Trmt112 Gene Expression in Mouse Embryonic Development
Mouse Trmt112, the homologous gene of yeast Trm112 (tRNA methyltransferase 11-2), was initially cloned from RIKEN with uncertain function. The yeast TRM112 is now known to play important roles in RNA methylation. Here, we studied the expression of Trmt112 by in situ hybridization and quantitative re...
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description | Mouse Trmt112, the homologous gene of yeast Trm112 (tRNA methyltransferase 11-2), was initially cloned from RIKEN with uncertain function. The yeast TRM112 is now known to play important roles in RNA methylation. Here, we studied the expression of Trmt112 by in situ hybridization and quantitative real-time RT-PCR (QRT-PCR). A higher expression level of Trmt112 was observed in the brain and nervous system by whole mount in situ hybridization from embryonic day 10.5 (E10.5) to E11.5. At later developmental stages E13.5 and E16.5, abundant expression was prominently found in various organs and tissues including developing brain, nervous system, thymus, lung, liver, intestine, kidney, and cartilage. Furthermore, Trmt112 was persistently expressed from E9.5 to E18.5 on whole embryos and highly expressed in multiple organs at E12.5, E15.5 and E18.5 by QRT-PCR. These results showed that Trmt112 gene was highly and ubiquitously expressed during mouse embryonic development, implying that it might be involved in the morphogenesis of diverse organs and tissues and numerous physiological functions. |
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The yeast TRM112 is now known to play important roles in RNA methylation. Here, we studied the expression of Trmt112 by in situ hybridization and quantitative real-time RT-PCR (QRT-PCR). A higher expression level of Trmt112 was observed in the brain and nervous system by whole mount in situ hybridization from embryonic day 10.5 (E10.5) to E11.5. At later developmental stages E13.5 and E16.5, abundant expression was prominently found in various organs and tissues including developing brain, nervous system, thymus, lung, liver, intestine, kidney, and cartilage. Furthermore, Trmt112 was persistently expressed from E9.5 to E18.5 on whole embryos and highly expressed in multiple organs at E12.5, E15.5 and E18.5 by QRT-PCR. 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Cytochem.</addtitle><description>Mouse Trmt112, the homologous gene of yeast Trm112 (tRNA methyltransferase 11-2), was initially cloned from RIKEN with uncertain function. The yeast TRM112 is now known to play important roles in RNA methylation. Here, we studied the expression of Trmt112 by in situ hybridization and quantitative real-time RT-PCR (QRT-PCR). A higher expression level of Trmt112 was observed in the brain and nervous system by whole mount in situ hybridization from embryonic day 10.5 (E10.5) to E11.5. At later developmental stages E13.5 and E16.5, abundant expression was prominently found in various organs and tissues including developing brain, nervous system, thymus, lung, liver, intestine, kidney, and cartilage. Furthermore, Trmt112 was persistently expressed from E9.5 to E18.5 on whole embryos and highly expressed in multiple organs at E12.5, E15.5 and E18.5 by QRT-PCR. These results showed that Trmt112 gene was highly and ubiquitously expressed during mouse embryonic development, implying that it might be involved in the morphogenesis of diverse organs and tissues and numerous physiological functions.</description><subject>in situ hybridization</subject><subject>mouse development</subject><subject>QRT-PCR</subject><subject>Regular</subject><subject>TRM112</subject><issn>0044-5991</issn><issn>1347-5800</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqFkUFv1DAQhS1ERZeFA38AReJCD2nHHjtxLlSoLaVSKy7lbHmdSTerxF7sbEX_Pd7dsgIuXMbSm0_PM_MYe8fhlIuqPrNLd8o5yPoFm3GUdak0wEs2A5CyVE3Dj9nrlFYAPOvyFTsWotIKFc5YdR_HiXNRXJOn4urnOlJKffBF74u7sElZGxfxKfjeFZf0SENYj-SnN-yos0Oit8_vnH3_cnV_8bW8_XZ9c_H5tnQVNlNZuVYAoVtAS9iIhcZWgtLaOrTCasudgFa3mrdKO6e7RnZCdVkSFenKIs7Zp73verMYqXX562gHs479aOOTCbY3f3d8vzQP4dEgVgpBZIOPzwYx_NhQmszYJ0fDYD3l9QyvFUrNUcP_URD5erreoR_-QVdhE32-hOFSaomwLXN2sqdcDClF6g5zczDb4EwOzuyCy-z7Pxc9kL-TysD5HlilyT7QAbBx6t1AOyupjNiWneWh45Y2GvL4C1aKqJ4</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>Gu, Tiantian</creator><creator>He, Hongjuan</creator><creator>Zhang, Yan</creator><creator>Han, Zhengbin</creator><creator>Hou, Guangyuan</creator><creator>Zeng, Tiebo</creator><creator>Liu, Qi</creator><creator>Wu, Qiong</creator><general>JAPAN SOCIETY OF HISTOCHEMISTRY AND CYTOCHEMISTRY</general><general>Japan Science and Technology Agency</general><general>Japan Society of Histochemistry and Cytochemistry</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>RC3</scope><scope>5PM</scope></search><sort><creationdate>20120101</creationdate><title>Trmt112 Gene Expression in Mouse Embryonic Development</title><author>Gu, Tiantian ; He, Hongjuan ; Zhang, Yan ; Han, Zhengbin ; Hou, Guangyuan ; Zeng, Tiebo ; Liu, Qi ; Wu, Qiong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c639t-6cd20e3cb0de392b83d40588ac3a2a8a1c20d8d81d58cc8f94f25f0d826e86a33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>in situ hybridization</topic><topic>mouse development</topic><topic>QRT-PCR</topic><topic>Regular</topic><topic>TRM112</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gu, Tiantian</creatorcontrib><creatorcontrib>He, Hongjuan</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Han, Zhengbin</creatorcontrib><creatorcontrib>Hou, Guangyuan</creatorcontrib><creatorcontrib>Zeng, Tiebo</creatorcontrib><creatorcontrib>Liu, Qi</creatorcontrib><creatorcontrib>Wu, Qiong</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>Genetics Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>ACTA HISTOCHEMICA ET CYTOCHEMICA</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gu, Tiantian</au><au>He, Hongjuan</au><au>Zhang, Yan</au><au>Han, Zhengbin</au><au>Hou, Guangyuan</au><au>Zeng, Tiebo</au><au>Liu, Qi</au><au>Wu, Qiong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Trmt112 Gene Expression in Mouse Embryonic Development</atitle><jtitle>ACTA HISTOCHEMICA ET CYTOCHEMICA</jtitle><addtitle>Acta Histochem. Cytochem.</addtitle><date>2012-01-01</date><risdate>2012</risdate><volume>45</volume><issue>2</issue><spage>113</spage><epage>119</epage><pages>113-119</pages><issn>0044-5991</issn><eissn>1347-5800</eissn><abstract>Mouse Trmt112, the homologous gene of yeast Trm112 (tRNA methyltransferase 11-2), was initially cloned from RIKEN with uncertain function. The yeast TRM112 is now known to play important roles in RNA methylation. Here, we studied the expression of Trmt112 by in situ hybridization and quantitative real-time RT-PCR (QRT-PCR). A higher expression level of Trmt112 was observed in the brain and nervous system by whole mount in situ hybridization from embryonic day 10.5 (E10.5) to E11.5. At later developmental stages E13.5 and E16.5, abundant expression was prominently found in various organs and tissues including developing brain, nervous system, thymus, lung, liver, intestine, kidney, and cartilage. 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subjects | in situ hybridization mouse development QRT-PCR Regular TRM112 |
title | Trmt112 Gene Expression in Mouse Embryonic Development |
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