Genome-wide identification, characterization, and expression analysis of lineage-specific genes within zebrafish
- Authors
- Yang, L., Zou, M., Fu, B., and He, S.
- ID
- ZDB-PUB-130213-3
- Date
- 2013
- Source
- BMC Genomics 14(1): 65 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Animals
- Base Composition
- Chromosomes/genetics
- Conserved Sequence
- Evolution, Molecular*
- Exons/genetics
- Female
- Gene Duplication/genetics
- Gene Expression Profiling*
- Genomics*
- Male
- Organ Specificity
- RNA, Messenger/genetics
- RNA, Messenger/metabolism
- Reproduction/genetics
- Spatio-Temporal Analysis
- Species Specificity
- Zebrafish/genetics*
- Zebrafish/growth & development
- Zebrafish/physiology
- PubMed
- 23368736 Full text @ BMC Genomics
Background
The genomic basis of teleost phenotypic complexity remains obscure, despite increasing availability of genome and transcriptome sequence data. Fish-specific genome duplication cannot provide sufficient explanation for the morphological complexity of teleosts, considering the relatively large number of extinct basal ray-finned fishes.
Results
In this study, we performed comparative genomic analysis to discover the Conserved Teleost-Specific Genes (CTSGs) and orphan genes within zebrafish and found that these two sets of lineage-specific genes may have played important roles during zebrafish embryogenesis. Lineage-specific genes within zebrafish share many of the characteristics of their counterparts in other species: shorter length, fewer exon numbers, higher GC content, and fewer of them have transcript support. Chromosomal location analysis indicated that neither the CTSGs nor the orphan genes were distributed evenly in the chromosomes of zebrafish. The significant enrichment of immunity proteins in CTSGs annotated by gene ontology (GO) or predicted ab initio may imply that defense against pathogens may be an important reason for the diversification of teleosts. The evolutionary origin of the lineage-specific genes was determined and a very high percentage of lineage-specific genes were generated via gene duplications. The temporal and spatial expression profile of lineage-specific genes obtained by expressed sequence tags (EST) and RNA-seq data revealed two novel properties: in addition to being highly tissue-preferred expression, lineage-specific genes are also highly temporally restricted, namely they are expressed in narrower time windows than evolutionarily conserved genes and are specifically enriched in later-stage embryos and early larval stages.
Conclusions
Our study provides the first systematic identification of two different sets of lineage-specific genes within zebrafish and provides valuable information leading towards a better understanding of the molecular mechanisms of the genomic basis of teleost phenotypic complexity for future studies.