is an essential yeast gene encoding a component of different LSM complexes involved in the regulation of mRNA splicing, stability, and translation. In previous papers, we reported that the expression in of the gene lacking the C-terminal Q/N-rich domain in an null strain () restored cell viability. Nevertheless, in this transformed strain, we observed some phenotypes that are typical markers of regulated cell death, reactive oxygen species (ROS), and oxidated RNA accumulation. In this paper, we report that a similar truncation operated in the gene confers on cells the same phenotypes observed with the gene. Up until now, there was no evidence of the direct involvement of in autophagy. Here we found that the mutant showed a block in the autophagic process and was very sensitive to nitrogen starvation or treatment with low doses of rapamycin, an inducer of autophagy. Moreover, both during nitrogen starvation and aging, the mutant accumulated cytoplasmic autophagy-related structures, suggesting a role of Lsm4 in a later step of the autophagy process.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530990 | PMC |
http://dx.doi.org/10.3390/ijms241813708 | DOI Listing |
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