Toward defining the transcriptional ecosystem
定义转录生态系统
基本信息
- 批准号:RGPIN-2019-06490
- 负责人:
- 金额:$ 3.06万
- 依托单位:
- 依托单位国家:加拿大
- 项目类别:Discovery Grants Program - Individual
- 财政年份:2020
- 资助国家:加拿大
- 起止时间:2020-01-01 至 2021-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Rationale. Following environmental perturbations, cells must quickly react to ensure a proper gene response. Gene responses depend on transcription factor recruiting the transcription machinery and coregulators to regulatory regions. In the nucleus, the genome architecture creates proximity between regulatory regions of multiple genes forming local microenvironments. Recent evidence suggests that transcription coregulators are highly mobile within these enclosed microenvironments. This is conceptually reminiscent of ecosystems found in nature where multiple populations create dynamic interplays to share resources and maintain homeostasis. Whether or not a pool of transcription coregulators is assigned and traded between groups of connected genes is an open question.
Objectives. The long-term goal of our research program is to demonstrate the existence of transcriptional ecosystem equilibriums between genes sharing the same physical environment. During the first 5 years, our goal will be to establish that transcription coregulators are mobile entities within a group of genes. Our central hypothesis is that transcription coregulators are traded between genes to sustain the response to environmental perturbations. To test our model, we are proposing two specific objectives:
Objective 1 Determine the response of group of genes to concomitant signals. Competition for resources is an important feature of natural ecosystems. Using environmental perturbations, we will investigate how group of genes react to concomitant signals. This will allow us to determine the presence of competitive and synergistic gene environments.
Objective 2 Establish the range of action of the transcriptional resources. Transcription machinery and coregulators are highly dynamic entities. We will use their mobility to identify connected genes sharing transcriptional resources. To do so, we will target the dCas9 fused to BirA to biotinylate proteins surrounding designated promoters and measure spreading to connected genes.
Expected Outcomes. We will establish a new conceptual framework where genes are part of an ecosystem in which transcription coregulators are limiting and therefore travel from gene to gene. We will determine if competition for transcription machinery and coregulators exist which will be crucial to understand how a cell integrates concomitant signals. We will experimentally confirm the travelling of coregulators between genes. Lastly, we will determine if highly expressed genes are used as a transcriptional resources reservoir to sustain gene responses.
Impact. With these discoveries, we will move our research field from semi-stable transcriptional models to biochemical equilibriums. This will redefine the notion of direct and indirect targets since a gene will not have to be directly occupied by an activated transcription factor to be regulated.
理由。环境扰动后,细胞必须快速做出反应,以确保适当的基因反应。基因反应取决于转录因子将转录机制和共调节子招募到调节区域。在细胞核中,基因组结构在形成局部微环境的多个基因的调控区域之间建立了邻近性。最近的证据表明转录共调节因子在这些封闭的微环境中具有高度的流动性。这在概念上让人想起自然界中发现的生态系统,其中多个种群创造动态相互作用以共享资源和维持体内平衡。转录共调节子库是否在相连基因组之间分配和交易是一个悬而未决的问题。
目标。我们研究计划的长期目标是证明共享相同物理环境的基因之间存在转录生态系统平衡。 在前 5 年中,我们的目标是确定转录辅助调节子是一组基因内的移动实体。我们的中心假设是转录共调节因子在基因之间交换以维持对环境扰动的反应。为了测试我们的模型,我们提出两个具体目标:
目标 1 确定基因组对伴随信号的反应。资源竞争是自然生态系统的一个重要特征。利用环境扰动,我们将研究一组基因如何对伴随信号做出反应。这将使我们能够确定竞争性和协同性基因环境的存在。
目标 2 确定转录资源的作用范围。转录机器和核心调节器是高度动态的实体。我们将利用它们的移动性来识别共享转录资源的连接基因。为此,我们将靶向与 BirA 融合的 dCas9,对指定启动子周围的蛋白质进行生物素化,并测量向连接基因的扩散。
预期结果。我们将建立一个新的概念框架,其中基因是生态系统的一部分,其中转录共调节因子受到限制,因此在基因之间传播。我们将确定是否存在转录机制和共调节子的竞争,这对于理解细胞如何整合伴随信号至关重要。我们将通过实验确认共调节子在基因之间的移动。最后,我们将确定高表达基因是否被用作转录资源库来维持基因反应。
影响。有了这些发现,我们将把我们的研究领域从半稳定转录模型转向生化平衡。这将重新定义直接和间接靶标的概念,因为基因不必直接被激活的转录因子占据才能受到调节。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Bilodeau, Steve其他文献
Cooperation between Cyclin E and p27Kip1 in Pituitary Tumorigenesis
- DOI:
10.1210/me.2010-0091 - 发表时间:
2010-09-01 - 期刊:
- 影响因子:0
- 作者:
Roussel-Gervais, Audrey;Bilodeau, Steve;Drouin, Jacques - 通讯作者:
Drouin, Jacques
Enhancer decommissioning by LSD1 during embryonic stem cell differentiation.
- DOI:
10.1038/nature10805 - 发表时间:
2012-02-01 - 期刊:
- 影响因子:64.8
- 作者:
Whyte, Warren A.;Bilodeau, Steve;Orlando, David A.;Hoke, Heather A.;Frampton, Garrett M.;Foster, Charles T.;Cowley, Shaun M.;Young, Richard A. - 通讯作者:
Young, Richard A.
SetDB1 contributes to repression of genes encoding developmental regulators and maintenance of ES cell state
- DOI:
10.1101/gad.1837309 - 发表时间:
2009-11-01 - 期刊:
- 影响因子:10.5
- 作者:
Bilodeau, Steve;Kagey, Michael H.;Young, Richard A. - 通讯作者:
Young, Richard A.
Distinct Developmental Roles of Cell Cycle Inhibitors p57Kip2 and p27Kip1 Distinguish Pituitary Progenitor Cell Cycle Exit from Cell Cycle Reentry of Differentiated Cells
- DOI:
10.1128/mcb.01885-08 - 发表时间:
2009-04-01 - 期刊:
- 影响因子:5.3
- 作者:
Bilodeau, Steve;Roussel-Gervais, Audrey;Drouin, Jacques - 通讯作者:
Drouin, Jacques
Glucocorticoid stimulation induces regionalized gene responses within topologically associating domains.
- DOI:
10.3389/fgene.2023.1237092 - 发表时间:
2023 - 期刊:
- 影响因子:3.7
- 作者:
Tav, Christophe;Fournier, Eric;Fournier, Michele;Khadangi, Fatemeh;Baguette, Audrey;Cote, Maxime C.;Silveira, Maruhen A. D.;Berube-Simard, Felix-Antoine;Bourque, Guillaume;Droit, Arnaud;Bilodeau, Steve - 通讯作者:
Bilodeau, Steve
Bilodeau, Steve的其他文献
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{{ truncateString('Bilodeau, Steve', 18)}}的其他基金
Toward defining the transcriptional ecosystem
定义转录生态系统
- 批准号:
RGPIN-2019-06490 - 财政年份:2022
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Toward defining the transcriptional ecosystem
定义转录生态系统
- 批准号:
RGPIN-2019-06490 - 财政年份:2021
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Toward defining the transcriptional ecosystem
定义转录生态系统
- 批准号:
RGPIN-2019-06490 - 财政年份:2019
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Development of new technologies to study the connection between chromosome architecture and regulation of the gene expression program
开发新技术来研究染色体结构与基因表达程序调控之间的联系
- 批准号:
436266-2013 - 财政年份:2018
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Development of new technologies to study the connection between chromosome architecture and regulation of the gene expression program
开发新技术来研究染色体结构与基因表达程序调控之间的联系
- 批准号:
436266-2013 - 财政年份:2017
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Development of new technologies to study the connection between chromosome architecture and regulation of the gene expression program
开发新技术来研究染色体结构与基因表达程序调控之间的联系
- 批准号:
436266-2013 - 财政年份:2016
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Development of new technologies to study the connection between chromosome architecture and regulation of the gene expression program
开发新技术来研究染色体结构与基因表达程序调控之间的联系
- 批准号:
436266-2013 - 财政年份:2015
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Development of new technologies to study the connection between chromosome architecture and regulation of the gene expression program
开发新技术来研究染色体结构与基因表达程序调控之间的联系
- 批准号:
436266-2013 - 财政年份:2014
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
Development of new technologies to study the connection between chromosome architecture and regulation of the gene expression program
开发新技术来研究染色体结构与基因表达程序调控之间的联系
- 批准号:
436266-2013 - 财政年份:2013
- 资助金额:
$ 3.06万 - 项目类别:
Discovery Grants Program - Individual
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