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通过对出芽率和细胞生长折线图进行分析,我们发现在敲除193C基因前期促进细胞分裂,保持高细胞活性;后期一定程度减缓了细胞活性,出芽率也有所降低。对RPL36B和其IncRNA的YPL250W-A敲除可以延长细胞活性,维持较高细胞出芽率,从而延缓细胞衰老过程。同时,我发现敲除YPL250W-A基因在早期细胞活性有所降低,后期细胞活性上升;同时,出芽率在后期也有所上升,我推断敲除250W延缓了细胞的衰老,

Through the analysis of the budding rate and cell growth line graphs, we found that knocking out the 193C gene promotes cell division in the early stages and maintains high cell viability. However, in the later stages, it somewhat slows down cellular activity, resulting in a decrease in the budding rate. The knockout of RPL36B and its IncRNA YPL250W-A can extend cell viability and maintain a higher budding rate, thereby delaying the aging process of cells. At the same time, I observed that knocking out the YPL250W-A gene initially reduces cell viability but increases it in later stages; additionally, the budding rate also rises in later stages. I infer that knocking out 250W delays cellular aging.


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