Abstract

The activity of genes controlling organ development may be associated with the redox state of subregions within the meristem. Glutaredoxins react to the level of oxidative potential and can reduce cysteine dithiols, in some cases to activate specific transcription factors. In Arabidopsis, loss of function of the glutaredoxin ROXY1 or the trihelix transcription factor PETAL LOSS (PTL) each results in reduced numbers of petals. Here, genetic studies have revealed that loss of petals in ptl mutant plants depends on ROXY1 function. The two genes also act together to restrain stamen-identifying C function from entering the outer whorls. On the other hand, they suppress growth between sepals and in sepal margins, with ROXY1 action partially redundant to that of PTL. Genetic interactions with aux1 mutations indicate that auxin activity is reduced in the petal whorl of roxy1 mutants as in ptl mutants. However, it is apparently increased in the sepal whorl of triple mutants associated with the ectopic outgrowth of sepal margins, and of finger-like extensions of inter-sepal zones that in 20% of cases are topped with bunches of ectopic sepals. These interactions may be indirect, although PTL and ROXY1 proteins can interact directly when co-expressed in a transient assay. Changes of conserved cysteines within PTL to similar amino acids that cannot be oxidized did not block its function. It may be in some cases that under reducing conditions ROXY1 binds PTL and activates it by reducing specific conserved cysteines, thus resulting in growth suppression.

Highlights

  • Meristems are the ultimate source of all plant tissues

  • We further showed that PETAL LOSS (PTL) and ROXY1 proteins can bind following transient co-expression, and that three conserved cysteines in PTL can be changed to serine or alanine without losing petal initiation function

  • The number of second whorl organs was similar in roxy1-3 and ptl-1 roxy1-3 mutant flowers, their identity was affected in the double mutant plants (Supplementary Table S3)

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Summary

Introduction

Meristems are the ultimate source of all plant tissues. Primary meristems are characterized by a core of slowly dividing stem cells surrounded by regions of growth, organogenesis, and eventually cellular differentiation (Sablowski, 2010). Specific transcription factors and signal molecules have been uncovered in Arabidopsis that maintain the stem cell population, especially members of the homeodomain WUSCHEL (WUS) family in association with CLAVATA (CLV) signaling molecules (Schoof et al, 2000). Another homeodomain transcription factor, SHOOT MERISTEMLESS (STM), maintains the undifferentiated peripheral zone, with its function fading as organ primordia. Boundaries between developing organ primordia are reinforced by dampening of cell divisions associated with expression of CUP-SHAPED COTYLEDON (CUC) genes of the NAC transcription factor family (Aida et al, 1997). More recent understanding of mechanisms of meristem development has built on these foundation studies (for reviews, see Žádníková and Simon, 2014; Hepworth and Pautot, 2015; Galli and Gallivotti, 2016)

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