Chromosome-level genome assembly for the Aldabra giant tortoise enables insights into the genetic health of a threatened population. (12th October 2022)

• Record Type: Journal Article
• Authors: Çilingir, F Gözde; A'Bear, Luke; Hansen, Dennis; Davis, Leyla R; Bunbury, Nancy; Ozgul, Arpat; Croll, Daniel; Grossen, Christine
• Is Part Of: GigaScience. Volume 11(2022)
• Publication Date: 2022-10-12
• Subjects: Aldabrachelys gigantea -- conservation management -- rewilding -- genome assembly -- HiFi sequencing -- Hi-C sequencing -- reference genome; Information storage and retrieval systems -- Research -- Periodicals; Biology -- Research -- Periodicals; Medical sciences -- Research -- Periodicals; Database management -- Periodicals; 570.285
• DOI: 10.1093/gigascience/giac090
• Languages: English
• ISSNs: 2047-217X

Abstract

Abstract: Background: The Aldabra giant tortoise ( Aldabrachelys gigantea ) is one of only two giant tortoise species left in the world. The species is endemic to Aldabra Atoll in Seychelles and is listed as Vulnerable on the International Union for Conservation of Nature Red List (v2.3) due to its limited distribution and threats posed by climate change. Genomic resources for A. gigantea are lacking, hampering conservation efforts for both wild and ex situ populations. A high-quality genome would also open avenues to investigate the genetic basis of the species' exceptionally long life span. Findings: We produced the first chromosome-level de novo genome assembly of A. gigantea using PacBio High-Fidelity sequencing and high-throughput chromosome conformation capture. We produced a 2.37-Gbp assembly with a scaffold N50 of 148.6 Mbp and a resolution into 26 chromosomes. RNA sequencing–assisted gene model prediction identified 23, 953 protein-coding genes and 1.1 Gbp of repetitive sequences. Synteny analyses among turtle genomes revealed high levels of chromosomal collinearity even among distantly related taxa. To assess the utility of the high-quality assembly for species conservation, we performed a low-coverage resequencing of 30 individuals from wild populations and two zoo individuals. Our genome-wide population structure analyses detected genetic population structure in the wild and identified the most likely origin of the zoo-housed individuals. We further identified putatively deleterious mutations to be monitored. Conclusions: We establish a high-quality chromosome-level reference genome for A. gigantea and one of the most complete turtle genomes available. We show that low-coverage whole-genome resequencing, for which alignment to the reference genome is a necessity, is a powerful tool to assess the population structure of the wild population and reveal the geographic origins of ex situ individuals relevant for genetic diversity management and rewilding efforts.