Transcriptome analysis of five ovarian stages reveals gonad maturation in female Macrobrachium nipponense
release_iytmkte2rzhonowoo7gwic7qyi
by
Yuning Zhang,
Sufei Jiang,
Hui Qiao,
Yiwei Xiong,
Hongtuo Fu,
Wenyi Zhang,
Yongsheng Gong,
Shubo Jin,
Yan Wu
Abstract
<jats:title>Abstract</jats:title><jats:sec>
<jats:title>Background</jats:title>
<jats:italic>Macrobrachium nipponense</jats:italic> is an economically important species of freshwater shrimp in China. Unlike other marine shrimps, the ovaries in adult female <jats:italic>M. nipponense</jats:italic> can mature rapidly and periodically during the reproductive period, but the resulting high stocking densities and environmental deterioration can negatively impact the harvest yield and economic benefits. To better understand ovary development in female <jats:italic>M. nipponense</jats:italic>, we performed systematic transcriptome sequencing of five different stages of ovarian maturation.
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<jats:title>Results</jats:title>
We obtained 255,966 Gb of high quality transcriptome data from 15 samples. Of the 105,082 unigenes that were selected, 30,878 were successfully annotated. From these unigenes, we identified 17 differentially expressed genes and identified three distinct gene expression patterns related to different biological processes. We found that cathepins, legumains, and cystatin were enriched in the lysosome pathway, and they are related to vitellogenin hydrolysis. Additionally, we found that myosin heavy chain 67 participated in oocyte excretion.
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<jats:title>Conclusions</jats:title>
We provide the first detailed transcriptome data relating to the ovarian maturation cycle in <jats:italic>M. nipponense</jats:italic>. Our results provide important reference information about the genomics, molecular biology, physiology, and population genetics of <jats:italic>M. nipponense</jats:italic> and other crustaceans. It is conducive to further solve the problem of <jats:italic>M. nipponense</jats:italic> rapid ovarian maturation from the aspects of energy supply and cell division.
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