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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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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