Cargando…

Genome-Wide Identification of Binding Sites for SmTCP7a Transcription Factors of Eggplant during Bacterial Wilt Resistance by ChIP-Seq

Teosinte branched 1/cycloidea/proliferating cell factor (TCP) transcription factors play a key role in the regulation of plant biotic and abiotic stresses. In this study, our results show that SmTCP7a positively regulated bacterial wilt that was caused by Ralstonia solanacearum. ChIP-seq was conduct...

Descripción completa

Detalles Bibliográficos
Autores principales: Xiao, Xi’ou, Lin, Wenqiu, Feng, Enyou, Wu, Caiyu, Ou, Xiongchang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224693/
https://www.ncbi.nlm.nih.gov/pubmed/35743285
http://dx.doi.org/10.3390/ijms23126844
_version_ 1784733430786818048
author Xiao, Xi’ou
Lin, Wenqiu
Feng, Enyou
Wu, Caiyu
Ou, Xiongchang
author_facet Xiao, Xi’ou
Lin, Wenqiu
Feng, Enyou
Wu, Caiyu
Ou, Xiongchang
author_sort Xiao, Xi’ou
collection PubMed
description Teosinte branched 1/cycloidea/proliferating cell factor (TCP) transcription factors play a key role in the regulation of plant biotic and abiotic stresses. In this study, our results show that SmTCP7a positively regulated bacterial wilt that was caused by Ralstonia solanacearum. ChIP-seq was conducted to analyze the transcriptional regulation mechanism of SmTCP7a before (R0 h) and 48 h after infection (R48 h). SmTCP7a regulated a total of 92 and 91 peak-associated genes in R0 h and R48 h, respectively. A KEGG (Kyoto encyclopedia of genes and genomes) pathway analysis showed that phenylpropanoid biosynthesis, MAPK (mitogen-activated protein kinas) signaling pathway, plant hormone signal transduction and plant-pathogen interactions were involved. The difference in peaks between R0 h and R48 h showed that there were three peak-associated genes that were modulated by infection. A better understanding of the potential target genes of SmTCP7a in response to R. solanacearum will provide a comprehensive understanding of the SmTCP7a regulatory mechanism during the eggplant defense response to bacterial wilt.
format Online
Article
Text
id pubmed-9224693
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-92246932022-06-24 Genome-Wide Identification of Binding Sites for SmTCP7a Transcription Factors of Eggplant during Bacterial Wilt Resistance by ChIP-Seq Xiao, Xi’ou Lin, Wenqiu Feng, Enyou Wu, Caiyu Ou, Xiongchang Int J Mol Sci Article Teosinte branched 1/cycloidea/proliferating cell factor (TCP) transcription factors play a key role in the regulation of plant biotic and abiotic stresses. In this study, our results show that SmTCP7a positively regulated bacterial wilt that was caused by Ralstonia solanacearum. ChIP-seq was conducted to analyze the transcriptional regulation mechanism of SmTCP7a before (R0 h) and 48 h after infection (R48 h). SmTCP7a regulated a total of 92 and 91 peak-associated genes in R0 h and R48 h, respectively. A KEGG (Kyoto encyclopedia of genes and genomes) pathway analysis showed that phenylpropanoid biosynthesis, MAPK (mitogen-activated protein kinas) signaling pathway, plant hormone signal transduction and plant-pathogen interactions were involved. The difference in peaks between R0 h and R48 h showed that there were three peak-associated genes that were modulated by infection. A better understanding of the potential target genes of SmTCP7a in response to R. solanacearum will provide a comprehensive understanding of the SmTCP7a regulatory mechanism during the eggplant defense response to bacterial wilt. MDPI 2022-06-20 /pmc/articles/PMC9224693/ /pubmed/35743285 http://dx.doi.org/10.3390/ijms23126844 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Xiao, Xi’ou
Lin, Wenqiu
Feng, Enyou
Wu, Caiyu
Ou, Xiongchang
Genome-Wide Identification of Binding Sites for SmTCP7a Transcription Factors of Eggplant during Bacterial Wilt Resistance by ChIP-Seq
title Genome-Wide Identification of Binding Sites for SmTCP7a Transcription Factors of Eggplant during Bacterial Wilt Resistance by ChIP-Seq
title_full Genome-Wide Identification of Binding Sites for SmTCP7a Transcription Factors of Eggplant during Bacterial Wilt Resistance by ChIP-Seq
title_fullStr Genome-Wide Identification of Binding Sites for SmTCP7a Transcription Factors of Eggplant during Bacterial Wilt Resistance by ChIP-Seq
title_full_unstemmed Genome-Wide Identification of Binding Sites for SmTCP7a Transcription Factors of Eggplant during Bacterial Wilt Resistance by ChIP-Seq
title_short Genome-Wide Identification of Binding Sites for SmTCP7a Transcription Factors of Eggplant during Bacterial Wilt Resistance by ChIP-Seq
title_sort genome-wide identification of binding sites for smtcp7a transcription factors of eggplant during bacterial wilt resistance by chip-seq
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9224693/
https://www.ncbi.nlm.nih.gov/pubmed/35743285
http://dx.doi.org/10.3390/ijms23126844
work_keys_str_mv AT xiaoxiou genomewideidentificationofbindingsitesforsmtcp7atranscriptionfactorsofeggplantduringbacterialwiltresistancebychipseq
AT linwenqiu genomewideidentificationofbindingsitesforsmtcp7atranscriptionfactorsofeggplantduringbacterialwiltresistancebychipseq
AT fengenyou genomewideidentificationofbindingsitesforsmtcp7atranscriptionfactorsofeggplantduringbacterialwiltresistancebychipseq
AT wucaiyu genomewideidentificationofbindingsitesforsmtcp7atranscriptionfactorsofeggplantduringbacterialwiltresistancebychipseq
AT ouxiongchang genomewideidentificationofbindingsitesforsmtcp7atranscriptionfactorsofeggplantduringbacterialwiltresistancebychipseq