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Reverse Transcription of 18S rRNA with Poly(dT)18 and Other Homopolymers
Ribosomal 18S RNA is widely used as a housekeeping gene in expression studies, including end-point PCR, Northern analysis, and real-time experiments. However, there are two disadvantages and two points of error introduction in using 18S rRNA as a reference gene. First, 18S has no poly(A) tail, so it...
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Published in: | Plant molecular biology reporter 2013-02, Vol.31 (1), p.55-63 |
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creator | Bogdanović, Milica D. Dragićević, Milan B. Tanić, Nikola T. Todorović, Slađana I. Mišić, Danijela M. Živković, Suzana T. Tissier, Alain Simonović, Ana D. |
description | Ribosomal 18S RNA is widely used as a housekeeping gene in expression studies, including end-point PCR, Northern analysis, and real-time experiments. However, there are two disadvantages and two points of error introduction in using 18S rRNA as a reference gene. First, 18S has no poly(A) tail, so it is commonly reverse transcribed with specific primers or random hexamers, independently from poly(dT)-primed transcripts. Secondly, due to its abundance, the 18S cDNA must be extensively diluted to be comparable to the tested genes. In this study, 18S rRNA from five taxonomically diverse plant species, including
Physcomitrella patens
,
Adiantum capillus-veneris
,
Centaurium erythraea
,
Arabidopsis thaliana
, and
Zea mays
, was successfully reverse transcribed (RT) using poly(dT)
18
. As all other homopolymers, including poly(dA)
18
, poly(dC)
18
, and poly(dG)
18
, could serve as RT primers, it was concluded that homopolymers anneal by mispriming at the sites of complementary homopolymeric runs or segments rich in complementary base. Poly(dC)
18
was the most efficient as RT primer, and the only one which interfered with subsequent PCR, giving species-specific pattern of products. Poly(dT)-primed RT reactions were less efficient in comparison to specific primer or random hexamer-primed reactions. Homopolymeric priming of 18S in RT reactions is general in terms of RNA origin and the method of RNA isolation and is possibly applicable to other tailless housekeeping genes. |
doi_str_mv | 10.1007/s11105-012-0474-y |
format | article |
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Physcomitrella patens
,
Adiantum capillus-veneris
,
Centaurium erythraea
,
Arabidopsis thaliana
, and
Zea mays
, was successfully reverse transcribed (RT) using poly(dT)
18
. As all other homopolymers, including poly(dA)
18
, poly(dC)
18
, and poly(dG)
18
, could serve as RT primers, it was concluded that homopolymers anneal by mispriming at the sites of complementary homopolymeric runs or segments rich in complementary base. Poly(dC)
18
was the most efficient as RT primer, and the only one which interfered with subsequent PCR, giving species-specific pattern of products. Poly(dT)-primed RT reactions were less efficient in comparison to specific primer or random hexamer-primed reactions. Homopolymeric priming of 18S in RT reactions is general in terms of RNA origin and the method of RNA isolation and is possibly applicable to other tailless housekeeping genes.</description><identifier>ISSN: 0735-9640</identifier><identifier>EISSN: 1572-9818</identifier><identifier>DOI: 10.1007/s11105-012-0474-y</identifier><language>eng</language><publisher>New York: Springer-Verlag</publisher><subject>Bioinformatics ; Biomedical and Life Sciences ; Life Sciences ; Metabolomics ; Original Paper ; Plant Breeding/Biotechnology ; Plant Sciences ; Proteomics</subject><ispartof>Plant molecular biology reporter, 2013-02, Vol.31 (1), p.55-63</ispartof><rights>Springer-Verlag 2012</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c203y-b22333776992e433ed8d8435ab90e28dd17e455f91762e33cdc27974d53c01133</citedby><cites>FETCH-LOGICAL-c203y-b22333776992e433ed8d8435ab90e28dd17e455f91762e33cdc27974d53c01133</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Bogdanović, Milica D.</creatorcontrib><creatorcontrib>Dragićević, Milan B.</creatorcontrib><creatorcontrib>Tanić, Nikola T.</creatorcontrib><creatorcontrib>Todorović, Slađana I.</creatorcontrib><creatorcontrib>Mišić, Danijela M.</creatorcontrib><creatorcontrib>Živković, Suzana T.</creatorcontrib><creatorcontrib>Tissier, Alain</creatorcontrib><creatorcontrib>Simonović, Ana D.</creatorcontrib><title>Reverse Transcription of 18S rRNA with Poly(dT)18 and Other Homopolymers</title><title>Plant molecular biology reporter</title><addtitle>Plant Mol Biol Rep</addtitle><description>Ribosomal 18S RNA is widely used as a housekeeping gene in expression studies, including end-point PCR, Northern analysis, and real-time experiments. However, there are two disadvantages and two points of error introduction in using 18S rRNA as a reference gene. First, 18S has no poly(A) tail, so it is commonly reverse transcribed with specific primers or random hexamers, independently from poly(dT)-primed transcripts. Secondly, due to its abundance, the 18S cDNA must be extensively diluted to be comparable to the tested genes. In this study, 18S rRNA from five taxonomically diverse plant species, including
Physcomitrella patens
,
Adiantum capillus-veneris
,
Centaurium erythraea
,
Arabidopsis thaliana
, and
Zea mays
, was successfully reverse transcribed (RT) using poly(dT)
18
. As all other homopolymers, including poly(dA)
18
, poly(dC)
18
, and poly(dG)
18
, could serve as RT primers, it was concluded that homopolymers anneal by mispriming at the sites of complementary homopolymeric runs or segments rich in complementary base. Poly(dC)
18
was the most efficient as RT primer, and the only one which interfered with subsequent PCR, giving species-specific pattern of products. Poly(dT)-primed RT reactions were less efficient in comparison to specific primer or random hexamer-primed reactions. Homopolymeric priming of 18S in RT reactions is general in terms of RNA origin and the method of RNA isolation and is possibly applicable to other tailless housekeeping genes.</description><subject>Bioinformatics</subject><subject>Biomedical and Life Sciences</subject><subject>Life Sciences</subject><subject>Metabolomics</subject><subject>Original Paper</subject><subject>Plant Breeding/Biotechnology</subject><subject>Plant Sciences</subject><subject>Proteomics</subject><issn>0735-9640</issn><issn>1572-9818</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNp9kEtPAjEUhRujifj4Ae661EX13j5ouyRExYSIQVw3w7QjQ2BKWtTMv7cE167u4tzv5OQj5AbhHgH0Q0ZEUAyQM5Basv6EDFBpzqxBc0oGoIVidijhnFzkvIbCgDEDMpmH75ByoItUdblO7W7fxo7GhqJ5p2n-OqI_7X5F3-Kmv_WLOzS06jyd7Vch0Uncxl0JtqXhipw11SaH6797ST6eHhfjCZvOnl_GoymrOYieLTkXQmg9tJYHKUTwxhspVLW0ELjxHnWQSjUW9ZAHIWpfc2219ErUgCjEJcFjb51izik0bpfabZV6h-AOKtxRhSsq3EGF6wvDj0wuv91nSG4dv1JXZv4D_QJdC1-k</recordid><startdate>20130201</startdate><enddate>20130201</enddate><creator>Bogdanović, Milica D.</creator><creator>Dragićević, Milan B.</creator><creator>Tanić, Nikola T.</creator><creator>Todorović, Slađana I.</creator><creator>Mišić, Danijela M.</creator><creator>Živković, Suzana T.</creator><creator>Tissier, Alain</creator><creator>Simonović, Ana D.</creator><general>Springer-Verlag</general><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20130201</creationdate><title>Reverse Transcription of 18S rRNA with Poly(dT)18 and Other Homopolymers</title><author>Bogdanović, Milica D. ; Dragićević, Milan B. ; Tanić, Nikola T. ; Todorović, Slađana I. ; Mišić, Danijela M. ; Živković, Suzana T. ; Tissier, Alain ; Simonović, Ana D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c203y-b22333776992e433ed8d8435ab90e28dd17e455f91762e33cdc27974d53c01133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Bioinformatics</topic><topic>Biomedical and Life Sciences</topic><topic>Life Sciences</topic><topic>Metabolomics</topic><topic>Original Paper</topic><topic>Plant Breeding/Biotechnology</topic><topic>Plant Sciences</topic><topic>Proteomics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bogdanović, Milica D.</creatorcontrib><creatorcontrib>Dragićević, Milan B.</creatorcontrib><creatorcontrib>Tanić, Nikola T.</creatorcontrib><creatorcontrib>Todorović, Slađana I.</creatorcontrib><creatorcontrib>Mišić, Danijela M.</creatorcontrib><creatorcontrib>Živković, Suzana T.</creatorcontrib><creatorcontrib>Tissier, Alain</creatorcontrib><creatorcontrib>Simonović, Ana D.</creatorcontrib><collection>CrossRef</collection><jtitle>Plant molecular biology reporter</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bogdanović, Milica D.</au><au>Dragićević, Milan B.</au><au>Tanić, Nikola T.</au><au>Todorović, Slađana I.</au><au>Mišić, Danijela M.</au><au>Živković, Suzana T.</au><au>Tissier, Alain</au><au>Simonović, Ana D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Reverse Transcription of 18S rRNA with Poly(dT)18 and Other Homopolymers</atitle><jtitle>Plant molecular biology reporter</jtitle><stitle>Plant Mol Biol Rep</stitle><date>2013-02-01</date><risdate>2013</risdate><volume>31</volume><issue>1</issue><spage>55</spage><epage>63</epage><pages>55-63</pages><issn>0735-9640</issn><eissn>1572-9818</eissn><abstract>Ribosomal 18S RNA is widely used as a housekeeping gene in expression studies, including end-point PCR, Northern analysis, and real-time experiments. However, there are two disadvantages and two points of error introduction in using 18S rRNA as a reference gene. First, 18S has no poly(A) tail, so it is commonly reverse transcribed with specific primers or random hexamers, independently from poly(dT)-primed transcripts. Secondly, due to its abundance, the 18S cDNA must be extensively diluted to be comparable to the tested genes. In this study, 18S rRNA from five taxonomically diverse plant species, including
Physcomitrella patens
,
Adiantum capillus-veneris
,
Centaurium erythraea
,
Arabidopsis thaliana
, and
Zea mays
, was successfully reverse transcribed (RT) using poly(dT)
18
. As all other homopolymers, including poly(dA)
18
, poly(dC)
18
, and poly(dG)
18
, could serve as RT primers, it was concluded that homopolymers anneal by mispriming at the sites of complementary homopolymeric runs or segments rich in complementary base. Poly(dC)
18
was the most efficient as RT primer, and the only one which interfered with subsequent PCR, giving species-specific pattern of products. Poly(dT)-primed RT reactions were less efficient in comparison to specific primer or random hexamer-primed reactions. Homopolymeric priming of 18S in RT reactions is general in terms of RNA origin and the method of RNA isolation and is possibly applicable to other tailless housekeeping genes.</abstract><cop>New York</cop><pub>Springer-Verlag</pub><doi>10.1007/s11105-012-0474-y</doi><tpages>9</tpages></addata></record> |
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subjects | Bioinformatics Biomedical and Life Sciences Life Sciences Metabolomics Original Paper Plant Breeding/Biotechnology Plant Sciences Proteomics |
title | Reverse Transcription of 18S rRNA with Poly(dT)18 and Other Homopolymers |
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