Functional Specialization of the Mediator-Associated Kinases CDK8 and CDK19
介导相关激酶 CDK8 和 CDK19 的功能专业化
基本信息
- 批准号:1627615
- 负责人:
- 金额:$ 41.33万
- 依托单位:
- 依托单位国家:美国
- 项目类别:Continuing Grant
- 财政年份:2015
- 资助国家:美国
- 起止时间:2015-09-01 至 2017-02-28
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Intellectual Merit: A major challenge in modern biology is to elucidate the molecular mechanisms employed by cells to regulate expression of thousands of genes in various contexts. Accurate regulation of gene activity is a key element of every major biological process. Specialized protein machineries regulate gene activity by decoding the information carried in DNA to satisfy the ever-changing needs of the cell. One such protein complex, known as Mediator, is recognized as a critical regulator of gene activity from yeast to humans, yet little is known about its mechanism of action. This research project investigates the function of two proteins within the Mediator complex, CDK8 and CDK19. Preliminary results demonstrate that CDK8 and CDK19 regulate the activity of different groups of genes involved in diverse cellular functions. This project aims to define the molecular mechanisms by which CDK8 and CDK19 enable cells to adjust the activity of different gene sets in response to changes in the cellular environment. This research is expected to have a transformative impact on the understanding of Mediator in particular and the evolution of gene expression control mechanisms in general. Given the quasi-universal role of Mediator in the control of gene activity, the discoveries arising from this project will have far reaching implications in the fields of cellular and molecular biology. Moreover, the innovative techniques developed in this project for the study of Mediator in human cells will produce a positive ripple effect in the gene expression field by enabling similar studies of other gene regulators.Broader Impacts: This project is carried out by a teaching-research team that strongly promotes science education and diversity in academia. This collaborative team involves trainees at the undergraduate, graduate and post-doctoral levels who work in an environment displaying gender balance and inclusion of minorities. Both the host institution and the Principal Investigator participate actively in programs that aim to: a) increase the number of minority students earning PhDs, b) provide hands-on research experience to undergraduates, c) prepare undergraduate students to pursue PhDs in the biosciences, and d) increase the representation of women in leadership positions in academia. The success of these endeavors is documented by multiple undergraduate authors in the high impact publications from this laboratory and by the fact that most of the 30+ undergraduates trained in this group have advanced to graduate school, medical school or teaching positions. The Principal Investigator is an active member of the local Hispanic community and a recognized life science educator at the University of Colorado at Boulder, where he is the Instructor of a large undergraduate course and co-Instructor of several graduate courses. Members of this team promote scientific literacy in the public via regular contributions to the popular press and outreach activities at the state and national level.
智力价值:现代生物学的一个主要挑战是阐明细胞在各种情况下调节数千种基因表达的分子机制。基因活性的精确调控是每一个主要生物过程的关键要素。专门的蛋白质机器通过解码DNA中携带的信息来调节基因活动,以满足细胞不断变化的需求。一种这样的蛋白质复合物,被称为中介体,被认为是从酵母到人类的基因活动的关键调节器,但对其作用机制知之甚少。本研究项目研究了中介复合物中CDK8和CDK19两种蛋白的功能。初步结果表明,CDK8和CDK19调节参与不同细胞功能的不同基因群的活性。该项目旨在确定CDK8和CDK19使细胞能够调节不同基因组的活性以响应细胞环境变化的分子机制。这项研究预计将对理解调解人产生变革性的影响,特别是对基因表达控制机制的进化。鉴于中介体在基因活动控制中的准普遍作用,本项目的发现将在细胞和分子生物学领域产生深远的影响。此外,该项目开发的用于人类细胞中介体研究的创新技术将在基因表达领域产生积极的连锁反应,使其他基因调节因子的类似研究成为可能。更广泛的影响:该项目由一个大力促进科学教育和学术界多样性的教研团队开展。这个合作团队包括本科生、研究生和博士后,他们在一个显示性别平衡和包容少数民族的环境中工作。主办机构和首席研究员都积极参与旨在:a)增加少数民族学生获得博士学位的数量,b)为本科生提供实践研究经验,c)准备本科生攻读生物科学博士学位,d)增加女性在学术界领导职位的代表性。这些努力的成功被该实验室的多名本科生作者在高影响力的出版物中记录下来,而且在这个小组中接受培训的30多名本科生中,大多数已经升入研究生院、医学院或担任教职。首席研究员是当地西班牙裔社区的活跃成员,也是科罗拉多大学博尔德分校公认的生命科学教育家,在那里他是一门大型本科课程的讲师,也是几门研究生课程的联合讲师。该小组的成员通过定期向大众媒体投稿和在州和国家一级开展外联活动,促进公众的科学素养。
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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Joaquin Espinosa其他文献
Heritable Variation in Lymphocyte-Related Traits and Risk of Down Syndrome Acute Lymphoblastic Leukemia: A Mendelian Randomization Study
- DOI:
10.1182/blood-2023-188434 - 发表时间:
2023-11-02 - 期刊:
- 影响因子:
- 作者:
Yunqi Li;Melissa A. Richard;Linda Kachuri;Yao Yu;Ching-Ju Ruu Hsu;Tracie C. Rosser;Elizabeth J. Leslie;Meenakshi Devidas;Elizabeth A. Raetz;Mignon L. Loh;Stephen P. Hunger;Neetha Paul Eduthan;Matthew D. Galbraith;Joaquin Espinosa;Jun J. Yang;Stephanie L. Sherman;Chad D. Huff;Karen R. Rabin;Philip J. Lupo;Adam J. de Smith - 通讯作者:
Adam J. de Smith
Joaquin Espinosa的其他文献
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{{ truncateString('Joaquin Espinosa', 18)}}的其他基金
Systematic analysis of context-specific functions of transcriptional CDKs in human cells
人类细胞中转录 CDK 的上下文特定功能的系统分析
- 批准号:
1817582 - 财政年份:2018
- 资助金额:
$ 41.33万 - 项目类别:
Continuing Grant
Functional Specialization of the Mediator-Associated Kinases CDK8 and CDK19
介导相关激酶 CDK8 和 CDK19 的功能专业化
- 批准号:
1243522 - 财政年份:2013
- 资助金额:
$ 41.33万 - 项目类别:
Continuing Grant
Functional Studies of the CDK-module of the Human Mediator Complex
人类介导复合体 CDK 模块的功能研究
- 批准号:
0842974 - 财政年份:2009
- 资助金额:
$ 41.33万 - 项目类别:
Continuing Grant
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