Comparative transcriptome analysis of sex-biased genes in the ovary and testis of Helicoverpa armigera
Author of the article:LIU Xiang-Ya JIANG Ting XIAO Hai-Jun ZHANG Wan-Na
Author's Workplace:Institute of Entomology, Jiangxi Agricultural University, Nanchang 330045, China; Institute of Entomology, Jiangxi Agricultural University, Nanchang 330045, China; Institute of Entomology, Jiangxi Agricultural University, Nanchang 330045, China; Institute of Entomology, Jiangxi Agricultural University, Nanchang 330045, China;
Key Words:Helicoverpa armigera; RNA-Seq; reproduction; ovary; testis
Abstract:
[Objectives] The cotton bollworm, Helicoverpa armigera, is one of the most
serious pests of cotton, corn and many other crops in China. Although high
reproduction is the basis for outbreaks of this pest, information on
reproduction- related genes of this species is lacking. [Methods] We sequenced ovary and testis transcriptomes
of H. armigera on an Illumina HiSeq2500 platform and identified numerous
genes that may be involved in gonadal development, gametogenesis and
reproduction. [Results] Raw
reads were assembled into 100 603 unigenes with a mean length of 666.05 bp and an N50 of 1 114 bp. A
similarity search resulted in 52 071 unigenes being annotated, most of which
with reference to the Nr database. Gene expression in the ovary and testis were
then compared, and 7 714 differentially expressed genes (DEGs) were identified.
Among these genes, 3 288 were up-regulated in the ovary and 4 426 were
up-regulated in the testis. Based on KEGG enrichment analyses, the pathways
involved in the regulation of gonadal development and gametogenesis were
identified, including the “mTOR signaling”, the “Oocyte meiosis”, “Insulin
signaling” and “GnRH signaling”, pathways. To further screen the transcriptome
database, numerous DEGs involved in gonadal development and gametogenesis were
identified, including vitellogenin (Vg), vitellogenin receptor (VgR), chorion-related genes, testis-specific
serine/threonine- protein kinase and spermatogenesis-associated protein. Finally, twelve DEGs were selected for RT-qPCR analysis, the expression
patterns of which were consistent with the results obtained from transcriptome
sequencing. [Conclusion] This study acquired the transcriptome data and
identified a series of genes related to gonadal development, providing a basis
for exploring the mechanisms regulating reproduction in H. armigera.