ATHEROSCLEROSIS AND APOLIPOPROTEIN A-I REGULATION
动脉粥样硬化和载脂蛋白 A-I 调节
基本信息
- 批准号:3472493
- 负责人:
- 金额:$ 7.39万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1988
- 资助国家:美国
- 起止时间:1988-12-01 至 1993-11-30
- 项目状态:已结题
- 来源:
- 关键词:Cercopithecidae Macaca apolipoproteins atherosclerosis cardiovascular disorder epidemiology disease /disorder model genetic markers genetic regulatory element genetic transcription high density lipoproteins hypercholesterolemia liver messenger RNA molecular pathology restriction mapping small intestines species difference tissue /cell culture transcription factor
项目摘要
The incidence of premature coronary atherosclerosis in the human
population. Highly correlated to decreased concentrations of high
density lipoprotein or its major apolipoprotein A-I, this condition
is referred to as hypoalphalipoproteinemia. The goal of the
studies proposed in this application are to elucidate the molecular
mechanisms which are responsible for regulating the production of
high density lipoproteins at the level of apo-A-I gene expression.
In order to clearly define differences based on apo A-I gene
expression and to relate these differences to variation in apo A-
I production, a recently described model system will be used. It
is well established that the African green monkey develops a less
severe hypercholesterolemia and atherosclerosis than the cynomolgus
monkey when fed levels of cholesterol and fat resembling the North
American diet. An important feature of this difference is that
African green monkeys have a substantially higher (3 fold) level
of plasma HDL and apo A-I concentration than cynomolgus monkeys,
factors which may contribute to their greater ability to resist the
development of atherosclerosis. Furthermore, apo A-I mRNA
abundance in both the liver and small intestine have been found to
correlate with the level of hepatic apo A-I production and apo A-
I plasma concentration for both the African green and cynomolgus
monkey. The studies proposed in this application, therefore, will
seek to determine if this species-specific difference in the levels
of tissue apo A-I mRNA reflect differences in the regulation and
expression of the primate apo A-I gene. To do this, the apo A-I
gene will be isolated and sequenced from both African green and
cynomolgus monkeys. The degree of sequence homology between the
two species will be compared, as well as to the human apo A-I gene
sequence. Relative rates of apo A-I transcription will be measured
and, the apo A-I mRNA steady state abundance measurements will be
correlated to the rates of apo A-I gene transcription for liver and
small intestine in both species. 5'flanking sequences of the apo
A-I gene for both the African green and cynomolgus monkey will be
analyzed by deletion mapping analysis to identify regulatory
elements which responsible for species-specific expression of the
primate apo A-I gene. The entire apo A-I gene cluster will be
investigated in both primate species to determine whether apo A-I,
apo C-III and apo A-VI exists as a multi-gene family. The
knowledge gained by the completion of these studies will be used
to develop strategies for the treatment of hypoalphalipoproteinemia
and coronary heart disease.
人早发冠状动脉粥样硬化的发病率
人口 与高浓度
密度脂蛋白或其主要载脂蛋白A-I,这种情况
称为低脂蛋白血症。 的目标
在本申请中提出的研究是为了阐明
负责调节生产的机制
高密度脂蛋白在apo-A-I基因表达水平。
为了明确定义基于载脂蛋白A-I基因的差异,
表达,并将这些差异与载脂蛋白A的变化联系起来。
在生产中,将使用最近描述的模型系统。 它
非洲绿色猴的发育速度
严重的高胆固醇血症和动脉粥样硬化比食蟹猴
猴子当喂养的胆固醇和脂肪水平类似北方
美国饮食 这种差异的一个重要特征是,
非洲绿色猴的水平高得多(3倍)
血浆HDL和apo A-I浓度的显著性差异,
这些因素可能有助于他们更大的抵抗能力,
动脉粥样硬化的发展。 此外,载脂蛋白A-I mRNA
在肝脏和小肠中的丰度被发现,
与肝脏载脂蛋白A-I产生水平和载脂蛋白A-
非洲绿色和食蟹猴的I血浆浓度
猴子. 因此,本申请中提出的研究将
试图确定这种物种特异性的水平差异
组织载脂蛋白A-I mRNA的表达反映了调节的差异,
灵长类动物载脂蛋白A-I基因的表达。 为此,载脂蛋白A-I
将从非洲绿色和
食蟹猴 序列之间的同源性程度
两个物种将进行比较,以及人类载脂蛋白A-I基因
顺序 将测量载脂蛋白A-I转录的相对速率
并且,载脂蛋白A-I mRNA稳态丰度测量将是
与肝脏载脂蛋白A-I基因转录速率相关,
两个物种的小肠。 载脂蛋白5 '侧翼序列
非洲绿色猴和食蟹猴的A-I基因将被
通过缺失作图分析进行分析,以鉴定调控基因。
元件负责物种特异性表达的
灵长类载脂蛋白A-I基因。 整个载脂蛋白A-I基因簇
在两种灵长类动物中进行研究以确定载脂蛋白A-I,
apo C-III和apo A-VI作为多基因家族存在。 的
将使用完成这些研究获得的知识
制定治疗低脂蛋白血症的策略,
和冠心病。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Mary G Sorci-Thomas其他文献
Mary G Sorci-Thomas的其他文献
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{{ truncateString('Mary G Sorci-Thomas', 18)}}的其他基金
Role of Pcpe2 in Adipose Tissue Remodeling and Lipoprotein Metabolism
Pcpe2 在脂肪组织重塑和脂蛋白代谢中的作用
- 批准号:
10837655 - 财政年份:2023
- 资助金额:
$ 7.39万 - 项目类别:
Biogenesis of HDL Through Cholesterol Efflux and ApoA-I Structural Reorganization
HDL 通过胆固醇流出和 ApoA-I 结构重组的生物合成
- 批准号:
8874470 - 财政年份:2015
- 资助金额:
$ 7.39万 - 项目类别:
Structural Relationship Between APO A-1 Comformation and the Extent of Particle L
APO A-1 构象与颗粒 L 大小之间的结构关系
- 批准号:
7537462 - 财政年份:2008
- 资助金额:
$ 7.39万 - 项目类别:
STRUCTURE/FUNCTION RELATIONSHIPS OF APOLIPOPROTEIN A (APOA-1)
载脂蛋白 A (APOA-1) 的结构/功能关系
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6338878 - 财政年份:2000
- 资助金额:
$ 7.39万 - 项目类别:
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APO A-1 结构突变与动脉粥样硬化
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6527296 - 财政年份:2000
- 资助金额:
$ 7.39万 - 项目类别:
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