAEIL, SOLTANLOO HASAN. Identification of Pathways and Candidate Genes Associated with Resistance to Ascochyta Blight in a Mutant Chickpea Variety using RNA-Seq Analysis. JOURNAL OF CROP BREEDING[Internet]. 2020;12(33 ):69-75. Available from: https://sid.ir/paper/181083/en

    IEEE: Copy

    Masoumeh Sabokbari Abarghan, Khalil Zaynali Nezhad, ESMAEIL EBRAHIMIE, and HASAN SOLTANLOO, “Identification of Pathways and Candidate Genes Associated with Resistance to Ascochyta Blight in a Mutant Chickpea Variety using RNA-Seq Analysis,” JOURNAL OF CROP BREEDING, vol. 12, no. 33 , pp. 69–75, 2020, [Online]. Available: https://sid.ir/paper/181083/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