4.7 Article Data Paper

Chromosome-level genome assemblies of the malaria vectors Anopheles coluzzii and Anopheles arabiensis

Journal

GIGASCIENCE
Volume 10, Issue 3, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/gigascience/giab017

Keywords

Anopheles arabiensis; Anopheles coluzzii; malaria mosquito; genome assembly; Oxford nanopore sequencing; Hi-C chromosome conformation capture

Funding

  1. US National Institutes of Health (NIH) [R21AI135298]
  2. Government of the Russian Federation through the ITMO Fellowship and Professorship Program
  3. JetBrains Research
  4. Fralin Life Sciences Institute
  5. USDA National Institute of Food and Agriculture Hatch project [223822]

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The study successfully produced de novo chromosome-level genome assemblies for Anopheles coluzzii and Anopheles arabiensis using long-read Oxford Nanopore sequencing technology and Hi-C scaffolding approach. The new assemblies allowed for improved analysis of the genomes of these mosquito species, facilitating functional and population genomic studies in A. coluzzii and A. arabiensis.
Background: Anopheles coluzzii and Anopheles arabiensis belong to the Anopheles gambiae complex and are among the major malaria vectors in sub-Saharan Africa. However, chromosome-level reference genome assemblies are still lacking for these medically important mosquito species. Findings: In this study, we produced de novo chromosome-level genome assemblies for A. coluzzii and A. arabiensis using the long-read Oxford Nanopore sequencing technology and the Hi-C scaffolding approach. We obtained 273.4 and 256.8 Mb of the total assemblies for A. coluzzii and A. arabiensis, respectively. Each assembly consists of 3 chromosome-scale scaffolds (X, 2, 3), complete mitochondrion, and unordered contigs identified as autosomal pericentromeric DNA, X pericentromeric DNA, and Y sequences. Comparison of these assemblies with the existing assemblies for these species demonstrated that we obtained improved reference-quality genomes. The new assemblies allowed us to identify genomic coordinates for the breakpoint regions of fixed and polymorphic chromosomal inversions in A. coluzzii and A. arabiensis. Conclusion: The new chromosome-level assemblies will facilitate functional and population genomic studies in A. coluzzii and A. arabiensis. The presented assembly pipeline will accelerate progress toward creating high-quality genome references for other disease vectors.

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