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Standarizing in Planta Agrobacterium Tumefacience Mediated Genetic Transformation Protocol to Develop New Events by Transforming G. Hirsutum Cotton based on Cry1Ac-Cry1Ec Genes

Received: 13 July 2014    Accepted: 22 July 2014    Published: 10 August 2014
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Abstract

Cotton breeding for insect resistance has been limited by a lack of sufficient genetic variation in the existing germplasms. Therefore, genetic engineering provides the possibility of creating varieties carrying new properties coming even from heterologous source. Exogenous pesticidal transgenes can be introduced into plants. Agrobacterium mediated plant transformation offers advantages like reducing copy number of the transgene and little co-suppression. Inter specific hybrids are known to be more susceptible to biotic stress. It is hence important to develop Bt version for inter specific hybrid. Presently, the Bt gene commercialized are owned by private sector. It is necessary to develop public sector’s Bt event and commercialize them. UAS Dharwad is involved in developing public sector Bt cotton genotypes. One variety, RCR4 (Gossypium hirsutum, L.) was used in the present investigation. Cry1Ac-Cry1Ec genes are to control Helicoverpa armigera and Spodoptera litura. The seedlings in pots were co-cultivated with solid Agrobacterium culture after cutting the meristematic tip with sharp knife. The number of seedlings co-cultivated, number of seedlings established and the number of seedlings showing transformed status are presented in this study. PCR was performed to confirm the presence of the transgene in the plants that were selected to be advanced further. The results showed that non of plants had trangenes Cry1Ac- Cry1Ec as detected through PCR amplification. In planta genetic transformation was carried out and the plants were tested in T0 generation by means of PCR amplification for the genes Cry1Ac- Cry1Ec. The results obtained were not amplified the Cry1Ac- Cry1Ec. Hence the transformation of the genes was not up to mark and the plants of T1 generation are also not confirmed.

Published in American Journal of Life Sciences (Volume 2, Issue 4)
DOI 10.11648/j.ajls.20140204.11
Page(s) 190-199
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This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Genetic Transformation, Agrobacterium Tumefacience, G. Hirsutum, Cry1Ac-Cry1Ec Genes

References
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    Yanal A. Alkuddsi, Shreekanth S. Patil, S. M. Manjula, K. J. Pranesh, B. C. Patil. (2014). Standarizing in Planta Agrobacterium Tumefacience Mediated Genetic Transformation Protocol to Develop New Events by Transforming G. Hirsutum Cotton based on Cry1Ac-Cry1Ec Genes. American Journal of Life Sciences, 2(4), 190-199. https://doi.org/10.11648/j.ajls.20140204.11

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    ACS Style

    Yanal A. Alkuddsi; Shreekanth S. Patil; S. M. Manjula; K. J. Pranesh; B. C. Patil. Standarizing in Planta Agrobacterium Tumefacience Mediated Genetic Transformation Protocol to Develop New Events by Transforming G. Hirsutum Cotton based on Cry1Ac-Cry1Ec Genes. Am. J. Life Sci. 2014, 2(4), 190-199. doi: 10.11648/j.ajls.20140204.11

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    AMA Style

    Yanal A. Alkuddsi, Shreekanth S. Patil, S. M. Manjula, K. J. Pranesh, B. C. Patil. Standarizing in Planta Agrobacterium Tumefacience Mediated Genetic Transformation Protocol to Develop New Events by Transforming G. Hirsutum Cotton based on Cry1Ac-Cry1Ec Genes. Am J Life Sci. 2014;2(4):190-199. doi: 10.11648/j.ajls.20140204.11

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  • @article{10.11648/j.ajls.20140204.11,
      author = {Yanal A. Alkuddsi and Shreekanth S. Patil and S. M. Manjula and K. J. Pranesh and B. C. Patil},
      title = {Standarizing in Planta Agrobacterium Tumefacience Mediated Genetic Transformation Protocol to Develop New Events by Transforming G. Hirsutum Cotton based on Cry1Ac-Cry1Ec Genes},
      journal = {American Journal of Life Sciences},
      volume = {2},
      number = {4},
      pages = {190-199},
      doi = {10.11648/j.ajls.20140204.11},
      url = {https://doi.org/10.11648/j.ajls.20140204.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajls.20140204.11},
      abstract = {Cotton breeding for insect resistance has been limited by a lack of sufficient genetic variation in the existing germplasms. Therefore, genetic engineering provides the possibility of creating varieties carrying new properties coming even from heterologous source. Exogenous pesticidal transgenes can be introduced into plants. Agrobacterium mediated plant transformation offers advantages like reducing copy number of the transgene and little co-suppression. Inter specific hybrids are known to be more susceptible to biotic stress. It is hence important to develop Bt version for inter specific hybrid. Presently, the Bt gene commercialized are owned by private sector. It is necessary to develop public sector’s Bt event and commercialize them. UAS Dharwad is involved in developing public sector Bt cotton genotypes. One variety, RCR4 (Gossypium hirsutum, L.) was used in the present investigation. Cry1Ac-Cry1Ec genes are to control Helicoverpa armigera and Spodoptera litura. The seedlings in pots were co-cultivated with solid Agrobacterium culture after cutting the meristematic tip with sharp knife. The number of seedlings co-cultivated, number of seedlings established and the number of seedlings showing transformed status are presented in this study. PCR was performed to confirm the presence of the transgene in the plants that were selected to be advanced further. The results showed that non of plants had trangenes Cry1Ac- Cry1Ec as detected through PCR amplification. In planta genetic transformation was carried out and the plants were tested in T0 generation by means of PCR amplification for the genes Cry1Ac- Cry1Ec. The results obtained were not amplified the Cry1Ac- Cry1Ec. Hence the transformation of the genes was not up to mark and the plants of T1 generation are also not confirmed.},
     year = {2014}
    }
    

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    T1  - Standarizing in Planta Agrobacterium Tumefacience Mediated Genetic Transformation Protocol to Develop New Events by Transforming G. Hirsutum Cotton based on Cry1Ac-Cry1Ec Genes
    AU  - Yanal A. Alkuddsi
    AU  - Shreekanth S. Patil
    AU  - S. M. Manjula
    AU  - K. J. Pranesh
    AU  - B. C. Patil
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    PY  - 2014
    N1  - https://doi.org/10.11648/j.ajls.20140204.11
    DO  - 10.11648/j.ajls.20140204.11
    T2  - American Journal of Life Sciences
    JF  - American Journal of Life Sciences
    JO  - American Journal of Life Sciences
    SP  - 190
    EP  - 199
    PB  - Science Publishing Group
    SN  - 2328-5737
    UR  - https://doi.org/10.11648/j.ajls.20140204.11
    AB  - Cotton breeding for insect resistance has been limited by a lack of sufficient genetic variation in the existing germplasms. Therefore, genetic engineering provides the possibility of creating varieties carrying new properties coming even from heterologous source. Exogenous pesticidal transgenes can be introduced into plants. Agrobacterium mediated plant transformation offers advantages like reducing copy number of the transgene and little co-suppression. Inter specific hybrids are known to be more susceptible to biotic stress. It is hence important to develop Bt version for inter specific hybrid. Presently, the Bt gene commercialized are owned by private sector. It is necessary to develop public sector’s Bt event and commercialize them. UAS Dharwad is involved in developing public sector Bt cotton genotypes. One variety, RCR4 (Gossypium hirsutum, L.) was used in the present investigation. Cry1Ac-Cry1Ec genes are to control Helicoverpa armigera and Spodoptera litura. The seedlings in pots were co-cultivated with solid Agrobacterium culture after cutting the meristematic tip with sharp knife. The number of seedlings co-cultivated, number of seedlings established and the number of seedlings showing transformed status are presented in this study. PCR was performed to confirm the presence of the transgene in the plants that were selected to be advanced further. The results showed that non of plants had trangenes Cry1Ac- Cry1Ec as detected through PCR amplification. In planta genetic transformation was carried out and the plants were tested in T0 generation by means of PCR amplification for the genes Cry1Ac- Cry1Ec. The results obtained were not amplified the Cry1Ac- Cry1Ec. Hence the transformation of the genes was not up to mark and the plants of T1 generation are also not confirmed.
    VL  - 2
    IS  - 4
    ER  - 

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Author Information
  • Agricultural Research Station, University of Agricultural Sciences, Dharwad- 580005, Karnataka, India

  • Agricultural Research Station, University of Agricultural Sciences, Dharwad- 580005, Karnataka, India

  • Agricultural Research Station, University of Agricultural Sciences, Dharwad- 580005, Karnataka, India

  • Agricultural Research Station, University of Agricultural Sciences, Dharwad- 580005, Karnataka, India

  • Agricultural Research Station, University of Agricultural Sciences, Dharwad- 580005, Karnataka, India

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