ANALYSIS OF THE COX4/COX4AL BIDIRECTIONAL PROMOTER
ANALYSIS OF THE COX4/COX4AL BIDIRECTIONAL PROMOTER
批准号:
6588758
负责人:
NANCY J BACHMAN
金额:
$0.51万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-09-01 至 2003-08-31
关键词:
DNA footprinting HeLa cells Xenopus animal tissue chickens cytochrome oxidase enzyme structure gene expression genetic promoter element genetic regulatory element molecular cloning nucleic acid sequence polymerase chain reaction protein protein interaction protein structure function site directed mutagenesis yeast two hybrid system zebrafish
中文摘要
细胞色素c氧化酶是线粒体内膜的多亚基酶复合物,其将电子从细胞色素c转移到分子氧并以质子梯度保存能量。 细胞色素氧化酶(COX 4)的最大的核编码亚基(亚基IV)的人类基因的表征导致鉴定出一个功能未知的紧密连锁的表达基因。 COX 4相关基因座(COX 4AL)与COX 4以头对头排列连接,因此基因间区域(250-bp)可能起双向启动子的作用。 该项目的第一个目的是通过免疫荧光跟踪24 kDa编码蛋白的亚细胞位置,并通过使用遗传和生物化学方法确定其与其他细胞蛋白的关联,以确定COX 4AL的可能功能。 双向启动子通常编码具有相似或相关功能的蛋白质;因此,将测试COX 4AL与COX 4一样编码线粒体蛋白质的特定假设。 第二个目的是确定COX 4/COX 4AL基因间区域是否作为双向启动子发挥功能。 将使用人细胞中转染的启动子-报告基因构建体的遗传分析来鉴定每个基因表达所必需的启动子元件。 第三,COX 4/COX 4AL基因中的保守启动子元件将用于扫描其他协调控制的哺乳动物基因的启动子,包括其他核编码的细胞色素氧化酶亚基和双向控制基因的启动子,以鉴定调节基因表达的新因子或建立由良好表征的因子使用的新的控制模式。 长期目标是为人类基因组的功能数据库作出贡献的16号染色体区域编码细胞色素氧化酶亚基IV基因。 在理解人类疾病的分子基础方面的未来进展取决于具有人类基因和基因间区域的功能的完整目录,作为通过长时间序列数据的“路线图”。
英文摘要
Cytochrome c oxidase is the multisubunit enzyme complex of the mitochondrial inner membrane which transfers electrons from cytochrome c to molecular oxygen and conserves energy as a proton gradient. Characterization of the human gene for the largest nuclear-encoded subunit (subunit IV) of cytochrome oxidase (COX4) led to the identification of a closely linked expressed gene of unknown function. COX4-associated locus (COX4AL) is linked in a head-to-head arrangement with COX4 and thus the intergenic region (250-bp) likely functions as a bidirectional promoter. The first aim of this project is to determine a possible function of COX4AL by tracking the subcellular location of the 24-kDa encoded protein via immunofluorescence and by determining its association with other cellular proteins using genetic and biochemical approaches. Bidirectional promoters usually encode proteins of similar or related function; thus the specific hypothesis that COX4AL, like COX4, encodes a mitochondrial protein will be tested. A second aim is to ascertain whether the COX4/COX4AL intergenic region functions as a bidirectional promoter. Genetic analysis of transfected promoter-reporter gene constructs in human cells will be used to identify promoter elements essential to the expression of each gene. Third, conserved promoter elements in COX4/COX4AL genes will be used to scan the promoters of other coordinately controlled mammalian genes, including those for other nuclear-encoded cytochrome oxidase subunits and bidirectionally controlled genes, to identify new factors that regulate gene expression or to establish new patterns of control used by well-characterized factors. The long-term objective is to contribute to the functional database of the human genome for a region of chromosome 16 shown to encode the cytochrome oxidase subunit IV gene. Future progress in understanding the molecular bases for human disorders depends on having a complete catalog of the functions of human genes and intergenic regions as a "roadmap" through long stretches of sequence data.
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