Structure and Function of Tpn transposable elements in the Japanese morning glory
Structure and Function of Tpn transposable elements in the Japanese morning glory
批准号:
11640621
负责人:
NITASAKA Eiji
金额:
$2.43万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1999
资助国家:
日本
项目状态:
已结题
起止时间:
1999 至 2000
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Some mutations of the Japanese morning glory were known to be unstable somatically and germinally as caused by insertions of transposable elements. Until now, transposable elements that cause mutable phenotypes have been isolated from several genes. All of these elements belong to the En/Spm family by their structures. They all carried common 28-bp terminal inverted repeats (TIRs) and subterminal regions with many repeats. These transposable elements with common terminal sequences are termed Tpn1 family. All of them thought to be nonautonomous elements and these elements in mutable alleles are mobilized by autonoumous elements. The copy number of Tpn1 family was estimated between 500 and 1000 copies per haploid genome. Using probe of subterminal regions, we isolated more than 200 Tpn clones, and 128 clones were classified into 30 groups by their restriction maps. We decided the complete sequences of 19 representative Tpn clones from 30 groups. The comparison of their common regions among all Tpns indicates that the 5'-common regions including TIR, subterminal and non-repetitive regions are much longer than 3'-common regions. Interestingly, their internal sequences of Tpns were quite different among groups and were derived from host gene sequences. Another interesting feature of the Tpn1 family is the phylogenetic trees of each 5' and 3'common sequences did not make parallel relationships. By the linkage between 5'-subterminal regions and internal sequences, recombination events between different groups occurred in 3'-regions. We deduced a mechanism that Tpns incorporated host gene sequences in process of evolution from these findings. 3' protruding ends of Tpns mainly invades into homologous host genes as templates when Abortive Gap Repair events were occurred.
期刊论文(32)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
国立歴史民俗博物館編: "伝統の朝顔"国立歴史民俗博物館. 64 (1999)
日本国立历史博物馆编:《传统牵牛花》国立日本历史博物馆64(1999)。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
米田芳秋,仁田坂英二: "アサガオ画像データベース"(財)遺伝学普及会編. (2000)
Yoshiaki Yoneda、Eiji Nitazaka:《牵牛花图像数据库》,遗传学促进协会编辑(2000)。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
仁田坂英二: "伝統の朝顔III-芽生えから開花まで"国立歴史民俗博物館 編. 80 (2000)
日本国立历史博物馆编《传统牵牛花III-从萌芽到开花》80(2000)。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Shiraiwa, E.Nitasaka and T.Yamazaki: "Geko, a novel gene involved in olfaction in Drosophila melanogaster"J.Neurogenet. 14. 145-164 (2000)
Shiraiwa、E.Nitasaka 和 T.Yamazaki:“Geko,一种参与果蝇嗅觉的新基因”J.Neurogenet。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
E.Nitasaka: "Mutant strains of the Japanese morning glory."Strain maintenance and databank for life science (N.Nakatsuji ed. Kyoritsu press). 63-67 (2000)
E.Nitasaka:“日本牵牛花的突变菌株。”生命科学菌株维护和数据库(N.Nakatsuji ed. Kyoritsu press)。
DOI:
--
发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
共 25 条
Analyses of responsible genes of morphological mutants in the Japanese morning glory.
-
批准号:15570007
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.37万
-
财政年份:2003
-
负责人:NITASAKA Eiji
-
依托单位:
Analysis of autonomous element of Tpnl family in the Japanese morning glory
-
批准号:13640615
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$2.05万
-
财政年份:2001
-
负责人:NITASAKA Eiji
-
依托单位:
Genetical and molecular characterization of divers in Drosophila melanogaster
-
批准号:09640738
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$1.98万
-
财政年份:1997
-
负责人:NITASAKA Eiji
-
依托单位:
Genetical analysis of sexual behavior in Drosophila melanogasteranalyzes
-
批准号:07640822
-
项目类别:Grant-in-Aid for Scientific Research (C)
-
资助金额:$1.47万
-
财政年份:1995
-
负责人:NITASAKA Eiji
-
依托单位:
Development of transposon-vector-systems in insects.
-
批准号:07554067
-
项目类别:Grant-in-Aid for Scientific Research (A)
-
资助金额:$2.3万
-
财政年份:1995
-
负责人:NITASAKA Eiji
-
依托单位:
国内基金
海外基金
登录
查看更多内容
梅 毒 螺 旋 体 膜 脂 蛋 白 Tpn32 经 ERK1/2-NF- κB 调 控
ICAM-1/LFA-1 促血管损伤机制研究
-
批准号:2024JJ9412
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2024
-
负责人:黄洁丽 特
-
依托单位:
梅毒螺旋体促血管内皮损伤新机制:膜脂蛋白Tpn32通过诱导血管增生加剧血管炎症
-
批准号:2023JJ30534
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2023
-
负责人:谢亚锋
-
依托单位:
肠道菌群及代谢产物介导的AhR-ILC3s调控网络在TPN相关肠黏膜屏障功能损伤中的作用及机制研究
-
批准号:--
-
项目类别:面上项目
-
资助金额:55万元
-
批准年份:2021
-
负责人:王新颖
-
依托单位:
新型小分子化合物TPN10456在多发性硬化症发病中的作用和机理
-
批准号:31900658
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2019
-
负责人:吕婕
-
依托单位:
梅毒螺旋体膜脂蛋白Tpn32相互作用宿主蛋白的筛选及功能研究
-
批准号:81702046
-
项目类别:青年科学基金项目
-
资助金额:20.0万元
-
批准年份:2017
-
负责人:谢亚锋
-
依托单位:
TPN相关肠屏障损伤小鼠模型的建立与应用
-
批准号:81770531
-
项目类别:面上项目
-
资助金额:83.0万元
-
批准年份:2017
-
负责人:王新颖
-
依托单位:
双歧杆菌防治TPN所致肠菌移位及胆汁瘀积的实验研究
-
批准号:30271350
-
项目类别:面上项目
-
资助金额:19.0万元
-
批准年份:2002
-
负责人:蔡威
-
依托单位: