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Gene set: RAPAMYCIN_UP_PENG (C2:PERT:0015)
Standard nameRAPAMYCIN_UP_PENG
Systematic nameC2:PERT:0015
Brief descriptionGenes upregulated in response to rapamycin starvation
CategoryC2: Curated
Sub-categoryPERT: Experimental pertuberation
Full description or Abstract

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RAFT1/FRAP/mTOR is a key regulator of cell growth and division
and the mammalian target of rapamycin, an immunosuppressive and
anticancer drug. Rapamycin deprivation and nutrient deprivation
have similar effects on the activity of S6 kinase 1 (S6K1) and
4E-BP1, two downstream effectors of RAFT1, but the relationship
between nutrient- and rapamycin-sensitive pathways is unknown.
Using transcriptional profiling, we show that, in human BJAB B-lymphoma
cells and murine CTLL-2 T lymphocytes, rapamycin treatment affects
the expression of many genes involved in nutrient and protein
metabolism. The rapamycin-induced transcriptional profile is distinct
from those induced by glucose, glutamine, or leucine deprivation
but is most similar to that induced by amino acid deprivation.
In particular, rapamycin treatment and amino acid deprivation
up-regulate genes involved in nutrient catabolism and energy production
and down-regulate genes participating in lipid and nucleotide
synthesis and in protein synthesis, turnover, and folding. Surprisingly,
however, rapamycin had effects opposite from those of amino acid
starvation on the expression of a large group of genes involved
in the synthesis, transport, and use of amino acids. Supported
by measurements of nutrient use, the data suggest that RAFT1 is
an energy and nutrient sensor and that rapamycin mimics a signal
generated by the starvation of amino acids but that the signal
is unlikely to be the absence of amino acids themselves. These
observations underscore the importance of metabolism in controlling
lymphocyte proliferation and offer a novel explanation for immunosuppression
by rapamycin. 
Publication URL12101249
External linksna
Keywords & MeSH headingsGene Expression Profiling,P.H.S.,Human,Support,Down-Regulation/drug effects,Gene Expression,Sirolimus,B-Lymphocytes/cytology/drug effects/metabolism,Starvation,Mice,B-Cell/metabolism,deficiency,metabolism,Glucose,Cell Line,Lymphoma,Ribosomal Protein S6 Kinases/metabolism,pharmacology,T-Lymphocytes/cytology/drug effects/metabolism,Animals,Immunosuppressive Agents,drug effects,Signal Transduction/drug effects/physiology,Up-Regulation/drug effects,Carrier Proteins/metabolism
OrganismHuman
Contributed byBroad Institute
Source platformHG_U95Av2
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Genes

190 genes, 190 accessions (Toggle view)

AccessionGeneTitleLinks
H2BFS
BART1
PLTP
PDK2
DOK2
ADA
CMRF35
IGL@
C5orf7
APS
DAAM1
CFLAR
TOP2A
CIRBP
H2AFX
EIF3S6
MYC
HIST2H2AA
CUTL1
EMS1
PDLIM1
ALDH2
JUND
SMAP
TAF10
MEG3
ATP6AP1
CD48
BRD8
CD37
HDAC5
BRF1
P8
LOC51035
TP53
UCP2
C6orf80
ARHGAP1
GCN5L1
MUTYH
IFIT1
KCNMB1
POLD4
LTA
ASCL1
UBE2J1
PSG7
BCL6
CCNG1
MS4A1
BCL7A
PRKCB1
TNFRSF1A
SLC35E2
ZFP36L1
IL2RG
GMDS
PPP2R5A
RGS10
STAT2
HLA-DQA1
IL4R
EDG5
CRHR2
CAMK1
GPX6
MAP4K2
CENPF
NOTCH4
MUSK
RQCD1
KIFAP3
KIAA0342
TBC1D1
GRINL1A
KIAA1536
hnRNPA3
GNB3
CLOCK
JAK1
IGHG3
HIST1H2BK
SPOCK2
PTK2B
TK1
LRMP
IGSF4
BNIP3L
PIK3CG
PTPN18
RW1
HMMR
SASH1
DRAP1
QSCN6
DDX46
HSRNAFEV
IDH2
BTG2
ASS
BASP1
TCL1A
TCF20
YF13H12
MGC2650
RGS13
IGLJ3
IFNGR2
HMG20B
ATP6V0A2
DMBT1
C5orf13
HAGH
SSTR2
HIST1H2BI
URKL1
FKBP8
MS4A2
CTDSP2
BC-2
RASGRP3
HMGCS2
CBLB
FLJ13052
BCKDHA
MYO1F
AP4M1
HLA-F
ATP2A3
EPS15
ROCK1
TAZ
CNAP1
UROS
RELB
LANCL1
TNFRSF7
POU2F2
HLA-DPB1
CD53
Rab11-FIP3
FAIM2
EPB49
IGHM
SLC25A6
PSCD1
LY86
AKR7A2
ACADVL
TNFRSF5
BRD3
RHBDL1
ACINUS
RTN2
FANCG
HIST1H3H
KIAA0746
FUCA1
XK
ENPP2
TXNIP
CDT1
ERCC1
PTPRH
SURF1
ARPC3
HIST1H2BN
EVER1
HMGCL
CSNK1G2
RPA3
KCNH2
HBP1
HEC
MTMR2
KIAA0076
POU2AF1
LKAP
CD22
MDM4
DVL1
TRO
GMPR
TOP3B
GNG10
CRAT
SLC38A6
AES
LAPTM5
RBMS3


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