Medaka (Oryzias latipes) Olpax6.2 acquires maternal inheritance and germ cells expression, but functionally degenerate in the eye

•Olpax6.2 acquires maternal inheritance and germ cells expression.•During embryogenesis, the RNA expression of Olpax6.2 was concentrated into diencephalon whereas the RNA transcript of Olpax6.1 were enriched in eye.•Olpax6.1 is a key gene in eye development, while Olpax6.2 is functionally degenerate...

Full description

Saved in:
Bibliographic Details
Published inGene Vol. 872; p. 147439
Main Authors Pan, Qihua, Luo, Junzhi, Jiang, Yuewen, Wang, Zhi, Lu, Ke, Chen, Tiansheng
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier B.V 01.07.2023
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:•Olpax6.2 acquires maternal inheritance and germ cells expression.•During embryogenesis, the RNA expression of Olpax6.2 was concentrated into diencephalon whereas the RNA transcript of Olpax6.1 were enriched in eye.•Olpax6.1 is a key gene in eye development, while Olpax6.2 is functionally degenerated in the eye. Gene duplication provides raw material for the evolution of genetic and phenotypic complexity. It has remained a long-standing mystery how duplicated genes evolve into new genes by neofunctionalization via the acquisition of new expression and/or activity and simultaneous loss of the old expression and activity. Fishes have many gene duplicates from whole genome duplication, making them excellent for studying the evolution of gene duplicates. In the fish medaka (Oryzias latipes), an ancestral pax6 gene has given rise to Olpax6.1 and Olpax6.2. Here we report that medaka Olpax6.2 is evolving towards neofunctionalization. A chromosomal syntenic analysis indicated that Olpax6.1 and Olpax6.2 are structurally co-homologous to the single pax6 in other organisms. Interestingly, Olpax6.2 maintains all conserved coding exons but loses the non-coding exons of Olpax6.1, and has 4 promoters versus 8 in Olpax6.1. RT-PCR revealed that Olpax6.2 maintains expression in the brain eye, pancreas as Olpax6.1. Surprisingly, Olpax6.2 also exhibits maternal inheritance and gonadal expression by RT-PCR, in situ hybridization and RNA transcriptome analysis. The expression and distribution of Olpax6.2 is not different from Olpax6.1 in the adult brain, eye and pancreas, but exhibited overlapping and distinct expression in early embryogenesis. We show that ovarian Olpax6.2 expression occurs in female germ cells. Olpax6.2 knockout shows no obvious defect in eye development, while Olpax6.1 F0 mutant have severe defects in eye development. Thus, Olpax6.2 acquires maternal inheritance and germ cell expression, but functionally degenerates in the eye, making this gene as an excellent model to study the neofunctionalization of duplicated genes.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0378-1119
1879-0038
DOI:10.1016/j.gene.2023.147439