Functional study on a protein involved in meiotic chromosome distribution
Functional study on a protein involved in meiotic chromosome distribution
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
中文摘要
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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.
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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:
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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)
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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
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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。
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Saito T, Matsuda Y, Ito H, Fusaki N, Hori T, Yamamoto T.: "Localization of Zap70, the gene for a T cell-specific protein tyrosine kinase, to mouse and rat chromosomes by kinase, to mouse and rat chromosomes by fluorescence in situ hybridization and molecu
Saito T、Matsuda Y、Ito H、Fusaki N、Hori T、Yamamoto T.:“Zap70(T 细胞特异性蛋白酪氨酸激酶基因)通过激酶定位到小鼠和大鼠染色体,通过激酶定位到小鼠和大鼠染色体
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