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2023
DOI: 10.1128/spectrum.05058-22
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Genome-Wide Characterization of the RNA Exosome Complex in Relation to Growth, Development, and Pathogenicity of Fusarium graminearum

Abstract: The RNA exosome complex is the most versatile RNA degradation machinery in eukaryotes. However, little is known about how this complex regulates the development and pathogenicity of plant-pathogenic fungi.

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Cited by 4 publications
(6 citation statements)
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“…These downregulated proteins were implicated in a wide range of biological processes, including translation, ribosome biogenesis, the cell cycle, oxidative phosphorylation and TCA cycle, protein processing in endoplasmic reticulum, and exosome ( Supplementary Tables 4 , 5 ). Abnormalities of these cellular processes jeopardize cell growth and functions, from energy metabolism to pathogenicity ( Fernández-Álvarez et al, 2013 ; Koh and Sarin, 2018 ; Richardson, 2019 ; Zhao et al, 2021 ; Yuan et al, 2023 ). Of the SUMOylated proteins, CpSep1, CpSlt2, CpMK2, CpMK1, and Cdc48 have been shown to be virulence factors in C. parasitica ( Park et al, 2004 ; Choi et al, 2005 ; Ko et al, 2016 ; So et al, 2017 ; Jo et al, 2019 ).…”
Section: Discussionmentioning
confidence: 99%
“…These downregulated proteins were implicated in a wide range of biological processes, including translation, ribosome biogenesis, the cell cycle, oxidative phosphorylation and TCA cycle, protein processing in endoplasmic reticulum, and exosome ( Supplementary Tables 4 , 5 ). Abnormalities of these cellular processes jeopardize cell growth and functions, from energy metabolism to pathogenicity ( Fernández-Álvarez et al, 2013 ; Koh and Sarin, 2018 ; Richardson, 2019 ; Zhao et al, 2021 ; Yuan et al, 2023 ). Of the SUMOylated proteins, CpSep1, CpSlt2, CpMK2, CpMK1, and Cdc48 have been shown to be virulence factors in C. parasitica ( Park et al, 2004 ; Choi et al, 2005 ; Ko et al, 2016 ; So et al, 2017 ; Jo et al, 2019 ).…”
Section: Discussionmentioning
confidence: 99%
“…The total proteins (Input) and the proteins eluted from the agarose beads (IP) were analyzed by western blot using the anti-Myc and anti-GFP antibodies, respectively. 17 Quantification of Acetyl-CoA. Acetyl-CoA was assayed as previously reported.…”
Section: ■ Materials and Methodsmentioning
confidence: 99%
“…Total proteins were extracted from the strain expressing the pair of fusion constructs and were further incubated with the anti-GFP agarose beads (SM038001, Smart-Lifesciences) at 4 °C for 4 h following the standard procedure. The total proteins (Input) and the proteins eluted from the agarose beads (IP) were analyzed by western blot using the anti-Myc and anti-GFP antibodies, respectively …”
Section: Materials and Methodsmentioning
confidence: 99%
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“…The deletion mutant of Fgexosc1 was unable to form perithecia. Although the deletion mutant of FgexoscA exhibited normal perithecia formation, it showed a significant reduction in the quantity of ascospores generated compared to the wild-type strain PH-1 [50] (Supplementary Table S1).…”
Section: Genes Involves In the Formation Of Peritheciamentioning
confidence: 99%