Seven Lotus japonicus Genes Required for Transcriptional Reprogramming of the Root during Fungal and Bacterial SymbiosisW

A combined genetic and transcriptome analysis was performed to study the molecular basis of the arbuscular mycorrhiza (AM) symbiosis. By testing the AM phenotype of nodulation-impaired mutants and complementation analysis, we defined seven Lotus japonicus common symbiosis genes ( SYMRK , CASTOR , PO...

Full description

Saved in:
Bibliographic Details
Published inThe Plant cell Vol. 17; no. 8; pp. 2217 - 2229
Main Authors Kistner, Catherine, Winzer, Thilo, Pitzschke, Andrea, Mulder, Lonneke, Sato, Shusei, Kaneko, Takakazu, Tabata, Satoshi, Sandal, Niels, Stougaard, Jens, Webb, K. Judith, Szczyglowski, Krzysztof, Parniske, Martin
Format Journal Article
LanguageEnglish
Published American Society of Plant Biologists 01.08.2005
Online AccessGet full text

Cover

Loading…
More Information
Summary:A combined genetic and transcriptome analysis was performed to study the molecular basis of the arbuscular mycorrhiza (AM) symbiosis. By testing the AM phenotype of nodulation-impaired mutants and complementation analysis, we defined seven Lotus japonicus common symbiosis genes ( SYMRK , CASTOR , POLLUX , SYM3 , SYM6 , SYM15 , and SYM24 ) that are required for both fungal and bacterial entry into root epidermal or cortical cells. To describe the phenotype of these mutants at the molecular level, we screened for differentiating transcriptional responses of mutant and wild-type roots by large-scale gene expression profiling using cDNA-amplified fragment length polymorphism. Two percent of root transcripts was found to increase in abundance during AM development, from which a set of AM-regulated marker genes was established. A Ser-protease ( SbtS ) and a Cys-protease ( CysS ) were also activated during root nodule development. AM-induced transcriptional activation was abolished in roots carrying mutations in common symbiosis genes, suggesting a central position of these genes in a pathway leading to the transcriptional activation of downstream genes. By contrast, AM fungus-induced gene repression appeared to be unaffected in mutant backgrounds, which indicates the presence of additional independent signaling pathways.
Bibliography:The author responsible for distribution of materials integral to the findings presented in this article in accordance with the policy described in the Instructions for Authors (www.plantcell.org) is: Martin Parniske (parniske@lmu.de).
These authors contributed equally to this work.
Current address: MRC Geneservice, Rosalind Franklin Centre for Genomics Research, Wellcome Trust Genome Campus, Hinxton, Cambridge CB10 1SB, UK.
Article, publication date, and citation information can be found at www.plantcell.org/cgi/doi/10.1105/tpc.105.032714.
Current address: Ludwig-Maximilians-Universität München, Institut für Genetik, Maria Ward Straße 1a, D-80638 München, Germany.
Current address: Deutsche Forschungsgemeinschaft, Kennedyallee 40, 53175 Bonn, Germany.
Online version contains Web-only data.
Current address: Vienna BioCenter, Dr. Bohrgasse 9, A-1030 Vienna, Austria.
Current address: Laboratoire des Interactions Plantes-Microorganismes, CNRS-INRA, 31326 Castanet-Tolosan Cedex, France.
ISSN:1040-4651
1532-298X
DOI:10.1105/tpc.105.032714