Evidence map›Paper›PMID 40407927›Full record

ArticleMarine biotechnology (New York, N.Y.)2025

Genetic Basis of Low-Salinity Tolerance in the Pacific Oyster (Crassostrea gigas) as Revealed by Estimation of Genetic Parameters and Genome-Wide Association Study.

Xiaojie Han, Ben Yang, Chao Guo, Mengmeng Xu, Deqi Sun, Chengjun Zhi, Qi Li, Shikai Liu

Abstract read
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In one paragraph

Article in Marine biotechnology (New York, N.Y.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Genetic Structures ofAnimals : an open access journal from MDPI · 2026
    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

8 authors.

Xiaojie HanKey Laboratory of Mariculture, Ministry of Education, and College of Fisheries, Ocean University of China), Ocean University of China, Qingdao, 266003, Shandong, China.
Ben YangKey Laboratory of Mariculture, Ministry of Education, and College of Fisheries, Ocean University of China), Ocean University of China, Qingdao, 266003, Shandong, China.
Chao GuoKey Laboratory of Mariculture, Ministry of Education, and College of Fisheries, Ocean University of China), Ocean University of China, Qingdao, 266003, Shandong, China.
Mengmeng XuKey Laboratory of Mariculture, Ministry of Education, and College of Fisheries, Ocean University of China), Ocean University of China, Qingdao, 266003, Shandong, China.
Deqi SunKey Laboratory of Mariculture, Ministry of Education, and College of Fisheries, Ocean University of China), Ocean University of China, Qingdao, 266003, Shandong, China.
Chengjun ZhiKey Laboratory of Mariculture, Ministry of Education, and College of Fisheries, Ocean University of China), Ocean University of China, Qingdao, 266003, Shandong, China.
Qi LiKey Laboratory of Mariculture, Ministry of Education, and College of Fisheries, Ocean University of China), Ocean University of China, Qingdao, 266003, Shandong, China.
Shikai LiuKey Laboratory of Mariculture, Ministry of Education, and College of Fisheries, Ocean University of China), Ocean University of China, Qingdao, 266003, Shandong, China. liushk@ouc.edu.cn.

Funding

National Natural Science Foundation of China 32341060
6 · The paper itself

Abstract

The Pacific oyster (Crassostrea gigas), a species of significant economic importance in global aquaculture, faces increasing challenges due to climate change and salinity fluctuations in coastal environments. This study aims to explore the breeding potential of low salinity tolerance traits and dissect their genetic basis, thereby improving environmental adaptability and expanding aquaculture zones. A total of 845 oysters from 36 full families were exposed to a low-salinity challenge (10 practical salinity units) for assessing phenotypic variation, estimating genetic parameters, and dissecting the genetic basis of low-salinity tolerance. The variation in survival rates among families (0-27.27%) highlighted substantial phenotypic plasticity of low-salinity tolerance. Heritability estimates for low-salinity tolerance traits ranged from 0.141 to 0.277, indicating low to moderate level genetic control of the trait. The low genetic and phenotypic correlations were observed between low-salinity tolerance and growth traits. Using a high-throughput and cost-effective genotyping approach by low-coverage whole genome sequencing with genotype imputation, we genotyped 297 samples with contrasted performance in low-salinity tolerance and detected 3,830,446 high-quality single nucleotide polymorphisms (SNPs) for genetic analysis. Genome-wide association studies (GWAS) uncovered the polygenic architecture of low-salinity tolerance and identified 16 SNPs associated with eight genes involved in oxidative metabolism, transmembrane transport, and immune defense. This study performed the first estimation of genetic parameters for low-salinity tolerance in C. gigas and identified genetic markers and associated genes for the trait, providing valuable information toward genetic improvement of low-salinity tolerance in the oyster using both traditional and genomic selection breeding strategies.

Indexed as

CrassostreaSalt ToleranceAnimalsAquacultureBreedingGenome-Wide Association StudyGenotypePhenotypePolymorphism, Single NucleotideSalinityCrassostrea gigasGenetic correlationGWASHeritabilityLow salinity

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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.