A mouse model of acrodermatitis enteropathica

肠病性肢端皮炎小鼠模型

• 批准号: 7788831
• 负责人: GLEN K ANDREWS
• 金额: $ 30.93万
• 依托单位: UNIVERSITY OF KANSAS MEDICAL CENTER
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-04-01 至 2013-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7788831
• 关键词: 3' Untranslated Regions; A Mouse; Acinar Cell; Address; Affect; Alleles; Animals; Biochemical; Birth; Blood; Cells; Congenital Abnormality; Conserved Sequence; Data; Development; Diet; Dietary Zinc; Disease; Embryonic Development; Endoderm Cell; Enterocytes; Etiology; Excision; Extracellular Domain; Funding; Gene Expression Regulation; Gene Mutation; Genes; Genetic; Hereditary Disease; Homeostasis; Human; Human Genetics; Hypersensitivity; Intestines; Investigation; Ions; Knock-out; Knockout Mice; Mammals; Maps; Membrane; Messenger RNA; Metals; Molecular; Mus; Mutate; Mutation; N-terminal; Pancreas; Patients; Phenotype; Physiological; Play; Process; Proteins; Publishing; Regulation; Relative (related person); Research; Role; Site; Structure; Testing; Tissues; Visceral; Zinc; Zinc deficiency; acrodermatitis enteropathica; autosomal recessive trait; base; body system; cell type; gene function; in vivo; insight; mRNA Expression; member; mouse model; novel; public health relevance; response; solute; stem; uptake; zinc-binding protein

DESCRIPTION (provided by applicant): The overall long-term objective of our studies is to elucidate the molecular mechanisms involved in zinc homeostasis in mammals. Specifically, we have been studying the Zip4 gene, mutations in which cause the rare, autosomal recessive trait acrodermatitis enteropathica (AE), in humans. ZIP4 is a member of the solute carrier 39a superfamily of metal transporters, and we find that ZIP5 is a close relative. In this competing continuation, we propose to test the hypothesis that ZIP4 and ZIP5 both play central physiological roles in zinc homeostasis with ZIP4 being the major mechanism for uptake of limiting dietary zinc while ZIP5 plays a major role in the removal of zinc under zinc-replete conditions. The hypothesis that these proteins have opposing functions is based on our finding that they localize to opposite membranes of polarized intestinal enterocytes and visceral endoderm cells, cell-types critical for proper zinc homeostasis, and they show opposite responses to zinc availability in these cells. In the initial funding period we discovered that mouse Zip4 mRNA expression and ZIP4 and ZIP5 proteins are dynamically regulated by several novel posttranscriptional and opposing zinc-dependent mechanisms. We also discovered that the mouse Zip4 gene is essential for early embryonic development and that haploinsufficiency exerts pleiotropic effects on the development of several organ systems and causes hypersensitivity to dietary zinc deficiency. Thus, Zip4 is a critically important gene that warrants further investigation. There are no genetic data on ZIP5 function but its zinc-dependent regulation opposite to that of ZIP4 suggests that it may be very important. To further address the functions and mechanisms of regulation of these zinc transporters we will pursue the following specific aims: 1) Determine the effects of tissue-specific conditional knockouts of the Zip4 and/or Zip5 genes on zinc homeostasis in the mouse, and 2) Explore the zinc-dependent mechanisms of posttranscriptional zinc-regulation of ZIP4 and ZIP5. These studies will contribute to our understanding of the lethal human genetic disorder acrodermatitis enteropathica and provide important insights into the etiology of several birth defects, as well as contribute to our basic understanding of the molecular mechanisms governing mammalian zinc homeostasis. PUBLIC HEALTH RELEVANCE: These studies will contribute to our understanding of the lethal human genetic disorder called acrodermatitis enteropathica (AE). Understanding the molecular mechanisms that underlie this disease will also provide important insights into the etiology of several birth defects that we discovered to be associated with mutations of the AE gene in mice. In a global sense, these studies will contribute to our basic understanding of the molecular mechanisms governing the homeostasis of the essential metal zinc in mammals.

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锌稳态的分子机制。具体来说，我们一直在研究Zip 4基因，该基因突变导致人类罕见的常染色体隐性遗传性肠病性肢端皮炎（AE）。ZIP 4是溶质载体39 a金属转运蛋白超家族的成员，我们发现ZIP 5是一个近亲。在这种竞争的延续，我们建议测试的假设，ZIP 4和ZIP 5都发挥中央生理作用，锌稳态与ZIP 4是主要的机制，限制饮食锌的摄取，而ZIP 5起着重要作用，在锌的去除条件下，充满锌。这些蛋白质具有相反功能的假设是基于我们的发现，即它们定位于极化的肠上皮细胞和内脏内胚层细胞的相反膜，这些细胞类型对适当的锌稳态至关重要，并且它们对这些细胞中的锌可用性表现出相反的反应。在最初的资助期间，我们发现小鼠Zip 4 mRNA表达以及ZIP 4和ZIP 5蛋白质受到几种新的转录后和相反的锌依赖机制的动态调节。我们还发现小鼠Zip 4基因对早期胚胎发育是必不可少的，单倍不足对几个器官系统的发育产生多效性作用，并导致对膳食锌缺乏的超敏反应。因此，Zip 4是一个非常重要的基因，值得进一步研究。目前还没有关于ZIP 5功能的遗传数据，但其与ZIP 4相反的锌依赖性调节表明它可能非常重要。为了进一步阐明这些锌转运蛋白的功能和调控机制，我们将追求以下具体目标：1）确定组织特异性条件性敲除Zip 4和/或Zip 5基因对小鼠锌稳态的影响，和2）探索ZIP 4和ZIP 5转录后锌调控的锌依赖性机制。这些研究将有助于我们了解致命的人类遗传性疾病肠病性肢端皮炎，并提供了重要的见解，几个出生缺陷的病因，以及有助于我们的基本了解哺乳动物锌稳态的分子机制。公共卫生相关性：这些研究将有助于我们了解致命的人类遗传性疾病称为肢端皮炎肠病（AE）。了解这种疾病的分子机制也将提供重要的见解，我们发现与小鼠AE基因突变相关的几种出生缺陷的病因。从整体意义上讲，这些研究将有助于我们对哺乳动物体内必需金属锌稳态的分子机制的基本理解。