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Shahmoradi Ghahe, S.

Publications and source records attributed to Shahmoradi Ghahe, S..

2 recordsLinked to original sources

Rpl40/eL40 ribosomal protein paralogs couple cytosolic translation to mitochondrial proteome and lipid homeostasis

Ribosomal protein paralogs are increasingly implicated in the regulation of cellular metabolism and mitochondrial function. However, the mechanisms linking paralog composition of ribosomes to mitochondrial physiology remain largely unclear. Here, we investigate the two Rpl40 paralogs in the budding yeast Saccharomyces cerevisiae and find that deletion of either paralog induces compensatory upregulation of the remaining gene and causes mild mitochondrial stress. Despite this shared phenotype, the mutants display distinct mitochondrial adaptations. Loss of Rpl40a is accompanied by increased abundance of mitochondrial proteins, including MICOS components, whereas loss of Rpl40b leads to reduced levels of mitochondrial inner membrane proteins, including the translocase Tim22 and carrier proteins, together with increased sensitivity to membrane stress. Notably, the two mutants show opposing changes in triglyceride abundance, pointing to paralog-specific control of lipid metabolic remodeling during mitochondrial stress. These findings suggest that Rpl40 paralogs differentially modulate cellular adaptation to mitochondrial stress, linking ribosome composition to mitochondrial proteostasis and lipid homeostasis.

biochemistry↗

Identification of a non-canonical function of prefoldin subunit 5 in proteasome assembly

The prefoldin complex is a heterohexameric, evolutionarily conserved co-chaperone that assists in the folding of polypeptides downstream of the protein translation machinery. Loss of prefoldin function leads to impaired solubility of cellular proteins. The degradation of proteins by the proteasome is an integral part of protein homeostasis. Failure of regulated protein degradation can lead to the accumulation of misfolded and defective proteins. We show that prefoldin subunit 5 is required for proteasome activity by contributing to the assembly of the 26S proteasome. In particular, we found that the absence of prefoldin subunit 5 impairs the formation of the Rpt ring subcomplex of the proteasome. Concomitant deletion of PFD5 and HSM3, a chaperone for assembly of the ATPase subunits comprising the Rpt ring, exacerbates this effect, suggesting a synergistic relationship between the two factors in proteasome assembly. Thus, our findings reveal a regulatory mechanism wherein prefoldin subunit 5 plays a crucial role in maintaining proteasome integrity, thereby influencing the degradation of proteins.

molecular biology↗