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Gene set: GLUCOSE_DOWN_PENG (C2:PERT:0022)
Standard nameGLUCOSE_DOWN_PENG
Systematic nameC2:PERT:0022
Brief descriptionGenes downregulated in response to glucose 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

157 genes, 157 accessions (Toggle view)

AccessionGeneTitleLinks
DKK4
HEAB
EIF2B4
FZR1
ELMO1
ATP5J
PHB
CALM1
SLA
ILK
PDAP2
SSTR5
NMU
UCHL1
DAPK2
KIAA1041
AGL
RAP1A
TNNT1
FUS
SF3A3
HLF
ARPC5
KIAA0150
PRKCBP1
ADCYAP1
TERF2
BMP1
TEGT
MSH2
SCN4A
NUP98
ID2
POLG
ITGB7
NAP1L1
MYCN
CCNG1
KIAA0284
G3BP
CAPZA1
SFRS1
ELL
MRPS18B
RAB1A
EIF3S3
GC20
PPP2R5A
PTGER3
GCDH
MAP4
DPYSL2
SMC4L1
WBSCR1
ARTN
RAB2
HIP1R
CD47
ASF1A
TRAF5
DVL3
ADNP
RAB9A
ZFY
CDC2
AAMP
SFRS2
ATP2A2
ARF4
DYRK1A
ERAL1
GTF2A2
VNN2
RB1
RRBP1
NFYB
H2AV
DKFZp434I1916
POGZ
IFI16
DKFZP547E1010
USP33
FUBP1
EHD1
HSRNAFEV
MAD2L1
ESPL1
GABARAP
TIMM17A
SH2B
GJB5
MGC8721
ABO
ECE2
UBE2N
SSBP1
FOLR1
BCL2
DNAJA1
PDCD4
BFSP2
RNF6
PURB
PAPSS1
BAZ1A
ACK1
C1orf8
MKI67
MICB
CREM
COMT
DEK
SIAT4C
USP12
MTVR1
KIAA1093
SLC25A5
HTR1B
CD86
CCT4
ATP6V0B
EDG4
RAB31
TUBB5
E2F4
MAGED1
WEE1
RANBP2
BPAG1
ARHGEF6
PICALM
PRKCABP
GORASP2
RBBP4
SMC5L1
E2F1
TXNIP
KIF11
XRCC5
HNRPR
PSMA5
SEC24C
RPA3
DNAJB6
CDC7
RPLP2
GPR3
RAB5A
MYEF2
ZFR
SFN
GMPR
AF1Q
SLC12A4
FOSL2
OIP5
STK6


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