Virus-induced gene silencing in Medicago truncatula and Lathyrus odorata

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Virus-induced gene silencing in Medicago truncatula and Lathyrus odorata. / Grønlund, Mette; Kjær, Gabriela Didina Constantin; Piednoir, Elodie; Kovacev, Jordan; Johansen, Elisabeth; Lund, Ole Søgaard.

I: Virus Research, Bind 135, Nr. 2, 2008, s. 345-349.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Grønlund, M, Kjær, GDC, Piednoir, E, Kovacev, J, Johansen, E & Lund, OS 2008, 'Virus-induced gene silencing in Medicago truncatula and Lathyrus odorata', Virus Research, bind 135, nr. 2, s. 345-349. https://doi.org/10.1016/j.virusres.2008.04.005

APA

Grønlund, M., Kjær, G. D. C., Piednoir, E., Kovacev, J., Johansen, E., & Lund, O. S. (2008). Virus-induced gene silencing in Medicago truncatula and Lathyrus odorata. Virus Research, 135(2), 345-349. https://doi.org/10.1016/j.virusres.2008.04.005

Vancouver

Grønlund M, Kjær GDC, Piednoir E, Kovacev J, Johansen E, Lund OS. Virus-induced gene silencing in Medicago truncatula and Lathyrus odorata. Virus Research. 2008;135(2):345-349. https://doi.org/10.1016/j.virusres.2008.04.005

Author

Grønlund, Mette ; Kjær, Gabriela Didina Constantin ; Piednoir, Elodie ; Kovacev, Jordan ; Johansen, Elisabeth ; Lund, Ole Søgaard. / Virus-induced gene silencing in Medicago truncatula and Lathyrus odorata. I: Virus Research. 2008 ; Bind 135, Nr. 2. s. 345-349.

Bibtex

@article{5344c260a1c411ddb6ae000ea68e967b,
title = "Virus-induced gene silencing in Medicago truncatula and Lathyrus odorata",
abstract = "Virus-induced gene silencing (VIGS) has become an important reverse genetics tool for functional genomics. VIGS vectors based on Pea early browning virus (PEBV, genus Tobravirus) and Bean pod mottle virus (genus Comovirus) are available for the legume species Pisum sativum and Glycine max, respectively. With the aim of extending the application of the PEBV VIGS vector to other legumes, we examined susceptibility of 99 accessions representing 24 legume species including 21 accessions of Medicago truncatula and 38 accessions Lotus japonicus. Infectivity of PEBV was tested by agro-inoculation with a vector carrying the complete {\ss}-glucuronidase (GUS) coding sequence. In situ histochemical staining analysis indicated that 4 of 21 M. truncatula and three of three Lathyrus odorata accessions were infected systemically by GUS tagged PEBV, while none of 38 L. japonicus accessions displayed GUS staining of either inoculated or uninoculated leaves. Agro-inoculation of plants representing PEBV-GUS susceptible M. truncatula and L. odorata accessions with PEBV carrying a fragment of Phytoene desaturase (PDS) resulted in development of a bleaching phenotype suggesting a down-regulation of PDS expression. In M. truncatula this was supported by quantification of PDS mRNA levels by real-time PCR",
keywords = "Former LIFE faculty, Reverse genetics, Leguminosae",
author = "Mette Gr{\o}nlund and Kj{\ae}r, {Gabriela Didina Constantin} and Elodie Piednoir and Jordan Kovacev and Elisabeth Johansen and Lund, {Ole S{\o}gaard}",
year = "2008",
doi = "10.1016/j.virusres.2008.04.005",
language = "English",
volume = "135",
pages = "345--349",
journal = "Virus Research",
issn = "0168-1702",
publisher = "Elsevier",
number = "2",

}

RIS

TY - JOUR

T1 - Virus-induced gene silencing in Medicago truncatula and Lathyrus odorata

AU - Grønlund, Mette

AU - Kjær, Gabriela Didina Constantin

AU - Piednoir, Elodie

AU - Kovacev, Jordan

AU - Johansen, Elisabeth

AU - Lund, Ole Søgaard

PY - 2008

Y1 - 2008

N2 - Virus-induced gene silencing (VIGS) has become an important reverse genetics tool for functional genomics. VIGS vectors based on Pea early browning virus (PEBV, genus Tobravirus) and Bean pod mottle virus (genus Comovirus) are available for the legume species Pisum sativum and Glycine max, respectively. With the aim of extending the application of the PEBV VIGS vector to other legumes, we examined susceptibility of 99 accessions representing 24 legume species including 21 accessions of Medicago truncatula and 38 accessions Lotus japonicus. Infectivity of PEBV was tested by agro-inoculation with a vector carrying the complete ß-glucuronidase (GUS) coding sequence. In situ histochemical staining analysis indicated that 4 of 21 M. truncatula and three of three Lathyrus odorata accessions were infected systemically by GUS tagged PEBV, while none of 38 L. japonicus accessions displayed GUS staining of either inoculated or uninoculated leaves. Agro-inoculation of plants representing PEBV-GUS susceptible M. truncatula and L. odorata accessions with PEBV carrying a fragment of Phytoene desaturase (PDS) resulted in development of a bleaching phenotype suggesting a down-regulation of PDS expression. In M. truncatula this was supported by quantification of PDS mRNA levels by real-time PCR

AB - Virus-induced gene silencing (VIGS) has become an important reverse genetics tool for functional genomics. VIGS vectors based on Pea early browning virus (PEBV, genus Tobravirus) and Bean pod mottle virus (genus Comovirus) are available for the legume species Pisum sativum and Glycine max, respectively. With the aim of extending the application of the PEBV VIGS vector to other legumes, we examined susceptibility of 99 accessions representing 24 legume species including 21 accessions of Medicago truncatula and 38 accessions Lotus japonicus. Infectivity of PEBV was tested by agro-inoculation with a vector carrying the complete ß-glucuronidase (GUS) coding sequence. In situ histochemical staining analysis indicated that 4 of 21 M. truncatula and three of three Lathyrus odorata accessions were infected systemically by GUS tagged PEBV, while none of 38 L. japonicus accessions displayed GUS staining of either inoculated or uninoculated leaves. Agro-inoculation of plants representing PEBV-GUS susceptible M. truncatula and L. odorata accessions with PEBV carrying a fragment of Phytoene desaturase (PDS) resulted in development of a bleaching phenotype suggesting a down-regulation of PDS expression. In M. truncatula this was supported by quantification of PDS mRNA levels by real-time PCR

KW - Former LIFE faculty

KW - Reverse genetics

KW - Leguminosae

U2 - 10.1016/j.virusres.2008.04.005

DO - 10.1016/j.virusres.2008.04.005

M3 - Journal article

C2 - 18495283

VL - 135

SP - 345

EP - 349

JO - Virus Research

JF - Virus Research

SN - 0168-1702

IS - 2

ER -

ID: 8114450