金属硫蛋白-转甲状腺素融合基因在转基因小鼠中的活性。质粒序列对组织特异性表达的可能影响。

Molecular biology & medicine Pub Date : 1989-08-01
H Sasaki, M Nakazato, M J Saraiva, H Matsuo, Y Sakaki
{"title":"金属硫蛋白-转甲状腺素融合基因在转基因小鼠中的活性。质粒序列对组织特异性表达的可能影响。","authors":"H Sasaki,&nbsp;M Nakazato,&nbsp;M J Saraiva,&nbsp;H Matsuo,&nbsp;Y Sakaki","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>Three strains of transgenic mice carrying the mouse metallothionein-I (MT) promoter fused to the human transthyretin (TTR) structural gene plus pUC plasmid sequences were investigated for expression of the fusion gene. Human TTR was inducible in the serum of at least two strains and the fusion gene mRNA was detected in several tissues of all the strains. The testis showed constitutive mRNA synthesis, while the intestine and some other tissues showed inducible expression. Unexpectedly, however, the fusion gene activity was grossly suppressed in the liver and kidney of all the strains. Available data suggest that this suppression results from the presence of the plasmid sequences. Analysis of tissue DNAs shows that the methylation status of the promoter sequences varies from strain to strain, depending on their chromosomal position, and that some CpG sites in the proximal portion of the promoter are not methylated at all in the liver and kidney of two strains. These findings suggest that the plasmid sequences suppress the MT promoter activity in some specific tissues by a mechanism that does not involve DNA methylation.</p>","PeriodicalId":77573,"journal":{"name":"Molecular biology & medicine","volume":"6 4","pages":"345-53"},"PeriodicalIF":0.0000,"publicationDate":"1989-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Activity of a metallothionein-transthyretin fusion gene in transgenic mice. Possible effect of plasmid sequences on tissue-specific expression.\",\"authors\":\"H Sasaki,&nbsp;M Nakazato,&nbsp;M J Saraiva,&nbsp;H Matsuo,&nbsp;Y Sakaki\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Three strains of transgenic mice carrying the mouse metallothionein-I (MT) promoter fused to the human transthyretin (TTR) structural gene plus pUC plasmid sequences were investigated for expression of the fusion gene. Human TTR was inducible in the serum of at least two strains and the fusion gene mRNA was detected in several tissues of all the strains. The testis showed constitutive mRNA synthesis, while the intestine and some other tissues showed inducible expression. Unexpectedly, however, the fusion gene activity was grossly suppressed in the liver and kidney of all the strains. Available data suggest that this suppression results from the presence of the plasmid sequences. Analysis of tissue DNAs shows that the methylation status of the promoter sequences varies from strain to strain, depending on their chromosomal position, and that some CpG sites in the proximal portion of the promoter are not methylated at all in the liver and kidney of two strains. These findings suggest that the plasmid sequences suppress the MT promoter activity in some specific tissues by a mechanism that does not involve DNA methylation.</p>\",\"PeriodicalId\":77573,\"journal\":{\"name\":\"Molecular biology & medicine\",\"volume\":\"6 4\",\"pages\":\"345-53\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1989-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Molecular biology & medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Molecular biology & medicine","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

研究了三株携带小鼠金属硫蛋白i (MT)启动子与人甲状腺转甲素(TTR)结构基因融合的转基因小鼠,以及pUC质粒序列对融合基因的表达。人类TTR至少在两株菌株的血清中可诱导,且在所有菌株的多个组织中均检测到融合基因mRNA。睾丸为组成型mRNA合成,而肠和其他部分组织为诱导型表达。然而,出乎意料的是,融合基因的活性在所有菌株的肝脏和肾脏中都被严重抑制。现有数据表明,这种抑制是由于质粒序列的存在。对组织dna的分析表明,启动子序列的甲基化状态因菌株而异,这取决于它们的染色体位置,并且在两株菌株的肝脏和肾脏中,启动子近端部分的一些CpG位点根本没有甲基化。这些发现表明,在某些特定组织中,质粒序列通过不涉及DNA甲基化的机制抑制MT启动子活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Activity of a metallothionein-transthyretin fusion gene in transgenic mice. Possible effect of plasmid sequences on tissue-specific expression.

Three strains of transgenic mice carrying the mouse metallothionein-I (MT) promoter fused to the human transthyretin (TTR) structural gene plus pUC plasmid sequences were investigated for expression of the fusion gene. Human TTR was inducible in the serum of at least two strains and the fusion gene mRNA was detected in several tissues of all the strains. The testis showed constitutive mRNA synthesis, while the intestine and some other tissues showed inducible expression. Unexpectedly, however, the fusion gene activity was grossly suppressed in the liver and kidney of all the strains. Available data suggest that this suppression results from the presence of the plasmid sequences. Analysis of tissue DNAs shows that the methylation status of the promoter sequences varies from strain to strain, depending on their chromosomal position, and that some CpG sites in the proximal portion of the promoter are not methylated at all in the liver and kidney of two strains. These findings suggest that the plasmid sequences suppress the MT promoter activity in some specific tissues by a mechanism that does not involve DNA methylation.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信