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GmSnRK1.1, a Sucrose Non-fermenting-1(SNF1)-Related Protein Kinase, Promotes Soybean Resistance to Phytophthora sojae.

Identifieur interne : 000489 ( Main/Exploration ); précédent : 000488; suivant : 000490

GmSnRK1.1, a Sucrose Non-fermenting-1(SNF1)-Related Protein Kinase, Promotes Soybean Resistance to Phytophthora sojae.

Auteurs : Le Wang [République populaire de Chine] ; Huiyu Wang [République populaire de Chine] ; Shengfu He [République populaire de Chine] ; Fanshan Meng [République populaire de Chine] ; Chuanzhong Zhang [République populaire de Chine] ; Sujie Fan [République populaire de Chine] ; Junjiang Wu [République populaire de Chine] ; Shuzhen Zhang [République populaire de Chine] ; Pengfei Xu [République populaire de Chine]

Source :

RBID : pubmed:31428116

Abstract

Phytophthora root and stem rot, a destructive disease of soybean [Glycine max (L.) Merr.], is caused by the oomycete Phytophthora sojae. However, how the disease resistance mechanisms of soybean respond to P. sojae infection remains unclear. Previously, we showed that GmWRKY31, which interacts with a sucrose non-fermenting-1(SNF1)-related protein kinase (SnRK), enhances resistance to P. sojae in soybean. Here, we report that the membrane-localized SnRK GmSnRK1.1 is involved in the soybean host response to P. sojae. The overexpression of GmSnRK1.1 (GmSnRK1.1-OE) increased soybean resistance to P. sojae, and the RNA interference (RNAi)-mediated silencing of GmSnRK1.1 (GmSnRK1.1-R) reduced resistance to P. sojae. Moreover, the activities and transcript levels of the antioxidant enzymes superoxide dismutase and peroxidase were markedly higher in the GmSnRK1.1-OE transgenic soybean plants than in the wild type (WT), but were reduced in the GmSnRK1.1-R plants. Several isoflavonoid phytoalexins related genes GmPAL, GmIFR, Gm4CL and GmCHS were significantly higher in "Suinong 10" and GmSnRK1.1-OE lines than these in "Dongnong 50," and were significantly lower in GmSnRK1.1-R lines. In addition, the accumulation of salicylic acid (SA) and the expression level of the SA biosynthesis-related gene were significantly higher in the GmSnRK1.1-OE plants than in the WT and GmSnRK1.1-R plants, moreover, SA biosynthesis inhibitor treated GmSnRK1.1-R lines plants displayed clearly increased pathogen biomass compared with H2O-treated plants after 24 h post-inoculation. These results showed that GmSnRK1.1 positively regulates soybean resistance to P. sojae, potentially functioning via effects on the expression of SA-related genes and increased accumulation of SA.

DOI: 10.3389/fpls.2019.00996
PubMed: 31428116
PubMed Central: PMC6688127


Affiliations:


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<div type="abstract" xml:lang="en">Phytophthora root and stem rot, a destructive disease of soybean [
<i>Glycine max</i>
(L.) Merr.], is caused by the oomycete
<i>Phytophthora sojae</i>
. However, how the disease resistance mechanisms of soybean respond to
<i>P. sojae</i>
infection remains unclear. Previously, we showed that GmWRKY31, which interacts with a sucrose non-fermenting-1(SNF1)-related protein kinase (SnRK), enhances resistance to
<i>P. sojae</i>
in soybean. Here, we report that the membrane-localized SnRK GmSnRK1.1 is involved in the soybean host response to
<i>P. sojae</i>
. The overexpression of
<i>GmSnRK1.1</i>
(
<i>GmSnRK1.1</i>
-OE) increased soybean resistance to
<i>P. sojae</i>
, and the RNA interference (RNAi)-mediated silencing of
<i>GmSnRK1.1</i>
(
<i>GmSnRK1.1</i>
-R) reduced resistance to
<i>P. sojae</i>
. Moreover, the activities and transcript levels of the antioxidant enzymes superoxide dismutase and peroxidase were markedly higher in the
<i>GmSnRK1.1</i>
-OE transgenic soybean plants than in the wild type (WT), but were reduced in the
<i>GmSnRK1.1</i>
-R plants. Several isoflavonoid phytoalexins related genes
<i>GmPAL</i>
,
<i>GmIFR</i>
,
<i>Gm4CL</i>
and
<i>GmCHS</i>
were significantly higher in "Suinong 10" and
<i>GmSnRK1.1</i>
-OE lines than these in "Dongnong 50," and were significantly lower in
<i>GmSnRK1.1</i>
-R lines. In addition, the accumulation of salicylic acid (SA) and the expression level of the SA biosynthesis-related gene were significantly higher in the
<i>GmSnRK1.1</i>
-OE plants than in the WT and
<i>GmSnRK1.1</i>
-R plants, moreover, SA biosynthesis inhibitor treated
<i>GmSnRK1.1</i>
-R lines plants displayed clearly increased pathogen biomass compared with H
<sub>2</sub>
O-treated plants after 24 h post-inoculation. These results showed that GmSnRK1.1 positively regulates soybean resistance to
<i>P. sojae</i>
, potentially functioning via effects on the expression of SA-related genes and increased accumulation of SA.</div>
</front>
</TEI>
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<DateRevised>
<Year>2020</Year>
<Month>09</Month>
<Day>29</Day>
</DateRevised>
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<Volume>10</Volume>
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<Year>2019</Year>
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<Title>Frontiers in plant science</Title>
<ISOAbbreviation>Front Plant Sci</ISOAbbreviation>
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<ArticleTitle>GmSnRK1.1, a Sucrose Non-fermenting-1(SNF1)-Related Protein Kinase, Promotes Soybean Resistance to
<i>Phytophthora sojae</i>
.</ArticleTitle>
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<Abstract>
<AbstractText>Phytophthora root and stem rot, a destructive disease of soybean [
<i>Glycine max</i>
(L.) Merr.], is caused by the oomycete
<i>Phytophthora sojae</i>
. However, how the disease resistance mechanisms of soybean respond to
<i>P. sojae</i>
infection remains unclear. Previously, we showed that GmWRKY31, which interacts with a sucrose non-fermenting-1(SNF1)-related protein kinase (SnRK), enhances resistance to
<i>P. sojae</i>
in soybean. Here, we report that the membrane-localized SnRK GmSnRK1.1 is involved in the soybean host response to
<i>P. sojae</i>
. The overexpression of
<i>GmSnRK1.1</i>
(
<i>GmSnRK1.1</i>
-OE) increased soybean resistance to
<i>P. sojae</i>
, and the RNA interference (RNAi)-mediated silencing of
<i>GmSnRK1.1</i>
(
<i>GmSnRK1.1</i>
-R) reduced resistance to
<i>P. sojae</i>
. Moreover, the activities and transcript levels of the antioxidant enzymes superoxide dismutase and peroxidase were markedly higher in the
<i>GmSnRK1.1</i>
-OE transgenic soybean plants than in the wild type (WT), but were reduced in the
<i>GmSnRK1.1</i>
-R plants. Several isoflavonoid phytoalexins related genes
<i>GmPAL</i>
,
<i>GmIFR</i>
,
<i>Gm4CL</i>
and
<i>GmCHS</i>
were significantly higher in "Suinong 10" and
<i>GmSnRK1.1</i>
-OE lines than these in "Dongnong 50," and were significantly lower in
<i>GmSnRK1.1</i>
-R lines. In addition, the accumulation of salicylic acid (SA) and the expression level of the SA biosynthesis-related gene were significantly higher in the
<i>GmSnRK1.1</i>
-OE plants than in the WT and
<i>GmSnRK1.1</i>
-R plants, moreover, SA biosynthesis inhibitor treated
<i>GmSnRK1.1</i>
-R lines plants displayed clearly increased pathogen biomass compared with H
<sub>2</sub>
O-treated plants after 24 h post-inoculation. These results showed that GmSnRK1.1 positively regulates soybean resistance to
<i>P. sojae</i>
, potentially functioning via effects on the expression of SA-related genes and increased accumulation of SA.</AbstractText>
</Abstract>
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</AffiliationInfo>
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<LastName>Wang</LastName>
<ForeName>Huiyu</ForeName>
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</AffiliationInfo>
</Author>
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<LastName>He</LastName>
<ForeName>Shengfu</ForeName>
<Initials>S</Initials>
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</AffiliationInfo>
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</AffiliationInfo>
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</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Fan</LastName>
<ForeName>Sujie</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Soybean Research Institute/Key Laboratory of Soybean Biology of Chinese Education Ministry, Northeast Agricultural University, Harbin, China.</Affiliation>
</AffiliationInfo>
<AffiliationInfo>
<Affiliation>College of Agronomy, Plant Biotechnology Center, Jilin Agricultural University, Changchun, China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Wu</LastName>
<ForeName>Junjiang</ForeName>
<Initials>J</Initials>
<AffiliationInfo>
<Affiliation>Soybean Research Institute of Heilongjiang Academy of Agricultural Sciences, Key Laboratory of Soybean Cultivation of Ministry of Agriculture P. R. China, Harbin, China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Zhang</LastName>
<ForeName>Shuzhen</ForeName>
<Initials>S</Initials>
<AffiliationInfo>
<Affiliation>Soybean Research Institute/Key Laboratory of Soybean Biology of Chinese Education Ministry, Northeast Agricultural University, Harbin, China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y">
<LastName>Xu</LastName>
<ForeName>Pengfei</ForeName>
<Initials>P</Initials>
<AffiliationInfo>
<Affiliation>Soybean Research Institute/Key Laboratory of Soybean Biology of Chinese Education Ministry, Northeast Agricultural University, Harbin, China.</Affiliation>
</AffiliationInfo>
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