Your browser doesn't support javascript.
loading
Interplay of gene expression and regulators under salinity stress in gill of Labeo rohita.
Harshini, Vemula; Shukla, Nitin; Raval, Ishan; Kumar, Sujit; Shrivastava, Vivek; Chaudhari, Aparna; Patel, Amrutlal K; Joshi, Chaitanya G.
Afiliação
  • Harshini V; Gujarat Biotechnology Research Centre, Sector 11, Gandhinagar, 382010, Gujarat, India.
  • Shukla N; Gujarat Biotechnology Research Centre, Sector 11, Gandhinagar, 382010, Gujarat, India.
  • Raval I; Gujarat Biotechnology Research Centre, Sector 11, Gandhinagar, 382010, Gujarat, India.
  • Kumar S; Postgraduate Institute of Fisheries Education and Research, Kamdhenu University, Himmatnagar, 383010, Gujarat, India.
  • Shrivastava V; Postgraduate Institute of Fisheries Education and Research, Kamdhenu University, Himmatnagar, 383010, Gujarat, India.
  • Chaudhari A; Central Institute of Fisheries Education, Mumbai, 400061, Maharashtra, India.
  • Patel AK; Gujarat Biotechnology Research Centre, Sector 11, Gandhinagar, 382010, Gujarat, India. jd2@gbrc.res.in.
  • Joshi CG; Gujarat Biotechnology Research Centre, Sector 11, Gandhinagar, 382010, Gujarat, India. director@gbrc.res.in.
BMC Genomics ; 24(1): 336, 2023 Jun 19.
Article em En | MEDLINE | ID: mdl-37337199
ABSTRACT

BACKGROUND:

Labeo 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.

RESULTS:

Comprehensive 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.

CONCLUSION:

Altogether, 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.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs / RNA Longo não Codificante Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs / RNA Longo não Codificante Limite: Animals Idioma: En Ano de publicação: 2023 Tipo de documento: Article