Evidence map›Paper›PMID 40928031›Full record

ArticleAdvanced science (Weinheim, Baden-Wurttemberg, Germany)2025

Patterns and Processes of Genomic Evolution Inferred From the Ten Smallest Vertebrate Genomes.

Kaiqiang Liu, Qian Wang, Ning Wang, Lingfeng Meng, Shuo Li, Hong-Yan Wang, Yuyan Liu, Qian Liu, Yangqing Zhang, Lucas B Doretto and 13 more

Abstract read
In one paragraph

Article in Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Patterns and Processes of Genomic Evolution Inferred From the Ten Smallest Vertebrate Genomes.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors.

Kaiqiang LiuState Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong, 266071, China.
Qian WangState Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong, 266071, China.
Ning WangDepartment of Biophysics and Biochemistry, Karolinska Institute, Stockholm, 17177, Sweden.
Lingfeng MengBGI-Qingdao, BGI-Shenzhen, Qingdao, Shandong, 266555, China.
Shuo LiState Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong, 266071, China.
Hong-Yan WangState Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong, 266071, China.
Yuyan LiuState Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong, 266071, China.
Qian LiuState Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong, 266071, China.
Yangqing ZhangState Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong, 266071, China.
Lucas B DorettoState Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong, 266071, China.
Mengqi ZhangBGI-Qingdao, BGI-Shenzhen, Qingdao, Shandong, 266555, China.
Yating QinBGI-Qingdao, BGI-Shenzhen, Qingdao, Shandong, 266555, China.
Shanshan PanBGI-Qingdao, BGI-Shenzhen, Qingdao, Shandong, 266555, China.
Shenglei HanState Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong, 266071, China.
Weijing LiState Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong, 266071, China.
Shanshan LiuBGI-Qingdao, BGI-Shenzhen, Qingdao, Shandong, 266555, China.
Fengtao GaoWeifang Municipal Key Laboratory of Fishery Resources Development & Comprehensive Utilization, College of Biology and Oceanography, Weifang University, Weifang, 261053, China.
Axel MeyerDepartment of Biology, University of Konstanz, 78457, Konstanz, Germany.
Jussi TaipaleDepartment of Biophysics and Biochemistry, Karolinska Institute, Stockholm, 17177, Sweden.
Guangyi FanBGI-Qingdao, BGI-Shenzhen, Qingdao, Shandong, 266555, China.
Manfred SchartlDevelopmental Biochemistry, Biozentrum, University of Würzburg, 97074, Würzburg, Germany.
Jilin ZhangTung Biomedical Sciences Centre, City University of Hong Kong, Hong Kong S.A.R, 999077, China.
Changwei ShaoState Key Laboratory of Mariculture Biobreeding and Sustainable Goods, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, Shandong, 266071, China.ORCID https://orcid.org/0000-0002-6953-2203

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pufferfish exhibit the smallest vertebrate genomes, making them ideal models for investigating evolutionary patterns and processes that affect genome size. While the Takifugu rubripes genome was fully sequenced two decades ago, key evolutionary drivers remain elusive. We sequenced 10 pufferfish genomes and generated 35 transcriptomes and 13 methylomes to understand genomic evolutionary mechanisms. Comparative genomics revealed that transposable element suppression-rather than lineage-specific conserved element loss-primarily underlies genome compaction. This is mediated by reductions in transposon-associated enzymes that limit transposable element propagation and modify DNA repair mechanisms that promote genomic streamlining. Based on resolved phylogeny among nine Takifugu, it is found that introgression drives speciation of T. niphobles and T. oblongus, while long-term linked selection dominates divergence in other species. Positive selection analyses highlighted mechanotransduction pathway genes (integrins, ion channel transport) that are functionally convergent with mammalian lung cell mechanisms, potentially supporting inflation-based anti-predatory strategies. Additionally, positive selection variants in genes that control lineage-specific skin patterning and coloration, which are either selected for or are rewired in regulatory processes, might suggest a role for pigmentation during the rapid speciation of this lineage. This findings shed light on mechanisms enabling extreme vertebrate genome compaction and provide insights for genome engineering applications.

Indexed as

Evolution, MolecularGenomeTetraodontiformesVertebratesAnimalsDNA Transposable ElementsGenomicsPhylogenySelection, GeneticTakifuguDNA Transposable Elementsgenome evolutionmost compact genomepufferfish genome

Identifiers

PMID40928031
PMCPMC12520575

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Registered trials

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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.