ENHANCERS INCREASE THE PROBABILITY BUT NOT THE LEVEL OF GENE-EXPRESSION

被引:244
作者
WALTERS, MC
FIERING, S
EIDEMILLER, J
MAGIS, W
GROUDINE, M
MARTIN, DIK
机构
[1] UNIV WASHINGTON,SCH MED,FRED HUTCHINSON CANC RES CTR,SEATTLE,WA 98104
[2] UNIV WASHINGTON,SCH MED,DEPT PEDIAT,SEATTLE,WA 98104
[3] UNIV WASHINGTON,SCH MED,DEPT RADIAT ONCOL,SEATTLE,WA 98104
关键词
D O I
10.1073/pnas.92.15.7125
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We have studied enhancer function in transient and stable expression assays in mammalian cells by using systems that distinguish expressing from nonexpressing cells. When expression is studied in this way, enhancers are found to increase the probability of a construct being active but not the level of expression per template. In stably integrated constructs, large differences in expression level are observed but these are not related to the presence of an enhancer. Together with earlier studies, these results suggest that enhancers act to affect a binary (on/off) switch in transcriptional activity. Although this idea challenges the widely accepted model of enhancer activity, it is consistent with much, if not all, experimental evidence on this subject. We hypothesize that enhancers act to increase the probability of forming a stably active template. When randomly integrated into the genome, enhancers may affect a metastable state of repression/activity, permitting expression in regions that would not permit activity of an isolated promoter.
引用
收藏
页码:7125 / 7129
页数:5
相关论文
共 30 条
[1]   EXPRESSION OF A BETA-GLOBIN GENE IS ENHANCED BY REMOTE SV40 DNA-SEQUENCES [J].
BANERJI, J ;
RUSCONI, S ;
SCHAFFNER, W .
CELL, 1981, 27 (02) :299-308
[2]   HETEROGENEITY OF SINGLE-CELL CYTOKINE GENE-EXPRESSION IN CLONAL T-CELL POPULATIONS [J].
BUCY, RP ;
PANOSKALTSISMORTARI, A ;
HUANG, GQ ;
LI, JM ;
KARR, L ;
ROSS, M ;
RUSSELL, JH ;
MURPHY, KM ;
WEAVER, CT .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (04) :1251-1262
[3]   A 5' ELEMENT OF THE CHICKEN BETA-GLOBIN DOMAIN SERVES AS AN INSULATOR IN HUMAN ERYTHROID-CELLS AND PROTECTS AGAINST POSITION EFFECT IN DROSOPHILA [J].
CHUNG, JH ;
WHITELEY, M ;
FELSENFELD, G .
CELL, 1993, 74 (03) :505-514
[4]   VARIED INTERACTIONS BETWEEN PROVIRUSES AND ADJACENT HOST CHROMATIN [J].
CONKLIN, KF ;
GROUDINE, M .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (11) :3999-4007
[5]   THE BICOID PROTEIN IS A POSITIVE REGULATOR OF HUNCHBACK TRANSCRIPTION IN THE EARLY DROSOPHILA EMBRYO [J].
DRIEVER, W ;
NUSSLEINVOLHARD, C .
NATURE, 1989, 337 (6203) :138-143
[6]   CONTROL OF GLOBIN GENE-TRANSCRIPTION [J].
EVANS, T ;
FELSENFELD, G ;
REITMAN, M .
ANNUAL REVIEW OF CELL BIOLOGY, 1990, 6 :95-124
[7]   CHROMOSOMAL POSITION EFFECTS DETERMINE TRANSCRIPTIONAL POTENTIAL OF INTEGRATED MAMMARY-TUMOR VIRUS-DNA [J].
FEINSTEIN, SC ;
ROSS, SR ;
YAMAMOTO, KR .
JOURNAL OF MOLECULAR BIOLOGY, 1982, 156 (03) :549-565
[8]   SINGLE CELL ASSAY OF A TRANSCRIPTION FACTOR REVEALS A THRESHOLD IN TRANSCRIPTION ACTIVATED BY SIGNALS EMANATING FROM THE T-CELL ANTIGEN RECEPTOR [J].
FIERING, S ;
NORTHROP, JP ;
NOLAN, GP ;
MATTILA, PS ;
CRABTREE, GR ;
HERZENBERG, LA .
GENES & DEVELOPMENT, 1990, 4 (10) :1823-1834
[9]   IMPROVED FACS-GAL - FLOW CYTOMETRIC ANALYSIS AND SORTING OF VIABLE EUKARYOTIC CELLS EXPRESSING REPORTER GENE CONSTRUCTS [J].
FIERING, SN ;
ROEDERER, M ;
NOLAN, GP ;
MICKLEM, DR ;
PARKS, DR ;
HERZENBERG, LA .
CYTOMETRY, 1991, 12 (04) :291-301
[10]   PROMOTER TRAPS IN EMBRYONIC STEM-CELLS - A GENETIC SCREEN TO IDENTIFY AND MUTATE DEVELOPMENTAL GENES IN MICE [J].
FRIEDRICH, G ;
SORIANO, P .
GENES & DEVELOPMENT, 1991, 5 (09) :1513-1523