AH RECEPTOR IN NONMAMMALIAN MODELS
AH RECEPTOR IN NONMAMMALIAN MODELS
批准号:
2907732
负责人:
Mark E Hahn
金额:
$19.41万
依托单位国家:
美国
项目类别:
财政年份:
1992
资助国家:
美国
项目状态:
已结题
起止时间:
1992-12-10 至 2002-08-31
关键词:
affinity labeling aromatic hydrocarbon receptor biochemical evolution biological signal transduction carbopolycyclic compound complementary DNA dioxins environmental toxicology gene expression genetic mapping genetic promoter element genetic transcription human tissue ligands medaka molecular cloning nucleic acid sequence protein sequence protein structure function receptor expression reporter genes species difference toxicant interaction transcription factor trout /salmon zebrafish
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION: (Adapted from the Investigator's Abstract) The aryl hydrocarbon
receptor (AHR) is a ligand-activated transcription factor through which
halogenated aromatic hydrocarbons, such as 2,3,7,8-tetrachlorodibenzo-p-dioxin
(TCDD), cause altered gene expression and toxicity. The AHR belongs to the
basic-helix-loop-helix/Per-ARNT-Sim (bHLH-PAS) family of transcriptional
regulatory proteins, whose members play key roles in development, circadian
rhythmicity, and environmental homeostasis. However, the normal cellular
function of the AHR is not yet known, despite extensive studies of the AHR in
mammals, including AHR-null mice.
Fish and non-mammalian vertebrates are being used increasingly as model systems
in toxicology and carcinogenesis research, in developmental biology, and as
sentinels of environmental quality. Proper interpretation of results obtained
in such models requires an understanding of the similarities and differences in
molecular mechanisms between humans and fish. In the preceding grant period, we
identified an AHR homolog (AHR1) as well as a novel AHR-related gene (AHR2) in
bony and cartilaginous fish. Fish AHR1 and AHR2 both exhibit specific,
high-affinity binding to [3H]TCDD. Phylogenetic analyses show that an AHR gene
duplication occurred early in vertebrate evolution, suggesting that two AHR
genes could exist in other vertebrates, including humans (PNAS (1997)
94:13743). To fully understand TCDD effects in humans, it is critical to
establish whether humans possess a second AHR and, if so, whether it functions
as a ligand-activated transcription factor like AHR1. If an AHR2 is not present
in humans, it is important to determine the functional relationships between
fish AHR1/AHRs and the human AHR in order to assess the value of fish as models
in environmental health research.
The overall objectives of the proposed research is to assess the similarities
and differences in components and mechanisms of AHR-dependent signal
transduction between humans and fish used as models in toxicology. We will
determine the diversity and function of AHR genes in fish species commonly used
as aquatic models, test the hypothesis that a second AHR-like gene exists in
humans, and compare the function of fish and human AHRs.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Understanding the origins and mechanisms of aryl hydrocarbon receptor promiscuity
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批准号:10679532
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项目类别:
-
资助金额:$51.1万
-
财政年份:2023
-
负责人:Mark E Hahn
-
依托单位:
Mechanisms Controlling Sensitivity and Resistance to Dioxin-like Compounds: Role of AIP
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批准号:10538943
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项目类别:
-
资助金额:$183.94万
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财政年份:2022
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负责人:Mark E Hahn
-
依托单位:
Gene-by-environment interactions that affect exposure-mediated congenital heart disease
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批准号:10216463
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项目类别:
-
资助金额:$64.43万
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财政年份:2021
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负责人:Mark E Hahn
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依托单位:
Gene-by-environment interactions that affect exposure-mediated congenital heart disease
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批准号:10655611
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项目类别:
-
资助金额:$62.37万
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财政年份:2021
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负责人:Mark E Hahn
-
依托单位:
Project 3: Cellular and Molecular Mechanisms Underlying Long-term Effects of Early Life Exposure to HAB Toxins
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批准号:10434783
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项目类别:
-
资助金额:$14.47万
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财政年份:2018
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负责人:Mark E Hahn
-
依托单位:
Project 3: Cellular and Molecular Mechanisms Underlying Long-term Effects of Early Life Exposure to HAB Toxins
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批准号:10223309
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项目类别:
-
资助金额:$14.15万
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财政年份:2018
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负责人:Mark E Hahn
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依托单位:
microRNAs in Developmental Toxicology
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批准号:7642973
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项目类别:
-
资助金额:$17.06万
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财政年份:2009
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负责人:Mark E Hahn
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依托单位:
Mechanisms of Embryo Response to Oxidative Stress
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批准号:8244524
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项目类别:
-
资助金额:$37.08万
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财政年份:2009
-
负责人:Mark E Hahn
-
依托单位:
Mechanisms of Embryo Response to Oxidative Stress
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批准号:8051862
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项目类别:
-
资助金额:$38.07万
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财政年份:2009
-
负责人:Mark E Hahn
-
依托单位:
Mechanisms of Embryo Response to Oxidative Stress
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批准号:8450175
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项目类别:
-
资助金额:$36.92万
-
财政年份:2009
-
负责人:Mark E Hahn
-
依托单位:
Mechanisms of Embryo Response to Oxidative Stress
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批准号:7655110
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项目类别:
-
资助金额:$37.62万
-
财政年份:2009
-
负责人:Mark E Hahn
-
依托单位:
microRNAs in Developmental Toxicology
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批准号:7894697
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项目类别:
-
资助金额:$17.27万
-
财政年份:2009
-
负责人:Mark E Hahn
-
依托单位:
AH RECEPTOR IN NONMAMMALIAN SPECIES
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批准号:2155134
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项目类别:
-
资助金额:$10.67万
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财政年份:1992
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负责人:Mark E Hahn
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依托单位:
AHR Signaling in Mammalian and Non-Mammalian Models
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批准号:8588318
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项目类别:
-
资助金额:$38.22万
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财政年份:1992
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负责人:Mark E Hahn
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依托单位:
AHR signaling in Mammalian and Non-Mammalian Models
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批准号:6761716
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项目类别:
-
资助金额:$33.94万
-
财政年份:1992
-
负责人:Mark E Hahn
-
依托单位:
AH RECEPTOR IN NON-MAMMALIAN SPECIES
-
批准号:3465419
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项目类别:
-
资助金额:$11.95万
-
财政年份:1992
-
负责人:Mark E Hahn
-
依托单位:
AH RECEPTOR IN NON-MAMMALIAN MODELS
-
批准号:6178332
-
项目类别:
-
资助金额:$23.75万
-
财政年份:1992
-
负责人:Mark E Hahn
-
依托单位:
AHR signaling in Mammalian and Non-Mammalian Models
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批准号:6892101
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项目类别:
-
资助金额:$34.63万
-
财政年份:1992
-
负责人:Mark E Hahn
-
依托单位:
AHR signaling in Mammalian and Non-Mammalian Models
-
批准号:7226219
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项目类别:
-
资助金额:$34.07万
-
财政年份:1992
-
负责人:Mark E Hahn
-
依托单位:
AH RECEPTOR IN NON-MAMMALIAN MODELS
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批准号:6382151
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项目类别:
-
资助金额:$21.2万
-
财政年份:1992
-
负责人:Mark E Hahn
-
依托单位:
海外基金