Ribosome-binding protein 1 maintains peroxisome biogenesis

Peroxisomes are single-membrane-bound organelles essential for human health, yet the mechanisms of peroxisome biogenesis are not fully understood. Here using a systematic double screening approach, we identified ribosome-binding protein 1 (RRBP1) as a novel peroxisome biogenesis factor in human cells. Deletion of RRBP1 in HEK293T cells led to a reduction in both peroxisome number and peroxisomal protein levels as well as in defects in processing of peroxisomal matrix proteins, such as ACOX1 and thiolase. However, cell proliferation and protein translation were not altered in cells lacking RRBP1. RRBP1 depletion did not affect peroxisome-endoplasmic reticulum (ER) contact sites, and pexophagy did not contribute to the reduction of peroxisomes in RRBP1 knockout cells. Instead, in the absence of RRBP1, peroxisomal proteins were processed by proteasomal degradation, suggesting that RRBP1 plays a role in the insertion of these proteins into ER membranes and their stabilization. Altogether, our results show that RRBP1 promotes peroxisome biogenesis in human cells, highlighting the power of systematic approaches in discovering novel factors of organellar biogenesis.

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Publication Details

Journal
Journal of Cell Science
Published
2024-12-15
DOI
https://doi.org/10.1242/jcs.264075
Citations
1
Primary Topic
Peroxisome Proliferator-Activated Receptors
Type
article
Field-Weighted Citation Impact
0.23
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article

Ribosome-binding protein 1 maintains peroxisome biogenesis

Eija Jokitalo, Pekka Katajisto, Tamara Somborac, Anı Akpınar et al.
1 citations
Journal of Cell Science
Peroxisome Proliferator-Activated Receptors
0.23
article

Ribosome-binding protein 1 maintains peroxisome biogenesis

Eija Jokitalo, Pekka Katajisto, Tamara Somborac, Anı Akpınar, Ville O. Paavilainen, Helena Vihinen, Anja Paatero, Svetlana Konovalova, Kaneez Fatima
article en
1 citations

Abstract

Peroxisomes are single-membrane-bound organelles essential for human health, yet the mechanisms of peroxisome biogenesis are not fully understood. Here using a systematic double screening approach, we identified ribosome-binding protein 1 (RRBP1) as a novel peroxisome biogenesis factor in human cells. Deletion of RRBP1 in HEK293T cells led to a reduction in both peroxisome number and peroxisomal protein levels as well as in defects in processing of peroxisomal matrix proteins, such as ACOX1 and thiolase. However, cell proliferation and protein translation were not altered in cells lacking RRBP1. RRBP1 depletion did not affect peroxisome-endoplasmic reticulum (ER) contact sites, and pexophagy did not contribute to the reduction of peroxisomes in RRBP1 knockout cells. Instead, in the absence of RRBP1, peroxisomal proteins were processed by proteasomal degradation, suggesting that RRBP1 plays a role in the insertion of these proteins into ER membranes and their stabilization. Altogether, our results show that RRBP1 promotes peroxisome biogenesis in human cells, highlighting the power of systematic approaches in discovering novel factors of organellar biogenesis.

Journal of Cell ScienceVol. 138(24)
University of Helsinki (FI), Helsinki Institute of Physics (FI)
Openalex Percentile: Top 39%
Peroxisome Proliferator-Activated Receptors
0.23
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