The Beginning of the End: A Chromosomal Assembly of the New World Malaria Mosquito Ends with a Novel Telomere

Author:

Compton Austin12,Liang Jiangtao23,Chen Chujia24,Lukyanchikova Varvara235,Qi Yumin12,Potters Mark12,Settlage Robert6,Miller Dustin7,Deschamps Stéphane8,Mao Chunhong9,Llaca Victor8,Sharakhov Igor V23410,Tu Zhijian124

Affiliation:

1. Department of Biochemistry, Virginia Tech, Blacksburg, VA24061

2. Fralin Life Science Institute, Virginia Tech, Blacksburg, VA24061

3. Department of Entomology, Virginia Tech, Blacksburg, VA24061

4. Genetics Bioinformatics and Computational Biology PhD program, Virginia Tech, Blacksburg, VA 24061

5. Institute of Cytology and Genetics SB RAS, Novosibirsk, Russia

6. Advanced Research Computing, Virginia Tech, Blacksburg, VA24061

7. MR4 Program, Center for Disease Control Foundation CDCF, Atlanta, GA30329

8. Corteva Agriscience, Johnston, IA 50131

9. Biocomplexity Institute & Initiative, University of Virginia, Charlottesville, VA 22911

10. Department of Genetics and Cell Biology, Tomsk State University, Tomsk, Russia

Abstract

Abstract Chromosome level assemblies are accumulating in various taxonomic groups including mosquitoes. However, even in the few reference-quality mosquito assemblies, a significant portion of the heterochromatic regions including telomeres remain unresolved. Here we produce a de novo assembly of the New World malaria mosquito, Anopheles albimanus by integrating Oxford Nanopore sequencing, Illumina, Hi-C and optical mapping. This 172.6 Mbps female assembly, which we call AalbS3, is obtained by scaffolding polished large contigs (contig N50 = 13.7 Mbps) into three chromosomes. All chromosome arms end with telomeric repeats, which is the first in mosquito assemblies and represents a significant step toward the completion of a genome assembly. These telomeres consist of tandem repeats of a novel 30-32 bp Telomeric Repeat Unit (TRU) and are confirmed by analyzing the termini of long reads and through both chromosomal in situ hybridization and a Bal31 sensitivity assay. The AalbS3 assembly included previously uncharacterized centromeric and rDNA clusters and more than doubled the content of transposable elements and other repetitive sequences. This telomere-to-telomere assembly, although still containing gaps, represents a significant step toward resolving biologically important but previously hidden genomic components. The comparison of different scaffolding methods will also inform future efforts to obtain reference-quality genomes for other mosquito species.

Publisher

Oxford University Press (OUP)

Subject

Genetics(clinical),Genetics,Molecular Biology

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