Analysis of the function of transcription clongation factor S-II family based on the structural analyzes
基于结构分析的转录延伸因子S-II家族功能分析
基本信息
- 批准号:07307023
- 负责人:
- 金额:$ 14.85万
- 依托单位:
- 依托单位国家:日本
- 项目类别:Grant-in-Aid for Scientific Research (A)
- 财政年份:1995
- 资助国家:日本
- 起止时间:1995 至 1996
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
In order to elucidate the significance of function and structure of tissue-specific transcription clongation factor S-II family, we tried to isolate the various S-II family and to analyze the structure-function relationships by several methods.1) Isolation and characterization of tissue-specific S-II family from various organs.Human testis-specific S-II was isolated through the interaction with TFIIB by two-hybrid systems and three types of tissue-specific S-II family are obtained from mouse and rat by RT-RCR method. It was found that expression of mouse testis-specific S-II is restricted to testicular germ cells during and after meiosis in the course of spermatogenesis.2) Genetical analysis of structure and function of S-II family.To elucidate the in vivo function of S-II,we tried to set up S.pombe system. Moreover, it was found that there are three other S-II family members from S.cerevisiae genomes.
为了阐明组织特异性转录克隆因子S-II家族的功能和结构的意义,我们尝试用几种方法分离不同的S-II家族并分析其结构与功能的关系:1)从不同器官中分离和鉴定组织特异性S-II家族。通过RT-RCR方法从小鼠和大鼠中获得特异性S-II家族。结果表明,小鼠睾丸特异性S-II基因在精子发生过程中的表达仅限于减数分裂前后的睾丸生殖细胞。2)S-II基因家族结构与功能的遗传学分析为了阐明S-II基因的体内功能,我们尝试建立粟酒裂殖酵母系统。此外,发现存在来自酿酒酵母基因组的其他三个S-II家族成员。
项目成果
期刊论文数量(45)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
T.Kuzuhara & M.Horikoshi: "Isolation and characterization of a cDNA enconding a human TFIID subunit containing a variety of putative structural motifs including direct repeats" Biol.Pharm.Bull.19. 122-126 (1996)
葛原
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S.Hasegawa, B.Choi & M.Horikoshi: "Isolation of Xenopus lacvis TFIID subunit p22 reveals two distinct structural regions" Gene. 169. 285-286 (1996)
长谷川、崔 B
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N.Adachi,T.Kubo & S.Natori: "Purification,characterization,and cDNA cloning of ABP-2(Arylphorin gene-specific binding protein-2)that specifically binds to the ABP-1-binding sequence in the arylphorin gene of sarcophaga peregrina" J.Biochem.120. 1239-1246
安达N·久保
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T. Yamamoto et al.: "Rapid preparation of plasmid templates suitable for a DNA sequencer without RNase treatment" Nucleic Acids Res.23. 3351-3352 (1995)
T. Yamamoto 等人:“快速制备适合 DNA 测序仪且无需 RNase 处理的质粒模板”Nucleic Acids Res.23。
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R.Mizutani,et al.: "Three-dimensional structures of the Fab fragment of murinc N1G9 antibody from primary immune response and of its complex with (4-hydroxy-3-nitrophenyl) acctatc" J.Mol.Biol.254. 208-222 (1995)
R.Mizutani 等人:“来自初级免疫反应的鼠 N1G9 抗体的 Fab 片段及其与 (4-羟基-3-硝基苯基) acctatc 复合物的三维结构”J.Mol.Biol.254。
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HORIKOSHI Masami其他文献
HORIKOSHI Masami的其他文献
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{{ truncateString('HORIKOSHI Masami', 18)}}的其他基金
Elucidation of the mechanism of nucleosomal structural change mediated by histone modifications
阐明组蛋白修饰介导的核小体结构变化机制
- 批准号:
21370052 - 财政年份:2009
- 资助金额:
$ 14.85万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Analysis of the mechanism of establishment of chromosomal functioning regions through nucleosomal structural changes
通过核小体结构变化建立染色体功能区的机制分析
- 批准号:
19370049 - 财政年份:2007
- 资助金额:
$ 14.85万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Analysis of the mechanism of eukaryotic transcription initiation and its regulation based on the TATA box-binding factor TFIID
基于TATA盒结合因子TFIID分析真核转录起始及其调控机制
- 批准号:
09480159 - 财政年份:1997
- 资助金额:
$ 14.85万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Analysis of the mechanism of eukaryotic transcription initiation and its regulation based on the TATA box-binding factor TFIID
基于TATA盒结合因子TFIID分析真核转录起始及其调控机制
- 批准号:
08458191 - 财政年份:1996
- 资助金额:
$ 14.85万 - 项目类别:
Grant-in-Aid for Scientific Research (B)
Basic research for development of new type of drugs based on the mechanism of transcriptional regulation
基于转录调控机制的新型药物开发基础研究
- 批准号:
06557127 - 财政年份:1994
- 资助金额:
$ 14.85万 - 项目类别:
Grant-in-Aid for Developmental Scientific Research (B)
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