A tiling microarray for global analysis of chloroplast genome expression in cucumber and other plants

<p>Abstract</p> <p>Plastids are small organelles equipped with their own genomes (plastomes). Although these organelles are involved in numerous plant metabolic pathways, current knowledge about the transcriptional activity of plastomes is limited. To solve this problem, we constru...

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Main Authors: Pląder Wojciech, Urbaniak Radosław, Guzowska-Nowowiejska Magdalena, Żmieńko Agnieszka, Formanowicz Piotr, Figlerowicz Marek
Format: Article
Language:English
Published: BMC 2011-09-01
Series:Plant Methods
Online Access:http://www.plantmethods.com/content/7/1/29
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spelling doaj-342c9768133c4b41aa926b9ffc52f2382020-11-25T01:13:46ZengBMCPlant Methods1746-48112011-09-01712910.1186/1746-4811-7-29A tiling microarray for global analysis of chloroplast genome expression in cucumber and other plantsPląder WojciechUrbaniak RadosławGuzowska-Nowowiejska MagdalenaŻmieńko AgnieszkaFormanowicz PiotrFiglerowicz Marek<p>Abstract</p> <p>Plastids are small organelles equipped with their own genomes (plastomes). Although these organelles are involved in numerous plant metabolic pathways, current knowledge about the transcriptional activity of plastomes is limited. To solve this problem, we constructed a plastid tiling microarray (PlasTi-microarray) consisting of 1629 oligonucleotide probes. The oligonucleotides were designed based on the cucumber chloroplast genomic sequence and targeted both strands of the plastome in a non-contiguous arrangement. Up to 4 specific probes were designed for each gene/exon, and the intergenic regions were covered regularly, with 70-nt intervals. We also developed a protocol for direct chemical labeling and hybridization of as little as 2 micrograms of chloroplast RNA. We used this protocol for profiling the expression of the cucumber chloroplast plastome on the PlasTi-microarray. Owing to the high sequence similarity of plant plastomes, the newly constructed microarray can be used to study plants other than cucumber. Comparative hybridization of chloroplast transcriptomes from cucumber, <it>Arabidopsis</it>, tomato and spinach showed that the PlasTi-microarray is highly versatile.</p> http://www.plantmethods.com/content/7/1/29
collection DOAJ
language English
format Article
sources DOAJ
author Pląder Wojciech
Urbaniak Radosław
Guzowska-Nowowiejska Magdalena
Żmieńko Agnieszka
Formanowicz Piotr
Figlerowicz Marek
spellingShingle Pląder Wojciech
Urbaniak Radosław
Guzowska-Nowowiejska Magdalena
Żmieńko Agnieszka
Formanowicz Piotr
Figlerowicz Marek
A tiling microarray for global analysis of chloroplast genome expression in cucumber and other plants
Plant Methods
author_facet Pląder Wojciech
Urbaniak Radosław
Guzowska-Nowowiejska Magdalena
Żmieńko Agnieszka
Formanowicz Piotr
Figlerowicz Marek
author_sort Pląder Wojciech
title A tiling microarray for global analysis of chloroplast genome expression in cucumber and other plants
title_short A tiling microarray for global analysis of chloroplast genome expression in cucumber and other plants
title_full A tiling microarray for global analysis of chloroplast genome expression in cucumber and other plants
title_fullStr A tiling microarray for global analysis of chloroplast genome expression in cucumber and other plants
title_full_unstemmed A tiling microarray for global analysis of chloroplast genome expression in cucumber and other plants
title_sort tiling microarray for global analysis of chloroplast genome expression in cucumber and other plants
publisher BMC
series Plant Methods
issn 1746-4811
publishDate 2011-09-01
description <p>Abstract</p> <p>Plastids are small organelles equipped with their own genomes (plastomes). Although these organelles are involved in numerous plant metabolic pathways, current knowledge about the transcriptional activity of plastomes is limited. To solve this problem, we constructed a plastid tiling microarray (PlasTi-microarray) consisting of 1629 oligonucleotide probes. The oligonucleotides were designed based on the cucumber chloroplast genomic sequence and targeted both strands of the plastome in a non-contiguous arrangement. Up to 4 specific probes were designed for each gene/exon, and the intergenic regions were covered regularly, with 70-nt intervals. We also developed a protocol for direct chemical labeling and hybridization of as little as 2 micrograms of chloroplast RNA. We used this protocol for profiling the expression of the cucumber chloroplast plastome on the PlasTi-microarray. Owing to the high sequence similarity of plant plastomes, the newly constructed microarray can be used to study plants other than cucumber. Comparative hybridization of chloroplast transcriptomes from cucumber, <it>Arabidopsis</it>, tomato and spinach showed that the PlasTi-microarray is highly versatile.</p>
url http://www.plantmethods.com/content/7/1/29
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