课题基金 / 基金详情

Functional study on a protein involved in meiotic chromosome distribution

Functional study on a protein involved in meiotic chromosome distribution
参与减数分裂染色体分布的蛋白质的功能研究
批准号:
07808083
负责人:
SAITO Toshiyuki
金额:
$1.34万
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
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

项目摘要

项目成果

SAITO Toshiyuki的其他基金

相似基金

相关文献

中文摘要
翻译
减数分裂是维持遗传信息世代不变的基本过程。虽然我们认为着丝粒在染色体分离中起着关键作用,但这一过程的生化细节却鲜为人知。在本研究的初始阶段,报告者假设在减数分裂中发生着丝粒的独特调控,因为减数分裂与染色体减半过程的有丝分裂明显不同。首先,他从睾丸中筛选编码DNA结合蛋白的DNA。Alphoid基因组dna作为靶蛋白的亲和材料固定在支撑基质上。将亲和柱的蛋白部分注射到小鼠体内,获得免疫血清。在大肠杆菌宿主中检测到多个表达重组蛋白的cDNA克隆。全长cDNA测序表明,该基因产物是一种富含谷氨酸的蛋白质(今天称为TRIM41)。通过荧光原位杂交确定该基因定位于人类染色体5q35.3。随后,他预期该蛋白与着丝粒区结合,并利用大鼠睾丸进行了免疫化学检测实验。与他的假设相反,该蛋白在成熟精子尾部的中间部分检测到非常强烈。减数分裂染色体的着丝粒在标本中表现出轻微的荧光信号。目前,TRIM41蛋白与着丝粒的假设作用之间的关系尚不清楚。
英文摘要
Meiosis is a basic process to maintain the genetic information constant through generations. Although we consider that centromere will play a key role in the separation of chromosomes, biochemical details of the process is little known. The reporter assumed at the initial phase of this study that an unique regulation of centromeres occurs in meiosis because meiosis is clearly distinguished from mitosis for the half-decreasing process of chromosomes. First, he screened cDNAs which code for DNA binding proteins from testis. Alphoid genomic DNAs were immobilized to supporting matrices as affinity materials for the target proteins. The resultant protein fraction of the affinity column work was injected into mice and immunized sera were obtained. The sera detected several cDNA clones which express recombinant proteins in E. coli host. Sequencing of a full-length cDNA shouwed that the gene product is a glutamic acid-rich protein (today the protein is known as TRIM41). The author determined that the gene is mapped to human chromosome 5q35.3 by fluorescence in situ hybridization. He then expected that the protein binds centromere region and performed immunochemical detection experiments using rat testis. In contrast of his assumption, the protein detected very strongly at mid-piece of matured sperm tail. Centromeres of meiotic chromosomes exhibited slight fluorescence signals in the specimen. At present, relation between TRIM41 protein and an assumed role of centromeres is unknown.
期刊论文(9)
专著(0)
科研奖励(0)
会议论文
Saito T, Seki N, Matsuda Y, Kitahara M, Murata M, Kanda N, Nomura N, Yamamoto T, Hori TA.: "Identification of the human ERK gene as a putative receptor tyrosine kinase and its chromosomal localization to 1p36.1 : a comparative mapping of human, mouse, and
Saito T、Seki N、Matsuda Y、Kitahara M、Murata M、Kanda N、Nomura N、Yamamoto T、Hori TA.:“人类 ERK 基因作为假定受体酪氨酸激酶的鉴定及其对 1p36.1 的染色体定位:
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Matsuda Y, Saito T, Fujimoto J, Yamamoto T.: "Chromosomal mapping of the mouse and rat brt genes."Genomics.. 40. 181-184 (1997)
Matsuda Y、Saito T、Fujimoto J、Yamamoto T.:“小鼠和大鼠 brt 基因的染色体图谱。”基因组学.. 40. 181-184 (1997)
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
SAITO.T,Matsuda,Y.Ito.H.Fusaki,N.Hori.T.and Yamamoto,T.: "Localization of Zy70,the game for a Tuil-specific pretein tyrssine kinase,to more and rat chromosaines by flucrescin in sifa hybridigation and melinkien linhas" Mammilian Gen. 8. 45-46 (1997)
SAITO.T、Matsuda、Y.Ito.H.Fusaki、N.Hori.T. 和 Yamamoto,T.:“Zy70(Tuil 特异性蛋白酪氨酸激酶的游戏)通过荧光素定位到更多和大鼠染色体
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
Yamauchi Masatake: "Isolation of human purH gene expressed in the rodent transformant cells by subtractive enrichment of 3'-untranslated region of human transcript."DNA Res. 2. 269-275 (1995)
Yamauchi Masatake:“通过消减富集人类转录本的 3-非翻译区,分离在啮齿动物转化细胞中表达的人类 purH 基因。”DNA Res。
DOI: --
发表时间:
期刊:
影响因子: --
作者: []
通讯作者:
共 9 条
    Imaging analysis of autophagy between periodontitis and dementia
    • 批准号:
      15K15775
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.33万
    • 财政年份:
      2015
    • 负责人:
      SAITO Toshiyuki
    • 依托单位:
    Cohort study on the relationship between oral health and systemic health in Goto City
    • 批准号:
      26293443
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $10.4万
    • 财政年份:
      2014
    • 负责人:
      SAITO Toshiyuki
    • 依托单位:
    Transcriptome analysis of leukocytes from sarcoma patients for helpful biomarkers
    • 批准号:
      25670544
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.33万
    • 财政年份:
      2013
    • 负责人:
      SAITO Toshiyuki
    • 依托单位:
    Imaging analysis of periodontitis and NASH related mechanism in 3D incubating system
    • 批准号:
      25670895
    • 项目类别:
      Grant-in-Aid for Challenging Exploratory Research
    • 资助金额:
      $2.41万
    • 财政年份:
      2013
    • 负责人:
      SAITO Toshiyuki
    • 依托单位:
    国内基金
    海外基金
    细胞有丝分裂过程中Aurora-A激酶驱动内质网动态形变促进染色体排列的机制研究
    • 批准号:
      32100589
    • 项目类别:
      青年科学基金项目(C类)
    • 资助金额:
      30.0万元
    • 批准年份:
      2021
    • 负责人:
      张炜
    • 依托单位:
    细胞核分布基因C样蛋白2在胞质分裂过程中的作用及机制研究
    • 批准号:
      32070709
    • 项目类别:
      面上项目
    • 资助金额:
      58.0万元
    • 批准年份:
      2020
    • 负责人:
      杨月红
    • 依托单位:
    异染色质蛋白HP1与ATRX结合在有丝分裂期维护染色体稳定性的分子机制研究
    • 批准号:
      32000499
    • 项目类别:
      青年科学基金项目
    • 资助金额:
      24.0万元
    • 批准年份:
      2020
    • 负责人:
      易琦
    • 依托单位:
    用一种新的方法研究Bub1调控有丝分裂的分子机制
    • 批准号:
      31970666
    • 项目类别:
      面上项目
    • 资助金额:
      58.0万元
    • 批准年份:
      2019
    • 负责人:
      张刚
    • 依托单位: