Exportin 1 modulates life span by regulating nucleolar dynamics via the autophagy protein LGG-1/GABARAP

Author:

Kumar Anita V.1ORCID,Kang Taewook2ORCID,Thakurta Tara G.1,Ng Celeste1,Rogers Aric N.3ORCID,Larsen Martin R.2ORCID,Lapierre Louis R.1ORCID

Affiliation:

1. Department of Molecular Biology, Cell Biology, and Biochemistry, Brown University, 185 Meeting St., Providence, RI 02912, USA.

2. Department of Biochemistry and Molecular Biology, University of Southern Denmark, Odense, Denmark.

3. MDI Biological Laboratory, 159 Old Bar Harbor Rd., Salisbury Cove, ME 04672, USA.

Abstract

Altered nucleolar and ribosomal dynamics are key hallmarks of aging, but their regulation remains unclear. Building on the knowledge that the conserved nuclear export receptor Exportin 1 (XPO-1/XPO1) modulates proteostasis and life span, we systematically analyzed the impact of nuclear export on protein metabolism. Using transcriptomic and subcellular proteomic analyses in nematodes, we demonstrate that XPO-1 modulates the nucleocytoplasmic distribution of key proteins involved in nucleolar dynamics and ribosome function, including fibrillarin (FIB-1/FBL) and RPL-11 (RPL11). Silencing xpo-1 led to marked reduction in global translation, which was accompanied by decreased nucleolar size and lower fibrillarin levels. A targeted screen of known proteostatic mediators revealed that the autophagy protein LGG-1/GABARAP modulates nucleolar size by regulating RPL-11 levels, linking specific protein degradation to ribosome metabolism. Together, our study reveals that nucleolar size and life span are regulated by LGG-1/GABARAP via ribosome protein surveillance.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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