Metabolism. Lysosomal amino acid transporter SLC38A9 signals arginine sufficiency to mTORC1.

Shuyu Wang(Howard Hughes Medical Institute), Zhi-Yang Tsun(Broad Institute), Rachel L. Wolfson(Massachusetts Institute of Technology), Kuang Shen(Howard Hughes Medical Institute), Gregory A. Wyant(Massachusetts Institute of Technology), Molly Plovanich(Harvard University), Elizabeth D. Yuan(Broad Institute), Tony D. Jones(Massachusetts Institute of Technology), Lynne Chantranupong(Allen Institute), William C. Comb(Massachusetts Institute of Technology), Timothy C. Wang(Howard Hughes Medical Institute), Liron Bar‐Peled(Massachusetts Institute of Technology), Roberto Zoncu(Whitehead Institute for Biomedical Research), Christoph Straub(Harvard University), Choah Kim(Whitehead Institute for Biomedical Research), Jiwon V. Park(Broad Institute), Bernardo L. Sabatini(Howard Hughes Medical Institute), David M. Sabatini(Broad Institute)
PubMed
January 9, 2015
Cited by 819Open Access
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Abstract

The mechanistic target of rapamycin complex 1 (mTORC1) protein kinase is a master growth regulator that responds to multiple environmental cues. Amino acids stimulate, in a Rag-, Ragulator-, and vacuolar adenosine triphosphatase-dependent fashion, the translocation of mTORC1 to the lysosomal surface, where it interacts with its activator Rheb. Here, we identify SLC38A9, an uncharacterized protein with sequence similarity to amino acid transporters, as a lysosomal transmembrane protein that interacts with the Rag guanosine triphosphatases (GTPases) and Ragulator in an amino acid-sensitive fashion. SLC38A9 transports arginine with a high Michaelis constant, and loss of SLC38A9 represses mTORC1 activation by amino acids, particularly arginine. Overexpression of SLC38A9 or just its Ragulator-binding domain makes mTORC1 signaling insensitive to amino acid starvation but not to Rag activity. Thus, SLC38A9 functions upstream of the Rag GTPases and is an excellent candidate for being an arginine sensor for the mTORC1 pathway.


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