Independence Award
- First Rank - Second Rank - Third Rank
Labour Award
- First Rank - Second Rank -Third Rank
National Award
- Study on food stuff for animal(2005)
- Study on rice breeding for export and domestic consumption(2005)
VIFOTEC Award
- Hybrid Maize by Single Cross V2002 (2003)
- Tomato Grafting to Manage Ralstonia Disease(2005)
- Cassava variety KM140(2010)
![]() |
|
![]() |
|
RNAi and genome editing of sugarcane: Progress and prospects
Tuesday, 2025/03/18 | 08:19:33
|
||||||||||||||||||||||||||||||||||||||||
Eleanor Brant, Evelyn Zuniga-Soto, Fredy Altpeter The Plant Journal; 7 March 2025; https://doi.org/10.1111/tpj.70048 SUMMARYSugarcane, which provides 80% of global table sugar and 40% of biofuel, presents unique breeding challenges due to its highly polyploid, heterozygous, and frequently aneuploid genome. Significant progress has been made in developing genetic resources, including the recently completed reference genome of the sugarcane cultivar R570 and pan-genomic resources from sorghum, a closely related diploid species. Biotechnological approaches including RNA interference (RNAi), overexpression of transgenes, and gene editing technologies offer promising avenues for accelerating sugarcane improvement. These methods have successfully targeted genes involved in important traits such as sucrose accumulation, lignin biosynthesis, biomass oil accumulation, and stress response. One of the main transformation methods—biolistic gene transfer or Agrobacterium-mediated transformation—coupled with efficient tissue culture protocols, is typically used for implementing these biotechnology approaches. Emerging technologies show promise for overcoming current limitations. The use of morphogenic genes can help address genotype constraints and improve transformation efficiency. Tissue culture-free technologies, such as spray-induced gene silencing, virus-induced gene silencing, or virus-induced gene editing, offer potential for accelerating functional genomics studies. Additionally, novel approaches including base and prime editing, orthogonal synthetic transcription factors, and synthetic directed evolution present opportunities for enhancing sugarcane traits. These advances collectively aim to improve sugarcane's efficiency as a crop for both sugar and biofuel production. This review aims to discuss the progress made in sugarcane methodologies, with a focus on RNAi and gene editing approaches, how RNAi can be used to inform functional gene targets, and future improvements and applications.
See https://onlinelibrary.wiley.com/doi/full/10.1111/tpj.70048
Figure 1: Strategies for generation, screening, and confirmation of transgene-free sugarcane plants. Cas9 RNP and nCas-base editor RNP systems could be used alongside guide RNAs to generate transgene-free sugarcane plants. Biolistics and PEG-mediated transformation are the two available methods for RNP delivery, with biolistic transformation holding the benefit of fewer somaclonal variations and accelerated plant regeneration. Capillary electrophoresis, high-resolution melt analysis (HRMA), or Cas9 RNP assays could then be used to screen for mutants with non-selectable phenotypes, followed by Sanger Sequencing or Next Generation Sequencing (NGS) technologies to confirm mutation sequence and size. A selectable phenotype can be generated via nCas base editor-mediated precision nucleotide substitutions in genes like acetolactate synthase conferring a selectable herbicide-resistant phenotype. This will facilitate recovery of co-edited target genes and streamline the analysis of regenerated plants.
|
||||||||||||||||||||||||||||||||||||||||
![]() ![]() ![]() |
||||||||||||||||||||||||||||||||||||||||
[ Other News ]___________________________________________________
|