2022
DOI: 10.1016/j.molp.2022.09.017
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Regulation of floral senescence in Arabidopsis by coordinated action of CONSTANS and jasmonate signaling

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Cited by 20 publications
(14 citation statements)
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“…Out of the 12, WRKY57 and WRKY60 were selected as our primary candidates to regulate IDA because i) their own upregulation preceded the induction of IDA , and ii) WRKY57 and WRKY60 had been highlighted in the list of most significantly regulated genes of the AZ transcriptome (Cai and Lashbrook, 2008). Besides, WRKY57 is involved in balancing jasmonic acid and auxin signaling in leaves during senescence, is a negative regulator of biotic stress resistance and its overexpression confers drought tolerance – processes previously linked to IDA signaling and abscission (Jiang et al, 2012; Jiang et al, 2014; Jiang and Yu, 2016; Serrano-Bueno et al, 2022). Similarly, WRKY60 is involved in immunity, and ABA signaling in osmotic and salt stress (Xu et al, 2006; Chen et al, 2010; Liu et al, 2012).…”
Section: Resultsmentioning
confidence: 99%
“…Out of the 12, WRKY57 and WRKY60 were selected as our primary candidates to regulate IDA because i) their own upregulation preceded the induction of IDA , and ii) WRKY57 and WRKY60 had been highlighted in the list of most significantly regulated genes of the AZ transcriptome (Cai and Lashbrook, 2008). Besides, WRKY57 is involved in balancing jasmonic acid and auxin signaling in leaves during senescence, is a negative regulator of biotic stress resistance and its overexpression confers drought tolerance – processes previously linked to IDA signaling and abscission (Jiang et al, 2012; Jiang et al, 2014; Jiang and Yu, 2016; Serrano-Bueno et al, 2022). Similarly, WRKY60 is involved in immunity, and ABA signaling in osmotic and salt stress (Xu et al, 2006; Chen et al, 2010; Liu et al, 2012).…”
Section: Resultsmentioning
confidence: 99%
“…CO function is strongly regulated at both the transcriptional and post-translational levels in Arabidopsis , indicating that the photoperiodic pathway has been subjected to high selective pressure (Romero and Valverde, 2009)◻. Other than flowering transition and reproductive development, no other functions have been described for CO, but recent studies suggested that it could regulate floral jasmonate signaling (Serrano-Bueno et al, 2022) and circadian genes (Gnesutta et al, 2017)◻. Here, we show that CO alters the circadian clock by binding to the promoters of key clock-related genes, revealing an undescribed function.…”
Section: Discussionmentioning
confidence: 99%
“…CO encodes a protein with two conserved protein domains: two B-boxes located at the amino terminus, involved in protein-protein interactions, and a carboxyl CCT (CONSTANS, CO LIKE, TIMING OF CAB1) domain, which includes a nuclear transport signal and mediates interactions with DNA and diverse proteins (Laubinger et al, 2006; Valverde, 2011)◻. Recently, a role for the central part of CO in regulating floral senescence has been proposed (Serrano-Bueno et al, 2022). CO is a hub in the photoperiodic regulatory network; it receives signals from a multitude of different pathways, such as day length and circadian clock (Serrano-Bueno et al, 2021), and triggers the expression of the florigen FLOWERING LOCUS T ( FT ), which induces flower differentiation (Ahn et al, 2008)◻.…”
Section: Introductionmentioning
confidence: 99%
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