2019
DOI: 10.1104/pp.19.00917
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MADS78 and MADS79 Are Essential Regulators of Early Seed Development in Rice

Abstract: MADS box transcription factors (TFs) are subdivided into type I and II based on phylogenetic analysis. The type II TFs regulate floral organ identity and flowering time, but type I TFs are relatively less characterized. Here, we report the functional characterization of two type I MADS box TFs in rice (Oryza sativa), MADS78 and MADS79. Transcript abundance of both these genes in developing seed peaked at 48 h after fertilization and was suppressed by 96 h after fertilization, corresponding to syncytial and cel… Show more

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Cited by 45 publications
(45 citation statements)
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References 87 publications
(117 reference statements)
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“…The event is finely orchestrated at the genetic and epigenetic levels (Folsom et al, ). CMT3 (Folsom et al, ; Lindroth et al, ), DRM3 (Sharma et al, ), KRP3 (Mizutani, Naganuma, Tsutsumi, & Saitoh, ), and several type‐I MADS‐box transcription factors, MADS78 , MADS 79 , MADS 87 , and MADS 89 (Chen et al, ; Folsom et al, ; Kang, Steffen, Portereiko, Lloyd, & Drews, ; Paul et al, ; Steffen, Kang, Portereiko, Lloyd, & Drews, ), show expression specific to the syncytial phase, and decline with the progression of cellularization. Thus, we referred these as syncytial‐associated genes (Figure ).…”
Section: Resultsmentioning
confidence: 99%
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“…The event is finely orchestrated at the genetic and epigenetic levels (Folsom et al, ). CMT3 (Folsom et al, ; Lindroth et al, ), DRM3 (Sharma et al, ), KRP3 (Mizutani, Naganuma, Tsutsumi, & Saitoh, ), and several type‐I MADS‐box transcription factors, MADS78 , MADS 79 , MADS 87 , and MADS 89 (Chen et al, ; Folsom et al, ; Kang, Steffen, Portereiko, Lloyd, & Drews, ; Paul et al, ; Steffen, Kang, Portereiko, Lloyd, & Drews, ), show expression specific to the syncytial phase, and decline with the progression of cellularization. Thus, we referred these as syncytial‐associated genes (Figure ).…”
Section: Resultsmentioning
confidence: 99%
“…Samples were transferred to xylene (100%) for 2 hr, followed by transfer to 500 µl of a 1:1 mixture of xylene and paraplast tablets and stored at 60°C. Finally, samples were transferred to and embedded in paraplast (Paul et al, ). Cross sections (10 µm) were obtained using a rotary microtome (Leica RM2125 RTS).…”
Section: Methodsmentioning
confidence: 99%
“…After fertilization, many type I MADS-box genes are transiently activated during cellularization ( Bemer et al., 2010 ; Zhang et al., 2018b ), possibly antagonizing FIS–PRC2 ( Pires, 2014 ). Aberrant activation of type I MADS s has been found to be associated with cellularization failure in Arabidopsis and rice ( Walia et al., 2009 ; Ishikawa et al., 2011 ; Zhang et al., 2018b ; Paul et al., 2020 ). For instance, agamous-like 62 ( agl62 ) and agl80 mutants exhibit precocious cellularization ( Portereiko et al., 2006 ; Kang et al., 2008 ), and the seed failures of the mea mutant and interspecific hybrids that are caused by delayed cellularization can be alleviated by the inactivation of PHERE1 ( PHE1 ), AGL62 , and AGL90 in Arabidopsis ( Köhler et al., 2003a ; Walia et al., 2009 ).…”
Section: Introductionmentioning
confidence: 99%
“…Delayed cellularization is also associated with increased auxin concentrations in Arabidopsis (Figueiredo et al ., 2016; Batista et al ., 2019). It is feasible that higher auxin concentrations in Fie1 ‐deficient, overproliferating coenocytic endosperm inhibit cell wall formation and increase auxin transport to seed coat tissue, resulting in cellular expansion and hence larger cell size (Batista et al ., 2019; Paul et al ., 2020a). The potential mechanistic link between Fie1 and auxin accumulation and transport needs further examination.…”
Section: Discussionmentioning
confidence: 99%