Suppression of the pathogen-inducible Medicago truncatula putative protease-inhibitor MtTi2 does not influence root infection by Aphanomyces euteiches but results in transcriptional changes from wildtype roots

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OriginalspracheEnglisch
Seiten (von - bis)84-95
Seitenumfang12
FachzeitschriftPlant science
Jahrgang173
Ausgabenummer2
PublikationsstatusVeröffentlicht - 1 Aug. 2007
Extern publiziertJa

Abstract

During the parasitic interaction between the model legume Medicago truncatula and the oomycete Aphanomyces euteiches, a plant protease inhibitor (PI)-encoding gene, MtTi2, was found to be induced. Sequence and database analyses showed that MtTi2 belongs to a group of at least four PIs, which are all specifically expressed upon pathogen infection or elicitor treatment. Reporter analysis showed that the MtTi2 promoter is activated in infected root tissues and revealed a distinct promoter area involved in this transcriptional induction. In order to elucidate the function of MtTi2, RNAi-mediated silencing experiments were carried out. After introduction of double-stranded MtTi2 RNA into M. truncatula roots, no endogenous transcripts were observed, indicating efficient gene suppression. Since some plant protease inhibitors were shown to suppress pathogen growth, the MtTi2i-phenotype was analyzed with respect to pathogen spreading after root infection. No altered pathogen development was observed in MtTi2i-roots as compared to control roots, indicating that MtTi2 does not directly influence the pathogen. In order to investigate whether suppression of MtTi2 results in transcriptional changes, transcriptome profiles of MtTi2i roots and control roots were analyzed using an 8000 gene M. truncatula microarray. A cluster analysis of genes regulated in roots upon infection in two MtTi2i-lines or two vector lines revealed groups of genes showing different regulation in MtTi2i- and wild type roots. Hence, it is likely that MtTi2 has endogenous functions other than directly suppressing the pathogen. Furthermore, the transcriptome approach revealed insight into the transcriptional changes in response to A. euteiches infection.

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Suppression of the pathogen-inducible Medicago truncatula putative protease-inhibitor MtTi2 does not influence root infection by Aphanomyces euteiches but results in transcriptional changes from wildtype roots. / Nyamsuren, Oyunbileg; Firnhaber, Christian; Hohnjec, Natalija et al.
in: Plant science, Jahrgang 173, Nr. 2, 01.08.2007, S. 84-95.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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title = "Suppression of the pathogen-inducible Medicago truncatula putative protease-inhibitor MtTi2 does not influence root infection by Aphanomyces euteiches but results in transcriptional changes from wildtype roots",
abstract = "During the parasitic interaction between the model legume Medicago truncatula and the oomycete Aphanomyces euteiches, a plant protease inhibitor (PI)-encoding gene, MtTi2, was found to be induced. Sequence and database analyses showed that MtTi2 belongs to a group of at least four PIs, which are all specifically expressed upon pathogen infection or elicitor treatment. Reporter analysis showed that the MtTi2 promoter is activated in infected root tissues and revealed a distinct promoter area involved in this transcriptional induction. In order to elucidate the function of MtTi2, RNAi-mediated silencing experiments were carried out. After introduction of double-stranded MtTi2 RNA into M. truncatula roots, no endogenous transcripts were observed, indicating efficient gene suppression. Since some plant protease inhibitors were shown to suppress pathogen growth, the MtTi2i-phenotype was analyzed with respect to pathogen spreading after root infection. No altered pathogen development was observed in MtTi2i-roots as compared to control roots, indicating that MtTi2 does not directly influence the pathogen. In order to investigate whether suppression of MtTi2 results in transcriptional changes, transcriptome profiles of MtTi2i roots and control roots were analyzed using an 8000 gene M. truncatula microarray. A cluster analysis of genes regulated in roots upon infection in two MtTi2i-lines or two vector lines revealed groups of genes showing different regulation in MtTi2i- and wild type roots. Hence, it is likely that MtTi2 has endogenous functions other than directly suppressing the pathogen. Furthermore, the transcriptome approach revealed insight into the transcriptional changes in response to A. euteiches infection.",
keywords = "Aphanomyces euteiches, Medicago truncatula, Microarrays, Protease inhibitor, RNAi",
author = "Oyunbileg Nyamsuren and Christian Firnhaber and Natalija Hohnjec and Anke Becker and Helge K{\"u}ster and Franziska Krajinski",
note = "Funding information: This work was supported by the Grain Legumes Integrated Project (FOOD-CT-2004-506223) an EU FP6 project. Oyunbileg Nyamsuren was supported by a World Laboratory Scholarship.",
year = "2007",
month = aug,
day = "1",
doi = "10.1016/j.plantsci.2007.04.002",
language = "English",
volume = "173",
pages = "84--95",
journal = "Plant science",
issn = "0168-9452",
publisher = "Elsevier Ireland Ltd",
number = "2",

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TY - JOUR

T1 - Suppression of the pathogen-inducible Medicago truncatula putative protease-inhibitor MtTi2 does not influence root infection by Aphanomyces euteiches but results in transcriptional changes from wildtype roots

AU - Nyamsuren, Oyunbileg

AU - Firnhaber, Christian

AU - Hohnjec, Natalija

AU - Becker, Anke

AU - Küster, Helge

AU - Krajinski, Franziska

N1 - Funding information: This work was supported by the Grain Legumes Integrated Project (FOOD-CT-2004-506223) an EU FP6 project. Oyunbileg Nyamsuren was supported by a World Laboratory Scholarship.

PY - 2007/8/1

Y1 - 2007/8/1

N2 - During the parasitic interaction between the model legume Medicago truncatula and the oomycete Aphanomyces euteiches, a plant protease inhibitor (PI)-encoding gene, MtTi2, was found to be induced. Sequence and database analyses showed that MtTi2 belongs to a group of at least four PIs, which are all specifically expressed upon pathogen infection or elicitor treatment. Reporter analysis showed that the MtTi2 promoter is activated in infected root tissues and revealed a distinct promoter area involved in this transcriptional induction. In order to elucidate the function of MtTi2, RNAi-mediated silencing experiments were carried out. After introduction of double-stranded MtTi2 RNA into M. truncatula roots, no endogenous transcripts were observed, indicating efficient gene suppression. Since some plant protease inhibitors were shown to suppress pathogen growth, the MtTi2i-phenotype was analyzed with respect to pathogen spreading after root infection. No altered pathogen development was observed in MtTi2i-roots as compared to control roots, indicating that MtTi2 does not directly influence the pathogen. In order to investigate whether suppression of MtTi2 results in transcriptional changes, transcriptome profiles of MtTi2i roots and control roots were analyzed using an 8000 gene M. truncatula microarray. A cluster analysis of genes regulated in roots upon infection in two MtTi2i-lines or two vector lines revealed groups of genes showing different regulation in MtTi2i- and wild type roots. Hence, it is likely that MtTi2 has endogenous functions other than directly suppressing the pathogen. Furthermore, the transcriptome approach revealed insight into the transcriptional changes in response to A. euteiches infection.

AB - During the parasitic interaction between the model legume Medicago truncatula and the oomycete Aphanomyces euteiches, a plant protease inhibitor (PI)-encoding gene, MtTi2, was found to be induced. Sequence and database analyses showed that MtTi2 belongs to a group of at least four PIs, which are all specifically expressed upon pathogen infection or elicitor treatment. Reporter analysis showed that the MtTi2 promoter is activated in infected root tissues and revealed a distinct promoter area involved in this transcriptional induction. In order to elucidate the function of MtTi2, RNAi-mediated silencing experiments were carried out. After introduction of double-stranded MtTi2 RNA into M. truncatula roots, no endogenous transcripts were observed, indicating efficient gene suppression. Since some plant protease inhibitors were shown to suppress pathogen growth, the MtTi2i-phenotype was analyzed with respect to pathogen spreading after root infection. No altered pathogen development was observed in MtTi2i-roots as compared to control roots, indicating that MtTi2 does not directly influence the pathogen. In order to investigate whether suppression of MtTi2 results in transcriptional changes, transcriptome profiles of MtTi2i roots and control roots were analyzed using an 8000 gene M. truncatula microarray. A cluster analysis of genes regulated in roots upon infection in two MtTi2i-lines or two vector lines revealed groups of genes showing different regulation in MtTi2i- and wild type roots. Hence, it is likely that MtTi2 has endogenous functions other than directly suppressing the pathogen. Furthermore, the transcriptome approach revealed insight into the transcriptional changes in response to A. euteiches infection.

KW - Aphanomyces euteiches

KW - Medicago truncatula

KW - Microarrays

KW - Protease inhibitor

KW - RNAi

UR - http://www.scopus.com/inward/record.url?scp=34250793438&partnerID=8YFLogxK

U2 - 10.1016/j.plantsci.2007.04.002

DO - 10.1016/j.plantsci.2007.04.002

M3 - Article

AN - SCOPUS:34250793438

VL - 173

SP - 84

EP - 95

JO - Plant science

JF - Plant science

SN - 0168-9452

IS - 2

ER -

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