Dynamic miRNA-mRNA interactions coordinate gene expression in adult Anopheles gambiae.

microRNAs (miRNAs) are increasingly recognized as important regulators of many biological processes in mosquitoes, vectors of numerous devastating infectious diseases. Identification of bona fide targets remains the bottleneck for functional studies of miRNAs. In this study, we used CLEAR-CLIP assay...

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Main Authors: Xiaonan Fu, Pengcheng Liu, George Dimopoulos, Jinsong Zhu
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2020-04-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1008765
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spelling doaj-3f0e3766dbc34b898e0c7015b67a09f62021-04-21T13:52:33ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042020-04-01164e100876510.1371/journal.pgen.1008765Dynamic miRNA-mRNA interactions coordinate gene expression in adult Anopheles gambiae.Xiaonan FuPengcheng LiuGeorge DimopoulosJinsong ZhumicroRNAs (miRNAs) are increasingly recognized as important regulators of many biological processes in mosquitoes, vectors of numerous devastating infectious diseases. Identification of bona fide targets remains the bottleneck for functional studies of miRNAs. In this study, we used CLEAR-CLIP assays to systematically analyze miRNA-mRNA interactions in adult female Anopheles gambiae mosquitoes. Thousands of miRNA-target pairs were captured after direct ligation of the miRNA and its cognate target transcript in endogenous Argonaute-miRNA-mRNA complexes. Using two interactions detected in this manner, miR-309-SIX4 and let-7-kr-h1, we demonstrated the reliability of this experimental approach in identifying in vivo gene regulation by miRNAs. The miRNA-mRNA interaction dataset provided an invaluable opportunity to decipher targeting rules of mosquito miRNAs. Enriched motifs in the diverse targets of each miRNA indicated that the majority of mosquito miRNAs rely on seed-based canonical target recognition, while noncanonical miRNA binding sites are widespread and often contain motifs complementary to the central or 3' ends of miRNAs. The time-lapse study of miRNA-target interactomes in adult female mosquitoes revealed dynamic miRNA regulation of gene expression in response to varying nutritional sources and physiological demands. Interestingly, some miRNAs exhibited flexibility to use distinct sequences at different stages for target recognition. Furthermore, many miRNA-mRNA interactions displayed stage-specific patterns, especially for those genes involved in metabolism, suggesting that miRNAs play critical roles in precise control of gene expression to cope with enormous physiological demands associated with egg production. The global mapping of miRNA-target interactions contributes to our understanding of miRNA targeting specificity in non-model organisms. It also provides a roadmap for additional studies focused on regulatory functions of miRNAs in Anopheles gambiae.https://doi.org/10.1371/journal.pgen.1008765
collection DOAJ
language English
format Article
sources DOAJ
author Xiaonan Fu
Pengcheng Liu
George Dimopoulos
Jinsong Zhu
spellingShingle Xiaonan Fu
Pengcheng Liu
George Dimopoulos
Jinsong Zhu
Dynamic miRNA-mRNA interactions coordinate gene expression in adult Anopheles gambiae.
PLoS Genetics
author_facet Xiaonan Fu
Pengcheng Liu
George Dimopoulos
Jinsong Zhu
author_sort Xiaonan Fu
title Dynamic miRNA-mRNA interactions coordinate gene expression in adult Anopheles gambiae.
title_short Dynamic miRNA-mRNA interactions coordinate gene expression in adult Anopheles gambiae.
title_full Dynamic miRNA-mRNA interactions coordinate gene expression in adult Anopheles gambiae.
title_fullStr Dynamic miRNA-mRNA interactions coordinate gene expression in adult Anopheles gambiae.
title_full_unstemmed Dynamic miRNA-mRNA interactions coordinate gene expression in adult Anopheles gambiae.
title_sort dynamic mirna-mrna interactions coordinate gene expression in adult anopheles gambiae.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2020-04-01
description microRNAs (miRNAs) are increasingly recognized as important regulators of many biological processes in mosquitoes, vectors of numerous devastating infectious diseases. Identification of bona fide targets remains the bottleneck for functional studies of miRNAs. In this study, we used CLEAR-CLIP assays to systematically analyze miRNA-mRNA interactions in adult female Anopheles gambiae mosquitoes. Thousands of miRNA-target pairs were captured after direct ligation of the miRNA and its cognate target transcript in endogenous Argonaute-miRNA-mRNA complexes. Using two interactions detected in this manner, miR-309-SIX4 and let-7-kr-h1, we demonstrated the reliability of this experimental approach in identifying in vivo gene regulation by miRNAs. The miRNA-mRNA interaction dataset provided an invaluable opportunity to decipher targeting rules of mosquito miRNAs. Enriched motifs in the diverse targets of each miRNA indicated that the majority of mosquito miRNAs rely on seed-based canonical target recognition, while noncanonical miRNA binding sites are widespread and often contain motifs complementary to the central or 3' ends of miRNAs. The time-lapse study of miRNA-target interactomes in adult female mosquitoes revealed dynamic miRNA regulation of gene expression in response to varying nutritional sources and physiological demands. Interestingly, some miRNAs exhibited flexibility to use distinct sequences at different stages for target recognition. Furthermore, many miRNA-mRNA interactions displayed stage-specific patterns, especially for those genes involved in metabolism, suggesting that miRNAs play critical roles in precise control of gene expression to cope with enormous physiological demands associated with egg production. The global mapping of miRNA-target interactions contributes to our understanding of miRNA targeting specificity in non-model organisms. It also provides a roadmap for additional studies focused on regulatory functions of miRNAs in Anopheles gambiae.
url https://doi.org/10.1371/journal.pgen.1008765
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