Evidence map›Paper›PMID 29914359›Full record

ArticleBMC genomics2018

Liver transcriptome analysis reveals extensive transcriptional plasticity during acclimation to low salinity in Cynoglossus semilaevis.

Yufeng Si, Haishen Wen, Yun Li, Feng He, Jifang Li, Siping Li, Huiwen He

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2018. 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
4.1field-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, 87 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 1 institution in 1 country.

Yufeng SiThe Key Laboratory of Mariculture (Ocean University of China), Ministry of Education, Ocean University of China, Qingdao, People's Republic of China.
Haishen WenThe Key Laboratory of Mariculture (Ocean University of China), Ministry of Education, Ocean University of China, Qingdao, People's Republic of China. wenhaishen@ouc.edu.cn.ORCID http://orcid.org/0000-0003-2520-685X
Yun LiThe Key Laboratory of Mariculture (Ocean University of China), Ministry of Education, Ocean University of China, Qingdao, People's Republic of China. yunli0116@ouc.edu.cn.
Feng HeThe Key Laboratory of Mariculture (Ocean University of China), Ministry of Education, Ocean University of China, Qingdao, People's Republic of China.
Jifang LiThe Key Laboratory of Mariculture (Ocean University of China), Ministry of Education, Ocean University of China, Qingdao, People's Republic of China.
Siping LiThe Key Laboratory of Mariculture (Ocean University of China), Ministry of Education, Ocean University of China, Qingdao, People's Republic of China.
Huiwen HeThe Key Laboratory of Mariculture (Ocean University of China), Ministry of Education, Ocean University of China, Qingdao, People's Republic of China.
Ocean University of China · CN

Funding

Ministry of Education of the People's Republic of China 201712026Ministry of Science and Technology of the People's Republic of China 2012AA10A403National Natural Science Foundation of China 4147611
6 · The paper itself

Abstract

backgroundSalinity is an important abiotic stress that influences the physiological and metabolic activity, reproduction, growth and development of marine fish. It has been suggested that half-smooth tongue sole (Cynoglossus semilaevis), a euryhaline fish species, uses a large amount of energy to maintain osmotic pressure balance when exposed to fluctuations in salinity. To delineate the molecular response of C. semilaevis to different levels of salinity, we performed RNA-seq analysis of the liver to identify the genes and molecular and biological processes involved in responding to salinity changes.

resultsThe present study yielded 330.4 million clean reads, of which 83.9% were successfully mapped to the reference genome of C. semilaevis. One hundred twenty-eight differentially expressed genes (DEGs), including 43 up-regulated genes and 85 down-regulated genes, were identified. These DEGs were highly represented in metabolic pathways, steroid biosynthesis, terpenoid backbone biosynthesis, butanoate metabolism, glycerolipid metabolism and the 2-oxocarboxylic acid metabolism pathway. In addition, genes involved in metabolism, osmoregulation and ion transport, signal transduction, immune response and stress response, and cytoskeleton remodeling were affected during acclimation to low salinity. Genes acat2, fdps, hmgcr, hmgcs1, mvk, pmvk, ebp, lss, dhcr7, and dhcr24 were up-regulated and abat, ddc, acy1 were down-regulated in metabolic pathways. Genes aqp10 and slc6a6 were down-regulated in osmoregulation and ion transport. Genes abat, fdps, hmgcs1, mvk, pmvk and dhcr7 were first reported to be associated with salinity adaptation in teleosts.

conclusionsOur results revealed that metabolic pathways, especially lipid metabolism were important for salinity adaptation. The candidate genes identified from this study provide a basis for further studies to investigate the molecular mechanism of salinity adaptation and transcriptional plasticity in marine fish.

Indexed as

Gene Expression RegulationTranscriptomeAcclimatizationAnimalsFish ProteinsFlatfishesGene Expression ProfilingGenomeHigh-Throughput Nucleotide SequencingLiverSalinitySequence Analysis, RNAFish ProteinsCynoglossus semilaevisLiverOsmoregulationRNA-seqSalinity adaptationTranscriptome

Identifiers

PMID29914359
PMCPMC6006554
OpenAlexW2808613754

What OpenQuestion holds

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LicenceCC BY
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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.