Identification of key drought stress-related genes in the hyacinth bean.

Hyacinth bean (Lablab purpureus [Linn.] Sweet) possesses excellent characteristics for field production, but the response of this plant to drought stress has not been described at the molecular level. Suppression subtraction hybridization (SSH) is an effective way to exploit key factors for plant re...

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Main Authors: Lu-Ming Yao, Biao Wang, Lin-Jing Cheng, Tian-Long Wu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3589356?pdf=render
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author Lu-Ming Yao
Biao Wang
Lin-Jing Cheng
Tian-Long Wu
author_facet Lu-Ming Yao
Biao Wang
Lin-Jing Cheng
Tian-Long Wu
author_sort Lu-Ming Yao
collection DOAJ
description Hyacinth bean (Lablab purpureus [Linn.] Sweet) possesses excellent characteristics for field production, but the response of this plant to drought stress has not been described at the molecular level. Suppression subtraction hybridization (SSH) is an effective way to exploit key factors for plant responses to drought stress that are involved in transcriptional and metabolic activities. In this study, forward and reverse SSH libraries were generated from root tissues of the drought-tolerant hyacinth bean genotype MEIDOU 2012 under water-stress conditions. A total of 1,287 unigenes (94 contigs and 1,193 singletons) were derived from sequence alignment and cluster assembly of 1400 ESTs, and 80.6% of those hit against NCBI non-redundant (nr) database with E value <1E-06. BLASTX analysis revealed that the majority top matches were proteins form Glycine max (L.) Merrill. (61.5%). According to a gene ontology (GO) functional classification, 816 functionally annotated unigenes were assigned to the biological process category (74.1%), and 83.9% of them classified into molecular function and 69.2% involved in cellular component. A total of 168 sequences were further annotated with 207 Enzyme Commission (EC) codes and mapped to 83 different KEGG pathways. Seventeen functionally relevant genes were found to be overrepresented under drought stress using enrichment analysis. Differential expression of unigenes were confirmed by quantitative real-time PCR assays, and their transcript profiles generally divided into three patterns, depending on the expression peaked levels after 6, 8 or 10 days dehydration, which indicated that these genes are functionally associated in the drought-stress response.
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spelling doaj.art-8f175596364e47dabeaaefb40b0f0b612022-12-22T01:52:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0183e5810810.1371/journal.pone.0058108Identification of key drought stress-related genes in the hyacinth bean.Lu-Ming YaoBiao WangLin-Jing ChengTian-Long WuHyacinth bean (Lablab purpureus [Linn.] Sweet) possesses excellent characteristics for field production, but the response of this plant to drought stress has not been described at the molecular level. Suppression subtraction hybridization (SSH) is an effective way to exploit key factors for plant responses to drought stress that are involved in transcriptional and metabolic activities. In this study, forward and reverse SSH libraries were generated from root tissues of the drought-tolerant hyacinth bean genotype MEIDOU 2012 under water-stress conditions. A total of 1,287 unigenes (94 contigs and 1,193 singletons) were derived from sequence alignment and cluster assembly of 1400 ESTs, and 80.6% of those hit against NCBI non-redundant (nr) database with E value <1E-06. BLASTX analysis revealed that the majority top matches were proteins form Glycine max (L.) Merrill. (61.5%). According to a gene ontology (GO) functional classification, 816 functionally annotated unigenes were assigned to the biological process category (74.1%), and 83.9% of them classified into molecular function and 69.2% involved in cellular component. A total of 168 sequences were further annotated with 207 Enzyme Commission (EC) codes and mapped to 83 different KEGG pathways. Seventeen functionally relevant genes were found to be overrepresented under drought stress using enrichment analysis. Differential expression of unigenes were confirmed by quantitative real-time PCR assays, and their transcript profiles generally divided into three patterns, depending on the expression peaked levels after 6, 8 or 10 days dehydration, which indicated that these genes are functionally associated in the drought-stress response.http://europepmc.org/articles/PMC3589356?pdf=render
spellingShingle Lu-Ming Yao
Biao Wang
Lin-Jing Cheng
Tian-Long Wu
Identification of key drought stress-related genes in the hyacinth bean.
PLoS ONE
title Identification of key drought stress-related genes in the hyacinth bean.
title_full Identification of key drought stress-related genes in the hyacinth bean.
title_fullStr Identification of key drought stress-related genes in the hyacinth bean.
title_full_unstemmed Identification of key drought stress-related genes in the hyacinth bean.
title_short Identification of key drought stress-related genes in the hyacinth bean.
title_sort identification of key drought stress related genes in the hyacinth bean
url http://europepmc.org/articles/PMC3589356?pdf=render
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AT linjingcheng identificationofkeydroughtstressrelatedgenesinthehyacinthbean
AT tianlongwu identificationofkeydroughtstressrelatedgenesinthehyacinthbean