DETERMINATION AND DIFFERENTIATION OF CARDIAC MYOCYTES
DETERMINATION AND DIFFERENTIATION OF CARDIAC MYOCYTES
批准号:
6054471
负责人:
David M BADER
金额:
$3.04万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
1989
资助国家:
美国
项目状态:
已结题
起止时间:
1989-07-01 至 2002-03-31
关键词:
DNA footprinting cardiac myocytes cell communication molecule cell differentiation cellular polarity chick embryo developmental genetics endoderm gel mobility shift assay gene expression genetic transcription heart rhythm molecular cloning myocardium myogenesis nonmammalian vertebrate embryology nucleic acid probes nucleic acid sequence southern blotting striated muscles transfection
中文摘要
控制心源性分化和心脏的机制
特异基因表达是未知的。 我们之前的数据显示,
心源性承诺的时间和胚胎期,
基因在发育中的心脏中被激活。 我们的数据表明,
心脏中肌肉基因表达的激活可能涉及独特的
在中胚层向肌细胞的初始转化后未观察到的机制。
最后,两个基因,心肌肌钙蛋白I(TnI)和心室肌球蛋白重
链1(VMHC 1),其在心肌形成的起始时被激活。
鉴别。 心肌肌钙蛋白I的表达是真实的,
而VMHC 1在所有纹状肌源性细胞中表达,
在肌源性分化的起始阶段,
立即局限于心室肌细胞。 我们建议确定
指导这两种心脏基因表达的调控序列
基因. 我们将:1)分离和表征5'和近端
心脏TnI和VMHC 1基因的序列,2)排除推定的
将与pTMG载体的lacZ报告基因融合的调节序列插入
心源性中胚层,分化的心肌细胞,骨骼肌源性
细胞和非肌原性细胞,以及3)鉴定
利用DNA足迹法研究调控元件中的DNA/蛋白质相互作用
和电泳迁移率变动分析。 我们的假设是
心肌肌钙蛋白I基因含有调控元件,
特异性表达,而VMHC 1基因含有指导
一个独特的普遍存在的表达阶段,随后是一个严格的心脏
具体阶段。 我们目前的目标是识别出
通过比较和对比假定的监管措施,
基因的元素,从而有助于确定
控制心脏特异性基因表达的分子机制,
心源性分化
英文摘要
The mechanisms which govern cardiogenic differentiation and cardiac--
specific gene expression are unknown. Our previous data have shown the
time of cardiogenic commitment and the embryonic period when cardiac
genes are activated in the developing heart. Our data suggest that the
activation of muscle gene expression in the heart may involve unique
mechanisms not seen after the initial conversion of mesoderm to myocyte.
Finally, two genes, cardiac troponin I (TnI) and ventricular myosin heavy
chain one (VMHC1) Which are activated at the initiation of cardiomyogenic
differentiation were identified. Cardiac TnI is expressed in a truly
cardiac-specific manner while VMHC1 is expressed in all striated myogenic
cells at the initiation of myogenic differentiation but then is
immediately restricted to ventricular myocytes. We propose to identify
regulatory sequences which direct the expression of these two cardiac
genes. We will: 1) isolate and characterize the 5' and proximal
sequences of the cardiac TnI and VMHC1 genes, 2) transfect putative
regulatory sequences fused to the lacZ reporter gene of pTMG vector into
cardiogenic mesoderm, differentiated cardiac myocytes, skeletal myogenic
cells and non-myogenic cells, and 3) identify specific regions of
DNA/protein interaction in the regulatory elements using DNA footprinting
and electrophoretic mobility shift assays. Our hypothesis is that the
cardiac TnI gene contains regulatory elements which confer cardiac
specific expression, while the VMHC1 gene contains sequences which direct
a unique ubiquitous phase of expression followed by a strict cardiac
specific phase. Our present goal is to identify the sequences which
direct these activities by comparing and contrasting putative regulatory
elements of the genes and thereby aid in the determination of the
molecular mechanisms which govern cardiac-specific gene expression and
cardiogenic differentiation.
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