A Mouse Model of Acrodermatitis Enteropathica
A Mouse Model of Acrodermatitis Enteropathica
批准号:
6596481
负责人:
GLEN K ANDREWS
金额:
$28.47万
依托单位国家:
美国
项目类别:
财政年份:
2003
资助国家:
美国
项目状态:
已结题
起止时间:
2003-04-01 至 2008-01-31
关键词:
acrodermatitis enteropathica cell membrane complementary DNA confocal scanning microscopy dietary trace element disease /disorder model gastrointestinal absorption /transport gene expression gene mutation gene targeting genetically modified animals green fluorescent proteins laboratory mouse messenger RNA metal metabolism northern blottings nutrition nutrition related tag polymerase chain reaction tissue /cell culture western blottings zinc
中文摘要
描述(由申请人提供):我们研究的总体长期目标是阐明哺乳动物体内锌稳态的分子机制。在此,我们建议研究罕见的常染色体隐性性状,肠病性肢端皮炎(AE)。AE的结果是无法吸收大量的膳食锌,并且在人类AE患者中发现了一个突变的候选基因。该基因编码金属转运蛋白ZIP基因超家族的一个成员,并被命名为hZIP4。我们将使用小鼠模型来验证这种假定的锌转运体在锌稳态中起核心生理作用的假设。目前还没有AE的小鼠模型,ZIP4的调控和功能也基本上一无所知。在初步研究中,我们克隆了小鼠ZIP4基因和cDNA,确定其在肠道中高表达,并证明mZIP4 mRNA在饮食缺锌期间显著上调。因此,本文的具体目的是:1)描述mZIP4原生突变体和AE突变体的金属转运特性;2)阐明金属调控mZIP4表达的机制;3)确定mZIP4基因靶向突变对小鼠锌稳态的影响。这个项目代表了博士实验室之间的合作努力。安德鲁斯,艾德和彼得森。作为私家侦探,安德鲁斯博士是哺乳动物胚胎发育和锌缺乏症方面的专家,也是基因表达的金属调控方面的专家。共同。他是ZIP转运蛋白功能和调控领域的专家和领导者。Peterson博士是珠蛋白基因座调控和小鼠基因敲除策略方面的专家。
英文摘要
DESCRIPTION (provided by applicant): The overall long-term objective of our studies is to elucidate the molecular mechanisms involved in zinc homeostasis in mammals. Herein, we propose to study the rare, autosomal recessive trait, acrodermatitis enteropathic (AE). AE results for the inability to absorb significant dietary zinc, and a candidate gene mutated in human patients with AE was just identified. This gene encodes a member of the ZIP gene superfamily of metal transporters and was named hZIP4. We will test the hypothesis that this putative zinc transporter plays a central physiological role in zinc homeostasis using the mouse model. No mouse models for AE exist and essentially nothing is known about the regulation and functions of ZIP4. In preliminary studies, we have cloned the mouse ZIP4 gene and cDNA, determined that it is highly expressed in the intestinal tract, and demonstrated that mZIP4 mRNA is dramatically up-regulated during periods of dietary zinc deficiency. Therefore, the specific aims of this proposal are to: 1) Delineate the metal transport properties of native and AE mutants of mZIP4; 2) elucidate the mechanisms of metallo-regulation of mZIP4 expression; and 3) determine the affects of targeted mutation of the mZIP4 gene on zinc homeostasis in the mouse. This project represents a collaborative effort between the laboratories of Drs. Andrews, Eide, and Peterson. The P.I., Dr. Andrews is an expert in mammalian embryonic development and zinc deficiency, and in metalloregulation of gene expression. The Co-I., Dr. Eide is an expert and leader in the field of ZIP transporter function and regulation, and Co-I., Dr. Peterson is an expert in globin locus regulation and mouse knockout strategies.
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A mouse model of acrodermatitis enteropathica
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批准号:7899452
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项目类别:
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资助金额:$10.0万
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财政年份:2009
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批准号:7788831
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资助金额:$30.93万
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批准号:6729892
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资助金额:$31.24万
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资助金额:$31.24万
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资助金额:$26.23万
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资助金额:$26.64万
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资助金额:$28.13万
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财政年份:2002
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依托单位:
Molecular Biology of Mammalian Zinc Homeostasis
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批准号:7070436
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项目类别:
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资助金额:$26.86万
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财政年份:2002
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负责人:GLEN K ANDREWS
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依托单位:
Molecular Biology of Mammalian Zinc Homeostasis
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批准号:6621949
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项目类别:
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资助金额:$23.36万
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财政年份:2002
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负责人:GLEN K ANDREWS
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依托单位:
ACUTE PANCREATITIS--ROLES OF CYTOKINES AND ANTIOXIDANTS
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批准号:2770532
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项目类别:
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资助金额:$16.64万
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财政年份:1995
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负责人:GLEN K ANDREWS
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依托单位:
ACUTE PANCREATITIS--ROLES OF CYTOKINES AND ANTIOXIDANTS
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批准号:2151210
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项目类别:
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资助金额:$17.39万
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财政年份:1995
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负责人:GLEN K ANDREWS
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依托单位:
ACUTE PANCREATITIS--ROLES OF CYTOKINES AND ANTIOXIDANTS
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批准号:2518495
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项目类别:
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资助金额:$16.01万
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财政年份:1995
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负责人:GLEN K ANDREWS
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依托单位:
ACUTE PANCREATITIS--ROLES OF CYTOKINES AND ANTIOXIDANTS
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批准号:2151209
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项目类别:
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资助金额:$16.73万
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财政年份:1995
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依托单位:
海外基金