Evidence map›Paper›PMID 31604932›Full record

ArticleNature communications2019

The allotetraploid origin and asymmetrical genome evolution of the common carp Cyprinus carpio.

Peng Xu, Jian Xu, Guangjian Liu, Lin Chen, Zhixiong Zhou, Wenzhu Peng, Yanliang Jiang, Zixia Zhao, Zhiying Jia, Yonghua Sun and 11 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 117 papers.

0numbers the graph read from it
0cells of the map it votes in
117citing papers in PubMed
32.6field-weighted citation impact, top 1% of its field
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

117 citing papers in PubMed, 239 citations in OpenAlex.

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  19. Phylogenetic networks empower biodiversity research.Proceedings of the National Academy of Sciences of the United States of America · 2025
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57 more citing papers are in PubMed but not listed here.

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

21 authors at 6 institutions in 1 country.

Peng XuKey Laboratory of Aquatic Genomics, Ministry of Agriculture, Chinese Academy of Fishery Sciences, Fengtai, Beijing, 100141, China. xupeng77@xmu.edu.cn.ORCID http://orcid.org/0000-0002-1531-5078
Jian XuKey Laboratory of Aquatic Genomics, Ministry of Agriculture, Chinese Academy of Fishery Sciences, Fengtai, Beijing, 100141, China.
Guangjian LiuNovogene Bioinformatics Institute, Beijing, 100029, China.ORCID http://orcid.org/0000-0001-6306-5870
Lin ChenState Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Xiamen University, Xiamen, 361102, China.
Zhixiong ZhouState Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Xiamen University, Xiamen, 361102, China.
Wenzhu PengState Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Xiamen University, Xiamen, 361102, China.
Yanliang JiangKey Laboratory of Aquatic Genomics, Ministry of Agriculture, Chinese Academy of Fishery Sciences, Fengtai, Beijing, 100141, China.
Zixia ZhaoKey Laboratory of Aquatic Genomics, Ministry of Agriculture, Chinese Academy of Fishery Sciences, Fengtai, Beijing, 100141, China.
Zhiying JiaHeilongjiang River Fishery Research Institute, Chinese Academy of Fishery Sciences, Harbin, 150001, China.
Yonghua SunKey Laboratory of Biodiversity and Conservation of Aquatic Organisms, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, China.ORCID http://orcid.org/0000-0001-9368-6969
Yidi WuState Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Xiamen University, Xiamen, 361102, China.
Baohua ChenState Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Xiamen University, Xiamen, 361102, China.
Fei PuState Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Xiamen University, Xiamen, 361102, China.ORCID http://orcid.org/0000-0002-7472-7638
Jianxin FengHenan Academy of Fishery Sciences, Zhengzhou, 450044, China.
Jing LuoState Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, School of Life Sciences, Center for Life Sciences, Yunnan University, Kunming, 650091, China.
Jing ChaiState Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, School of Life Sciences, Center for Life Sciences, Yunnan University, Kunming, 650091, China.
Hanyuan ZhangKey Laboratory of Aquatic Genomics, Ministry of Agriculture, Chinese Academy of Fishery Sciences, Fengtai, Beijing, 100141, China.
Hui WangState Key Laboratory of Marine Environmental Science, College of Ocean and Earth Sciences, Xiamen University, Xiamen, 361102, China.
Chuanju DongCollege of Fisheries, Henan Normal University, Xinxiang, Henan, 453007, China.ORCID http://orcid.org/0000-0001-9232-8609
Wenkai JiangNovogene Bioinformatics Institute, Beijing, 100029, China.ORCID http://orcid.org/0000-0001-8863-3117
Xiaowen SunHeilongjiang River Fishery Research Institute, Chinese Academy of Fishery Sciences, Harbin, 150001, China.
Xiamen University · CNChinese Academy of Fishery Sciences · CNNovogene Bioinformatics Institute · CNYunnan University · CNChinese Academy of Sciences · CNHenan Normal University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Common carp (Cyprinus carpio) is an allotetraploid species derived from recent whole genome duplication and provides a model to study polyploid genome evolution in vertebrates. Here, we generate three chromosome-level reference genomes of C. carpio and compare to related diploid Cyprinid genomes. We identify a Barbinae lineage as potential diploid progenitor of C. carpio and then divide the allotetraploid genome into two subgenomes marked by a distinct genome similarity to the diploid progenitor. We estimate that the two diploid progenitors diverged around 23 Mya and merged around 12.4 Mya based on the divergence rates of homoeologous genes and transposable elements in two subgenomes. No extensive gene losses are observed in either subgenome. Instead, we find gene expression bias across surveyed tissues such that subgenome B is more dominant in homoeologous expression. CG methylation in promoter regions may play an important role in altering gene expression in allotetraploid C. carpio.

Indexed as

GenomePolyploidyAnimalsCarpsEvolution, MolecularPhylogenySequence Analysis, RNA

Identifiers

PMID31604932
PMCPMC6789147
OpenAlexW2980212815

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.