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Hidden genomic features of an invasive malaria vector, Anopheles stephensi, revealed by a chromosome-level genome assembly

BACKGROUND: The mosquito Anopheles stephensi is a vector of urban malaria in Asia that recently invaded Africa. Studying the genetic basis of vectorial capacity and engineering genetic interventions are both impeded by limitations of a vector’s genome assembly. The existing assemblies of An. stephen...

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Autores principales: Chakraborty, Mahul, Ramaiah, Arunachalam, Adolfi, Adriana, Halas, Paige, Kaduskar, Bhagyashree, Ngo, Luna Thanh, Jayaprasad, Suvratha, Paul, Kiran, Whadgar, Saurabh, Srinivasan, Subhashini, Subramani, Suresh, Bier, Ethan, James, Anthony A., Emerson, J. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876825/
https://www.ncbi.nlm.nih.gov/pubmed/33568145
http://dx.doi.org/10.1186/s12915-021-00963-z
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author Chakraborty, Mahul
Ramaiah, Arunachalam
Adolfi, Adriana
Halas, Paige
Kaduskar, Bhagyashree
Ngo, Luna Thanh
Jayaprasad, Suvratha
Paul, Kiran
Whadgar, Saurabh
Srinivasan, Subhashini
Subramani, Suresh
Bier, Ethan
James, Anthony A.
Emerson, J. J.
author_facet Chakraborty, Mahul
Ramaiah, Arunachalam
Adolfi, Adriana
Halas, Paige
Kaduskar, Bhagyashree
Ngo, Luna Thanh
Jayaprasad, Suvratha
Paul, Kiran
Whadgar, Saurabh
Srinivasan, Subhashini
Subramani, Suresh
Bier, Ethan
James, Anthony A.
Emerson, J. J.
author_sort Chakraborty, Mahul
collection PubMed
description BACKGROUND: The mosquito Anopheles stephensi is a vector of urban malaria in Asia that recently invaded Africa. Studying the genetic basis of vectorial capacity and engineering genetic interventions are both impeded by limitations of a vector’s genome assembly. The existing assemblies of An. stephensi are draft-quality and contain thousands of sequence gaps, potentially missing genetic elements important for its biology and evolution. RESULTS: To access previously intractable genomic regions, we generated a reference-grade genome assembly and full transcript annotations that achieve a new standard for reference genomes of disease vectors. Here, we report novel species-specific transposable element (TE) families and insertions in functional genetic elements, demonstrating the widespread role of TEs in genome evolution and phenotypic variation. We discovered 29 previously hidden members of insecticide resistance genes, uncovering new candidate genetic elements for the widespread insecticide resistance observed in An. stephensi. We identified 2.4 Mb of the Y chromosome and seven new male-linked gene candidates, representing the most extensive coverage of the Y chromosome in any mosquito. By tracking full-length mRNA for > 15 days following blood feeding, we discover distinct roles of previously uncharacterized genes in blood metabolism and female reproduction. The Y-linked heterochromatin landscape reveals extensive accumulation of long-terminal repeat retrotransposons throughout the evolution and degeneration of this chromosome. Finally, we identify a novel Y-linked putative transcription factor that is expressed constitutively throughout male development and adulthood, suggesting an important role. CONCLUSION: Collectively, these results and resources underscore the significance of previously hidden genomic elements in the biology of malaria mosquitoes and will accelerate the development of genetic control strategies of malaria transmission. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-00963-z.
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spelling pubmed-78768252021-02-11 Hidden genomic features of an invasive malaria vector, Anopheles stephensi, revealed by a chromosome-level genome assembly Chakraborty, Mahul Ramaiah, Arunachalam Adolfi, Adriana Halas, Paige Kaduskar, Bhagyashree Ngo, Luna Thanh Jayaprasad, Suvratha Paul, Kiran Whadgar, Saurabh Srinivasan, Subhashini Subramani, Suresh Bier, Ethan James, Anthony A. Emerson, J. J. BMC Biol Research Article BACKGROUND: The mosquito Anopheles stephensi is a vector of urban malaria in Asia that recently invaded Africa. Studying the genetic basis of vectorial capacity and engineering genetic interventions are both impeded by limitations of a vector’s genome assembly. The existing assemblies of An. stephensi are draft-quality and contain thousands of sequence gaps, potentially missing genetic elements important for its biology and evolution. RESULTS: To access previously intractable genomic regions, we generated a reference-grade genome assembly and full transcript annotations that achieve a new standard for reference genomes of disease vectors. Here, we report novel species-specific transposable element (TE) families and insertions in functional genetic elements, demonstrating the widespread role of TEs in genome evolution and phenotypic variation. We discovered 29 previously hidden members of insecticide resistance genes, uncovering new candidate genetic elements for the widespread insecticide resistance observed in An. stephensi. We identified 2.4 Mb of the Y chromosome and seven new male-linked gene candidates, representing the most extensive coverage of the Y chromosome in any mosquito. By tracking full-length mRNA for > 15 days following blood feeding, we discover distinct roles of previously uncharacterized genes in blood metabolism and female reproduction. The Y-linked heterochromatin landscape reveals extensive accumulation of long-terminal repeat retrotransposons throughout the evolution and degeneration of this chromosome. Finally, we identify a novel Y-linked putative transcription factor that is expressed constitutively throughout male development and adulthood, suggesting an important role. CONCLUSION: Collectively, these results and resources underscore the significance of previously hidden genomic elements in the biology of malaria mosquitoes and will accelerate the development of genetic control strategies of malaria transmission. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-021-00963-z. BioMed Central 2021-02-10 /pmc/articles/PMC7876825/ /pubmed/33568145 http://dx.doi.org/10.1186/s12915-021-00963-z Text en © The Author(s) 2021 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research Article
Chakraborty, Mahul
Ramaiah, Arunachalam
Adolfi, Adriana
Halas, Paige
Kaduskar, Bhagyashree
Ngo, Luna Thanh
Jayaprasad, Suvratha
Paul, Kiran
Whadgar, Saurabh
Srinivasan, Subhashini
Subramani, Suresh
Bier, Ethan
James, Anthony A.
Emerson, J. J.
Hidden genomic features of an invasive malaria vector, Anopheles stephensi, revealed by a chromosome-level genome assembly
title Hidden genomic features of an invasive malaria vector, Anopheles stephensi, revealed by a chromosome-level genome assembly
title_full Hidden genomic features of an invasive malaria vector, Anopheles stephensi, revealed by a chromosome-level genome assembly
title_fullStr Hidden genomic features of an invasive malaria vector, Anopheles stephensi, revealed by a chromosome-level genome assembly
title_full_unstemmed Hidden genomic features of an invasive malaria vector, Anopheles stephensi, revealed by a chromosome-level genome assembly
title_short Hidden genomic features of an invasive malaria vector, Anopheles stephensi, revealed by a chromosome-level genome assembly
title_sort hidden genomic features of an invasive malaria vector, anopheles stephensi, revealed by a chromosome-level genome assembly
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7876825/
https://www.ncbi.nlm.nih.gov/pubmed/33568145
http://dx.doi.org/10.1186/s12915-021-00963-z
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