PUBLICATION
Hundreds of LncRNAs Display Circadian Rhythmicity in Zebrafish Larvae
- Authors
- Mishra, S.K., Zhong, Z., Wang, H.
- ID
- ZDB-PUB-211129-63
- Date
- 2021
- Source
- Cells 10(11): (Journal)
- Registered Authors
- Wang, Han, Zhong, Zhaomin
- Keywords
- bioinformatics, circadian clocks, circadian rhythmicity, lncRNA-encoded peptides, lncRNAs, noncoding RNAs, zebrafish larvae
- MeSH Terms
-
- Animals
- Circadian Rhythm/genetics*
- Conserved Sequence
- Darkness
- Gene Expression Profiling
- Gene Expression Regulation
- Gene Ontology
- Humans
- Larva/genetics
- Larva/physiology
- Male
- Mice
- Models, Molecular
- Peptides/chemistry
- Peptides/genetics
- Peptides/metabolism
- Pineal Gland/metabolism
- RNA, Long Noncoding/genetics*
- RNA, Long Noncoding/metabolism
- Testis/metabolism
- Zebrafish/genetics*
- Zebrafish/physiology*
- PubMed
- 34831396 Full text @ Cells
Citation
Mishra, S.K., Zhong, Z., Wang, H. (2021) Hundreds of LncRNAs Display Circadian Rhythmicity in Zebrafish Larvae. Cells. 10(11):.
Abstract
Long noncoding RNAs (lncRNAs) have been shown to play crucial roles in various life processes, including circadian rhythms. Although next generation sequencing technologies have facilitated faster profiling of lncRNAs, the resulting datasets require sophisticated computational analyses. In particular, the regulatory roles of lncRNAs in circadian clocks are far from being completely understood. In this study, we conducted RNA-seq-based transcriptome analysis of zebrafish larvae under both constant darkness (DD) and constant light (LL) conditions in a circadian manner, employing state-of-the-art computational approaches to identify approximately 3220 lncRNAs from zebrafish larvae, and then uncovered 269 and 309 lncRNAs displaying circadian rhythmicity under DD and LL conditions, respectively, with 30 of them are coexpressed under both DD and LL conditions. Subsequently, GO, COG, and KEGG pathway enrichment analyses of all these circadianly expressed lncRNAs suggested their potential involvement in numerous biological processes. Comparison of these circadianly expressed zebrafish larval lncRNAs, with rhythmically expressed lncRNAs in the zebrafish pineal gland and zebrafish testis, revealed that nine (DD) and twelve (LL) larval lncRNAs are coexpressed in the zebrafish pineal gland and testis, respectively. Intriguingly, among peptides encoded by these coexpressing circadianly expressed lncRNAs, three peptides (DD) and one peptide (LL) were found to have the known domains from the Protein Data Bank. Further, the conservation analysis of these circadianly expressed zebrafish larval lncRNAs with human and mouse genomes uncovered one lncRNA and four lncRNAs shared by all three species under DD and LL conditions, respectively. We also investigated the conserved lncRNA-encoded peptides and found one peptide under DD condition conserved in these three species and computationally predicted its 3D structure and functions. Our study reveals that hundreds of lncRNAs from zebrafish larvae exhibit circadian rhythmicity and should help set the stage for their further functional studies.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping