Abstract
Biotechnological improvement of monocots is often hampered by the lack of efficient regeneration systems, requisite wound responses and low cell competence. Despite these limitations, the biolistic and Agrobacterium methods have been successfully used to produce several transgenic monocots by adjusting the parameters that govern efficient delivery and integration of transgene(s) into plant genome. It is now possible to transform even difficult monocots using tailor-made gene constructs and promoters, suitable A. tumefaciens strains and a proper understanding of the entire process. This success has been reviewed in the present article and a special emphasis was laid on the measures that were taken in overcoming the difficulties that arise due to the differential responses of monocots and dicots. This information is necessary for biotechnological improvement of still newer monocotyledonous plants that have been hitherto difficult to transform.
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Abbreviations
- FISH:
-
fluorescence in situ hybridization
- NLS:
-
nuclear localization signal
- NSE:
-
nuclear signal E1
- PEG:
-
polyethylene glycol
- vir:
-
virulence
References
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The authors are grateful to CSIR and the director, IHBT for providing the requisite facilities for carrying out this work. Priyanka Sood also acknowledges the Council of Scientific and Industrial Research (CSIR), India for providing financial assistance in the form of Senior Research Fellowship. IHBT Publication number: 0745.
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Sood, P., Bhattacharya, A. & Sood, A. Problems and possibilities of monocot transformation. Biol Plant 55, 1–15 (2011). https://doi.org/10.1007/s10535-011-0001-2
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DOI: https://doi.org/10.1007/s10535-011-0001-2