Aurore Claude-Taupin

Dr. Aurore Claude-Taupin


Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2020 in Developmental Cell
Verified
Journal Article
Closed access
JJJingyue Jia
Jingyue Jia
ACAurore Claude-Taupin
Aurore Claude-Taupin
YGYuexi Gu
Yuexi Gu
SCSeong Won Choi
Seong Won Choi
RPRyan Peters
Ryan Peters
VDVojo Deretic
Vojo Deretic

1 April 2018 in Molecular Cell
Verified
Journal Article
Closed access
JJJingyue Jia
Jingyue Jia
YAYakubu Princely Abudu
Yakubu Princely Abudu
ACAurore Claude-Taupin
Aurore Claude-Taupin
YGYuexi Gu
Yuexi Gu
SKSuresh Kumar
Suresh Kumar
VDVojo Deretic
Vojo Deretic

2 February 2018 in Journal of Cell Biology
Verified
Journal Article
Open access
PDF file
SKSuresh Kumar
Suresh Kumar
AJAshish Jain
Ashish Jain
FFFarzin Farzam
Farzin Farzam
JJJingyue Jia
Jingyue Jia
YGYuexi Gu
Yuexi Gu
VDVojo Deretic
Vojo Deretic
Autophagy is a conserved eukaryotic process with metabolic, immune, and general homeostatic functions in mammalian cells. Mammalian autophagosomes fuse with lysosomes in a SNARE-driven process that includes syntaxin 17 (Stx17). How Stx17 translocates to autophagosomes is unknown. In this study, we show that the mechanism of Stx17 recruitment to autophagosomes in human cells entails the small guanosine triphosphatase IRGM. Stx17 directly interacts with IRGM, and efficient Stx17 recruitment to autophagosomes requires IRGM. Both IRGM and Stx17 directly interact with mammalian Atg8 proteins, thus being guided to autophagosomes. We also show that Stx17 is significant in defense against infectious agents and that Stx17–IRGM interaction is targeted by an HIV virulence factor Nef.

5 November 2018 in Autophagy
Verified
Journal Article
Closed access
JJJingyue Jia
Jingyue Jia
YAYakubu Princely Abudu
Yakubu Princely Abudu
ACAurore Claude-Taupin
Aurore Claude-Taupin
YGYuexi Gu
Yuexi Gu
SKSuresh Kumar
Suresh Kumar
VDVojo Deretic
Vojo Deretic
The Ser/Thr protein kinase MTOR (mechanistic target of rapamycin kinase) regulates cellular metabolism and controls macroautophagy/autophagy. Autophagy has both metabolic and quality control functions, including recycling nutrients at times of starvation and removing dysfunctional intracellular organelles. Lysosomal damage is one of the strongest inducers of autophagy, and yet mechanisms of its activation in response to lysosomal membrane damage are not fully understood. Our recent study has uncovered a new signal transduction system based on cytosolic galectins that elicits autophagy by controlling master regulators of metabolism and autophagy, MTOR and AMPK, in response to lysosomal damage. Thus, intracellular galectins are not, as previously thought, passive tags recognizing damage to guide selective autophagy receptors, but control the activation state of AMPK and MTOR in response to endomembrane damage. Abbreviations: MTOR: mechanistic target of rapamycin kinase; AMPK: AMP-activated protein kinase / Protein Kinase AMP-Activated; SLC38A9: Solute Carrier Family 38 Member 9; APEX2: engineered ascorbate peroxidase 2; RRAGA/B: Ras Related GTP Binding A or B; LAMTOR1: Late Endosomal/Lysosomal Adaptor, MAPK and MTOR Activator 1; LGALS8: Lectin, Galactoside-Binding, Soluble, 8 / Galectin 8; LGALS9: Lectin, Galactoside-Binding, Soluble, 9 / Galectin 9; TAK1: TGF-Beta Activated Kinase 1 / Mitogen-Activated Protein Kinase Kinase Kinase 7 (MAP3K7); STK11/LKB1: Serine/Threonine Kinase 11 / Liver Kinase B1; ULK1: Unc-51 Like Autophagy Activating Kinase 1.

12 July 2021 in Nature Cell Biology
Verified
Journal Article
Closed access
PDF file
ACAurore Claude-Taupin
Aurore Claude-Taupin
JJJingyue Jia
Jingyue Jia
ZBZambarlal Bhujabal
Zambarlal Bhujabal
MGMeriem Garfa-Traoré
Meriem Garfa-Traoré
SKSuresh Kumar
Suresh Kumar
VDVojo Deretic
Vojo Deretic

1 November 2018 in Seminars in Cell & Developmental Biology
Verified
Journal Article
Closed access
ACAurore Claude-Taupin
Aurore Claude-Taupin
BBBhawana Bissa
Bhawana Bissa
JJJingyue Jia
Jingyue Jia
YGYuexi Gu
Yuexi Gu
VDVojo Deretic
Vojo Deretic