TY - JOUR
T1 - Intracellular lipid surveillance by small G protein geranylgeranylation
AU - Watterson, Abigail
AU - Tatge, Lexus
AU - Wajahat, Naureen
AU - Arneaud, Sonja L.B.
AU - Solano Fonseca, Rene
AU - Beheshti, Shaghayegh T.
AU - Metang, Patrick
AU - Mihelakis, Melina
AU - Zuurbier, Kielen R.
AU - Corley, Chase D.
AU - Dehghan, Ishmael
AU - McDonald, Jeffrey G.
AU - Douglas, Peter M.
N1 - Funding Information:
We thank A. Ghazi for the NHR-49::GFP (AGP33a) worm strain; M. Zerial for the PEPT-1::DsRed worm strain (MZE1); SunyBiotech for generation and validation of the rab-11.2(syb2999) (PHX2999) and GFP::RAB-11.1 (PHX4435) worm strains; the Caenorhabditis Genetics Center (CGC) for worm strains; A. Lemoff and the UT Southwestern Medical Center Mass Spectrometry Core for LC-MS/MS support; and M. Buszczak and M. Douglas for critical review of the manuscript. We acknowledge S. Schmid, K. Dean, R. Debose-Boyd, D. Russell and J. Goldstein for critical discussions. This work has been funded by the Clayton Foundation for Research, the Welch Foundation (I-2061-20210327), the NIH (R00AG042495, R01AG061338, and R56AG070167) and the Cancer Prevention Research Institute of Texas (RR150089). Schematics were created with BioRender.com.
Funding Information:
We thank A. Ghazi for the NHR-49::GFP (AGP33a) worm strain; M. Zerial for the PEPT-1::DsRed worm strain (MZE1); SunyBiotech for generation and validation of the rab-11.2(syb2999) (PHX2999) and GFP::RAB-11.1 (PHX4435) worm strains; the Caenorhabditis Genetics Center (CGC) for worm strains; A. Lemoff and the UT Southwestern Medical Center Mass Spectrometry Core for LC-MS/MS support; and M. Buszczak and M. Douglas for critical review of the manuscript. We acknowledge S. Schmid, K. Dean, R. Debose-Boyd, D. Russell and J. Goldstein for critical discussions. This work has been funded by the Clayton Foundation for Research, the Welch Foundation (I-2061-20210327), the NIH (R00AG042495, R01AG061338, and R56AG070167) and the Cancer Prevention Research Institute of Texas (RR150089). Schematics were created with BioRender.com.
Publisher Copyright:
© 2022, The Author(s), under exclusive licence to Springer Nature Limited.
PY - 2022/5/26
Y1 - 2022/5/26
N2 - Imbalances in lipid homeostasis can have deleterious effects on health1,2. Yet how cells sense metabolic demand due to lipid depletion and respond by increasing nutrient absorption remains unclear. Here we describe a mechanism for intracellular lipid surveillance in Caenorhabditis elegans that involves transcriptional inactivation of the nuclear hormone receptor NHR-49 through its cytosolic sequestration to endocytic vesicles via geranylgeranyl conjugation to the small G protein RAB-11.1. Defective de novo isoprenoid synthesis caused by lipid depletion limits RAB-11.1 geranylgeranylation, which promotes nuclear translocation of NHR-49 and activation of rab-11.2 transcription to enhance transporter residency at the plasma membrane. Thus, we identify a critical lipid sensed by the cell, its conjugated G protein, and the nuclear receptor whose dynamic interactions enable cells to sense metabolic demand due to lipid depletion and respond by increasing nutrient absorption and lipid metabolism.
AB - Imbalances in lipid homeostasis can have deleterious effects on health1,2. Yet how cells sense metabolic demand due to lipid depletion and respond by increasing nutrient absorption remains unclear. Here we describe a mechanism for intracellular lipid surveillance in Caenorhabditis elegans that involves transcriptional inactivation of the nuclear hormone receptor NHR-49 through its cytosolic sequestration to endocytic vesicles via geranylgeranyl conjugation to the small G protein RAB-11.1. Defective de novo isoprenoid synthesis caused by lipid depletion limits RAB-11.1 geranylgeranylation, which promotes nuclear translocation of NHR-49 and activation of rab-11.2 transcription to enhance transporter residency at the plasma membrane. Thus, we identify a critical lipid sensed by the cell, its conjugated G protein, and the nuclear receptor whose dynamic interactions enable cells to sense metabolic demand due to lipid depletion and respond by increasing nutrient absorption and lipid metabolism.
UR - http://www.scopus.com/inward/record.url?scp=85130296052&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85130296052&partnerID=8YFLogxK
U2 - 10.1038/s41586-022-04729-7
DO - 10.1038/s41586-022-04729-7
M3 - Article
C2 - 35585236
AN - SCOPUS:85130296052
SN - 0028-0836
VL - 605
SP - 736
EP - 740
JO - Nature
JF - Nature
IS - 7911
ER -