Abstract

BackgroundThe siRNA and piRNA pathways have been shown in insects to be essential for regulation of gene expression and defence against exogenous and endogenous genetic elements (viruses and transposable elements). The vast majority of endogenous small RNAs produced by the siRNA and piRNA pathways originate from repetitive or transposable elements (TE). In D. melanogaster, TE-derived endogenous siRNAs and piRNAs are involved in genome surveillance and maintenance of genome integrity. In the medically relevant malaria mosquito Anopheles gambiae TEs constitute 12-16% of the genome size. Genetic variations induced by TE activities are known to shape the genome landscape and to alter the fitness in An. gambiae.ResultsHere, using bioinformatics approaches we analyzed the small RNA data sets from 6 libraries formally reported in a previous study and examined the expression of the mixed germline/somatic siRNAs and piRNAs produced in adult An. gambiae females. We characterized a large population of TE-derived endogenous siRNAs and piRNAs, which constitutes 56-60% of the total siRNA and piRNA reads in the analysed libraries. Moreover, we identified a number of protein coding genes producing gene-specific siRNAs and piRNAs that were generally expressed at much lower levels than the TE-associated small RNAs. Detailed sequence analysis revealed that An. gambiae piRNAs were produced by both “ping-pong” dependent (TE-associated piRNAs) and independent mechanisms (genic piRNAs). Similarly to D. melanogaster, more than 90% of the detected piRNAs were produced from TE-associated clusters in An. gambiae. We also found that biotic stress as blood feeding and infection with Plasmodium parasite, the etiological agent of malaria, modulated the expression levels of the endogenous siRNAs and piRNAs in An. gambiae.ConclusionsWe identified a large and diverse set of the endogenously derived siRNAs and piRNAs that share common and distinct aspects of small RNA expression across insect species, and inferred their impact on TE and gene activity in An. gambiae. The TE-specific small RNAs produced by both the siRNA and piRNA pathways represent an important aspect of genome stability and genetic variation, which might have a strong impact on the evolution of the genome and vector competence in the malaria mosquitoes.Electronic supplementary materialThe online version of this article (doi:10.1186/s12864-015-1436-1) contains supplementary material, which is available to authorized users.

Highlights

  • The small interfering RNAs (siRNA) and P-element induced wiped testis (PIWI)-interacting RNA (piRNA) pathways have been shown in insects to be essential for regulation of gene expression and defence against exogenous and endogenous genetic elements

  • Using previously reported deep sequenced small RNA libraries [33] we examined the expression of endogenous siRNAs and PIWI-interacting RNA (piRNA) produced in adult An. gambiae females

  • Small RNA sequencing We performed analysis of small RNA populations recovered from the deep sequenced small RNA libraries published in [33] to determine i) diversity of the mixed germline/somatic endogenous siRNAs and piRNAs in An. gambiae adult females ii) how endogenous siRNAs and piRNAs respond to blood feeding and Plasmodium berghei infection

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Summary

Introduction

The siRNA and piRNA pathways have been shown in insects to be essential for regulation of gene expression and defence against exogenous and endogenous genetic elements (viruses and transposable elements). The vast majority of endogenous small RNAs produced by the siRNA and piRNA pathways originate from repetitive or transposable elements (TE). In the medically relevant malaria mosquito Anopheles gambiae TEs constitute 12-16% of the genome size. Small non-coding RNAs (ncRNAs) are involved in regulation of gene expression, RNA based immunity and activity of transposable elements (TEs) and their remnants. In D. melanogaster two small RNA silencing pathways, small interfering RNAs (siRNA) and piRNA (PIWI-interacting RNAs), regulate gene expression by silencing specific genes and TEs both in germline and soma [1,2,3,4,5,6,7]. Depletion of Ago-2 in An. gambiae and Ae. aegypti mosquitoes respectively infected with O’nyong-yong virus and Sindbis virus resulted in increased virus replication [8,9]

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