bioRxiv Science⌕ Search

bioRxiv · 10.1101/2025.03.14.643328

Genomic resources for curimba Prochilodus lineatus reveal a fractal pattern of hierarchical genetic population structure in mixed stocks across fish segregated by dams.

Abstract

Genomic resources, new microsatellite markers and a novel observation of a fractal pattern of the genetic population structure are presented for curimba Prochilodus lineatus, a suitable model organism for freshwater migratory species in South America. Our main goals were to investigate the presence of mixed fish stocks, the effects of isolation by dams and broodstocking over the genetic diversity for this species. We focused on the upper segment of the extremely fragmented Grande River, MG, Brazil, from the megadiverse continental La Plata Basin. Two main co-occurring genetically admixed stocks were identified by maximum likelihood estimation and iteratively unfolded with two further steps, through a hierarchical analysis of genetic structure. It consistently unveiled two newly defined internal groups, from the previously resolved clusters (23). We suggest this stratified pattern of mixed stocks from the main river channel may be attributed to the existence of different, well defined breeding grounds, nested within differential scales throughout this basin, arranged according to fractal geometry (1st order river, 2nd and 3rd order tributaries, and so on). This would imply in homing behaviour for this species. Our work also provides massive molecular data for this fish, including its first draft genome assembly and a valuable panel for the rapid and low-cost development of new microsatellite DNA markers. These findings will likely benefit researchers and environmental managers in tackling challenging issues regarding the conservation of Neotropical migratory fishes, as they support the hypothesis of the isolating effects of dams and broodstocking over genetic variability. More importantly, the results presented here point to the potential role of tributaries of different orders in harbouring genetically diverse populations of migratory freshwater fishes.

Source connections

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Yazbeck, G. M., Nascimento, G. A. S., Carvalho, L. C., Graciano, R. C. D., Santos, R., Oliveira, R. S.. 2025-03-17. Genomic resources for curimba Prochilodus lineatus reveal a fractal pattern of hierarchical genetic population structure in mixed stocks across fish segregated by dams.. https://doi.org/10.1101/2025.03.14.643328

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related preprints

Large language model-based bibliometric evaluation of population descriptors in human genetics

As the use of population descriptors such as race, ethnicity, and ancestry have become increasingly common in modern genetics research, there have been growing calls to critically examine their use. Most notably, in 2023, the National Academies of Science, Engineering, and Medicine (NASEM) published a report titled Using Population Descriptors in Genetics and Genomics Research: A New Framework for an Evolving Field, which included eight specific and actionable recommendations for researchers to implement the ethical and accurate use of population descriptors in genetic research. Here, we use the 2023 NASEM report as a benchmark to analyze the use of population descriptors in genome-wide association studies (GWAS). We develop a general toolkit for large language model-based bibliometrics, operationalize the report's recommendations into an evaluation framework, and apply this framework to evaluate all 4,007 papers from the GWAS Catalog published between 2007 and 2025 with full text available on PubMedCentral. We find significant improvements in adherence to NASEM report recommendations over time. However, most improvements predate the publication of the NASEM report itself, suggesting the report functioned primarily as a synthesis of existing best practices rather than a catalyst for change. We conclude by highlighting opportunities for growth in the field of human genetics.

genetics↗

Mitigating biases of rescaling in forward-in-time population genetic simulations

Forward-in-time population genetic simulations are widely used in evolutionary analyses, but simulating large populations and long genomic regions remains computationally demanding. To reduce this cost, parameter rescaling is widely employed, in which the original evolutionary process is approximated by one with a smaller population size and fewer generations. Recently, several studies using the SLiM simulator have raised concerns about the accuracy of this rescaling approach. In this study, we show that many of the biases reported in these studies can be mitigated by using a different simulation algorithm. These results reveal that the accuracy of parameter rescaling depends on how well the simulation algorithm preserves diffusion-limit properties under rescaling.

genetics↗

OPA1 controls mitochondrial dysfunction-driven liver fibrosis in MASLD

Progressive hepatic fibrosis is the principal determinant of morbidity and mortality in metabolic dysfunction-associated steatotic liver disease and steatohepatitis (MASLD/MASH). Mitochondrial dysfunction is a hallmark of MASH, and the release of mitochondrial damage-associated molecular patterns (mito-DAMPs) from injured hepatocytes can promote fibrosis. However, how mitochondrial dynamics and quality control shape the fibrotic response in MASLD/MASH remains unclear. Here, through large-scale genomic analyses of mitochondrial genes governing mitophagy, fusion and fission in human MASLD, with a power-equivalent sample size of approximately 700,000 individuals, we identify a strong association between hepatic fibrosis and the mitochondrial fusion factor dynamin-like GTPase optic atrophy 1 (OPA1). OPA1 transcripts and protein abundance in the liver epithelium were progressively dysregulated with advancing fibrosis. In mice, hepatocyte-specific OPA1 loss alone was sufficient to induce hepatic stellate cell activation and fibrosis in zone 3, promoted the release of mito-DAMPs into the circulation and exacerbated fibrosis in experimental MASH. These findings identify OPA1 as a central regulator of the hepatic fibrotic response and connect defective mitochondrial homeostasis to mito-DAMP release, hepatic stellate cell activation and fibrosis in MASLD.

genetics↗