Abstract

MicroRNAs (miRNAs) are non-coding small RNAs (sRNAs) that regulate gene expression in a wide range of eukaryotes. In this study, we analyzed regulatory sRNAs in Penicillium chrysogenum, the industrial producer of the β-lactam antibiotic penicillin. To identify sRNAs and microRNA-like RNAs (milRNAs) on a global approach, two sRNA sequencing libraries were constructed. One library was created with pooled total RNA, obtained from twelve differently grown cultures (RNA Mix), and the other with total RNA from a single submerged cultivation (∆ku70FRT2). Illumina sequencing of both RNA libraries produced 84,322,825 mapped reads. To distinguish between Dicer-dependent and independent sRNA formation, we further constructed two single dicer gene mutants (∆dcl2 and ∆dcl1) and a dicer double mutant (∆dcl2∆dcl1) and analyzed an sRNA library from the Dicer-deficient double-mutant. We identified 661 Dicer-dependent loci and in silico prediction revealed 34 milRNAs. Northern blot hybridization of two milRNAs provided evidence for mature milRNAs that are processed either in a complete or partial Dicer-dependent manner from an RNA precursor. Identified milRNAs share typical characteristics of previously discovered fungal milRNAs, like a strong preference for a 5' uracil and the typical length distribution. The detection of potential milRNA target sites in the genome suggests that milRNAs might play a role in posttranscriptional gene regulation. Our data will further increase our knowledge of sRNA dependent gene regulation processes, which is an important prerequisite to develop more effective strategies for improving industrial fermentations with P. chrysogenum.

Highlights

  • Small regulatory RNAs are short non-coding RNAs ranging in size from 17 to 29 nt that mediate RNA interference (RNAi)

  • For RNA isolation, the industrial laboratory strain P2niaD18 was grown on four different media and harvested at three different time points

  • Two further small RNA libraries were generated from submerged cultures of Δku70FRT2 and Dicer-double mutant Δku70FRT2Δdcl2Δdcl1, hereafter referred to as Δdcl2Δdcl1

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Summary

Introduction

Small regulatory RNAs are short non-coding RNAs ranging in size from 17 to 29 nt that mediate RNA interference (RNAi). RNAs (piwiRNAs), short interfering RNAs (siRNAs), and microRNAs (miRNAs) Their endogenous or extrinsic origins and different biogenesis pathways can distinguish these sRNAs from each other. SiRNAs and miRNAs are usually derived from double stranded RNAs (dsRNAs) that are processed by Dicer-like proteins, while piwiRNAs originate Dicer-independently from a single stranded RNA (ssRNA) [4,5]. Besides exogenous siRNAs that mediate silencing of selfish genetic elements, endogenous siRNAs have been reported that regulate expression of endogenous genes in animals, plants, and fungi. These siRNAs originate from exonic regions (exonic-siRNAs), and target the mRNAs of protein coding genes from which they were produced [5,7,8,9]

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