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Development of transgenic mice expressing human complement modulator

Development of transgenic mice expressing human complement modulator
表达人类补体调节剂的转基因小鼠的开发
批准号:
06454718
负责人:
OKABE Masaru
金额:
$3.9万
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (B)
财政年份:
1994
资助国家:
日本
项目状态:
已结题
起止时间:
1994 至 1995

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中文摘要
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英文摘要
Production of transgenic mice which express CD46The construct to make transgenic mice were checked using CHO cells in vitro. The checked construct which is consisted with SV40 SR alpha promoter and CD46 were used in transgenic mouse experiment. However, all the transgenic mice produced by this construct did not express CD46 on their cell surface. On the course of finding the cause of this silent expression, it was found that when the cytosolic tail of CD46 were eliminated, the rest of the CD46 were expressed. Further experiment using transgenic mice also revealed that the origin of the silencer effect is derived form the nontranslated 3' region of the CD46 gene. By making the transgenic mice lacking CD46 3' untranslated region, we could produce the mice which express the CD46 on the cell surface.Cloning of CD46 genomic gene.The expression pattern of the above mentioned transgenic mice were limited to muscle, pancreas, lung and some more organs, and not strongly on the blood cells. The virus infection test was performed, but until now a very concrete evidence of the infection is not obtained. Therefore, to express CD46 as in the natural CD46 expressing cells, we cloned the genomic CD46 from human genomic library. At the present moment, we are now producing CD46 transgenic mice driven under CD46 promoter.The role of CD46 in fertilization.CD46 was shown to act in the complement regulation and also in sperm-egg fusion. In the seminal fluid, there are considerable amount of CD46. The CD46 in the seminal fluid was shown to exist on prostasome membrane and has an effect on complement regulation. The role of the prostasome CD46 was suggested to protecting sperm from complement attack in the vagina and uterus.
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D.Watanabe et al.,: "characterization of the testis-specific gene ‘calmegin'promoter sebuene and its activity defined by transgenic mause expeniments" FEBS Lett.,. 368. 509-512 (1995)
D. Watanabe 等人:“睾丸特异性基因 ‘calmegin’ 启动子辛丁烯的表征及其通过转基因 mause 实验定义的活性” FEBS Lett., 368. 509-512 (1995)
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通讯作者:
M. Ikawa, et al.,: "Greentlaorescent protein as a marker intransgenic mice;" Develop. Growth Differ.,. 37. 455-459 (1995)
M. Ikawa 等人:“Greentlaorescent 蛋白作为转基因小鼠的标记;”
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通讯作者:
M.Ikawa, K.Kominami, Y.Yoshimura, K.Tanaka, Y.Nishimune and M.Okabe: "A rapid and non-invasive selection of transgenic embryos before implantation using green fluorescent protein (GFP)" FEBS Lett.375. 125-128 (1995)
M.Ikawa、K.Kominami、Y.Yoshimura、K.Tanaka、Y.Nishimune 和 M.Okabe:“使用绿色荧光蛋白 (GFP) 在植入前快速、非侵入性地选择转基因胚胎”FEBS Lett.375。
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通讯作者:
K.Ohashi, F.Saji, A.Wakimoto, T.Tsutsui, T.Nakazawa, M.Okabe, T.Mimura and O.Tanizawa: "Selection of acrosome-reacted sperm with MH61-Immunobeads" Am.Soc.Androl.15. 78-82 (1994)
K.Ohashi、F.Saji、A.Wakimoto、T.Tsutsui、T.Nakazawa、M.Okabe、T.Mimura 和 O.Tanizawa:“用 MH61-Immunobeads 选择顶体反应精子”Am.Soc.Androl。
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21
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      2002
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