EventsCells, Cells and Nothing but Cells: Discoveries, Challenges and Directions
Published
This submission belongs to the session CELLS_S3. Cellular Metabolism of the event Cells, Cells and Nothing but Cells: Discoveries, Challenges and Directions
Published date
07 Feb, 2023
Academic Editor
author-avatarAlexander E. Kalyuzhny
Citation
Nazela Ahmed Chowdhury, Fatema Akter Sadia, Ismat Jahan Anee, Ashfaqul Muid Khandaker, The Effect of RAS2 Gene Mutation in Yeast Model, in Proceedings of Cells, Cells and Nothing but Cells: Discoveries, Challenges and Directions, 6 March–8 March 2023, MDPI: Basel, Switzerland
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The Effect of RAS2 Gene Mutation in Yeast Model

1. Branch of Genetics and Molecular Biology, Department of Zoology, University of Dhaka, Dhaka-1000, Bangladesh, Bangladesh
2. Branch of Genetics and Molecular Biology, Department of Zoology, University of Dhaka, Dhaka-1000, Bangladesh
Abstract

More than 30% of all human malignancies are brought about by mutation in RAS proto-oncogenes (HRAS, KRAS, and NRAS) that are greatly conserved in yeast (RAS1 and RAS2). This makes yeast an efficient single-celled eukaryotic model organism to study their functions. In this current investigation, the null mutation of RAS2 gene was analyzed to find out its deleterious consequences in yeast cells based on their ability to utilize glycerol as its respiratory substrate, mtDNA mutation rate, mtDNA abundance and distribution pattern. Mutant cells grown in YPEG plates demonstrated slight respiratory deficiency than the wild type. Erythromycin-resistant assay was carried out to analyze the spontaneous mitochondrial DNA mutation rate in ras2 mutant and was found greater than the wild type. In addition, the mitochondrial DNA of both strains was also visualized under a fluorescence microscope using DAPI fluorescent stain. It was observed that mtDNA abundance was much lower than that of the wild type. Thus, the present investigation revealed that the deletion of RAS2 gene resulted in mtDNA mutation and depletion.

Keywords
Mutation
RAS proto-oncogenes
S. cerevisiae
Mitochondrial DNA
Cancer
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