In silico Design and Validation of CRISPR/Cas9 gRNAs for Enhancing Drought Tolerance and Yield in Rice
Shafana S
Centre of Plant Biotechnology & Molecular Biology, College of Agriculture, Kerala Agricultural University, Vellanikkara, Thrissur, Kerala - 680656, India.
Kripa Pappachan
Centre of Plant Biotechnology & Molecular Biology, College of Agriculture, Kerala Agricultural University, Vellanikkara, Thrissur, Kerala - 680656, India.
Abida P.S *
Centre of Plant Biotechnology & Molecular Biology, College of Agriculture, Kerala Agricultural University, Vellanikkara, Thrissur, Kerala - 680656, India.
Acharya Arpita
Centre of Plant Biotechnology & Molecular Biology, College of Agriculture, Kerala Agricultural University, Vellanikkara, Thrissur, Kerala - 680656, India.
G Bhavya
Centre of Plant Biotechnology & Molecular Biology, College of Agriculture, Kerala Agricultural University, Vellanikkara, Thrissur, Kerala - 680656, India.
Melna Mary C.J
Centre of Plant Biotechnology & Molecular Biology, College of Agriculture, Kerala Agricultural University, Vellanikkara, Thrissur, Kerala - 680656, India.
*Author to whom correspondence should be addressed.
Abstract
Rice is a staple food crop globally, and its yield is significantly impacted by drought, posing a threat to food security. Several genes have been implicated in drought response and yield regulation, which can be targeted using CRISPR/Cas9 genome editing techniques to develop improved rice cultivars. This study aimed to design guide RNAs (gRNAs) for drought-responsive and yield-determining genes in rice, including flavanone 3-hydroxylase-1 (OsF3H-1), chalcone synthase 31 (OsCHS31), nodulin/SWEET12 (OsSWEET12), MYB47, and OsKALA3, utilizing bioinformatics tools. Genome sequences were retrieved from the Rice Genome Annotation Project (RGAP) and the Rice Annotation Project Database (RAP-DB). Optimal gRNAs were designed using the CRISPR-P v2 tool and evaluated based on parameters such as GC content, off-target score, on-target score, and genome location. The structural stability of the selected gRNAs was validated using the Mathews Lab RNA secondary structure prediction tool. Most gRNAs, except those targeting OsF3H-1, exhibited low self-folding probabilities and energy levels within acceptable ranges, indicating favorable structural stability. However, the OsF3H-1 gRNAs demonstrated higher susceptibility to self-folding, requiring further refinement. The designed gRNAs provide a strong foundation for future CRISPR/Cas9-based genome editing experiments. These findings pave the way for engineering rice to develop stress-resilient and high-yielding varieties, contributing to enhanced agricultural sustainability and global food security.
Keywords: Genome editing, Drought, CRISPR/Cas9, flavanone 3-hydroxylase, OsF3H-1, chalcone synthase 31, OsCHS31, nodulin/SWEET12, MYB47, OsKALA3