Cargando…

Cloning and Characterization of Two MAPK Genes UeKpp2 and UeKpp6 in Ustilago esculenta

Ustilago esculenta, resembling a fungal endophyte in Zizania latifolia, inhibits the host plant flowering and induces the host stems to swell and form edible galls. It is well believed that when and how the fungus infects and proliferates in the host plants during the host development is of importan...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Yafen, Ge, Qianwen, Cao, Qianchao, Cui, Haifeng, Hu, Peng, Yu, Xiaoping, Ye, Zihong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018589/
https://www.ncbi.nlm.nih.gov/pubmed/29594403
http://dx.doi.org/10.1007/s00284-018-1483-3
_version_ 1783334985238839296
author Zhang, Yafen
Ge, Qianwen
Cao, Qianchao
Cui, Haifeng
Hu, Peng
Yu, Xiaoping
Ye, Zihong
author_facet Zhang, Yafen
Ge, Qianwen
Cao, Qianchao
Cui, Haifeng
Hu, Peng
Yu, Xiaoping
Ye, Zihong
author_sort Zhang, Yafen
collection PubMed
description Ustilago esculenta, resembling a fungal endophyte in Zizania latifolia, inhibits the host plant flowering and induces the host stems to swell and form edible galls. It is well believed that when and how the fungus infects and proliferates in the host plants during the host development is of importance in the edible gall formation. Mitogen-activated protein kinases (MAPKs) have been found to play an important role in sensing environment cues and regulating infection. Two MAPK genes UeKpp2 and UeKpp6 from U. esculenta were cloned and suggested to be involved in the Fus3/Kss1 pathway by a phylogenetic analysis with the neighbor-joining method. Quantitative RT-PCR (qRT-PCR) analyses indicated that expression of UeKpp2 and UeKpp6 were induced during mating and infection processes, and their expression patterns displayed differentially under different carbon and nitrogen sources. In addition, subcellular localization of UeKpp2 or UeKpp6 fused with the reporter green fluoresce protein was observed by confocal laser scanning microscope, and yeast two-hybrid assays were carried out. Results showed that both UeKpp2 and UeKpp6 were located in cytoplasm and interacted with UePrf1, indicating their involvement in hyphal growth and host–pathogen regulation. Only UeKpp2 but not UeKpp6 interacted with the upstream MAPK kinase UeFuz7, implying an additional MAPK pathway, in which UeKpp6 involved, existed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00284-018-1483-3) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6018589
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Springer US
record_format MEDLINE/PubMed
spelling pubmed-60185892018-07-11 Cloning and Characterization of Two MAPK Genes UeKpp2 and UeKpp6 in Ustilago esculenta Zhang, Yafen Ge, Qianwen Cao, Qianchao Cui, Haifeng Hu, Peng Yu, Xiaoping Ye, Zihong Curr Microbiol Article Ustilago esculenta, resembling a fungal endophyte in Zizania latifolia, inhibits the host plant flowering and induces the host stems to swell and form edible galls. It is well believed that when and how the fungus infects and proliferates in the host plants during the host development is of importance in the edible gall formation. Mitogen-activated protein kinases (MAPKs) have been found to play an important role in sensing environment cues and regulating infection. Two MAPK genes UeKpp2 and UeKpp6 from U. esculenta were cloned and suggested to be involved in the Fus3/Kss1 pathway by a phylogenetic analysis with the neighbor-joining method. Quantitative RT-PCR (qRT-PCR) analyses indicated that expression of UeKpp2 and UeKpp6 were induced during mating and infection processes, and their expression patterns displayed differentially under different carbon and nitrogen sources. In addition, subcellular localization of UeKpp2 or UeKpp6 fused with the reporter green fluoresce protein was observed by confocal laser scanning microscope, and yeast two-hybrid assays were carried out. Results showed that both UeKpp2 and UeKpp6 were located in cytoplasm and interacted with UePrf1, indicating their involvement in hyphal growth and host–pathogen regulation. Only UeKpp2 but not UeKpp6 interacted with the upstream MAPK kinase UeFuz7, implying an additional MAPK pathway, in which UeKpp6 involved, existed. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s00284-018-1483-3) contains supplementary material, which is available to authorized users. Springer US 2018-03-28 2018 /pmc/articles/PMC6018589/ /pubmed/29594403 http://dx.doi.org/10.1007/s00284-018-1483-3 Text en © The Author(s) 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Article
Zhang, Yafen
Ge, Qianwen
Cao, Qianchao
Cui, Haifeng
Hu, Peng
Yu, Xiaoping
Ye, Zihong
Cloning and Characterization of Two MAPK Genes UeKpp2 and UeKpp6 in Ustilago esculenta
title Cloning and Characterization of Two MAPK Genes UeKpp2 and UeKpp6 in Ustilago esculenta
title_full Cloning and Characterization of Two MAPK Genes UeKpp2 and UeKpp6 in Ustilago esculenta
title_fullStr Cloning and Characterization of Two MAPK Genes UeKpp2 and UeKpp6 in Ustilago esculenta
title_full_unstemmed Cloning and Characterization of Two MAPK Genes UeKpp2 and UeKpp6 in Ustilago esculenta
title_short Cloning and Characterization of Two MAPK Genes UeKpp2 and UeKpp6 in Ustilago esculenta
title_sort cloning and characterization of two mapk genes uekpp2 and uekpp6 in ustilago esculenta
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6018589/
https://www.ncbi.nlm.nih.gov/pubmed/29594403
http://dx.doi.org/10.1007/s00284-018-1483-3
work_keys_str_mv AT zhangyafen cloningandcharacterizationoftwomapkgenesuekpp2anduekpp6inustilagoesculenta
AT geqianwen cloningandcharacterizationoftwomapkgenesuekpp2anduekpp6inustilagoesculenta
AT caoqianchao cloningandcharacterizationoftwomapkgenesuekpp2anduekpp6inustilagoesculenta
AT cuihaifeng cloningandcharacterizationoftwomapkgenesuekpp2anduekpp6inustilagoesculenta
AT hupeng cloningandcharacterizationoftwomapkgenesuekpp2anduekpp6inustilagoesculenta
AT yuxiaoping cloningandcharacterizationoftwomapkgenesuekpp2anduekpp6inustilagoesculenta
AT yezihong cloningandcharacterizationoftwomapkgenesuekpp2anduekpp6inustilagoesculenta