NEUROBIOLOGY OF MARCKS--A MACS MUTANT MOUSE MODEL
马克斯的神经生物学——MACS突变小鼠模型
基本信息
- 批准号:2842866
- 负责人:
- 金额:$ 27.35万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:1998
- 资助国家:美国
- 起止时间:1998-08-10 至 2001-07-31
- 项目状态:已结题
- 来源:
- 关键词:alanine biological signal transduction electrophysiology enzyme substrate fatty acylation gene expression genotype hippocampus laboratory mouse learning long term potentiation membrane activity memory model design /development mossy fiber myristates neural plasticity neurobiology polymerase chain reaction protein kinase C quantitative trait loci visual perception
项目摘要
MARCKS (Myristoylated Alanine Rich C Kinase Substrate) is the most
prominent phosphoprotein substrate for protein kinase C in brain.
Accumulating data have indicated a role for MARCKS in transducing
extracellular signals for the regulation of actin-membrane plasticity
and cellular processes associated with dynamic regulation of the
neuronal cytoskeleton and synaptic restructuring, e.g., brain
development and neurotransmitter signaling. Additional evidence from
our laboratory has demonstrated a role for MARCKS in the hippocampus as
a target for the long-term action of chronic lithium in the brain. With
the recent creation of a mutant mouse model for the Macs gene which has
now been backcrossed onto a C57BL/6 background to the eighth generation,
MARCKS has been shown to play a critical role in brain development.
Recent data from our laboratory have demonstrated for the first time
that the distribution of MARCKS mRNA in brain is preferentially
expressed in limbic and limbic-related regions of the brain, with a
specific cellular distribution in hippocampus of both rat and mouse
brain. In preliminary data, we have also demonstrated that MARCKS is
expressed in a gene-dose dependent fashion in adult Macs null/+
heterozygotes, and that the approximately 50 percent reduction of MARCKS
expression is associated with hippocampal mossy fiber hyperplasia, as
well as enhanced spatial learning (Sections C.8b and C.9). These
findings take on further significance in light of our current additional
data demonstrating that DBA/2 mice which demonstrate hippocampal mossy
fiber hypoplasia and significant spatial learning deficits, also show
a significant elevation in hippocampal MARCKS as compared to C57BL/6
mice. This proposal outlines a three year interdisciplinary research
strategy, in conjunction with the Center for Mammalian Genetics, to
create mice expressing levels of MARCKS varying from 50 percent (Macs
null/+) to 260 percent (MARCKS Tg+/+) of that expressed by wild-type
mice. In these mice we will investigate the functional consequences of
both under and over-expression of MARCKS on hippocampal mossy fiber
development, hippocampal LTP electrophysiology, and spatial learning.
In addition, we will assess the genetic basis of this interstrain
variation in MARCKS expression and identify the positions of
quantitative trait loci controlling MARCKS expression among backcross
and/or F2 intercross progeny of DBA/2 and C57BL/6. Once the genetic
basis of this variation is evident, we will determine if the same loci
cosegregate with the length of the mossy fiber infrapyramidal projection
and spatial learning in hybrid progeny expressing highest vs. lowest
MARCKS. The outlined series of studies are designed to examine a direct
role for MARCKS in neuroplastic events in brain related to hippocampal
development and learning/memory, and assess the extent to which these
complex phenotypic traits are linked to the Macs gene itself and/or
interactive gene modifiers.
Marcks(肉豆蔻酰化丙氨酸富C激酶底物)是最多的
大脑中蛋白激酶C的显著磷蛋白底物。
越来越多的数据表明,Marcks在转换过程中发挥了作用
肌动蛋白-膜可塑性调节的细胞外信号
和细胞过程与细胞的动态调节有关
神经元细胞骨架和突触重构,例如脑
发育和神经递质信号。补充证据来自
我们的实验室已经证明了Marcks在海马体中的作用
这是慢性锂在大脑中长期作用的目标。使用
最近建立了Macs基因的突变小鼠模型,该模型具有
现已回交到C57BL/6背景的第八代,
马克斯已被证明在大脑发育中起着关键作用。
我们实验室的最新数据首次证明了
MARCKS基因在脑内的分布优先
在大脑的边缘和边缘相关区域表达,具有
大鼠和小鼠海马区特异性细胞分布
大脑。在初步数据中,我们还证明了马克是
成人MACs Null/+以基因剂量依赖性方式表达
杂合子,Marcks大约50%的减少
表达与海马苔藓纤维增生有关,AS
以及加强空间学习(C.8b和C.9节)。这些
鉴于我们目前的额外研究,这些发现具有进一步的意义
数据显示,DBA/2小鼠表现出海马苔藓
纤维发育不全和显著的空间学习障碍,也显示
与C57BL/6相比,海马区Marcks显著升高
老鼠。这份提案概述了一项为期三年的跨学科研究
战略,与哺乳动物遗传学中心合作,以
创建表达Marcks水平从50%(Mac)变化的小鼠
空/+)到260%(Marcks Tg+/+)的野生型表达
老鼠。在这些小鼠中,我们将研究
MARCKS在海马苔藓纤维上的低表达和高表达
发育、海马LTP电生理学和空间学习。
此外,我们还将评估这种中间菌株的遗传基础。
Marcks基因表达的变异及其定位
控制回交MARCKS表达的数量性状基因座
和/或DBA/2与C57BL/6的F2杂交后代。
这种变异的基础是显而易见的,我们将确定是否相同的基因座
与苔藓纤维锥体下部投射的长度共分离
杂交后代的空间学习表现为最高与最低
马克。概述的一系列研究旨在检查直接
MARCKS在脑内与海马区相关的神经再生事件中的作用
发展和学习/记忆,并评估这些因素的程度
复杂的表型性状与macs基因本身和/或
互动式基因修饰物。
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)
数据更新时间:{{ journalArticles.updateTime }}
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
数据更新时间:{{ journalArticles.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ monograph.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ sciAawards.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ conferencePapers.updateTime }}
{{ item.title }}
- 作者:
{{ item.author }}
数据更新时间:{{ patent.updateTime }}
Robert H. Lenox其他文献
A device for the automated monitoring of stereotypic behavior
- DOI:
10.1016/s0278-5846(82)80105-x - 发表时间:
1982-01-01 - 期刊:
- 影响因子:
- 作者:
Mark R. Brann;Molly Finnerty;Robert H. Lenox;Yigal H. Ehrlich - 通讯作者:
Yigal H. Ehrlich
Protein phosphorylation mediates effects of isoproterenol on adenylate cyclase activity in rat cortical membranes
- DOI:
10.1007/bf00965475 - 发表时间:
1981-07-01 - 期刊:
- 影响因子:3.800
- 作者:
Scott R. Whittemore;Robert H. Lenox;Edith D. Hendley;Yigal H. Ehrlich - 通讯作者:
Yigal H. Ehrlich
Changes in brain levels of cyclic nucleotides and gamma-aminobutyric acid in barbiturate dependence and withdrawal.
巴比妥依赖性和戒断时大脑中环核苷酸和γ-氨基丁酸水平的变化。
- DOI:
- 发表时间:
1979 - 期刊:
- 影响因子:5
- 作者:
Robert H. Lenox;H. L. Wray;G. Kant;T. Hawkins;James L. Meyerhoff - 通讯作者:
James L. Meyerhoff
Dopamine diffusion after microwave fixation at 986 MHz
- DOI:
10.1007/bf00964646 - 发表时间:
1979-08-01 - 期刊:
- 影响因子:3.800
- 作者:
G. Jean Kant;Robert H. Lenox;James L. Meyerhoff - 通讯作者:
James L. Meyerhoff
Robert H. Lenox的其他文献
{{
item.title }}
{{ item.translation_title }}
- DOI:
{{ item.doi }} - 发表时间:
{{ item.publish_year }} - 期刊:
- 影响因子:{{ item.factor }}
- 作者:
{{ item.authors }} - 通讯作者:
{{ item.author }}
{{ truncateString('Robert H. Lenox', 18)}}的其他基金
NEUROBIOLOGY OF MARCKS--A MACS MUTANT MOUSE MODEL
马克斯的神经生物学——MACS突变小鼠模型
- 批准号:
2891174 - 财政年份:1998
- 资助金额:
$ 27.35万 - 项目类别:
NEUROBIOLOGY OF MARCKS--A MACS MUTANT MOUSE MODEL
马克斯的神经生物学——MACS突变小鼠模型
- 批准号:
6186780 - 财政年份:1998
- 资助金额:
$ 27.35万 - 项目类别:
LITHIUM REGULATION OF BRAIN PROTEIN KINASE C SUBSTRATES
锂对脑蛋白激酶 C 底物的调节
- 批准号:
2675560 - 财政年份:1996
- 资助金额:
$ 27.35万 - 项目类别:
LITHIUM REGULATION OF BRAIN PROTEIN KINASE C SUBSTRATES
锂对脑蛋白激酶 C 底物的调节
- 批准号:
2416194 - 财政年份:1996
- 资助金额:
$ 27.35万 - 项目类别:
LITHIUM REGULATION OF BRAIN PROTEIN KINASE C SUBSTRATES
锂对脑蛋白激酶 C 底物的调节
- 批准号:
2256433 - 财政年份:1996
- 资助金额:
$ 27.35万 - 项目类别:
LITHIUM REGULATION OF BRAIN PROTEIN KINASE C SUBSTRATES
锂对脑蛋白激酶 C 底物的调节
- 批准号:
3430347 - 财政年份:1993
- 资助金额:
$ 27.35万 - 项目类别:
LITHIUM REGULATION OF BRAIN PROTEIN KINASE C SUBSTRATES
锂对脑蛋白激酶 C 底物的调节
- 批准号:
3430346 - 财政年份:1993
- 资助金额:
$ 27.35万 - 项目类别:
LITHIUM REGULATION OF BRAIN PROTEIN KINASE C SUBSTRATES
锂对脑蛋白激酶 C 底物的调节
- 批准号:
2249459 - 财政年份:1993
- 资助金额:
$ 27.35万 - 项目类别:
MOLECULAR MECHANISMS OF LITHIUM ACTION IN AFFECTIVE ILLN
锂在情感疾病中作用的分子机制
- 批准号:
3380266 - 财政年份:1987
- 资助金额:
$ 27.35万 - 项目类别:
MOLECULAR MECHANISMS OF LITHIUM ACTION IN AFFECTIVE ILLN
锂在情感疾病中作用的分子机制
- 批准号:
3380265 - 财政年份:1987
- 资助金额:
$ 27.35万 - 项目类别:
相似海外基金
ROLE OF CELL ADHESION IN BIOLOGICAL SIGNAL TRANSDUCTION
细胞粘附在生物信号转导中的作用
- 批准号:
6238317 - 财政年份:1997
- 资助金额:
$ 27.35万 - 项目类别:
ROLE OF CELL ADHESION IN BIOLOGICAL SIGNAL TRANSDUCTION
细胞粘附在生物信号转导中的作用
- 批准号:
5210031 - 财政年份:
- 资助金额:
$ 27.35万 - 项目类别:














{{item.name}}会员




