Integration of molecular biology tools for identifying promoters and genes abundantly expressed in flowers of <it>Oncidium </it>Gower Ramsey

<p>Abstract</p> <p>Background</p> <p>Orchids comprise one of the largest families of flowering plants and generate commercially important flowers. However, model plants, such as <it>Arabidopsis thaliana </it>do not contain all plant genes, and agronomic and...

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Main Authors: Tung Shu-Yun, Chou Shu-Jen, Shen Shu-Chen, Liu Nien-Tze, Wu Fu-Hui, Liao De-Chih, Hsu Chen-Tran, Yang Chang-Hsien, Chan Ming-Tsair, Lin Choun-Sea
Format: Article
Language:English
Published: BMC 2011-04-01
Series:BMC Plant Biology
Online Access:http://www.biomedcentral.com/1471-2229/11/60
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author Tung Shu-Yun
Chou Shu-Jen
Shen Shu-Chen
Liu Nien-Tze
Wu Fu-Hui
Liao De-Chih
Hsu Chen-Tran
Yang Chang-Hsien
Chan Ming-Tsair
Lin Choun-Sea
author_facet Tung Shu-Yun
Chou Shu-Jen
Shen Shu-Chen
Liu Nien-Tze
Wu Fu-Hui
Liao De-Chih
Hsu Chen-Tran
Yang Chang-Hsien
Chan Ming-Tsair
Lin Choun-Sea
author_sort Tung Shu-Yun
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>Orchids comprise one of the largest families of flowering plants and generate commercially important flowers. However, model plants, such as <it>Arabidopsis thaliana </it>do not contain all plant genes, and agronomic and horticulturally important genera and species must be individually studied.</p> <p>Results</p> <p>Several molecular biology tools were used to isolate flower-specific gene promoters from <it>Oncidium </it>'Gower Ramsey' (<it>Onc</it>. GR). A cDNA library of reproductive tissues was used to construct a microarray in order to compare gene expression in flowers and leaves. Five genes were highly expressed in flower tissues, and the subcellular locations of the corresponding proteins were identified using lip transient transformation with fluorescent protein-fusion constructs. BAC clones of the 5 genes, together with 7 previously published flower- and reproductive growth-specific genes in <it>Onc</it>. GR, were identified for cloning of their promoter regions. Interestingly, 3 of the 5 novel flower-abundant genes were putative trypsin inhibitor (<it>TI</it>) genes (<it>OnTI1</it>, <it>OnTI2 </it>and <it>OnTI3</it>), which were tandemly duplicated in the same BAC clone. Their promoters were identified using transient GUS reporter gene transformation and stable <it>A. thaliana </it>transformation analyses.</p> <p>Conclusions</p> <p>By combining cDNA microarray, BAC library, and bombardment assay techniques, we successfully identified flower-directed orchid genes and promoters.</p>
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spelling doaj.art-07136c9e6ffb4caaa0dde210f5e8b6832022-12-21T22:11:52ZengBMCBMC Plant Biology1471-22292011-04-011116010.1186/1471-2229-11-60Integration of molecular biology tools for identifying promoters and genes abundantly expressed in flowers of <it>Oncidium </it>Gower RamseyTung Shu-YunChou Shu-JenShen Shu-ChenLiu Nien-TzeWu Fu-HuiLiao De-ChihHsu Chen-TranYang Chang-HsienChan Ming-TsairLin Choun-Sea<p>Abstract</p> <p>Background</p> <p>Orchids comprise one of the largest families of flowering plants and generate commercially important flowers. However, model plants, such as <it>Arabidopsis thaliana </it>do not contain all plant genes, and agronomic and horticulturally important genera and species must be individually studied.</p> <p>Results</p> <p>Several molecular biology tools were used to isolate flower-specific gene promoters from <it>Oncidium </it>'Gower Ramsey' (<it>Onc</it>. GR). A cDNA library of reproductive tissues was used to construct a microarray in order to compare gene expression in flowers and leaves. Five genes were highly expressed in flower tissues, and the subcellular locations of the corresponding proteins were identified using lip transient transformation with fluorescent protein-fusion constructs. BAC clones of the 5 genes, together with 7 previously published flower- and reproductive growth-specific genes in <it>Onc</it>. GR, were identified for cloning of their promoter regions. Interestingly, 3 of the 5 novel flower-abundant genes were putative trypsin inhibitor (<it>TI</it>) genes (<it>OnTI1</it>, <it>OnTI2 </it>and <it>OnTI3</it>), which were tandemly duplicated in the same BAC clone. Their promoters were identified using transient GUS reporter gene transformation and stable <it>A. thaliana </it>transformation analyses.</p> <p>Conclusions</p> <p>By combining cDNA microarray, BAC library, and bombardment assay techniques, we successfully identified flower-directed orchid genes and promoters.</p>http://www.biomedcentral.com/1471-2229/11/60
spellingShingle Tung Shu-Yun
Chou Shu-Jen
Shen Shu-Chen
Liu Nien-Tze
Wu Fu-Hui
Liao De-Chih
Hsu Chen-Tran
Yang Chang-Hsien
Chan Ming-Tsair
Lin Choun-Sea
Integration of molecular biology tools for identifying promoters and genes abundantly expressed in flowers of <it>Oncidium </it>Gower Ramsey
BMC Plant Biology
title Integration of molecular biology tools for identifying promoters and genes abundantly expressed in flowers of <it>Oncidium </it>Gower Ramsey
title_full Integration of molecular biology tools for identifying promoters and genes abundantly expressed in flowers of <it>Oncidium </it>Gower Ramsey
title_fullStr Integration of molecular biology tools for identifying promoters and genes abundantly expressed in flowers of <it>Oncidium </it>Gower Ramsey
title_full_unstemmed Integration of molecular biology tools for identifying promoters and genes abundantly expressed in flowers of <it>Oncidium </it>Gower Ramsey
title_short Integration of molecular biology tools for identifying promoters and genes abundantly expressed in flowers of <it>Oncidium </it>Gower Ramsey
title_sort integration of molecular biology tools for identifying promoters and genes abundantly expressed in flowers of it oncidium it gower ramsey
url http://www.biomedcentral.com/1471-2229/11/60
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