Evidence map›Paper›PMID 37493868›Full record

ArticleMarine biotechnology (New York, N.Y.)2023

Whole Transcriptome Analysis Reveals the Global Molecular Responses of mRNAs, lncRNAs, miRNAs, circRNAs, and Their ceRNA Networks to Salinity Stress in Hong Kong Oysters, Crassostrea hongkongensis.

Salifu Ibrahim, Chuangye Yang, Chenyang Yue, Xinyu Song, Yuewen Deng, Qi Li, Wengang Lü

Abstract read
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In one paragraph

Article in Marine biotechnology (New York, N.Y.), 2023. 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
4.8field-weighted citation impact, top 5% 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

2 citing papers in PubMed, 20 citations in OpenAlex.

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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

7 authors at 2 institutions in 1 country.

Salifu Ibrahim *Guangdong Marine Invertebrates Science and Technology Innovation Center, Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China.
Chuangye Yang *Pearl Breeding and Processing Engineering Technology Research Centre of Guangdong Province, Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China.
Chenyang YueGuangdong Marine Invertebrates Science and Technology Innovation Center, Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China. yuechenyang1992@gdou.edu.cn.
Xinyu SongGuangdong Marine Invertebrates Science and Technology Innovation Center, Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China.
Yuewen DengPearl Breeding and Processing Engineering Technology Research Centre of Guangdong Province, Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China.
Qi LiKey Laboratory of Mariculture, Ministry of Education, Ocean University of China, Qingdao, 266003, China.
Wengang LüGuangdong Marine Invertebrates Science and Technology Innovation Center, Fisheries College, Guangdong Ocean University, Zhanjiang, 524088, China.
Guangdong Ocean University · CNOcean University of China · CN

Funding

Chinese Ministry of Science and Technology through the National Key Research and Development Program of China 2018YFD0901401Department of Education of Guangdong Province 2021KCXTD026GuangDong Basic and Applied Basic Research Foundation 2022A1515110002Science and Technology Program of Zhanjiang City 2021E05029the project of the Innovation Team for the Innovation and Utilization of Economic Animal Germplasm in the South China Sea 2021KCXTD026
6 · The paper itself

Abstract

The Hong Kong oyster, Crassostrea hongkongensis, is an estuarine bivalve with remarkable commercial value in South China, and the increase of salinity in estuaries during the dry season has posed a major threat to the oyster farming. To explore the global transcriptional response to salinity stress, a whole-transcriptome analysis was performed with the gills of oysters in 6‰, 18‰, and 30‰ filtered seawater. Overall, 2243, 194, 371, and 167 differentially expressed mRNAs (DEmRNAs), differentially expressed long non-coding RNAs (DElncRNAs), differentially expressed circular RNAs (DEcircRNAs), and differentially expressed microRNAs (DEmiRNAs) were identified, respectively. Based on GO enrichment and KEGG pathway analysis, these important DEmRNAs, DElncRNAs, DEcircRNAs, and DEmiRNAs were predicted to be mainly involved in amino acids metabolism, microtubule movement, and immune defense. This demonstrated the complexity of dynamic transcriptomic profiles of C. hongkongensis in response to salinity fluctuation. The regulatory relationships of DEmiRNAs-DEmRNAs, DElncRNAs-DEmiRNAs, and DEcircRNAs-DEmiRNAs were also predicted, and finally, a circRNA-associated competing endogenous RNA (ceRNA) network was constructed, consisting of six DEcircRNAs, eight DEmiRNAs, and five DEmRNAs. The key roles of taurine and hypotaurine metabolism and phenylalanine metabolism were highlighted in this ceRNA network, which was consistent with the major contribution of free amino acids to intracellular osmolality and cell volume regulation. Collectively, this study provides comprehensive data, contributing to the exploration of coding and non-coding RNAs in C. hongkongensis salinity response. The results would benefit the understanding of the response mechanism of bivalves against salinity fluctuation, and provide clues for genetic improvement of C. hongkongensis with hyper-salinity tolerance.

Indexed as

CrassostreaMicroRNAsRNA, Long NoncodingAnimalsGene Expression ProfilingGene Regulatory NetworksHong KongRNA, CircularRNA, MessengerSalt StressTranscriptomeMicroRNAsRNA, CircularRNA, Long NoncodingRNA, MessengerCeRNACrassostrea hongkongensisSalt stressWhole transcriptome analysis

Identifiers

PMID37493868
OpenAlexW4385264838

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.