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:2891174
- 负责人:
- 金额:$ 24.15万
- 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(富含豆蔻酰化丙氨酸的C激酶底物)是目前
脑中蛋白激酶C的主要磷蛋白底物。
积累的数据表明MARCKS在转导中的作用,
调节肌动蛋白膜可塑性的细胞外信号
以及与细胞内代谢的动态调节相关的细胞过程。
神经元细胞骨架和突触重构,例如,大脑
发育和神经递质信号传导。 其他证据来自
我们的实验室已经证明了MARCKS在海马体中的作用,
慢性锂在大脑中长期作用的目标。 与
最近建立的Macs基因突变小鼠模型,
现在已经在C57 BL/6背景上回交到第八代,
MARCKS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
MARCKS mRNA在脑内的分布优先于
在大脑的边缘和边缘相关区域表达,
大鼠和小鼠海马内特异性细胞分布
个脑袋 在初步数据中,我们还证明了MARCKS是
在成人Macs null/+中以基因剂量依赖性方式表达
杂合子,并且MARCKS的大约50%的减少
表达与海马苔藓纤维增生有关,因为
以及增强的空间学习(第C.8b和C.9节)。 这些
根据我们目前的额外研究,
数据表明,显示海马苔藓的DBA/2小鼠
纤维发育不全和显著的空间学习缺陷,也表明
与C57 BL/6相比,海马MARCKS显著升高
小鼠该计划将进行为期三年的跨学科研究。
该战略与哺乳动物遗传学中心合作,
制造表达MARCKS水平从50%(Macs)到100%(Macs)不等的小鼠。
null/+)至野生型表达的260%(MARCKS Tg+/+)
小鼠 在这些小鼠中,我们将研究
海马苔藓纤维上MARCKS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表达的变化,并确定
回交中控制MARCKS表达的数量性状基因座
和/或DBA/2和C57 BL/6的F2互交后代。 一旦基因
这种变化的基础是显而易见的,我们将确定是否相同的位点
与苔藓纤维锥体下投射的长度共分离
和空间学习在杂交后代中表达最高与最低
马克。 概述的一系列研究旨在检查一个直接的
MARCKS在海马神经可塑性事件中的作用
发展和学习/记忆,并评估在何种程度上,这些
复杂的表型性状与Macs基因本身和/或
相互作用的基因修饰剂。
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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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
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{{ 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:
6186780 - 财政年份:1998
- 资助金额:
$ 24.15万 - 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:
2842866 - 财政年份:1998
- 资助金额:
$ 24.15万 - 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:
$ 24.15万 - 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:
$ 24.15万 - 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:
$ 24.15万 - 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:
$ 24.15万 - 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:
$ 24.15万 - 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:
$ 24.15万 - 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:
$ 24.15万 - 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:
$ 24.15万 - 项目类别:
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