Effects of the Atrial Natriuretic Factor enhancer and the 5'HS4 insulator on the probability of gene expression.
Effects of the Atrial Natriuretic Factor enhancer and the 5'HS4 insulator on the probability of gene expression.
批准号:
nhmrc : 109003
负责人:
David Martin
金额:
$35.65万
依托单位国家:
澳大利亚
项目类别:
NHMRC Project Grants
财政年份:
2000
资助国家:
澳大利亚
项目状态:
已结题
起止时间:
2000-01-01 至 2002-12-31
中文摘要
复杂的生物体包含许多不同类型的细胞,这些细胞可以具有完全不同的外观和功能。所有这些细胞都含有相同的基因;它们之间的差异是通过选择性地使用基因来实现的。完成基因选择性使用的方法是理解复杂生物体如何发育,以及这种发育如何在癌症、心脏病和其他常见疾病中出错的关键。大量证据表明,基因调控是通过蛋白质因子与基因两侧DNA片段的相互作用来完成的。我们工作的一个基础假设是,侧翼DNA元素的作用主要是增加基因活跃而不是沉默的可能性。我们将询问,当心脏受到压力时,从小鼠心房利钠因子(ANF)基因中去除一个已知的调节元件是否会降低心房利钠因子在心脏细胞中表达的可能性。这项实验还将揭示人类一种极其常见的疾病状态(心脏肥厚)。在第二个实验中,我们将使用我们开发的一个新的实验系统来询问基因调控元件是否能够调节基因的表达量,以及打开基因。我们之前的工作表明情况并非如此,但我们希望进行更严格的测试。另一种假设是,没有DNA元件能够完全保护转移的基因不受周围调控元件的影响。因此,我们将测试一种DNA元件,该元件已被提议将任何基因与周围基因的所有影响隔离开来,并询问它是否能够在基因组的任何位置创建一个自主表达的基因。因为它们处理的是所有基因共有的功能,这些实验将提供适用于操纵基因表达的广泛努力的信息。
英文摘要
Complex organisms contain many different types of cells, which can have completely different appearances and functions. All of these cells contain the same genes; the differences between them are achieved by the selective use of the genes. The means by which the selective use of genes is accomplished is a key to understanding how complex organisms develop, and how that development goes awry in cancer, heart disease, and other common disorders. A very large body of evidence indicates that gene regulation is accomplished by the interaction of protein factors with segments of DNA flanking the gene. One hypothesis underlying our work is that the flanking DNA elements act primarily to increase the probability that a gene will be active rather than silent. We will ask if removing a known regulatory element from the gene for Atrial Natriuretic Factor (ANF) in mice reduces the likelihood of ANF being expressed by heart cells when the heart is stressed. This experiment will also shed new light on an extremely common disease state in humans (cardiac hypertrophy). In a second experiment, we will use a new experimental system we have developed to ask if a gene regulatory element is able to dial up the amount of expression from a gene, as well as to switch the gene on. Our previous work suggested this was not the case, but we wish to conduct a more rigorous test. Another hypothesis is that no DNA element is able to completely shield a transferred gene from the regulatory elements surrounding it. Accordingly, we will test a DNA element that has been proposed to insulate any gene from all influences of surrounding genes, and ask if it is able to create an autonomously expressing gene at any site within the genome. Because they deal with functions that are common to all genes, these experiments will provide information that should be applicable to a broad array of efforts to manipulate gene expression.
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