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Dynamic expression of miRNAs across immature and adult stages of the malaria mosquito Anopheles stephensi

BACKGROUND: MicroRNAs are small non-coding RNAs that are involved in various biological processes including insect development. Anopheles stephensi serves as primary vector of malaria parasite in Asia and exhibits holometabolous life cycle that involves four different stages of development. Regulati...

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Autores principales: Jain, Shanu, Rana, Vandita, Tridibes, Adak, Sunil, Sujatha, Bhatnagar, Raj K
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418096/
https://www.ncbi.nlm.nih.gov/pubmed/25888742
http://dx.doi.org/10.1186/s13071-015-0772-y
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author Jain, Shanu
Rana, Vandita
Tridibes, Adak
Sunil, Sujatha
Bhatnagar, Raj K
author_facet Jain, Shanu
Rana, Vandita
Tridibes, Adak
Sunil, Sujatha
Bhatnagar, Raj K
author_sort Jain, Shanu
collection PubMed
description BACKGROUND: MicroRNAs are small non-coding RNAs that are involved in various biological processes including insect development. Anopheles stephensi serves as primary vector of malaria parasite in Asia and exhibits holometabolous life cycle that involves four different stages of development. Regulation and role of mosquito miRNAs during various stages of mosquito development remain largely unknown. METHODS: High throughput small RNA sequencing was employed for identification and profiling of miRNAs across immature and adult stages of malaria vector, which were further validated using Northern hybridization and real time PCR. Target prediction and pathway analysis was carried out to understand the role of regulated miRNAs in insect development. Degradome sequencing was employed to identify cleaved targets of some regulated miRNAs. Loss of function strategy was employed for miR-989 to understand its probable role in female reproductive process. RESULTS: Small RNA sequencing and data analysis revealed 111 and 14 known and novel miRNAs respectively across all stages of Anopheles stephensi. Nine miRNAs showed gender specific regulation across different stages of mosquito development. Analysis of miRNAs revealed regulation of 24 and 26 miRNAs across different stages of male and female mosquito development respectively. mRNA targets and significant pathways targeted by regulated miRNAs were identified for each stage of mosquito development. Degradome sequencing revealed twenty nine cleaved targets of insect miRNAs. MicroRNA-989 showed significant up-regulation in the adult female as compared to adult male mosquito. Knockdown of miR-989 expression in adult female using miRNA specific antagomir affected targets playing roles in protein binding, proteolysis and nucleic acid binding in ovary tissue of female mosquito post blood feeding. CONCLUSIONS: This is the first comprehensive effort to understand regulation of Anopheles stephensi miRNAs across developmental stages of male and female mosquito. Preliminary role of regulated miRNAs in mosquito development was revealed by target prediction and pathway analysis. MicroRNA-989 emerged to have important roles in adult female mosquitoes showing significant up-regulation which was further studied using miR-989 specific antagomir. This study provides insights into mosquito development and reproductive process and has implications for effective control of mosquito population required for reducing spread of mosquito-borne infectious diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-015-0772-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-44180962015-05-05 Dynamic expression of miRNAs across immature and adult stages of the malaria mosquito Anopheles stephensi Jain, Shanu Rana, Vandita Tridibes, Adak Sunil, Sujatha Bhatnagar, Raj K Parasit Vectors Research BACKGROUND: MicroRNAs are small non-coding RNAs that are involved in various biological processes including insect development. Anopheles stephensi serves as primary vector of malaria parasite in Asia and exhibits holometabolous life cycle that involves four different stages of development. Regulation and role of mosquito miRNAs during various stages of mosquito development remain largely unknown. METHODS: High throughput small RNA sequencing was employed for identification and profiling of miRNAs across immature and adult stages of malaria vector, which were further validated using Northern hybridization and real time PCR. Target prediction and pathway analysis was carried out to understand the role of regulated miRNAs in insect development. Degradome sequencing was employed to identify cleaved targets of some regulated miRNAs. Loss of function strategy was employed for miR-989 to understand its probable role in female reproductive process. RESULTS: Small RNA sequencing and data analysis revealed 111 and 14 known and novel miRNAs respectively across all stages of Anopheles stephensi. Nine miRNAs showed gender specific regulation across different stages of mosquito development. Analysis of miRNAs revealed regulation of 24 and 26 miRNAs across different stages of male and female mosquito development respectively. mRNA targets and significant pathways targeted by regulated miRNAs were identified for each stage of mosquito development. Degradome sequencing revealed twenty nine cleaved targets of insect miRNAs. MicroRNA-989 showed significant up-regulation in the adult female as compared to adult male mosquito. Knockdown of miR-989 expression in adult female using miRNA specific antagomir affected targets playing roles in protein binding, proteolysis and nucleic acid binding in ovary tissue of female mosquito post blood feeding. CONCLUSIONS: This is the first comprehensive effort to understand regulation of Anopheles stephensi miRNAs across developmental stages of male and female mosquito. Preliminary role of regulated miRNAs in mosquito development was revealed by target prediction and pathway analysis. MicroRNA-989 emerged to have important roles in adult female mosquitoes showing significant up-regulation which was further studied using miR-989 specific antagomir. This study provides insights into mosquito development and reproductive process and has implications for effective control of mosquito population required for reducing spread of mosquito-borne infectious diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13071-015-0772-y) contains supplementary material, which is available to authorized users. BioMed Central 2015-03-25 /pmc/articles/PMC4418096/ /pubmed/25888742 http://dx.doi.org/10.1186/s13071-015-0772-y Text en © Jain et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Jain, Shanu
Rana, Vandita
Tridibes, Adak
Sunil, Sujatha
Bhatnagar, Raj K
Dynamic expression of miRNAs across immature and adult stages of the malaria mosquito Anopheles stephensi
title Dynamic expression of miRNAs across immature and adult stages of the malaria mosquito Anopheles stephensi
title_full Dynamic expression of miRNAs across immature and adult stages of the malaria mosquito Anopheles stephensi
title_fullStr Dynamic expression of miRNAs across immature and adult stages of the malaria mosquito Anopheles stephensi
title_full_unstemmed Dynamic expression of miRNAs across immature and adult stages of the malaria mosquito Anopheles stephensi
title_short Dynamic expression of miRNAs across immature and adult stages of the malaria mosquito Anopheles stephensi
title_sort dynamic expression of mirnas across immature and adult stages of the malaria mosquito anopheles stephensi
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4418096/
https://www.ncbi.nlm.nih.gov/pubmed/25888742
http://dx.doi.org/10.1186/s13071-015-0772-y
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