Heterotrimeric G Protein Signaling in Arabidopsis
Heterotrimeric G Protein Signaling in Arabidopsis
批准号:
6513643
负责人:
ALAN M. JONES
金额:
$31.56万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-09-01 至 2006-08-31
关键词:
Arabidopsis G protein biological signal transduction cell proliferation confocal scanning microscopy gene expression guanine nucleotide binding protein hormone receptor indoleacetate phytohormones plant growth /development plant growth regulators polymerase chain reaction protein protein interaction protein structure function receptor coupling root seeds
中文摘要
描述(由申请人提供):在大多数后生动物中,不同的
异源三聚体 G 蛋白复合物将许多不同的上游信号耦合到
不同的下游效应子,如腺苷酸环化酶、离子通道和
磷脂酶。然而,在拟南芥中,只有一个规范
但控制不同植物的异源三聚体 G 蛋白复合物
回应。我们不知道这是如何实现的,也不知道是什么
受体激活该 G 蛋白复合物。我的最新技术进展
小组使用功能获得和功能丧失的方法来理解
拟南芥 G 蛋白亚基的功能将使我们能够确定
该 G 蛋白复合物在各种信号传导途径中的分子作用。那里
该项目的三个重点领域是:生长素对根部发育的控制,
下胚轴发育;以及种子发芽的多信号控制。
具体来说,我们将: 1. 确定 G 蛋白突变体的生长素反应性
和过度表达并检查控制种子的信号串扰
发芽,2. 识别和表征遗传和物理相互作用因素
Galpha 和 Gbeta 使用外源抑制子筛选(包括激活)
诱变和使用胞浆蛋白-蛋白相互作用测定,以及 3. 测试
使用反向遗传推定一小组候选 GPCR 的功能
接近。总之,目标是检验生长素利用的假设
信号转导中的异三聚体 G 蛋白。这项工作还解决了
信号串扰机制长期存在的问题。因为,单身
拟南芥异源三聚体 G 蛋白似乎是多重信号的核心
途径,利用拟南芥进行遗传学研究可能揭示其核心机制
信号集成,这可能会被普遍共享。
英文摘要
DESCRIPTION (provided by applicant): In most metazoans, different
heterotrimeric G protein complexes couple many different upstream signals to
different downstream effectors such as adenyl cyclase, ion channels, and
phospholipases. However, in Arabidopsis, there is only a single canonical
heterotrimeric G protein complex that nonetheless controls different plant
responses. We do not know how this is accomplished nor do we know what
receptors activate this G protein complex. Recent technical advances from my
group using both gain- and loss-of-function approaches to understand the
function of Arabidopsis G protein subunits will enable us to determine the
molecular role of this G protein complex in various signaling pathways. There
are three focus areas for this project: auxin control of root development,
hypocotyl development; and multi-signal control of seed germination.
Specifically, we will: 1. determine auxin responsiveness of G protein mutants
and overexpressors and examine the signal cross-talk controlling seed
germination, 2. identify and characterize genetic and physical interactors of
Galpha and Gbeta using extragenic suppressor screens including activation
mutagenesis and using cytosolic protein-protein interaction assays, and 3. test
putative functions of a small set of candidate GPCRs using reverse genetic
approaches. In summary, the goal is to test the hypothesis that auxin utilizes
heterotrimeric G proteins in signal transduction. This work also addresses a
longstanding problem on the mechanism of signal cross-talk. Because, the single
Arabidopsis heterotrimeric G protein appears to be central to multiple signal
pathways, genetic studies using Arabidopsis may reveal the core mechanism of
signal integration, which is likely to be shared universally.
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会议论文
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海外基金