Evidence map›Paper›PMID 41735841›Full record

ArticleBMC genomics2026

Genome-wide insights into adaptive divergence, historical demography, and habitat suitability of Ptychobarbus Kaznakovi and P. leptosomus.

Taiming Yan, Ping Chen, Huiling Wang, Mengna Chang, Qipeng Fu, Wenjie Luo, Fei Liu, Junjie Huang, Wenxiang Ding, Kuo Gao and 7 more

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Article in BMC genomics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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17 authors.

Taiming Yan *Fisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Ping Chen *Fisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Huiling WangFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Mengna ChangFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Qipeng FuFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Wenjie LuoFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Fei LiuFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Junjie HuangFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Wenxiang DingFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Kuo GaoFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Lin WenFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Jinxing XiongFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Haochen WangFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Rukui ZengYalong River Hydropower Development Company, Ltd, Chengdu, China.
Ziting TangFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China.
Zhi HeFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China. zhihe@sicau.edu.cn.
Deying YangFisheries College, Sichuan Agricultural University, 211 # Huimin Road, Chengdu, China. deyingyang@sicau.edu.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundOur previous study from 2024 indicated that Ptychobarbus leptosomus is a new species found only in the Yalong River (the largest tributary of the Jinsha River). P. leptosomus was historically classified as P. kaznakovi, which lives in the Jinsha River. To date, the evolutionary history and population dynamics of P. leptosomus and P. kaznakovi have not been reported. In our study, both species have similar morphologies, which may reflect gene flow between the two species. Genotyping-by-sequencing (GBS) technology was utilized to acquire whole-genome single-nucleotide polymorphism (SNP) markers, which were subsequently used to assess population structure, population dynamics, and adaptive differentiation.

resultsPhylogenetic and population structural analyses based on SNPs indicated that P. leptosomus is an independent Picea species. Additionally, P. kaznakov is more closely related to P. chungtienensis, which is consistent with its geographic distribution. The obvious gene flow from P. kaznakovi and P. chungtienensis branches to P. dipogon was detected. Historical population dynamics analysis revealed that tectonic events in the Shaluli Mountains and the Quaternary climate oscillation had important impacts on the current distribution patterns of the two species, which experienced similar population contraction and expansion processes. Local adaptation promoted differentiation between P. leptosomus and P. kaznakov. Genotype and environment association analysis revealed that 35,654 SNPs were related to environmental factors, mainly related to adaptation to precipitation seasonality and temperature seasonality. Selective elimination analysis revealed that the selected genes were enriched mainly in glycan biosynthesis and metabolism and growth hormone synthesis, secretion, and action (genes such as glycine decarboxylase (gldc), cyp51, igf-1, and tnf-α), which can help P. leptosomus and P. kaznakov adapt better to the water environment of the high mountains and valleys in the Shaluli Mountains.

conclusionsThis study emphasizes the significant role of geological and environmental changes in shaping the population history and evolutionary processes of P. kaznakovi and P. leptosomus, and deepens our understanding of the species classification of Ptychobarbus and provides a basis for future species protection.

Indexed as

Adaptation, PhysiologicalCyprinidaeEcosystemAnimalsGene FlowGenetics, PopulationPhylogenyPolymorphism, Single NucleotideHistorical population dynamicsP. leptosomusPopulation structurePtychobarbus kaznakoviSingle-nucleotide polymorphism (SNP)Whole-genome level

Identifiers

PMID41735841
PMCPMC13041509

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.