MG132‐induced progerin clearance is mediated by autophagy activation and splicing regulation
Abstract Hutchinson–Gilford progeria syndrome (HGPS) is a lethal premature and accelerated aging disease caused by a de novo point mutation in LMNA encoding A‐type lamins. Progerin, a truncated and toxic prelamin A issued from aberrant splicing, accumulates in HGPS cells' nuclei and is a hallma...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
Springer Nature
2017-09-01
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Series: | EMBO Molecular Medicine |
Subjects: | |
Online Access: | https://doi.org/10.15252/emmm.201607315 |