Viral-Mediated Noisy Gene Expression Reveals Biphasic E2f1 Response to MYC

被引:34
作者
Wong, Jeffrey V. [1 ,2 ]
Yao, Guang [2 ,3 ]
Nevins, Joseph R. [2 ,3 ]
You, Lingchong [1 ,2 ,4 ]
机构
[1] Duke Univ, Dept Biomed Engn, Durham, NC 27708 USA
[2] Duke Univ, Inst Genome Sci & Policy, Durham, NC 27708 USA
[3] Duke Univ, Dept Mol Genet & Microbiol, Durham, NC 27708 USA
[4] Duke Univ, Duke Ctr Syst Biol, Durham, NC 27708 USA
基金
美国国家卫生研究院;
关键词
CELL-CYCLE PROGRESSION; C-MYC; RETINOBLASTOMA PROTEIN; IN-VIVO; TRANSCRIPTIONAL ACTIVATION; GENOMIC TARGETS; RIBOSOMAL DNA; S-PHASE; APOPTOSIS; BINDING;
D O I
10.1016/j.molcel.2011.01.014
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Gene expression mediated by viral vectors is subject to cell-to-cell variability, which limits the accuracy of gene delivery. When coupled with single-cell measurements, however, such variability provides an efficient means to quantify signaling dynamics in mammalian cells. Here, we illustrate the utility of this approach by mapping the E2f1 response to MYC, serum stimulation, or both. Our results revealed an underappreciated mode of gene regulation: E2f1 expression first increased, then decreased as MYC input increased. This biphasic pattern was also reflected in other nodes of the network, including the miR-17-92 microRNA cluster and p19Arf. A mathematical model of the network successfully predicted modulation of the biphasic E2F response by serum and a CDK inhibitor. In addition to demonstrating how noise can be exploited to probe signaling dynamics, our results reveal how coordination of the MYC/RB/E2F pathway enables dynamic discrimination of aberrant and normal levels of growth stimulation.
引用
收藏
页码:275 / 285
页数:11
相关论文
共 74 条
[1]   Complex transcriptional regulatory mechanisms control expression of the E2F3 locus [J].
Adams, MR ;
Sears, R ;
Nuckolls, F ;
Leone, G ;
Nevins, JR .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (10) :3633-3639
[2]   THE C-MYC PROTEIN INDUCES CELL-CYCLE PROGRESSION AND APOPTOSIS THROUGH DIMERIZATION WITH MAX [J].
AMATI, B ;
LITTLEWOOD, TD ;
EVAN, GI ;
LAND, H .
EMBO JOURNAL, 1993, 12 (13) :5083-5087
[3]   ONCOGENIC ACTIVITY OF THE C-MYC PROTEIN REQUIRES DIMERIZATION WITH MAX [J].
AMATI, B ;
BROOKS, MW ;
LEVY, N ;
LITTLEWOOD, TD ;
EVAN, GI ;
LAND, H .
CELL, 1993, 72 (02) :233-245
[4]   TRANSCRIPTIONAL ACTIVATION BY THE HUMAN C-MYC ONCOPROTEIN IN YEAST REQUIRES INTERACTION WITH MAX [J].
AMATI, B ;
DALTON, S ;
BROOKS, MW ;
LITTLEWOOD, TD ;
EVAN, GI ;
LAND, H .
NATURE, 1992, 359 (6394) :423-426
[5]   c-Myc associates with ribosomal DNA and activates RNA polymerase I transcription [J].
Arabi, A ;
Wu, SQ ;
Ridderstråle, K ;
Bierhoff, H ;
Shiue, C ;
Fatyol, K ;
Fahlén, S ;
Hydbring, P ;
Söderberg, O ;
Grummt, I ;
Larsson, LG ;
Wright, APH .
NATURE CELL BIOLOGY, 2005, 7 (03) :303-310
[6]   p14ARF links the tumour suppressors RB and p53 [J].
Bates, S ;
Phillips, AC ;
Clark, PA ;
Stott, F ;
Peters, G ;
Ludwig, RL ;
Vousden, KH .
NATURE, 1998, 395 (6698) :124-125
[7]   Myc-mediated proliferation and lymphomagenesis, but not apoptosis, are compromised by E2F1 loss [J].
Baudino, TA ;
Maclean, KH ;
Brennan, J ;
Parganas, E ;
Yang, CY ;
Aslanian, A ;
Lees, JA ;
Sherr, CJ ;
Roussel, MF ;
Cleveland, JL .
MOLECULAR CELL, 2003, 11 (04) :905-914
[8]  
Bièche I, 1999, CANCER RES, V59, P2759
[9]   Putting tumours in context [J].
Bissell, MJ ;
Radisky, D .
NATURE REVIEWS CANCER, 2001, 1 (01) :46-54
[10]   MAX - A HELIX-LOOP-HELIX ZIPPER PROTEIN THAT FORMS A SEQUENCE-SPECIFIC DNA-BINDING COMPLEX WITH MYC [J].
BLACKWOOD, EM ;
EISENMAN, RN .
SCIENCE, 1991, 251 (4998) :1211-1217