Abstract

BackgroundThe control of gene expression in eukaryotic cells occurs both transcriptionally and post-transcriptionally. Although many genes are now known to be regulated at the translational level, in general, the mechanisms are poorly understood. We have previously presented polysomal gradient and array-based evidence that translational control is widespread in a significant number of genes when yeast cells are exposed to a range of stresses. Here we have re-examined these gene sets, considering the role of UTR sequences in the translational responses of these genes using recent large-scale datasets which define 5' and 3' transcriptional ends for many yeast genes. In particular, we highlight the potential role of 5' UTRs and upstream open reading frames (uORFs).ResultsWe show a highly significant enrichment in specific GO functional classes for genes that are translationally up- and down-regulated under given stresses (e.g. carbohydrate metabolism is up-regulated under amino acid starvation). Cross-referencing these data with the stress response data we show that translationally upregulated genes have longer 5' UTRs, consistent with their role in translational regulation. In the first genome-wide study of uORFs in a set of mapped 5' UTRs, we show that uORFs are rare, being statistically under-represented in UTR sequences. However, they have distinct compositional biases consistent with their putative role in translational control and are more common in genes which are apparently translationally up-regulated.ConclusionThese results demonstrate a central regulatory role for UTR sequences, and 5' UTRs in particular, highlighting the significant role of uORFs in post-transcriptional control in yeast. Yeast uORFs are more highly conserved than has been suggested, lending further weight to their significance as functional elements involved in gene regulation. It also suggests a more complex and novel mechanism of control, whereby uORFs permit genes to escape from a more general attenuation of translation under conditions of stress. However, since uORFs are relatively rare (only ~13% of yeast genes have them) there remain many unanswered questions as to how UTR elements can direct translational control of many hundreds of genes under stress.

Highlights

  • The control of gene expression in eukaryotic cells occurs both transcriptionally and posttranscriptionally

  • In particular we examine upstream open reading frames, which can affect the level of gene expression via a number of potential post-transcriptional mechanisms [5,6,24,25,26] These include mRNA degradation via the nonsense mediated decay pathway (NMD) [26], possible activities of the small peptides encoded by the uORF themselves [25], and mechanisms relating to the scanning of the transcript by the ribosome

  • In this study we have examined the role of upstream sequence elements in yeast untranslated region (UTR), considering whether they play a concerted role in regulation of gene expression under stress conditions

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Summary

Introduction

The control of gene expression in eukaryotic cells occurs both transcriptionally and posttranscriptionally. Much of this research has exploited advances in arraybased technologies to characterise how gene expression levels change during the cell cycle or in response to stresses or environmental changes [1,2], allowing transcriptional factors to be mapped to the genes they regulate [3,4]. These approaches only deliver regulatory control information at the transcriptional level. Mutations in UTRs can lead to serious pathology [18], demonstrating their importance to proper function in the cell

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