两个独立 Myh6-Cre 转基因小鼠品系的比较分析

Amanda Davenport , Chase W. Kessinger , Ryan D. Pfeiffer , Nikita Shah , Richard Xu , E. Dale Abel , Nathan R. Tucker , Zhiqiang Lin
{"title":"两个独立 Myh6-Cre 转基因小鼠品系的比较分析","authors":"Amanda Davenport ,&nbsp;Chase W. Kessinger ,&nbsp;Ryan D. Pfeiffer ,&nbsp;Nikita Shah ,&nbsp;Richard Xu ,&nbsp;E. Dale Abel ,&nbsp;Nathan R. Tucker ,&nbsp;Zhiqiang Lin","doi":"10.1016/j.jmccpl.2024.100081","DOIUrl":null,"url":null,"abstract":"<div><p>We have previously shown that the <em>Myh6</em> promoter drives Cre expression in a subset of male germ line cells in three independent <em>Myh6-Cre</em> mouse lines, including two transgenic lines and one knock-in allele. In this study, we further compared the tissue-specificity of the two <em>Myh6-Cre</em> transgenic mouse lines, <em>MDS Myh6-Cre and AUTR Myh6-Cre,</em> through examining the expression of tdTomato (tdTom) red fluorescence protein in multiple internal organs, including the heart, brain, liver, lung, pancreas and brown adipose tissue. Our results show that <em>MDS Myh6-Cre</em> mainly activates tdTom reporter in the heart, whereas <em>AUTR Myh6-Cre</em> activates tdTom expression significantly in the heart, and in the cells of liver, pancreas and brain. In the heart, similar to <em>MDS Myh6-Cre</em><strong>,</strong> <em>AUTR Myh6-Cre</em> activates tdTom in most cardiomyocytes. In the other organs, <em>AUTR Myh6-Cre</em> not only mosaically activates tdTom in some parenchymal cells, such as hepatocytes in the liver and neurons in the brain, but also turns on tdTom in some interstitial cells of unknown identity.</p></div>","PeriodicalId":73835,"journal":{"name":"Journal of molecular and cellular cardiology plus","volume":"9 ","pages":"Article 100081"},"PeriodicalIF":0.0000,"publicationDate":"2024-07-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S2772976124000217/pdfft?md5=dd1462761635d293fc8c059df82c8a5c&pid=1-s2.0-S2772976124000217-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Comparative analysis of two independent Myh6-Cre transgenic mouse lines\",\"authors\":\"Amanda Davenport ,&nbsp;Chase W. Kessinger ,&nbsp;Ryan D. Pfeiffer ,&nbsp;Nikita Shah ,&nbsp;Richard Xu ,&nbsp;E. Dale Abel ,&nbsp;Nathan R. Tucker ,&nbsp;Zhiqiang Lin\",\"doi\":\"10.1016/j.jmccpl.2024.100081\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We have previously shown that the <em>Myh6</em> promoter drives Cre expression in a subset of male germ line cells in three independent <em>Myh6-Cre</em> mouse lines, including two transgenic lines and one knock-in allele. In this study, we further compared the tissue-specificity of the two <em>Myh6-Cre</em> transgenic mouse lines, <em>MDS Myh6-Cre and AUTR Myh6-Cre,</em> through examining the expression of tdTomato (tdTom) red fluorescence protein in multiple internal organs, including the heart, brain, liver, lung, pancreas and brown adipose tissue. Our results show that <em>MDS Myh6-Cre</em> mainly activates tdTom reporter in the heart, whereas <em>AUTR Myh6-Cre</em> activates tdTom expression significantly in the heart, and in the cells of liver, pancreas and brain. In the heart, similar to <em>MDS Myh6-Cre</em><strong>,</strong> <em>AUTR Myh6-Cre</em> activates tdTom in most cardiomyocytes. In the other organs, <em>AUTR Myh6-Cre</em> not only mosaically activates tdTom in some parenchymal cells, such as hepatocytes in the liver and neurons in the brain, but also turns on tdTom in some interstitial cells of unknown identity.</p></div>\",\"PeriodicalId\":73835,\"journal\":{\"name\":\"Journal of molecular and cellular cardiology plus\",\"volume\":\"9 \",\"pages\":\"Article 100081\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-07-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.sciencedirect.com/science/article/pii/S2772976124000217/pdfft?md5=dd1462761635d293fc8c059df82c8a5c&pid=1-s2.0-S2772976124000217-main.pdf\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of molecular and cellular cardiology plus\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2772976124000217\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of molecular and cellular cardiology plus","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2772976124000217","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

我们之前已经证明,在三个独立的Myh6-Cre小鼠品系(包括两个转基因品系和一个基因敲入等位基因)中,Myh6启动子驱动Cre在雄性生殖系细胞亚群中的表达。在本研究中,我们通过检测tdTomato(tdTom)红色荧光蛋白在多个内脏器官(包括心、脑、肝、肺、胰腺和棕色脂肪组织)中的表达,进一步比较了两个Myh6-Cre转基因小鼠品系(MDS Myh6-Cre和AUTR Myh6-Cre)的组织特异性。我们的研究结果表明,MDS Myh6-Cre主要激活心脏中的tdTom报告基因,而AUTR Myh6-Cre则显著激活心脏、肝脏、胰腺和脑细胞中的tdTom表达。在心脏中,与MDS Myh6-Cre类似,AUTR Myh6-Cre也能激活大多数心肌细胞中的tdTom。在其他器官中,AUTR Myh6-Cre不仅在一些实质细胞(如肝脏中的肝细胞和大脑中的神经元)中镶嵌激活tdTom,而且还在一些身份不明的间质细胞中开启tdTom。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Comparative analysis of two independent Myh6-Cre transgenic mouse lines

Comparative analysis of two independent Myh6-Cre transgenic mouse lines

We have previously shown that the Myh6 promoter drives Cre expression in a subset of male germ line cells in three independent Myh6-Cre mouse lines, including two transgenic lines and one knock-in allele. In this study, we further compared the tissue-specificity of the two Myh6-Cre transgenic mouse lines, MDS Myh6-Cre and AUTR Myh6-Cre, through examining the expression of tdTomato (tdTom) red fluorescence protein in multiple internal organs, including the heart, brain, liver, lung, pancreas and brown adipose tissue. Our results show that MDS Myh6-Cre mainly activates tdTom reporter in the heart, whereas AUTR Myh6-Cre activates tdTom expression significantly in the heart, and in the cells of liver, pancreas and brain. In the heart, similar to MDS Myh6-Cre, AUTR Myh6-Cre activates tdTom in most cardiomyocytes. In the other organs, AUTR Myh6-Cre not only mosaically activates tdTom in some parenchymal cells, such as hepatocytes in the liver and neurons in the brain, but also turns on tdTom in some interstitial cells of unknown identity.

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
Journal of molecular and cellular cardiology plus
Journal of molecular and cellular cardiology plus Cardiology and Cardiovascular Medicine
自引率
0.00%
发文量
0
审稿时长
31 days
×
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