PROTEIN INTERACTIONS AND REPRESSION FUNCTION OF E1A
PROTEIN INTERACTIONS AND REPRESSION FUNCTION OF E1A
批准号:
2414212
负责人:
Elizabeth Moran
金额:
$29.49万
依托单位国家:
美国
项目类别:
财政年份:
1991
资助国家:
美国
项目状态:
已结题
起止时间:
1991-08-01 至 2001-04-30
中文摘要
描述:E1a相关蛋白,p300,与
癌症生物学家因为,作为转化功能的直接靶点
在腺病毒E1a基因中,它与两个细胞的调节有关
周期特异性和组织特异性基因表达。P300是高度
与CREB共激活因子CBP同源。CREB和CBP是主要的
环状AMP反应途径转录反应的介体。
P300和CBP之间的关系表明,它们的表现相似
功能。然而,它们是由不同的基因编码的,并且
初步临床证据表明,特定的代谢紊乱
与CBP的选择性丢失有关,表明p300和CBP不是
功能上是多余的。调查人员发现了一种新的270千道尔顿
与P300和CBP都相关的产品。P270特别是
有趣的是,它作为紧密连接的组件存在于细胞中
相关的一系列蛋白质。此外,他们还确定了一个突出的
这个复合体的成员,被称为BRG1。BRG1蛋白产物是一种
转录激活因子--基因表达途径的调节因子
随着发育和分化,推测有一种DNA解旋酶。这个
具有这种活性的p207/BRG1复合体。这一点的认定
互动应该为理解
P300和BRG1家族的分子作用机制
这些蛋白质似乎是基因表达的关键调节因子
控制细胞增殖和分化的途径。
英文摘要
DESCRIPTION: The E1A-associated protein, p300, is of major interest to
cancer biologists because, as a direct target of the transforming functions
of the adenovirus E1A gene, it is implicated in the regulation of both cell
cycle specific and tissue specific gene expression. p300 is highly
homologous to the CREB coactivator, CBP. CREB and CBP are the major
mediators of the transcriptional response to cyclic AMP-responsive pathways.
The relationship between p300 and CBP suggests that they perform, similar
functions. Nevertheless, they are encoded by different genes, and
preliminary clinical evidence indicates that specific metabolic disorders
are linked with selective loss of CBP, indicating that p300 and CBP are not
functionally redundant. The investigators identified a new 270 kilodalton
product that is related to both p300 and CBP. p270 is particularly
interesting because it exists in cells as a component of a tightly
associated series of proteins. Moreover they have identified a prominent
member of this complex as BRG1. The BRG1 protein product is a
transcriptional activator, a regulator of gene expression pathways linked
with the development and differentiation, and a putative DNA helicase. The
p207/BRG1 complexes with this activity intact. The identification of this
interaction should open the way to understanding a major part of the
molecular mechanisms of action of the p300 and BRG1 families, two families
of proteins that appear to be pivotal regulators of gene expression in
pathways controlling cell proliferation and differentiation.
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批准号:2096547
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资助金额:$26.13万
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PROTEIN INTERACTIONS AND REPRESSION FUNCTION OF THE E1A
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批准号:3198310
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项目类别:
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资助金额:$25.15万
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PROTEIN INTERACTIONS AND REPRESSION FUNCTION OF E1A
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依托单位:
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海外基金