Click
here to close Hello! We notice that
you are using Internet Explorer, which is not supported by Echinobase
and may cause the site to display incorrectly. We suggest using a
current version of Chrome,
FireFox,
or Safari.
???displayArticle.abstract???
A model was built to examine the kinetics of regulatory cascades such as occur in developmental gene networks. The model relates occupancy of cis-regulatory target sites to transcriptional initiation rate, and thence to RNA and protein output. The model was used to simulate regulatory cascades in which genes encoding transcription factors are successively activated. Using realistic parameter ranges based on extensive earlier measurements in sea urchin embryos, we find that transitions of regulatory states occur sharply in these simulations, with respect to time or changing transcription factor concentrations. As is often observed in developing systems, the simulated regulatory cascades display a succession of gene activations separated by delays of some hours. The most important causes of this behavior are cooperativity in the assembly of cis-regulatory complexes and the high specificity of transcription factors for their target sites. Successive transitions in state occur long in advance of the approach to steady-state levels of the molecules that drive the process. The kinetics of such developmental systems thus depend mainly on the initial output rates of genes activated in response to the advent of new transcription factors.
Ackers,
Quantitative model for gene regulation by lambda phage repressor.
1982, Pubmed
Ackers,
Quantitative model for gene regulation by lambda phage repressor.
1982,
Pubmed
Arenas-Mena,
Spatial expression of Hox cluster genes in the ontogeny of a sea urchin.
2000,
Pubmed
,
Echinobase
Aronson,
Rates of RNA chain growth in developing sea urchin embryos.
1977,
Pubmed
,
Echinobase
Braun,
Combinatorial action of HNF3 and Sp family transcription factors in the activation of the rabbit uteroglobin/CC10 promoter.
1998,
Pubmed
Busby,
Transcription in developing sea urchins: electron microscopic analysis of cleavage, gastrula and prism stages.
1980,
Pubmed
,
Echinobase
Cabrera,
Regulation of cytoplasmic mRNA prevalence in sea urchin embryos. Rates of appearance and turnover for specific sequences.
1984,
Pubmed
,
Echinobase
Calzone,
Gene regulatory factors of the sea urchin embryo. I. Purification by affinity chromatography and cloning of P3A2, a novel DNA-binding protein.
1991,
Pubmed
,
Echinobase
Calzone,
Developmental appearance of factors that bind specifically to cis-regulatory sequences of a gene expressed in the sea urchin embryo.
1988,
Pubmed
,
Echinobase
Coffman,
SpRunt-1, a new member of the runt domain family of transcription factors, is a positive regulator of the aboral ectoderm-specific CyIIIA gene in sea urchin embryos.
1996,
Pubmed
,
Echinobase
Cutting,
Rare maternal mRNAs code for regulatory proteins that control lineage-specific gene expression in the sea urchin embryo.
1990,
Pubmed
,
Echinobase
Davidson,
A provisional regulatory gene network for specification of endomesoderm in the sea urchin embryo.
2002,
Pubmed
,
Echinobase
Davidson,
A genomic regulatory network for development.
2002,
Pubmed
,
Echinobase
Davidson,
Regulatory gene networks and the properties of the developmental process.
2003,
Pubmed
Driever,
The bicoid protein is a positive regulator of hunchback transcription in the early Drosophila embryo.
1989,
Pubmed
Emerson,
Interaction of specific nuclear factors with the nuclease-hypersensitive region of the chicken adult beta-globin gene: nature of the binding domain.
1985,
Pubmed
Garrity,
Interleukin-2 transcription is regulated in vivo at the level of coordinated binding of both constitutive and regulated factors.
1994,
Pubmed
Gregory,
Functional interaction of GATA1 with erythroid Krüppel-like factor and Sp1 at defined erythroid promoters.
1996,
Pubmed
Hernandez-Munain,
Cooperation among multiple transcription factors is required for access to minimal T-cell receptor alpha-enhancer chromatin in vivo.
1998,
Pubmed
Höög,
Gene regulatory factors of the sea urchin embryo. II. Two dissimilar proteins, P3A1 and P3A2, bind to the same target sites that are required for early territorial gene expression.
1991,
Pubmed
,
Echinobase
Ito,
The TRAP/SMCC/Mediator complex and thyroid hormone receptor function.
2001,
Pubmed
Lee,
Modulation of sea urchin actin mRNA prevalence during embryogenesis: nuclear synthesis and decay rate measurements of transcripts from five different genes.
1992,
Pubmed
,
Echinobase
Lin,
The general affinity of lac repressor for E. coli DNA: implications for gene regulation in procaryotes and eucaryotes.
1975,
Pubmed
Malik,
Transcriptional regulation through Mediator-like coactivators in yeast and metazoan cells.
2000,
Pubmed
Mao,
Functional and physical interactions between mammalian achaete-scute homolog 1 and myocyte enhancer factor 2A.
1996,
Pubmed
Martinez,
SpHmx, a sea urchin homeobox gene expressed in embryonic pigment cells.
1997,
Pubmed
,
Echinobase
Miller,
Morphological studies of transcription.
1972,
Pubmed
Sigvardsson,
Early B-cell factor, E2A, and Pax-5 cooperate to activate the early B cell-specific mb-1 promoter.
2002,
Pubmed
Sugawara,
Cooperativity between the J and S elements of class II major histocompatibility complex genes as enhancers in normal and class II-negative patient and mutant B cell lines.
1995,
Pubmed
Thanos,
Virus induction of human IFN beta gene expression requires the assembly of an enhanceosome.
1995,
Pubmed
Wang,
SpZ12-1, a negative regulator required for spatial control of the territory-specific CyIIIa gene in the sea urchin embryo.
1995,
Pubmed
,
Echinobase
Yuh,
Cis-regulatory logic in the endo16 gene: switching from a specification to a differentiation mode of control.
2001,
Pubmed
,
Echinobase
Yuh,
Genomic cis-regulatory logic: experimental and computational analysis of a sea urchin gene.
1998,
Pubmed
,
Echinobase
Zeller,
Developmental utilization of SpP3A1 and SpP3A2: two proteins which recognize the same DNA target site in several sea urchin gene regulatory regions.
1995,
Pubmed
,
Echinobase