Developmental RNA-Seq transcriptomics of haploid germ cells and spermatozoa uncovers novel pathways associated with teleost spermiogenesis.
Júlia Castro-ArnauFrançois ChauvignéJèssica Gómez GarridoAnna Esteve-CodinaMarc DabadTyler S AliotoRoderick Nigel FinnJoan CerdàPublished in: Scientific reports (2022)
In non-mammalian vertebrates, the molecular mechanisms involved in the transformation of haploid germ cells (HGCs) into spermatozoa (spermiogenesis) are largely unknown. Here, we investigated this process in the marine teleost gilthead seabream (Sparus aurata) through the examination of the changes in the transcriptome between cell-sorted HGCs and ejaculated sperm (SPZ EJ ). Samples were collected under strict quality controls employing immunofluorescence microscopy as well as by determining the sperm motion kinematic parameters by computer-assisted sperm analysis. Deep sequencing by RNA-seq identified a total of 7286 differentially expressed genes (DEGs) (p-value < 0.01) between both cell types, of which nearly half were upregulated in SPZ EJ compared to HCGs. In addition, approximately 9000 long non-coding RNAs (lncRNAs) were found, of which 56% were accumulated or emerged de novo in SPZ EJ . The upregulated transcripts are involved in transcriptional and translational regulation, chromatin and cytoskeleton organization, metabolic processes such as glycolysis and oxidative phosphorylation, and also include a number of ion and water channels, exchangers, transporters and receptors. Pathway analysis conducted on DEGs identified 37 different signaling pathways enriched in SPZ EJ , including 13 receptor pathways, from which the most predominant correspond to the chemokine and cytokine, gonadotropin-releasing hormone receptor and platelet derived growth factor signaling pathways. Our data provide new insight into the mRNA and lncRNA cargos of teleost spermatozoa and uncover the possible involvement of novel endocrine mechanisms during the differentiation and maturation of spermatozoa.
Keyphrases
- single cell
- rna seq
- induced apoptosis
- growth factor
- high throughput
- long non coding rna
- signaling pathway
- gene expression
- cell cycle arrest
- genome wide
- endoplasmic reticulum stress
- transcription factor
- poor prognosis
- dna damage
- cell death
- stem cells
- epithelial mesenchymal transition
- high speed
- single molecule
- electronic health record
- dna methylation
- cell therapy
- machine learning
- embryonic stem cells
- long noncoding rna
- artificial intelligence
- binding protein
- atomic force microscopy
- upper limb
- mesenchymal stem cells