Abstract

Floral organ shedding is a cell separation event preceded by cell-wall loosening and generally accompanied by cell expansion. Mutations in NEVERSHED (NEV) or INFLORESCENCE DEFICIENT IN ABSCISSION (IDA) block floral organ abscission in Arabidopsis thaliana. NEV encodes an ADP-ribosylation factor GTPase-activating protein, and cells of nev mutant flowers display membrane-trafficking defects. IDA encodes a secreted peptide that signals through the receptor-like kinases HAESA (HAE) and HAESA-LIKE2 (HSL2). Analyses of single and double mutants revealed unique features of the nev and ida phenotypes. Cell-wall loosening was delayed in ida flowers. In contrast, nev and nev ida mutants displayed ectopic enlargement of abscission zone (AZ) cells, indicating that cell expansion alone is not sufficient to trigger organ loss. These results suggest that NEV initially prevents precocious cell expansion but is later integral for cell separation. IDA is involved primarily in the final cell separation step. A mutation in KNOTTED-LIKE FROM ARABIDOPSIS THALIANA1 (KNAT1), a suppressor of the ida mutant, could not rescue the abscission defects of nev mutant flowers, indicating that NEV-dependent activity downstream of KNAT1 is required. Transcriptional profiling of mutant AZs identified gene clusters regulated by IDA-HAE/HSL2. Several genes were more strongly downregulated in nev-7 compared with ida and hae hsl2 mutants, consistent with the rapid inhibition of organ loosening in nev mutants, and the overlapping roles of NEV and IDA in cell separation. A model of the crosstalk between the IDA signalling pathway and NEV-mediated membrane traffic during floral organ abscission is presented.

Highlights

  • Plants have the ability to abscise whole organs once their purpose has been served (Roberts et al, 2002; Lewis et al, 2006)

  • Distinct pBS profiles indicate where in the abscission process a given gene exerts its influence. bop1 bop2 mutant flowers with defects in abscission zone (AZ) formation display relatively high and constant pBS levels that reflect an absolute block in the abscission process (McKim et al, 2008), while delayed abscission4 flowers show an initial increase in pBS followed by a decline, suggesting decreased sensitivity to triggers of the process, including changes in response to auxin, ethylene, and jasmonic acid (Patterson and Bleecker, 2004; Patterson et al, 2007; Kim et al, 2013)

  • Many ethylene receptor mutants display a delay in the initial decrease in pBS; the profile is similar to wild type, suggesting a role in the timing of abscission (Patterson et al, 2007). ida and hae hsl2 represent a fourth, V-shaped profile with a delayed pBS decrease, and a subsequent increase starting one to two positions after organ shedding in the wild type (Butenko et al, 2003; Cho et al, 2008)

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Summary

Introduction

Plants have the ability to abscise whole organs once their purpose has been served (Roberts et al, 2002; Lewis et al, 2006). Sensitized AZs are responsive to the small peptide INFLORESCENCE DEFICIENT IN ABSCISSION (IDA), which relays a signal through the two closely related leucine-rich-repeat receptor-like kinases (LRR-RLKs) HAESA (HAE) and HAESA-LIKE2 (HSL2) (Cho et al, 2008; McKim et al, 2008; Stenvik et al, 2008; Butenko et al, 2009). Overexpression of IDA (IDAOE) using the cauliflower mosaic virus 35S promoter leads to early abscission of floral organs with enlargement of the AZ region, secretion of arabinogalactan protein (AGP), and ectopic abscission of branches and cauline leaves (Stenvik et al, 2006) These phenotypes are lost for IDAOE in an hae hsl background, consistent with IDA serving as the ligand of HAE/HSL2 (Cho et al, 2008; Stenvik et al, 2008).

Materials and methods
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