Analysis of developmental genetic system using small teleost fish as vertebrate model systems
Analysis of developmental genetic system using small teleost fish as vertebrate model systems
批准号:
12202004
负责人:
TAKEDA Hiroyuki
金额:
$133.63万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research on Priority Areas
财政年份:
2000
资助国家:
日本
项目状态:
已结题
起止时间:
2000 至 2004
中文摘要
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英文摘要
In the present study, we focused on the medaka that became an attractive model organism for the study of vertebrate early development and genome evolution. The following three groups were jointed, aiming at the establishment of comprehensive resources for medaka developmental genetics as well as structural and functional analyses of developmentally important genes in medaka.1. Takeda and NaruseTo strengthen the study of medaka developmental genetics, Takeda's laboratory has conducted a large-scale isolation of ESTs from medaka embryos and developed tools that facilitate mutant analysis such as rapid mapping system, M-markers and microarray with 8,000 uni-genes. These resources are accelerating medaka mutant analyses and made an important contribution to the medaka genome sequencing project.2. HoriHori's laboratory analyzed the organization of the entire hox gene loci. Together with the information in the Fugu genome database and in the Danio genome database, the physical maps of three fish genomes were constructed and compared one another. Not only numbers of hox genes but also the distances between the neighboring hox genes are highly similar between medaka and fugu. As for six clusters, Aa, Ab, Ba, Bb, Ca and Da that are commonly present in the three fishes, only few or no differences were found in each cluster. Thus, the hox gene sets should have been well conserved once they had been established in respective species.3. KudoKudo's laboratory has screened for mutants that are defective in organogenesis and fin regeneration in the medaka, using ethylnitrosourea (ENU) as a mutagen. A total of 386 mutagenized genomes were scored to identify 151 mutations affecting organogenesis, and 16 mutations affecting the fin regeneration were identified. In parallel, they isolated 20,000 ESTs from re-generating fins, representing about 3,000 uni-genes.
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Matsuda, M.: "DMY is a Y-specific DM-domain gene required for male development in the medaka fish."Nature. 417. 559-563 (2002)
Matsuda, M.:“DMY 是青鳉鱼雄性发育所需的 Y 特异性 DM 结构域基因。”《自然》。
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DOI:
10.1002/dvdy.20181
发表时间:
2004-12-01
期刊:
DEVELOPMENTAL DYNAMICS
影响因子:
2.5
作者:
[Kawakami, A, Fukazawa, T, Takeda, H]
通讯作者:
Takeda, H
Takuya Sakaguchi: "Expression of zebrafish BTG-b, anti-proliferative cofactor, during early embryogenesis"Mechanisms of Development. (in press). (2001)
Takuya Sakaguchi:“斑马鱼 BTG-b(抗增殖辅因子)在早期胚胎发生过程中的表达”发育机制。
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Naruse, K.: "Medaka genomics : a bridge between mutant phenotypes and gene function"Mechanisms of Development. (印刷中). (2004)
Naruse, K.:“青鳉基因组学:突变表型和基因功能之间的桥梁”发展机制(2004 年出版)。
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Sakaguchi, T: "Formation and patterning roles of the yolk syncytial layer. (Review)"Pattern Formation in Zebrafish. 1-14 (2002)
Sakaguchi,T:“卵黄合胞体层的形成和图案形成作用。(评论)”斑马鱼的图案形成。
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