IDENTIFICATION OF DEVELOPMENTAL CONTROL GENES USING YAC TRANSGENIC MICE
IDENTIFICATION OF DEVELOPMENTAL CONTROL GENES USING YAC TRANSGENIC MICE
批准号:
07044282
负责人:
YAMAMURA Ken-ichi
金额:
$3.2万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for international Scientific Research
财政年份:
1995
资助国家:
日本
项目状态:
已结题
起止时间:
1995 至 1996
中文摘要
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英文摘要
In this project, we try to establish an experimental approach coupling positional cloning and transgenic technologies for identification and isolation of mutated genes. Recent advances in genome analysis technologies enable us to isolate large size mammalian genomic DNA into YAC (Yeast artificial chromosome) or BAC (bacterial artificial chromosome) vectors. In combination with efficient genetic mapping techniques, it is feasible to map any mutation on mouse chromosome, and narrow down the region containing mutated gene to submega base range. However, identifying the relevant mutated gene can still be a formidable task, and a conventional method of identifying a gene by searching DNA sequence differences between mutant and wild-type may not always be possible. In those cases, alternative approach utilizing transgenic technologies would have potential to define the location of a gene on a large genomic DNA,i.e.introducing YAC or BACs containing genomic fragments harboring candidate genes … More into mutant mice and scoring for the rescue of the phenotype. We are now trying to identify mutated genes for developmental mutations such as t^<w5>, quaking both in the T/t complex of mouse Chromosome 17, and tk (tail kinks) on Chromosome 9. In each case, we have narrowed down the region where mutated gene resides to several hundred kb to 1 Mb. In order to find the mutated genes for these mutations, we first established the methodologies for production of transgenic mice carrying YAC or BAC DNA.YAC or BAC DNAs were prepared as follows ; an agarose plug containing YAC or BAC DNA was run on a pulsed field gel, and a band corresponding YAC/BAC clone waw excised and treated with agarase. After the enzyme digestion, released DNAs were washed and concentrated by a filtration apparatus. DNA solution of 5ng/mul was microinjected into mouse fertilized eggs. When a YAC clone with 650kb insert derived from the t^<w5> region was injected, we could establish three lines of transgenics carrying -270kb, -380kb and -450kb, respectively. Also, we have produced two transgenic mice, and found that both of mice contained intact, 150kb BAC clone derived from tail kinks region. Using these transgenic mice, we have begun breeding experiments to ask if these transgenes can rescue mutant phenotypes or not. Less
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共 18 条
Genetic studies on unique phenotypes in MSM/Ms mouse strain
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批准号:21220010
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项目类别:Grant-in-Aid for Scientific Research (S)
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资助金额:$134.78万
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财政年份:2009
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负责人:YAMAMURA Ken-ichi
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依托单位:
Identification of genes responsible for developmental mutant mice
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批准号:09044325
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批准号:04044136
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项目类别:Grant-in-Aid for international Scientific Research
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资助金额:$3.78万
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财政年份:1992
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负责人:YAMAMURA Ken-ichi
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Analysis on the molecular mechanism of development using insertional mutant mice.
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项目类别:Grant-in-Aid for international Scientific Research
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资助金额:$4.22万
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财政年份:1989
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负责人:YAMAMURA Ken-ichi
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依托单位:
Molecular genetic analysis of familial amyloidotic polyneuropathy
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批准号:63440082
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项目类别:Grant-in-Aid for General Scientific Research (A)
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资助金额:$1.34万
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财政年份:1988
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负责人:YAMAMURA Ken-ichi
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依托单位:
Production of a transgenic mouse model of familial amyloidotic polyneuropathy.
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批准号:61480439
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资助金额:$4.54万
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财政年份:1986
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负责人:YAMAMURA Ken-ichi
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依托单位:
国内基金
海外基金
利用羊八井(YAC+Tibet-III) 数据进行 10TeV 以上能量朝前区强子作用性质的研究
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批准号:11275212
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项目类别:面上项目
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批准年份:2012
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负责人:黄晶
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依托单位:
人XP21区多个基因的分子水平定位及X专性YAC克隆构建
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批准号:39180005
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资助金额:14.0万元
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批准年份:1991
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负责人:余龙
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依托单位: