An improved method for RNA isolation and cDNA library construction from immature seeds of <it>Jatropha curcas </it>L

<p>Abstract</p> <p>Background</p> <p>RNA quality and quantity is sometimes unsuitable for cDNA library construction, from plant seeds rich in oil, polysaccharides and other secondary metabolites. Seeds of jatropha (<it>Jatropha curcas </it>L.) are rich in fa...

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Main Authors: Kaur Jatinder, Gu Keyu, Sangha Jatinder, Yin Zhongchao
Format: Article
Language:English
Published: BMC 2010-05-01
Series:BMC Research Notes
Online Access:http://www.biomedcentral.com/1756-0500/3/126
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spelling doaj-88ba8842b9b348ed8d340f7315cf28c22020-11-25T02:20:20ZengBMCBMC Research Notes1756-05002010-05-013112610.1186/1756-0500-3-126An improved method for RNA isolation and cDNA library construction from immature seeds of <it>Jatropha curcas </it>LKaur JatinderGu KeyuSangha JatinderYin Zhongchao<p>Abstract</p> <p>Background</p> <p>RNA quality and quantity is sometimes unsuitable for cDNA library construction, from plant seeds rich in oil, polysaccharides and other secondary metabolites. Seeds of jatropha (<it>Jatropha curcas </it>L.) are rich in fatty acids/lipids, storage proteins, polysaccharides, and a number of other secondary metabolites that could either bind and/or co-precipitate with RNA, making it unsuitable for downstream applications. Existing RNA isolation methods and commercial kits often fail to deliver high-quality total RNA from immature jatropha seeds for poly(A)<sup>+ </sup>RNA purification and cDNA synthesis.</p> <p>Findings</p> <p>A protocol has been developed for isolating good quality total RNA from immature jatropha seeds, whereby a combination of the CTAB based RNA extraction method and a silica column of a commercial plant RNA extraction kit is used. The extraction time was reduced from two days to about 3 hours and the RNA was suitable for poly(A)<sup>+ </sup>RNA purification, cDNA synthesis, cDNA library construction, RT-PCR, and Northern hybridization. Based on sequence information from selected clones and amplified PCR product, the cDNA library seems to be a good source of full-length jatropha genes. The method was equally effective for isolating RNA from mustard and rice seeds.</p> <p>Conclusions</p> <p>This is a simple CTAB + silica column method to extract high quality RNA from oil rich immature jatropha seeds that is suitable for several downstream applications. This method takes less time for RNA extraction and is equally effective for other tissues where the quality and quantity of RNA is highly interfered by the presence of fatty acids, polysaccharides and polyphenols.</p> http://www.biomedcentral.com/1756-0500/3/126
collection DOAJ
language English
format Article
sources DOAJ
author Kaur Jatinder
Gu Keyu
Sangha Jatinder
Yin Zhongchao
spellingShingle Kaur Jatinder
Gu Keyu
Sangha Jatinder
Yin Zhongchao
An improved method for RNA isolation and cDNA library construction from immature seeds of <it>Jatropha curcas </it>L
BMC Research Notes
author_facet Kaur Jatinder
Gu Keyu
Sangha Jatinder
Yin Zhongchao
author_sort Kaur Jatinder
title An improved method for RNA isolation and cDNA library construction from immature seeds of <it>Jatropha curcas </it>L
title_short An improved method for RNA isolation and cDNA library construction from immature seeds of <it>Jatropha curcas </it>L
title_full An improved method for RNA isolation and cDNA library construction from immature seeds of <it>Jatropha curcas </it>L
title_fullStr An improved method for RNA isolation and cDNA library construction from immature seeds of <it>Jatropha curcas </it>L
title_full_unstemmed An improved method for RNA isolation and cDNA library construction from immature seeds of <it>Jatropha curcas </it>L
title_sort improved method for rna isolation and cdna library construction from immature seeds of <it>jatropha curcas </it>l
publisher BMC
series BMC Research Notes
issn 1756-0500
publishDate 2010-05-01
description <p>Abstract</p> <p>Background</p> <p>RNA quality and quantity is sometimes unsuitable for cDNA library construction, from plant seeds rich in oil, polysaccharides and other secondary metabolites. Seeds of jatropha (<it>Jatropha curcas </it>L.) are rich in fatty acids/lipids, storage proteins, polysaccharides, and a number of other secondary metabolites that could either bind and/or co-precipitate with RNA, making it unsuitable for downstream applications. Existing RNA isolation methods and commercial kits often fail to deliver high-quality total RNA from immature jatropha seeds for poly(A)<sup>+ </sup>RNA purification and cDNA synthesis.</p> <p>Findings</p> <p>A protocol has been developed for isolating good quality total RNA from immature jatropha seeds, whereby a combination of the CTAB based RNA extraction method and a silica column of a commercial plant RNA extraction kit is used. The extraction time was reduced from two days to about 3 hours and the RNA was suitable for poly(A)<sup>+ </sup>RNA purification, cDNA synthesis, cDNA library construction, RT-PCR, and Northern hybridization. Based on sequence information from selected clones and amplified PCR product, the cDNA library seems to be a good source of full-length jatropha genes. The method was equally effective for isolating RNA from mustard and rice seeds.</p> <p>Conclusions</p> <p>This is a simple CTAB + silica column method to extract high quality RNA from oil rich immature jatropha seeds that is suitable for several downstream applications. This method takes less time for RNA extraction and is equally effective for other tissues where the quality and quantity of RNA is highly interfered by the presence of fatty acids, polysaccharides and polyphenols.</p>
url http://www.biomedcentral.com/1756-0500/3/126
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