Evidence map›Paper›PMID 34320652›Full record

ArticleMolecular biology and evolution2021

Two Reference-Quality Sea Snake Genomes Reveal Their Divergent Evolution of Adaptive Traits and Venom Systems.

An Li, Junjie Wang, Kuo Sun, Shuocun Wang, Xin Zhao, Tingfang Wang, Liyan Xiong, Weiheng Xu, Lei Qiu, Yan Shang and 3 more

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

26 citing papers in PubMed, 46 citations in OpenAlex.

  1. Article
  2. Review
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  5. Article
  6. Sex Chromosome Turnovers and Stability in Snakes.Molecular biology and evolution · 2025
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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

13 authors at 4 institutions in 1 country.

An LiDepartment of Critical Care Medicine, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai, China.
Junjie WangDepartment of Critical Care Medicine, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai, China.
Kuo SunSchool of Pharmacy, Second Military Medical University, Shanghai, China.
Shuocun WangSchool of Medicine, Shanghai University, Shanghai, China.
Xin ZhaoDepartment of Critical Care Medicine, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai, China.
Tingfang WangSchool of Medicine, Shanghai University, Shanghai, China.
Liyan XiongSchool of Medicine, Shanghai University, Shanghai, China.
Weiheng XuSchool of Pharmacy, Second Military Medical University, Shanghai, China.
Lei QiuSchool of Pharmacy, Second Military Medical University, Shanghai, China.
Yan ShangDepartment of Respiratory and Critical Care Medicine, Changhai Hospital, Second Military Medical University, Shanghai, China.
Runhui LiuSchool of Pharmacy, Second Military Medical University, Shanghai, China.
Sheng WangDepartment of Critical Care Medicine, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai, China.
Yiming LuDepartment of Critical Care Medicine, Shanghai Tenth People's Hospital, School of Medicine, Tongji University, Shanghai, China.
Second Military Medical University · CNShanghai Tenth People's Hospital · CNShanghai University · CNTongji University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

True sea snakes (Hydrophiini) are among the last and most successful clades of vertebrates that show secondary marine adaptation, exhibiting diverse phenotypic traits and lethal venom systems. To better understand their evolution, we generated the first chromosome-level genomes of two representative Hydrophiini snakes, Hydrophis cyanocinctus and H. curtus. Through comparative genomics we identified a great expansion of the underwater olfaction-related V2R gene family, consisting of more than 1,000 copies in both snakes. A series of chromosome rearrangements and genomic structural variations were recognized, including large inversions longer than 30 megabase (Mb) on sex chromosomes which potentially affect key functional genes associated with differentiated phenotypes between the two species. By integrating multiomics we found a significant loss of the major weapon for elapid predation, three-finger toxin genes, which displayed a dosage effect in H. curtus. These genetic changes may imply mechanisms that drove the divergent evolution of adaptive traits including prey preferences between the two closely related snakes. Our reference-quality sea snake genomes also enrich the repositories for addressing important issues on the evolution of marine tetrapods, and provide a resource for discovering marine-derived biological products.

Indexed as

HydrophiidaeAnimalsElapid VenomsEvolution, MolecularGenomePhenotypeElapid Venomschromosomal rearrangementsdivergent evolutiongenomic structural variationthree-finger toxintrue sea snakesV2R genes

Identifiers

PMID34320652
PMCPMC8557462
OpenAlexW3185146399

What OpenQuestion holds

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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.