两种水稻属鱼类70-kDa热休克蛋白(Hsp70) cdna的克隆与鉴定。

Idengaku zasshi Pub Date : 1995-06-01 DOI:10.1266/jjg.70.423
A Arai, K Naruse, H Mitani, A Shima
{"title":"两种水稻属鱼类70-kDa热休克蛋白(Hsp70) cdna的克隆与鉴定。","authors":"A Arai,&nbsp;K Naruse,&nbsp;H Mitani,&nbsp;A Shima","doi":"10.1266/jjg.70.423","DOIUrl":null,"url":null,"abstract":"<p><p>cDNA corresponding to two hsp70-related genes (OLHSC70 and CEHSC70) were isolated from two lines of cultured fish cells derived from the genus Oryzias. OLHSC70 was 2,261 bp in length and encoded a protein of 686 amino acids with a predicted molecular mass of 76,120 daltons. CEHSC70 was 2,114 bp in length and it lacked the 5' region found in OLHSC70. Two-dimensional electrophoresis revealed that Oryzias latipes has at least three heat-inducible proteins with molecular masses of about 70,000 daltons. One of these proteins (Hsp70.1) was barely expressed under normal conditions but its high-level expression was induced by hyperthermia. The other two proteins (Hsc70.1, and Hsc70.2) were constitutively expressed under normal conditions and only slightly enhanced levels were induced by hyperthermia. Transfection with the cloned sequence, RNA dot-blot analysis and the two-dimensional electrophoresis of proteins showed that OLHSC70 encoded Hsc70.1.</p>","PeriodicalId":13120,"journal":{"name":"Idengaku zasshi","volume":"70 3","pages":"423-33"},"PeriodicalIF":0.0000,"publicationDate":"1995-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1266/jjg.70.423","citationCount":"45","resultStr":"{\"title\":\"Cloning and characterization of cDNAs for 70-kDa heat-shock proteins (Hsp70) from two fish species of the genus Oryzias.\",\"authors\":\"A Arai,&nbsp;K Naruse,&nbsp;H Mitani,&nbsp;A Shima\",\"doi\":\"10.1266/jjg.70.423\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>cDNA corresponding to two hsp70-related genes (OLHSC70 and CEHSC70) were isolated from two lines of cultured fish cells derived from the genus Oryzias. OLHSC70 was 2,261 bp in length and encoded a protein of 686 amino acids with a predicted molecular mass of 76,120 daltons. CEHSC70 was 2,114 bp in length and it lacked the 5' region found in OLHSC70. Two-dimensional electrophoresis revealed that Oryzias latipes has at least three heat-inducible proteins with molecular masses of about 70,000 daltons. One of these proteins (Hsp70.1) was barely expressed under normal conditions but its high-level expression was induced by hyperthermia. The other two proteins (Hsc70.1, and Hsc70.2) were constitutively expressed under normal conditions and only slightly enhanced levels were induced by hyperthermia. Transfection with the cloned sequence, RNA dot-blot analysis and the two-dimensional electrophoresis of proteins showed that OLHSC70 encoded Hsc70.1.</p>\",\"PeriodicalId\":13120,\"journal\":{\"name\":\"Idengaku zasshi\",\"volume\":\"70 3\",\"pages\":\"423-33\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1995-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1266/jjg.70.423\",\"citationCount\":\"45\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Idengaku zasshi\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1266/jjg.70.423\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Idengaku zasshi","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1266/jjg.70.423","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 45

摘要

从两种培养的Oryzias属鱼细胞中分离到两个hsp70相关基因(OLHSC70和CEHSC70)的cDNA。OLHSC70全长2261 bp,编码686个氨基酸,预测分子量为76,120道尔顿。CEHSC70全长2114 bp,缺少OLHSC70的5′区。双向电泳结果表明,水稻至少有3个热诱导蛋白,分子量约为7万道尔顿。其中一种蛋白(Hsp70.1)在正常条件下几乎不表达,但高温诱导其高表达。另外两种蛋白(Hsc70.1和Hsc70.2)在正常条件下组成性表达,热疗诱导的表达水平仅略有提高。克隆序列转染、RNA点印迹分析和蛋白双向电泳显示,OLHSC70编码Hsc70.1。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Cloning and characterization of cDNAs for 70-kDa heat-shock proteins (Hsp70) from two fish species of the genus Oryzias.

cDNA corresponding to two hsp70-related genes (OLHSC70 and CEHSC70) were isolated from two lines of cultured fish cells derived from the genus Oryzias. OLHSC70 was 2,261 bp in length and encoded a protein of 686 amino acids with a predicted molecular mass of 76,120 daltons. CEHSC70 was 2,114 bp in length and it lacked the 5' region found in OLHSC70. Two-dimensional electrophoresis revealed that Oryzias latipes has at least three heat-inducible proteins with molecular masses of about 70,000 daltons. One of these proteins (Hsp70.1) was barely expressed under normal conditions but its high-level expression was induced by hyperthermia. The other two proteins (Hsc70.1, and Hsc70.2) were constitutively expressed under normal conditions and only slightly enhanced levels were induced by hyperthermia. Transfection with the cloned sequence, RNA dot-blot analysis and the two-dimensional electrophoresis of proteins showed that OLHSC70 encoded Hsc70.1.

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
期刊最新文献
Mitochondrial plasmid-like DNAs of the B1 family in the genus Oryza: sequence heterogeneity and evolution. Molecular clock for dating of divergence between animal phyla. Regional localization of rat and mouse protein-tyrosine phosphatase PTP alpha/LRP gene (Ptpra) by fluorescence in situ hybridization. Polymorphic distribution and molecular diversification of mitochondrial plasmid-like DNAs in the genus Oryza. Adaptive significance of amylase polymorphism in Drosophila. X. Analysis of alpha-amylase activity of two amylase variants in individual Drosophila subobscura flies.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1