CRISPR/Cas9 Directed Mutagenesis of in High Yielding Basmati Rice ( L.) Line and Comparative Proteome Profiling of Unveiled Changes Triggered by Mutations.

Int J Mol Sci

College of Agriculture, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangxi University, Nanning 530004, China.

Published: August 2020


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Article Abstract

In rice, semi-dwarfism is among the most required characteristics, as it facilitates better yields and offers lodging resistance. Here, semi-dwarf rice lines lacking any residual transgene-DNA and off-target effects were generated through CRISPR/Cas9-guided mutagenesis of the gene in a high yielding Basmati rice line, and the isobaric tags for relative and absolute quantification (iTRAQ) strategy was utilized to elucidate the proteomic changes in mutants. The results indicated the reduced gibberellins (GA and GA) levels, plant height (28.72%), and flag leaf length, while all the other traits remained unchanged. The expression was highly suppressed, and the mutants exhibited decreased cell length, width, and restored their plant height by exogenous GA treatment. Comparative proteomics of the wild-type and homozygous mutant line (GXU43_9) showed an altered level of 588 proteins, 273 upregulated and 315 downregulated, respectively. The identified differentially expressed proteins (DEPs) were mainly enriched in the carbon metabolism and fixation, glycolysis/gluconeogenesis, photosynthesis, and oxidative phosphorylation pathways. The proteins (Q6AWY7, Q6AWY2, Q9FRG8, Q6EPP9, Q6AWX8) associated with growth-regulating factors (, , , , and ) and GA (Q8RZ73, Q9AS97, Q69VG1, Q8LNJ6, Q0JH50, and Q5MQ85) were downregulated, while the abscisic stress-ripening protein 5 () and abscisic acid receptor () were upregulated in mutant lines. We integrated CRISPR/Cas9 with proteomic screening as the most reliable strategy for rapid assessment of the CRISPR experiments outcomes.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7504442PMC
http://dx.doi.org/10.3390/ijms21176170DOI Listing

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