Abstract

BackgroundThe CDC20 and Cdh1/CCS52 proteins are substrate determinants and activators of the Anaphase Promoting Complex/Cyclosome (APC/C) E3 ubiquitin ligase and as such they control the mitotic cell cycle by targeting the degradation of various cell cycle regulators. In yeasts and animals the main CDC20 function is the destruction of securin and mitotic cyclins. Plants have multiple CDC20 gene copies whose functions have not been explored yet. In Arabidopsis thaliana there are five CDC20 isoforms and here we aimed at defining their contribution to cell cycle regulation, substrate selectivity and plant development.Methodology/Principal FindingsStudying the gene structure and phylogeny of plant CDC20s, the expression of the five AtCDC20 gene copies and their interactions with the APC/C subunit APC10, the CCS52 proteins, components of the mitotic checkpoint complex (MCC) and mitotic cyclin substrates, conserved CDC20 functions could be assigned for AtCDC20.1 and AtCDC20.2. The other three intron-less genes were silent and specific for Arabidopsis. We show that AtCDC20.1 and AtCDC20.2 are components of the MCC and interact with mitotic cyclins with unexpected specificity. AtCDC20.1 and AtCDC20.2 are expressed in meristems, organ primordia and AtCDC20.1 also in pollen grains and developing seeds. Knocking down both genes simultaneously by RNAi resulted in severe delay in plant development and male sterility. In these lines, the meristem size was reduced while the cell size and ploidy levels were unaffected indicating that the lower cell number and likely slowdown of the cell cycle are the cause of reduced plant growth.Conclusions/SignificanceThe intron-containing CDC20 gene copies provide conserved and redundant functions for cell cycle progression in plants and are required for meristem maintenance, plant growth and male gametophyte formation. The Arabidopsis-specific intron-less genes are possibly “retrogenes” and have hitherto undefined functions or are pseudogenes.

Highlights

  • Consecutive and repeated action of ubiquitin activating (E1), ubiquitin conjugating (E2) and ubiquitin ligase (E3) enzymes leads to polyubiquitination and to degradation of target proteins by the 26S proteasome

  • We show that AtCDC20.1 and AtCDC20.2 are highly redundant mitotic cell cycle regulators that are expressed in tissues with high cell division activity and are required for normal plant development

  • Five CDC20 genes in Arabidopsis thaliana In the Arabidopsis genome six AtCDC20 genes were predicted by Capron et al [22]

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Summary

Introduction

Consecutive and repeated action of ubiquitin activating (E1), ubiquitin conjugating (E2) and ubiquitin ligase (E3) enzymes leads to polyubiquitination and to degradation of target proteins by the 26S proteasome. The APC/C complex is composed of at least 11 different core subunits, while the activity and substrate specificity of the APC/C are predominantly determined by two classes of activator proteins: CDC20 and CDH1, the latter known in plants as CCS52 [2]. Each of them targets the degradation of proteins containing the loosely defined RxxLxxxN/Q destruction box (D-box) sequence [3]. This sequence was first found in mitotic cyclins that bind to the RLV cyclin-binding motif, conserved in the last WD40 repeat of both the CDC20 and CDH1 proteins. The CDC20 and Cdh1/CCS52 proteins are substrate determinants and activators of the Anaphase Promoting Complex/Cyclosome (APC/C) E3 ubiquitin ligase and as such they control the mitotic cell cycle by targeting the degradation of various cell cycle regulators. In Arabidopsis thaliana there are five CDC20 isoforms and here we aimed at defining their contribution to cell cycle regulation, substrate selectivity and plant development

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