Oliver's mTOR Atlas Evidence Platform
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Marco Sardiello

Geneticist who, in Andrea Ballabio's group, helped show that lysosomal genes share a promoter motif and are switched on together by the transcription factor TFEB; his lab now works on lysosomal storage diseases, especially the neuronal ceroid lipofuscinoses.

Professor of Pediatrics, Division of Genetics and Genomic Medicine, Washington University School of Medicine in St. Louis · previously Department of Molecular and Human Genetics, Baylor College of Medicine, Houston · Telethon Institute of Genetics and Medicine (TIGEM), Naples

Sardiello Lab, Division of Genetics and Genomic Medicine, Department of Pediatrics, Washington University School of Medicine (St. Louis, Missouri, USA) ↗ ORCID0000-0001-6484-0250 ↗

Marco Sardiello Portrait: Baylor College of Medicine

Marco Sardiello was first author of the 2009 Science paper from Andrea Ballabio's group at TIGEM in Naples (SAR2009). The team found that most lysosomal genes are expressed in a coordinated way and share a promoter motif (later called the CLEAR element) bound by TFEB. When lysosomes were overloaded, TFEB moved into the nucleus, and extra TFEB increased lysosome numbers and degradation capacity in cultured cells. mTOR was not studied in this paper; later work tied TFEB to mTORC1.

After TIGEM, Sardiello ran a lab in the Department of Molecular and Human Genetics at Baylor College of Medicine in Houston and then moved to Washington University in St. Louis, where he is Professor of Pediatrics. His lab characterises poorly annotated genes linked to inherited disease, with a focus on lysosomal biology and the neuronal ceroid lipofuscinoses.

Milestones in the Atlas

A selection, not a full bibliography: only papers that meet the Atlas inclusion criteria.

YearEvidenceStudy
2009 M A gene network regulating lysosomal biogenesis and function SAR2009 First author: lysosomal genes form a coordinated network with a shared promoter motif regulated by TFEB, which drives lysosome biogenesis.

Co-authors in the Atlas

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