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 , Chase W. Kessinger , Ryan D. Pfeiffer , Nikita Shah , Richard Xu , E. Dale Abel , Nathan R. Tucker , 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 , Chase W. Kessinger , Ryan D. Pfeiffer , Nikita Shah , Richard Xu , E. Dale Abel , Nathan R. Tucker , 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}
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.