TY - JOUR
T1 - Who does TORC2 talk to?
AU - Xie, Jianling
AU - Wang, Xuemin
AU - Proud, Christopher G.
N1 - Funding Information:
The authors’ research on mTOR signalling is currently supported by the South Australian Health and Medical Research Institute. Due to space considerations, we have been unable to cite all the primary literature relating to TORC2, its control, and its functions.
Publisher Copyright:
© 2018 The Author(s).
PY - 2018/5/24
Y1 - 2018/5/24
N2 - The target of rapamycin (TOR) is a protein kinase that, by forming complexes with partner proteins, governs diverse cellular signalling networks to regulate a wide range of processes. TOR thus plays central roles in maintaining normal cellular functions and, when dysregulated, in diverse diseases. TOR forms two distinct types of multiprotein complexes (TOR complexes 1 and 2, TORC1 and TORC2). TORC1 and TORC2 differ in their composition, their control and their substrates, so that they play quite distinct roles in cellular physiology. Much effort has been focused on deciphering the detailed regulatory links within the TOR pathways and the structure and control of TOR complexes. In this review, we summarize recent advances in understanding mammalian (m) TORC2, its structure, its regulation, and its substrates, which link TORC2 signalling to the control of cell functions. It is now clear that TORC2 regulates several aspects of cell metabolism, including lipogenesis and glucose transport. It also regulates gene transcription, the cytoskeleton, and the activity of a subset of other protein kinases.
AB - The target of rapamycin (TOR) is a protein kinase that, by forming complexes with partner proteins, governs diverse cellular signalling networks to regulate a wide range of processes. TOR thus plays central roles in maintaining normal cellular functions and, when dysregulated, in diverse diseases. TOR forms two distinct types of multiprotein complexes (TOR complexes 1 and 2, TORC1 and TORC2). TORC1 and TORC2 differ in their composition, their control and their substrates, so that they play quite distinct roles in cellular physiology. Much effort has been focused on deciphering the detailed regulatory links within the TOR pathways and the structure and control of TOR complexes. In this review, we summarize recent advances in understanding mammalian (m) TORC2, its structure, its regulation, and its substrates, which link TORC2 signalling to the control of cell functions. It is now clear that TORC2 regulates several aspects of cell metabolism, including lipogenesis and glucose transport. It also regulates gene transcription, the cytoskeleton, and the activity of a subset of other protein kinases.
UR - http://www.scopus.com/inward/record.url?scp=85047998076&partnerID=8YFLogxK
U2 - 10.1042/BCJ20180130
DO - 10.1042/BCJ20180130
M3 - Review article
C2 - 29794170
AN - SCOPUS:85047998076
VL - 475
SP - 1721
EP - 1738
JO - Biochemical Journal
JF - Biochemical Journal
SN - 0264-6021
IS - 10
ER -