Chromosome-level genome assemblies of Southern pygmy perch ( Nannoperca australis ) and Yarra pygmy perch ( N. obscura ) reveal several miniaturization genes

Read full text
Authors: Jonathan Sandoval‐Castillo, Luciano Bellagamba Beheregaray
Cited by: 1
References: 76

Abstract

Freshwater biodiversity is declining at alarming rates, and the biological characteristics of small freshwater fishes make them particularly vulnerable to habitat degradation and fragmentation. Pygmy perches are small Australian fishes whose populations have recently undergone rapid declines due to human-induced pressures. They also exhibit paedomorphic miniaturization, an evolutionary phenomenon whose consequences for the persistence and diversification of freshwater fishes remain unclear. Genomic resources for pygmy perches would significantly enhance both conservation efforts and evolutionary research. Here, we describe chromosome-level genome assemblies for the Southern Pygmy Perch (Nannoperca australis) and the Yarra Pygmy Perch (N. obscura). We provide evidence for high synteny among percichthyid genomes and for positive selection on size- and growth-related genes in the pygmy perch lineage. The N. australis and N. obscura assemblies are 675.7 and 653.9 Mbp in length, with scaffold N50 values of 26.98 and 26.22 Mbp, respectively. Each assembly comprises 24 pseudo-chromosomes and 890 or 1,476 contigs, with repeat contents of 22.3% and 28.1%. We predicted 26,390 and 24,654 protein-coding genes, and BUSCO completeness scores for Teleostei genes were 96.9% and 96.5%, respectively for N. australis and N. obscura. Their genomes are comparable in quality to the best currently available percichthyid assemblies. These genomic resources will support conservation management efforts and provide a foundation for comparative studies on the adaptive significance of miniaturization.

Fields of Study & Subjects

Genomics and Phylogenetic Studies Genetic diversity and population structure Chromosomal and Genetic Variations

Publication details

Journal / source
Journal of Heredity
Publisher
Oxford University Press (OUP)
Publication date
8 July 2026
Language
EN