Synthesis of novel siRNAs having thymidine dimers consisting of a carbamate or a urea linkage at their 3′ overhang regions and their ability to suppress human RNase L protein expression
In order to examine the effect of modifications at the 3′ overhang regions of short interfering RNAs (siRNAs) on their gene-silencing activities, we designed and synthesized novel siRNAs having thymidine dimers consisting of a carbamate or a urea linkage at their 3′ overhang regions. Suppression of...
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Veröffentlicht in: | Biochemical and biophysical research communications 2005-05, Vol.330 (4), p.1168-1175 |
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creator | Ueno, Yoshihito Naito, Tomoharu Kawada, Koshi Shibata, Aya Kim, Hye-Sook Wataya, Yusuke Kitade, Yukio |
description | In order to examine the effect of modifications at the 3′ overhang regions of short interfering RNAs (siRNAs) on their gene-silencing activities, we designed and synthesized novel siRNAs having thymidine dimers consisting of a carbamate or a urea linkage at their 3′ overhang regions. Suppression of human RNase L protein expression by these siRNAs was analyzed by immunoblot with RNase L-specific antibody. It was found that, at 24
h post-transfection, the modified siRNAs having the thymidine dimers with the carbamate and urea linkage suppress the protein expression 78 and 37 times more efficiently than that with the natural phosphodiester linkage, respectively. Furthermore, the siRNA containing the carbamate linkage was 37 times more resistant to nucleolytic degradation by snake venom phosphodiesterase than the siRNA consisting of the natural phosphodiester linkage. Thus, the RNA duplexes having the thymidine dimers with the carbamate or urea linkage at their 3′ overhang regions will be promising candidates for novel siRNA molecules to down-regulate protein expression. |
doi_str_mv | 10.1016/j.bbrc.2005.03.100 |
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h post-transfection, the modified siRNAs having the thymidine dimers with the carbamate and urea linkage suppress the protein expression 78 and 37 times more efficiently than that with the natural phosphodiester linkage, respectively. Furthermore, the siRNA containing the carbamate linkage was 37 times more resistant to nucleolytic degradation by snake venom phosphodiesterase than the siRNA consisting of the natural phosphodiester linkage. Thus, the RNA duplexes having the thymidine dimers with the carbamate or urea linkage at their 3′ overhang regions will be promising candidates for novel siRNA molecules to down-regulate protein expression.</description><identifier>ISSN: 0006-291X</identifier><identifier>EISSN: 1090-2104</identifier><identifier>DOI: 10.1016/j.bbrc.2005.03.100</identifier><identifier>PMID: 15823566</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Carbamate ; Carbamates - chemistry ; Dimerization ; Endoribonucleases - antagonists & inhibitors ; Endoribonucleases - biosynthesis ; Humans ; Nucleic Acid Denaturation ; Phosphoric Diester Hydrolases - chemistry ; RNA, Small Interfering - chemical synthesis ; RNA, Small Interfering - metabolism ; RNA, Small Interfering - pharmacology ; RNAi ; RNase L ; siRNA ; Snake Venoms - enzymology ; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization ; Thymidine - chemistry ; Tumor Cells, Cultured ; Urea ; Urea - chemistry</subject><ispartof>Biochemical and biophysical research communications, 2005-05, Vol.330 (4), p.1168-1175</ispartof><rights>2005 Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c385t-1dd9b4907ffa64ff6ffc62f2bdca2a061f190268c6801adbde44342acf2ce2d83</citedby><cites>FETCH-LOGICAL-c385t-1dd9b4907ffa64ff6ffc62f2bdca2a061f190268c6801adbde44342acf2ce2d83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0006291X05005887$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15823566$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ueno, Yoshihito</creatorcontrib><creatorcontrib>Naito, Tomoharu</creatorcontrib><creatorcontrib>Kawada, Koshi</creatorcontrib><creatorcontrib>Shibata, Aya</creatorcontrib><creatorcontrib>Kim, Hye-Sook</creatorcontrib><creatorcontrib>Wataya, Yusuke</creatorcontrib><creatorcontrib>Kitade, Yukio</creatorcontrib><title>Synthesis of novel siRNAs having thymidine dimers consisting of a carbamate or a urea linkage at their 3′ overhang regions and their ability to suppress human RNase L protein expression</title><title>Biochemical and biophysical research communications</title><addtitle>Biochem Biophys Res Commun</addtitle><description>In order to examine the effect of modifications at the 3′ overhang regions of short interfering RNAs (siRNAs) on their gene-silencing activities, we designed and synthesized novel siRNAs having thymidine dimers consisting of a carbamate or a urea linkage at their 3′ overhang regions. Suppression of human RNase L protein expression by these siRNAs was analyzed by immunoblot with RNase L-specific antibody. It was found that, at 24
h post-transfection, the modified siRNAs having the thymidine dimers with the carbamate and urea linkage suppress the protein expression 78 and 37 times more efficiently than that with the natural phosphodiester linkage, respectively. Furthermore, the siRNA containing the carbamate linkage was 37 times more resistant to nucleolytic degradation by snake venom phosphodiesterase than the siRNA consisting of the natural phosphodiester linkage. Thus, the RNA duplexes having the thymidine dimers with the carbamate or urea linkage at their 3′ overhang regions will be promising candidates for novel siRNA molecules to down-regulate protein expression.</description><subject>Carbamate</subject><subject>Carbamates - chemistry</subject><subject>Dimerization</subject><subject>Endoribonucleases - antagonists & inhibitors</subject><subject>Endoribonucleases - biosynthesis</subject><subject>Humans</subject><subject>Nucleic Acid Denaturation</subject><subject>Phosphoric Diester Hydrolases - chemistry</subject><subject>RNA, Small Interfering - chemical synthesis</subject><subject>RNA, Small Interfering - metabolism</subject><subject>RNA, Small Interfering - pharmacology</subject><subject>RNAi</subject><subject>RNase L</subject><subject>siRNA</subject><subject>Snake Venoms - enzymology</subject><subject>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</subject><subject>Thymidine - chemistry</subject><subject>Tumor Cells, Cultured</subject><subject>Urea</subject><subject>Urea - chemistry</subject><issn>0006-291X</issn><issn>1090-2104</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc2O0zAUhSMEYsrAC7BAXrFruXZSJ5HYjEb8SdUgDSCxs27s69YlcYrtVHQ3zzRb3oYnwaWV2MHK8j3fObq6pyiec1hw4PLVdtF1QS8EwHIBZZ7Bg2LGoYW54FA9LGYAIOei5V8viicxbgE4r2T7uLjgy0aUSylnxc9PB582FF1ko2V-3FPPoru9uYpsg3vn1yxtDoMzzhMzbqAQmR59xtNRyxZkGkOHAyZiY8jfKRCy3vlvuCaGKfvJBVb-urtnOT1sMPsCrV1OYejNWcfO9S4dWBpZnHa7QDEvMA3o2e0NRmIrtgtjIucZ_fijZv_T4pHFPtKz83tZfHn75vP1-_nq47sP11eruS6bZZpzY9quaqG2FmVlrbRWS2FFZzQKBMktb0HIRssGOJrOUFWVlUBthSZhmvKyeHnKzSt8nygmNbioqe_R0zhFJeu6FLyq_wvyuimrumozKE6gDmOMgazaBTdgOCgO6tit2qpjt-rYrYIyzyCbXpzTp24g89dyLjMDr08A5WPsHQUVtSOvybhAOikzun_l_wZv_brt</recordid><startdate>20050520</startdate><enddate>20050520</enddate><creator>Ueno, Yoshihito</creator><creator>Naito, Tomoharu</creator><creator>Kawada, Koshi</creator><creator>Shibata, Aya</creator><creator>Kim, Hye-Sook</creator><creator>Wataya, Yusuke</creator><creator>Kitade, Yukio</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>7TM</scope><scope>7X8</scope></search><sort><creationdate>20050520</creationdate><title>Synthesis of novel siRNAs having thymidine dimers consisting of a carbamate or a urea linkage at their 3′ overhang regions and their ability to suppress human RNase L protein expression</title><author>Ueno, Yoshihito ; Naito, Tomoharu ; Kawada, Koshi ; Shibata, Aya ; Kim, Hye-Sook ; Wataya, Yusuke ; Kitade, Yukio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c385t-1dd9b4907ffa64ff6ffc62f2bdca2a061f190268c6801adbde44342acf2ce2d83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Carbamate</topic><topic>Carbamates - chemistry</topic><topic>Dimerization</topic><topic>Endoribonucleases - antagonists & inhibitors</topic><topic>Endoribonucleases - biosynthesis</topic><topic>Humans</topic><topic>Nucleic Acid Denaturation</topic><topic>Phosphoric Diester Hydrolases - chemistry</topic><topic>RNA, Small Interfering - chemical synthesis</topic><topic>RNA, Small Interfering - metabolism</topic><topic>RNA, Small Interfering - pharmacology</topic><topic>RNAi</topic><topic>RNase L</topic><topic>siRNA</topic><topic>Snake Venoms - enzymology</topic><topic>Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization</topic><topic>Thymidine - chemistry</topic><topic>Tumor Cells, Cultured</topic><topic>Urea</topic><topic>Urea - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ueno, Yoshihito</creatorcontrib><creatorcontrib>Naito, Tomoharu</creatorcontrib><creatorcontrib>Kawada, Koshi</creatorcontrib><creatorcontrib>Shibata, Aya</creatorcontrib><creatorcontrib>Kim, Hye-Sook</creatorcontrib><creatorcontrib>Wataya, Yusuke</creatorcontrib><creatorcontrib>Kitade, Yukio</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Nucleic Acids Abstracts</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>Ueno, Yoshihito</au><au>Naito, Tomoharu</au><au>Kawada, Koshi</au><au>Shibata, Aya</au><au>Kim, Hye-Sook</au><au>Wataya, Yusuke</au><au>Kitade, Yukio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of novel siRNAs having thymidine dimers consisting of a carbamate or a urea linkage at their 3′ overhang regions and their ability to suppress human RNase L protein expression</atitle><jtitle>Biochemical and biophysical research communications</jtitle><addtitle>Biochem Biophys Res Commun</addtitle><date>2005-05-20</date><risdate>2005</risdate><volume>330</volume><issue>4</issue><spage>1168</spage><epage>1175</epage><pages>1168-1175</pages><issn>0006-291X</issn><eissn>1090-2104</eissn><abstract>In order to examine the effect of modifications at the 3′ overhang regions of short interfering RNAs (siRNAs) on their gene-silencing activities, we designed and synthesized novel siRNAs having thymidine dimers consisting of a carbamate or a urea linkage at their 3′ overhang regions. Suppression of human RNase L protein expression by these siRNAs was analyzed by immunoblot with RNase L-specific antibody. It was found that, at 24
h post-transfection, the modified siRNAs having the thymidine dimers with the carbamate and urea linkage suppress the protein expression 78 and 37 times more efficiently than that with the natural phosphodiester linkage, respectively. Furthermore, the siRNA containing the carbamate linkage was 37 times more resistant to nucleolytic degradation by snake venom phosphodiesterase than the siRNA consisting of the natural phosphodiester linkage. Thus, the RNA duplexes having the thymidine dimers with the carbamate or urea linkage at their 3′ overhang regions will be promising candidates for novel siRNA molecules to down-regulate protein expression.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>15823566</pmid><doi>10.1016/j.bbrc.2005.03.100</doi><tpages>8</tpages></addata></record> |
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subjects | Carbamate Carbamates - chemistry Dimerization Endoribonucleases - antagonists & inhibitors Endoribonucleases - biosynthesis Humans Nucleic Acid Denaturation Phosphoric Diester Hydrolases - chemistry RNA, Small Interfering - chemical synthesis RNA, Small Interfering - metabolism RNA, Small Interfering - pharmacology RNAi RNase L siRNA Snake Venoms - enzymology Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization Thymidine - chemistry Tumor Cells, Cultured Urea Urea - chemistry |
title | Synthesis of novel siRNAs having thymidine dimers consisting of a carbamate or a urea linkage at their 3′ overhang regions and their ability to suppress human RNase L protein expression |
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