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5′-UTR and ORF elements, as well as the 3′-UTR regulate the translation of Cyclin
Mammalian oocyte maturation is wholly dependent on the translation of accumulated maternal transcripts. Therefore, measuring the translation of specific genes, especially Ccnb1 and Ccnb2, which are key regulators of the oocyte cell cycle in mice, is essential to monitor oocyte cell cycle progression...
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Published in: | Biochemical and biophysical research communications 2020-07, Vol.527 (4), p.968-973 |
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description | Mammalian oocyte maturation is wholly dependent on the translation of accumulated maternal transcripts. Therefore, measuring the translation of specific genes, especially Ccnb1 and Ccnb2, which are key regulators of the oocyte cell cycle in mice, is essential to monitor oocyte cell cycle progression. For this purpose, almost all previous research has used a reporter construct containing the 3′-untranslated region (UTR) of Ccnb. It is based on the concept that the 3′-UTR is the main modulator of translation. Here, we investigated the expression pattern of Renilla luciferase (RL) reporters combining the 5′-UTR and/or open reading frame (ORF) as well as the 3′-UTR (RL-3′, 5′-RL-3′, RL-ORF-3′, and 5′-RL-ORF-3′) of Ccnb1 and Ccnb2 in somatic cells and mouse oocytes. The addition of the 5′-UTR and/or ORF of Ccnb altered the expression of the RL-3′ reporter in HEK293T cells and mouse oocytes. The ORF tended to suppress RL expression, whereas the 5′-UTR enhanced the expression in most cases. The increased rate in expression was the highest when only the 3′-UTR of Ccnb1 (RL-3′) was used, whereas the 5′-RL-ORF-3′ reporter showed a relatively lower increase during oocyte maturation. For Ccnb2, the RL-ORF-3′ reporter showed the largest increase, and other reporters exhibited a similar increase in expression during oocyte maturation. Results show that the expression of these genes is modulated not only by the 3′-UTR but also by the 5′-UTR and ORF. Therefore, special caution should be taken when using only the 3′-UTR to monitor the expression of specific genes.
•The reporter containing 5′-UTR and/or ORF of Ccnb1 and Ccnb2, in addition to their 3′-UTR are differently expressed in HEK293T and mouse oocytes.•Reporters show varying translational expression patterns based on cell cycle stage.•Expression of these genes is modulated by the 5′-UTR, and ORF as well as the 3′-UTR.•Ccnb1 and Ccnb2 expression levels in vivo may not be recapitulated by a reporter gene with only 3′-UTR. |
doi_str_mv | 10.1016/j.bbrc.2020.04.151 |
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•The reporter containing 5′-UTR and/or ORF of Ccnb1 and Ccnb2, in addition to their 3′-UTR are differently expressed in HEK293T and mouse oocytes.•Reporters show varying translational expression patterns based on cell cycle stage.•Expression of these genes is modulated by the 5′-UTR, and ORF as well as the 3′-UTR.•Ccnb1 and Ccnb2 expression levels in vivo may not be recapitulated by a reporter gene with only 3′-UTR.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2020.04.151</identifier><identifier>PMID: 32439164</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>3' Untranslated Regions ; 5' Untranslated Regions ; Animals ; Cyclin B ; Cyclin B1 - genetics ; Cyclin B2 - genetics ; Female ; HEK293 Cells ; Humans ; Mice, Inbred C57BL ; Mouse oocyte ; Oocytes - metabolism ; Open reading frame ; Open Reading Frames ; Protein Biosynthesis ; Translational regulation ; Untranslated region</subject><ispartof>Biochemical and biophysical research communications, 2020-07, Vol.527 (4), p.968-973</ispartof><rights>2020 Elsevier Inc.</rights><rights>Copyright © 2020 Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-42b3996f2ac79d887b35fecf595a4e63d1f7ce9c25f806e62033dc7ca01d35843</citedby><cites>FETCH-LOGICAL-c356t-42b3996f2ac79d887b35fecf595a4e63d1f7ce9c25f806e62033dc7ca01d35843</cites><orcidid>0000-0003-3574-7668</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32439164$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kim, Boram</creatorcontrib><creatorcontrib>Kim, Hye Min</creatorcontrib><creatorcontrib>Kang, Min Kook</creatorcontrib><creatorcontrib>Sohn, Dong Hyun</creatorcontrib><creatorcontrib>Han, Seung Jin</creatorcontrib><title>5′-UTR and ORF elements, as well as the 3′-UTR regulate the translation of Cyclin</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>Mammalian oocyte maturation is wholly dependent on the translation of accumulated maternal transcripts. Therefore, measuring the translation of specific genes, especially Ccnb1 and Ccnb2, which are key regulators of the oocyte cell cycle in mice, is essential to monitor oocyte cell cycle progression. For this purpose, almost all previous research has used a reporter construct containing the 3′-untranslated region (UTR) of Ccnb. It is based on the concept that the 3′-UTR is the main modulator of translation. Here, we investigated the expression pattern of Renilla luciferase (RL) reporters combining the 5′-UTR and/or open reading frame (ORF) as well as the 3′-UTR (RL-3′, 5′-RL-3′, RL-ORF-3′, and 5′-RL-ORF-3′) of Ccnb1 and Ccnb2 in somatic cells and mouse oocytes. The addition of the 5′-UTR and/or ORF of Ccnb altered the expression of the RL-3′ reporter in HEK293T cells and mouse oocytes. The ORF tended to suppress RL expression, whereas the 5′-UTR enhanced the expression in most cases. The increased rate in expression was the highest when only the 3′-UTR of Ccnb1 (RL-3′) was used, whereas the 5′-RL-ORF-3′ reporter showed a relatively lower increase during oocyte maturation. For Ccnb2, the RL-ORF-3′ reporter showed the largest increase, and other reporters exhibited a similar increase in expression during oocyte maturation. Results show that the expression of these genes is modulated not only by the 3′-UTR but also by the 5′-UTR and ORF. Therefore, special caution should be taken when using only the 3′-UTR to monitor the expression of specific genes.
•The reporter containing 5′-UTR and/or ORF of Ccnb1 and Ccnb2, in addition to their 3′-UTR are differently expressed in HEK293T and mouse oocytes.•Reporters show varying translational expression patterns based on cell cycle stage.•Expression of these genes is modulated by the 5′-UTR, and ORF as well as the 3′-UTR.•Ccnb1 and Ccnb2 expression levels in vivo may not be recapitulated by a reporter gene with only 3′-UTR.</description><subject>3' Untranslated Regions</subject><subject>5' Untranslated Regions</subject><subject>Animals</subject><subject>Cyclin B</subject><subject>Cyclin B1 - genetics</subject><subject>Cyclin B2 - genetics</subject><subject>Female</subject><subject>HEK293 Cells</subject><subject>Humans</subject><subject>Mice, Inbred C57BL</subject><subject>Mouse oocyte</subject><subject>Oocytes - metabolism</subject><subject>Open reading frame</subject><subject>Open Reading Frames</subject><subject>Protein Biosynthesis</subject><subject>Translational regulation</subject><subject>Untranslated region</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kM1Kw0AQxxdRbP14AQ-SowcTZz-yzYIXKVaFQqG04G3ZbCaakiZ1N1V685l8JJ_ExLYePQ0z_ObPzI-QCwoRBSpvFlGaOhsxYBCBiGhMD0ifgoKQURCHpA8AMmSKPvfIifcLAEqFVMekx5ngikrRJ_P4-_MrnM-mgamyYDIdBVjiEqvGXwfGBx9Yll1tXjHge9Lhy7o0Df5OG2cq33ZFXQV1Hgw3tiyqM3KUm9Lj-a6ekvnofjZ8DMeTh6fh3Ti0PJZNKFjKlZI5M3agsiQZpDzO0eaxio1AyTOaDywqy-I8AYmSAeeZHVgDNONxIvgpudrmrlz9tkbf6GXhbXuzqbBee80ESA5CJaxF2Ra1rvbeYa5Xrlgat9EUdKdTL3SnU3c6NQjd6myXLnf563SJ2d_K3l8L3G4BbL98L9BpbwusLGaFQ9vorC7-y_8Bw8eF2A</recordid><startdate>20200705</startdate><enddate>20200705</enddate><creator>Kim, Boram</creator><creator>Kim, Hye Min</creator><creator>Kang, Min Kook</creator><creator>Sohn, Dong Hyun</creator><creator>Han, Seung Jin</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0003-3574-7668</orcidid></search><sort><creationdate>20200705</creationdate><title>5′-UTR and ORF elements, as well as the 3′-UTR regulate the translation of Cyclin</title><author>Kim, Boram ; Kim, Hye Min ; Kang, Min Kook ; Sohn, Dong Hyun ; Han, Seung Jin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-42b3996f2ac79d887b35fecf595a4e63d1f7ce9c25f806e62033dc7ca01d35843</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>3' Untranslated Regions</topic><topic>5' Untranslated Regions</topic><topic>Animals</topic><topic>Cyclin B</topic><topic>Cyclin B1 - genetics</topic><topic>Cyclin B2 - genetics</topic><topic>Female</topic><topic>HEK293 Cells</topic><topic>Humans</topic><topic>Mice, Inbred C57BL</topic><topic>Mouse oocyte</topic><topic>Oocytes - metabolism</topic><topic>Open reading frame</topic><topic>Open Reading Frames</topic><topic>Protein Biosynthesis</topic><topic>Translational regulation</topic><topic>Untranslated region</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kim, Boram</creatorcontrib><creatorcontrib>Kim, Hye Min</creatorcontrib><creatorcontrib>Kang, Min Kook</creatorcontrib><creatorcontrib>Sohn, Dong Hyun</creatorcontrib><creatorcontrib>Han, Seung Jin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Biochemical and biophysical research communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kim, Boram</au><au>Kim, Hye Min</au><au>Kang, Min Kook</au><au>Sohn, Dong Hyun</au><au>Han, Seung Jin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>5′-UTR and ORF elements, as well as the 3′-UTR regulate the translation of Cyclin</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2020-07-05</date><risdate>2020</risdate><volume>527</volume><issue>4</issue><spage>968</spage><epage>973</epage><pages>968-973</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>Mammalian oocyte maturation is wholly dependent on the translation of accumulated maternal transcripts. Therefore, measuring the translation of specific genes, especially Ccnb1 and Ccnb2, which are key regulators of the oocyte cell cycle in mice, is essential to monitor oocyte cell cycle progression. For this purpose, almost all previous research has used a reporter construct containing the 3′-untranslated region (UTR) of Ccnb. It is based on the concept that the 3′-UTR is the main modulator of translation. Here, we investigated the expression pattern of Renilla luciferase (RL) reporters combining the 5′-UTR and/or open reading frame (ORF) as well as the 3′-UTR (RL-3′, 5′-RL-3′, RL-ORF-3′, and 5′-RL-ORF-3′) of Ccnb1 and Ccnb2 in somatic cells and mouse oocytes. The addition of the 5′-UTR and/or ORF of Ccnb altered the expression of the RL-3′ reporter in HEK293T cells and mouse oocytes. The ORF tended to suppress RL expression, whereas the 5′-UTR enhanced the expression in most cases. The increased rate in expression was the highest when only the 3′-UTR of Ccnb1 (RL-3′) was used, whereas the 5′-RL-ORF-3′ reporter showed a relatively lower increase during oocyte maturation. For Ccnb2, the RL-ORF-3′ reporter showed the largest increase, and other reporters exhibited a similar increase in expression during oocyte maturation. Results show that the expression of these genes is modulated not only by the 3′-UTR but also by the 5′-UTR and ORF. Therefore, special caution should be taken when using only the 3′-UTR to monitor the expression of specific genes.
•The reporter containing 5′-UTR and/or ORF of Ccnb1 and Ccnb2, in addition to their 3′-UTR are differently expressed in HEK293T and mouse oocytes.•Reporters show varying translational expression patterns based on cell cycle stage.•Expression of these genes is modulated by the 5′-UTR, and ORF as well as the 3′-UTR.•Ccnb1 and Ccnb2 expression levels in vivo may not be recapitulated by a reporter gene with only 3′-UTR.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>32439164</pmid><doi>10.1016/j.bbrc.2020.04.151</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0003-3574-7668</orcidid></addata></record> |
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subjects | 3' Untranslated Regions 5' Untranslated Regions Animals Cyclin B Cyclin B1 - genetics Cyclin B2 - genetics Female HEK293 Cells Humans Mice, Inbred C57BL Mouse oocyte Oocytes - metabolism Open reading frame Open Reading Frames Protein Biosynthesis Translational regulation Untranslated region |
title | 5′-UTR and ORF elements, as well as the 3′-UTR regulate the translation of Cyclin |
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