Abstract

XRN4, the plant cytoplasmic homolog of yeast and metazoan XRN1, catalyzes exoribonucleolytic degradation of uncapped mRNAs from the 5′ end. Most studies of cytoplasmic XRN substrates have focused on polyadenylated transcripts, although many substrates are likely first deadenylated. Here, we report the global investigation of XRN4 substrates in both polyadenylated and nonpolyadenylated RNA to better understand the impact of the enzyme in Arabidopsis. RNA degradome analysis demonstrated that xrn4 mutants overaccumulate many more decapped deadenylated intermediates than those that are polyadenylated. Among these XRN4 substrates that have 5′ ends precisely at cap sites, those associated with photosynthesis, nitrogen responses and auxin responses were enriched. Moreover, xrn4 was found to be defective in the dark stress response and lateral root growth during N resupply, demonstrating that XRN4 is required during both processes. XRN4 also contributes to nonsense-mediated decay (NMD) and xrn4 accumulates 3′ fragments of select NMD targets, despite the lack of the metazoan endoribonuclease SMG6 in plants. Beyond demonstrating that XRN4 is a major player in multiple decay pathways, this study identified intriguing molecular impacts of the enzyme, including those that led to new insights about mRNA decay and discovery of functional contributions at the whole-plant level.

Highlights

  • Cytoplasmic mRNA decay is an important posttranscriptional step for controlling gene expression and eliminating undesirable or aberrant RNA

  • Using a multifaceted RNA degradome approach, we identified XRN4 substrates that led us to find that the response to dark stress and normal root growth during N resupply are compromised in xrn4 mutants

  • Because of the absence of SMG6 in plants, this argues for a novel mechanism initiating the decay of some nonsense-mediated decay (NMD) targets that are XRN4 substrates

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Summary

Introduction

Cytoplasmic mRNA decay is an important posttranscriptional step for controlling gene expression and eliminating undesirable or aberrant RNA. It is a complex process involving multiple pathways [1,2,3]. Deadenylated RNA can either be degraded in the 3 to 5 direction by the multimeric exosome complex or 5 to 3 after decapping [2]. Alternative pathways exist in which transcripts bypass deadenylation and undergo decapping followed by decay by XRN1 (e.g. during nonsense-mediated decay, NMD) or are cleaved internally (e.g. during small RNA-directed argonaute (AGO) cleavage) and are degraded exonucleolytically from the cleaved ends [2,8,9,10,11,12,13]

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