Evidence map›Paper›PMID 37337199›Full record

ArticleBMC genomics2023

Interplay of gene expression and regulators under salinity stress in gill of Labeo rohita.

Vemula Harshini, Nitin Shukla, Ishan Raval, Sujit Kumar, Vivek Shrivastava, Aparna Chaudhari, Amrutlal K Patel, Chaitanya G Joshi

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

3 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Physiological Thresholds and Adaptation Mechanisms of the Ili Perch (Animals : an open access journal from MDPI · 2025
    Article
  3. 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 at 3 institutions in 1 country.

Vemula HarshiniGujarat Biotechnology Research Centre, Sector 11, Gandhinagar, 382010, Gujarat, India.
Nitin ShuklaGujarat Biotechnology Research Centre, Sector 11, Gandhinagar, 382010, Gujarat, India.
Ishan RavalGujarat Biotechnology Research Centre, Sector 11, Gandhinagar, 382010, Gujarat, India.
Sujit KumarPostgraduate Institute of Fisheries Education and Research, Kamdhenu University, Himmatnagar, 383010, Gujarat, India.
Vivek ShrivastavaPostgraduate Institute of Fisheries Education and Research, Kamdhenu University, Himmatnagar, 383010, Gujarat, India.
Aparna ChaudhariCentral Institute of Fisheries Education, Mumbai, 400061, Maharashtra, India.
Amrutlal K PatelGujarat Biotechnology Research Centre, Sector 11, Gandhinagar, 382010, Gujarat, India. jd2@gbrc.res.in.
Chaitanya G JoshiGujarat Biotechnology Research Centre, Sector 11, Gandhinagar, 382010, Gujarat, India. director@gbrc.res.in.
Government of Gujarat · INKamdhenu University · INCentral Institute of Fisheries Education · IN

Funding

Government of Gujarat-Department of Science and Technology (GOG-DST) MB-18
6 · The paper itself

Abstract

backgroundLabeo rohita is the most preferred freshwater carp species in India. The concern of increasing salinity concentration in freshwater bodies due to climate change may greatly impact the aquatic environment. Gills are one of the important osmoregulatory organs and have direct contact with external environment. Hence, the current study is conducted to understand the gill transcriptomic response of L. rohita under hypersalinity environment.

resultsComprehensive analysis of differentially expressed long non-coding RNAs (lncRNAs), microRNAs (miRNAs) and mRNAs was performed in gills of L. rohita treated with 2, 4, 6 and 8ppt salinity concentrations. Networks of lncRNA-miRNA-mRNA revealed involvement of 20, 33, 52 and 61 differentially expressed lncRNAs, 11, 13, 26 and 21 differentially expressed miRNAs in 2, 4, 6 and 8ppt groups between control and treatment respectively. These lncRNA-miRNA pairs were regulating 87, 214, 499 and 435 differentially expressed mRNAs (DE mRNAs) in 2, 4, 6 and 8ppt treatments respectively. Functional analysis of these genes showed enrichment in pathways related to ion transportation and osmolyte production to cope with induced osmotic pressure due to high salt concentration. Pathways related to signal transduction (MAPK, FOXO and phosphatidylinositol signaling), and environmental information processing were also upregulated under hypersalinity. Energy metabolism and innate immune response pathways also appear to be regulated. Protein turnover was high at 8ppt as evidenced by enrichment of the proteasome and aminoacyl tRNA synthesis pathways, along with other enriched KEGG terms such as apoptosis, cellular senescence and cell cycle.

conclusionAltogether, the RNA-seq analysis provided valuable insights into competitive endogenous (lncRNA-miRNA-mRNA) regulatory network of L. rohita under salinity stress. L. rohita is adapting to the salinity stress by means of upregulating protein turnover, osmolyte production and removing the damaged cells using apoptotic pathway and regulating the cell growth and hence diverting the essential energy for coping with salinity stress.

Indexed as

MicroRNAsRNA, Long NoncodingAnimalsGene Regulatory NetworksGillsRNA, MessengerSalt StressTranscriptomeMicroRNAsRNA, Long NoncodingRNA, MessengerceRNA networkGill transcriptomeLabeo rohitaSalinity stress

Identifiers

PMID37337199
PMCPMC10278310
OpenAlexW4381252244

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.