Abstract

ObjectiveTo assess the differences in ovarian transcriptomes in Shan Ma ducks between their peak and late stages of egg production, and to obtain new transcriptomic data of these egg-producing ducks.MethodsThe Illumina HiSeq 2000 system was used for high throughput sequencing of ovarian transcriptomes from Shan Ma ducks at their peak or late stages of egg production.ResultsGreater than 93% of the sequencing data had a base quality score (Q score) that was not less than 20 (Q20). From ducks at their peak stage of egg production, 42,782,676 reads were obtained, with 4,307,499,083 bp sequenced. From ducks at their late stage of egg production, 45,316,166 reads were obtained, with 4,562,063,363 bp sequenced. A comparison of the two datasets identified 2,002 differentially expressed genes, with 790 upregulated and 1,212 downregulated. Further analysis showed that 1,645 of the 2,002 differentially expressed genes were annotated in the non-redundant (NR) database, with 646 upregulated and 999 downregulated. Among the differentially expressed genes with annotations in the NR database, 696 genes were functionally annotated in the clusters of orthologous groups of proteins database, involving 25 functional categories. One thousand two hundred four of the differentially expressed genes with annotations in the NR database were functionally annotated in the gene ontology (GO) database, and could be divided into three domains and 56 categories. The three domains were cellular component, molecular function, and biological process. Among the genes identified in the GO database, 451 are involved in development and reproduction. Analysis of the differentially expressed genes with annotations in the NR database against the Kyoto encyclopedia of genes and genomes database revealed that 446 of the genes could be assigned to 175 metabolic pathways, of which the peroxisome proliferator-activated receptor signaling pathway, insulin signaling pathway, fructose and mannose metabolic pathways, gonadotropin releasing hormone signaling pathway and transforming growth factor beta signaling pathway were significantly enriched.ConclusionThe differences in ovarian transcriptomes in Shan Ma ducks between their peak and late stages of egg production were elucidated, which greatly enriched the ovarian transcriptomic information of egg-producing ducks.

Highlights

  • Improving the reproductive performance of poultry is an important goal for genetic selection

  • Since ovarian function in poultry exerts a direct impact on egg production [1], poultry breeding scientists usually focus on the ovary to study egg production, including examination of the main genes controlling egg production and other related differentially expressed genes

  • Few reports are available in the literature regarding duck ovarian transcriptomes; and no reports exist on ovarian transcriptomic differences between Shan Ma ducks at peak and late stages of egg production

Read more

Summary

Introduction

Improving the reproductive performance of poultry is an important goal for genetic selection. Five of the differentially expressed genes (protein tyrosine kinase 2 beta [PTK2B], phospholipase C [PLCB], cytochrome P450 family 19 subfamily A [CYP19A], hydroxy-delta5-steroid dehydrogenase, 3 beta [HSD3B], and Insulin-like growth factor-binding protein 3 [IGFBP3]) and were confirmed to be involved in steroid hormone biosynthesis, gonadotropin releasing hormone (GnRH) signaling, prolactin signaling and ovary development. These genes have been extensively studied and are known to be important in mammalian female reproductive organogenesis and reproductive cycle regulation [6]. We sequenced the ovarian transcriptomes in Shan Ma ducks to assess basic information at different reproductive stages, screen for differentially expressed genes, and provide a foundation for future studies on genes related to reproductive performance and on the regulation of these genes at the molecular level

Methods
Discussion
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call