Abstract

Post-transcriptional control is nowadays considered a main checking point for correct gene regulation during development, and RNA binding proteins actively participate in this process. Arabidopsis thaliana FLOWERING LOCUS WITH KH DOMAINS (FLK) and PEPPER (PEP) genes encode RNA-binding proteins that contain three K-homology (KH)-domain, the typical configuration of Poly(C)-binding ribonucleoproteins (PCBPs). We previously demonstrated that FLK and PEP interact to regulate FLOWERING LOCUS C (FLC), a central repressor of flowering time. Now we show that FLK and PEP also play an important role in the maintenance of the C-function during floral organ identity by post-transcriptionally regulating the MADS-box floral homeotic gene AGAMOUS (AG). Previous studies have indicated that the KH-domain containing protein HEN4, in concert with the CCCH-type RNA binding protein HUA1 and the RPR-type protein HUA2, facilitates maturation of the AG pre-mRNA. In this report we show that FLK and PEP genetically interact with HEN4, HUA1, and HUA2, and that the FLK and PEP proteins physically associate with HUA1 and HEN4. Taken together, these data suggest that HUA1, HEN4, PEP and FLK are components of the same post-transcriptional regulatory module that ensures normal processing of the AG pre-mRNA. Our data better delineates the roles of PEP in plant development and, for the first time, links FLK to a morphogenetic process.

Highlights

  • Development of multicellular organisms relies on exquisitely controlled transcriptional and post-transcriptional regulatory actions to govern gene expression and accurately respond to endogenous and environmental fluctuations

  • In this work we have found that FLOWERING LOCUS WITH KH DOMAINS (FLK) and PEP play a pivotal role in flower organogenesis by post-transcriptionally regulating the MADS-box floral organ identity gene AGAMOUS (AG)

  • Our results reveal the existence of a post-transcriptional regulatory activity controlling key master genes for floral timing and flower morphogenesis, which might be instrumental for coordinating both developmental phases

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Summary

Introduction

Development of multicellular organisms relies on exquisitely controlled transcriptional and post-transcriptional regulatory actions to govern gene expression and accurately respond to endogenous and environmental fluctuations. FM identity genes, such as LEAFY (LFY) [2] and APETALA1 (AP1) [3], are crucial in activating the floral homeotic genes that specify identity of concentric whorls of organs in the Arabidopsis flower [1]. According to the ABC(E) model [4,5,6], the class A genes AP1 and AP2 specify sepals and, together with the B function genes PISTILLATA (PI) and AP3, contribute to petal identity. Co-expression of B-genes and the C-function gene AGAMOUS (AG) confer male stamen identity, while AG alone specifies female carpels, defining the pistil or gynoecium situated in the innermost whorl. With the exception of AP2 (an AP2/EREBP) [10,11], all floral homeotic genes encode type II MADSbox transcription factors, a lineage comprising central regulators in most aspects of plant development [9,12,13]

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