ENVIRONMENT & GLI GENES IN NORMAL DEVELOPMENT & DISEASE
环境
基本信息
- 批准号:6787335
- 负责人:
- 金额:$ 59.04万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2000
- 资助国家:美国
- 起止时间:2000-09-30 至 2006-07-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
Developmental pathways are networks of genes which act coordinately to establish the body plan. Disruptions of these genes, which can be associated with environmental exposures, can result in serious dysmorphogenesis or cancer in both children and adults. An important goal of environmental science ought to be reduction of these poor outcomes. This will require an understanding of the genes affected by specific exposures and the consequence of alterations in these genes or their products which in turn will require a complete biochemical understanding of the pathways critical in development. The ligand Sonic hedgehog, the receptors Patched and Smoothened, and the GLI family of transcription factors represent one such pathway critical to the normal development of many organs due to their regulation functions at the nexus of mesenchymal differentiation. Environmental exposure to jervine or UVA and UCB disrupts the pathway. Although some gene targets of the pathway are not known from work in Drosophila key downstream targets and upstream regulators remain to be elucidated in mammals and the roles of these molecules established in normal development in order to better understand their role in dysmorphogenesis and neoplasia. For example, basal cell carcinoma (BCC) is the most common cancer in man and mutations in Patched or over-expression of GLI are both strongly associated with BCC. Prostatic cancer is a serious problem in the US and our preliminary evidence suggests an association of GLI expression with prostatic cancer in humans. We have established a unique team of co- investigators of GLI expression with pro-static cancer in humans. We have established a unique team of co-investigators at Northwestern University who study the regulation and function of the homologues of the GLI genes in C. elegans, Drosophila, mouse, and human. We have previously worked together to collaborate on studies of these genes and these efforts will be greatly enhanced by the current program project allowing use of data from Drosophila and C. elegans in the design of experiments in mouse, or with human material. We are uniquely suited to establish the regulation of the GLI genes at a transcriptional, post- transcriptional, and functional (protein-protein interactions) level. The long term goals of our work will be to determine pathways of development involving GLI genes and their interactions with environmental exposure, in order to establish mechanisms of interact with downstream targets. These experiments will provide data of great significance to both normal development, birth defects, and cancer. The work will very likely provide important general models of transcription factor activity whose utility will extend to a wide variety of developmental, birth defects, and cancer. The work will very likely provide important general models of transcription factor activity whose utility will extend to a wide variety of developmental and cancer problems. Clearly understanding the pathways and the biochemical mechanism of action of developmental genes will be necessary in order to determine the role of environmental exposures on human health.
发育途径是由基因组成的网络,它们协调行动以建立身体计划。这些基因的中断可能与环境暴露有关,可能会导致严重的畸形发育或儿童和成人的癌症。环境科学的一个重要目标应该是减少这些糟糕的结果。这将需要了解受特定暴露影响的基因以及这些基因或其产物改变的后果,这反过来又需要对发育中至关重要的途径有一个完整的生化理解。配体Sonic Hedgehog、受体补丁和平滑以及GLI转录因子家族是对许多器官的正常发育至关重要的途径之一,因为它们在间充质分化的神经节上具有调节功能。环境暴露于球茎或UVA和UCB会扰乱这一途径。虽然该途径的一些基因靶点在果蝇中还不清楚,但在哺乳动物中关键的下游靶点和上游调节因子仍有待阐明,以及这些分子在正常发育中的作用,以便更好地了解它们在畸形发生和肿瘤发生中的作用。例如,基底细胞癌(BCC)是人类最常见的癌症,GLI的补丁或过度表达突变都与BCC密切相关。前列腺癌在美国是一个严重的问题,我们的初步证据表明,GLI的表达与人类前列腺癌有关。我们已经建立了一个独特的团队,共同研究GLI在人类前列腺癌中的表达。我们已经在西北大学建立了一个独特的合作研究团队,他们研究线虫、果蝇、小鼠和人类中GLI基因同源基因的调节和功能。我们之前曾在这些基因的研究上进行过合作,目前的计划项目将极大地加强这些努力,该计划允许在老鼠或人类材料的实验设计中使用来自果蝇和线虫的数据。我们特别适合在转录、转录后和功能(蛋白质-蛋白质相互作用)水平上建立GLI基因的调控。我们工作的长期目标将是确定涉及GLI基因的发育途径及其与环境暴露的相互作用,以便建立与下游靶标相互作用的机制。这些实验将为正常发育、出生缺陷和癌症提供具有重要意义的数据。这项工作很有可能提供转录因子活性的重要通用模型,其用途将扩展到各种发育、出生缺陷和癌症。这项工作很有可能提供转录因子活性的重要通用模型,其用途将扩展到各种发育和癌症问题。为了确定环境暴露对人类健康的作用,必须清楚地了解发育基因的作用途径和生化作用机制。
项目成果
期刊论文数量(6)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
CRISPR editing of the GLI1 first intron abrogates GLI1 expression and differentially alters lineage commitment.
- DOI:10.1002/stem.3341
- 发表时间:2021-05
- 期刊:
- 影响因子:0
- 作者:Galat Y;Gu H;Perepitchka M;Taylor R;Yoon JW;Glukhova XA;Li XN;Beletsky IP;Walterhouse DO;Galat V;Iannaccone PM
- 通讯作者:Iannaccone PM
p53 modulates the activity of the GLI1 oncogene through interactions with the shared coactivator TAF9.
- DOI:10.1016/j.dnarep.2015.06.006
- 发表时间:2015-10
- 期刊:
- 影响因子:3.8
- 作者:Yoon JW;Lamm M;Iannaccone S;Higashiyama N;Leong KF;Iannaccone P;Walterhouse D
- 通讯作者:Walterhouse D
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Philip M Iannaccone其他文献
GLI1 genotypes do not predict basal cell carcinoma risk: a case control study
- DOI:
10.1186/1476-4598-8-113 - 发表时间:
2009-11-30 - 期刊:
- 影响因子:33.900
- 作者:
Andrea Watson;Paul Kent;Murad Alam;Amy S Paller;David M Umbach;Joon Won Yoon;Philip M Iannaccone;David O Walterhouse - 通讯作者:
David O Walterhouse
Multiple Embryo Phenotype Associated with Nodal/Short earlethal Double Mutant Mice • 285
- DOI:
10.1203/00006450-199704001-00305 - 发表时间:
1997-04-01 - 期刊:
- 影响因子:3.100
- 作者:
Kristina C Pfendler;Michael R Kuehn;Philip M Iannaccone - 通讯作者:
Philip M Iannaccone
THE HUMAN ONCODEVELOPMENTAL PROTEIN GLI INTERACTS WITH GLI AND WITH CREB-BINDING PROTEIN. † 306
- DOI:
10.1203/00006450-199704001-00326 - 发表时间:
1997-04-01 - 期刊:
- 影响因子:3.100
- 作者:
Joon Won Yoon;Philip M Iannaccone;David O Walterhouse - 通讯作者:
David O Walterhouse
Philip M Iannaccone的其他文献
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{{ truncateString('Philip M Iannaccone', 18)}}的其他基金
EB 2019 Symposium: The Environment and Gene Expression, Role of the Epigenome
EB 2019 研讨会:环境与基因表达、表观基因组的作用
- 批准号:
9763048 - 财政年份:2019
- 资助金额:
$ 59.04万 - 项目类别:
Integrating cell sorting and tissue shaping mechanisms during cornea maturation
角膜成熟过程中整合细胞分选和组织塑造机制
- 批准号:
7979662 - 财政年份:2010
- 资助金额:
$ 59.04万 - 项目类别:
RAT RESOURCE AND RESEARCH CENTER: CLONING TECHNOLOGY
大鼠资源与研究中心:克隆技术
- 批准号:
7391988 - 财政年份:2006
- 资助金额:
$ 59.04万 - 项目类别:
RAT RESOURCE AND RESEARCH CENTER: CLONING TECHNOLOGY
大鼠资源与研究中心:克隆技术
- 批准号:
7153957 - 财政年份:2005
- 资助金额:
$ 59.04万 - 项目类别:
RAT RESOURCE AND RESEARCH CENTER: CLONING TECHNOLOGY
大鼠资源与研究中心:克隆技术
- 批准号:
6982672 - 财政年份:2004
- 资助金额:
$ 59.04万 - 项目类别:
ANIMAL MODELS BASED ON NUCLEAR TRANSFER IN THE RAT
基于大鼠核转移的动物模型
- 批准号:
6017410 - 财政年份:1998
- 资助金额:
$ 59.04万 - 项目类别:
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