Pere Puigserver

Pere Puigserver, Ph.D.

Professor of Cell Biology (Dana-Farber Cancer Institute)
Professor of Cell Biology (HMS)

Pere Puigserver, Ph.D. is Professor of Cell Biology at Harvard Medical School and Dana-Farber Cancer Institute. He received his PhD in Biochemistry from UIB (Spain) that included research at Stockholm University, following postdoctoral work at the Dana-Farber Cancer Institute. He joined the faculty of Cell Biology at Johns Hopkins University School of Medicine in 2002 and subsequently returned in 2006 to the Department of Cell Biology (Harvard Medical School) and Cancer Biology (Dana-Farber Cancer Institute).

The Puigserver Lab focuses on the regulatory molecular mechanisms of core metabolic processes that maintain cell homeostasis and phenotypes. The research program of the Puigserver Lab includes main areas such as 1) mitochondrial biology, 2) intermediary metabolism and, 3) cancer metabolism and energetics. In mitochondrial biology, particular interests are in the regulatory mechanisms that control mitochondrial energetics and biogenesis, with implications in a variety of diseases including metabolic and mitochondrial diseases. In intermediary metabolism, a major focus is in liver and adipose cells and their regulatory mechanisms that control nutrient-derived metabolic and energetic activities. In cancer metabolism and energetics, the Puigserver Lab addresses how these processes drive core cancer biology programs such as cell growth, survival and resistance mechanisms.  The Puigserver Lab uses a multidisciplinary experimental design and approaches including chemical and genetic screens in mammalian cells, quantitative metabolomics and proteomics, biochemistry, mouse pre-clinical models of obesity/diabetes, mitochondrial diseases and cancer.    

Dana Farber Cancer Institute

Dept. of Cell Biology, LC-6213

360 Longwood Avenue

Boston, MA 02115

Lab telephone: 617-582-7977

Lab fax: 617-632-5363

Foxo1 integrates insulin signaling with mitochondrial function in the liver.
Authors: Authors: Cheng Z, Guo S, Copps K, Dong X, Kollipara R, Rodgers JT, Depinho RA, Puigserver P, White MF.
Nat Med
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Antioxidant and oncogene rescue of metabolic defects caused by loss of matrix attachment.
Authors: Authors: Schafer ZT, Grassian AR, Song L, Jiang Z, Gerhart-Hines Z, Irie HY, Gao S, Puigserver P, Brugge JS.
Nature
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GCN5-mediated transcriptional control of the metabolic coactivator PGC-1beta through lysine acetylation.
Authors: Authors: Kelly TJ, Lerin C, Haas W, Gygi SP, Puigserver P.
J Biol Chem
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AMPK regulates energy expenditure by modulating NAD+ metabolism and SIRT1 activity.
Authors: Authors: Cantó C, Gerhart-Hines Z, Feige JN, Lagouge M, Noriega L, Milne JC, Elliott PJ, Puigserver P, Auwerx J.
Nature
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Insulin resistance: beta-arrestin development.
Authors: Authors: Rodgers JT, Puigserver P.
Cell Res
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A PGC-1alpha-O-GlcNAc transferase complex regulates FoxO transcription factor activity in response to glucose.
Authors: Authors: Housley MP, Udeshi ND, Rodgers JT, Shabanowitz J, Puigserver P, Hunt DF, Hart GW.
J Biol Chem
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Concurrent regulation of AMP-activated protein kinase and SIRT1 in mammalian cells.
Authors: Authors: Suchankova G, Nelson LE, Gerhart-Hines Z, Kelly M, Gauthier MS, Saha AK, Ido Y, Puigserver P, Ruderman NB.
Biochem Biophys Res Commun
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The genetic ablation of SRC-3 protects against obesity and improves insulin sensitivity by reducing the acetylation of PGC-1{alpha}.
Authors: Authors: Coste A, Louet JF, Lagouge M, Lerin C, Antal MC, Meziane H, Schoonjans K, Puigserver P, O'Malley BW, Auwerx J.
Proc Natl Acad Sci U S A
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O-GlcNAc regulates FoxO activation in response to glucose.
Authors: Authors: Housley MP, Rodgers JT, Udeshi ND, Kelly TJ, Shabanowitz J, Hunt DF, Puigserver P, Hart GW.
J Biol Chem
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Metabolic adaptations through the PGC-1 alpha and SIRT1 pathways.
Authors: Authors: Rodgers JT, Lerin C, Gerhart-Hines Z, Puigserver P.
FEBS Lett
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