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Lysosomes are organelles central to degradation and recycling processes in animal cells. Whether lysosomal activity is coordinated to respond to cellular needs remains unclear. We found that most lysosomal genes exhibit coordinated transcriptional behavior and are regulated by the transcription factor EB (TFEB). Under aberrant lysosomal storage conditions, TFEB translocated from the cytoplasm to the nucleus, resulting in the activation of its target genes. TFEB overexpression in cultured cells induced lysosomal biogenesis and increased the degradation of complex molecules, such as glycosaminoglycans and the pathogenic protein that causes Huntington's disease. Thus, a genetic program controls lysosomal biogenesis and function, providing a potential therapeutic target to enhance cellular clearing in lysosomal storage disorders and neurodegenerative diseases.
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Marco Sardiello
Washington University in St. Louis
Michela Palmieri
University of Modena and Reggio Emilia
Alberto di Ronza
Baylor College of Medicine
Science
University of Milan
Federico II University Hospital
Telethon Institute Of Genetics And Medicine
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Sardiello et al. (Thu,) studied this question.
synapsesocial.com/papers/69d7c8b433ca018b39ae2ce4 — DOI: https://doi.org/10.1126/science.1174447