College of Yingdong Life Science, Shaoguan University, Room C-304, Yingdong Building, No. 288, Daxue Road, Zhenjiang District, Shaoguan, 512005, Guangdong, China.
Genes Genomics. 2019 May;41(5):515-528. doi: 10.1007/s13258-019-00787-w. Epub 2019 Feb 14.
Molting is a critical developmental process for crustaceans, during which the claw muscles undergo periodic atrophy and restoration. But the mechanism underlying this special muscle reshuffle around ecdysis is not yet thoroughly understood.
To investigate the molecular mechanism underlying the muscle's reshuffle over the molting cycle of Chinese mitten crab Eriocheir sinensis.
The Illumina high-throughput sequencing technique were used to sequence the transcriptome of the whole claw muscles from Chinese mitten crab Eriocheir sinensis in three molting stages (inter-molt C stage, pre-molt D and post-molt A-B stage); the de novo assembly, annotation and functional evaluation of the contigs were performed with bioinformatics tools.
Totally 129,149 unigenes, 128,190 CDS, 33,770 SSRs and a large number of SNP sites were obtained, and 3700 and 12,771 differentially expressed genes (DEGs) were identified respectively in A-B and D stage compared with that in C stage. The identified DEGs were enriched to 746 and 1 408 GO terms respectively in A-B and D stage compared with C stage (p ≤ 0.05). KEGG pathway analysis showed that the DEGs were significantly enriched in 14 and 11 pathways in A-B vs C comparison and D vs C comparison (p ≤ 0.05), respectively. These DEGs are involved in several biological processes critical for the animal's growth and development, such as gene expression, protein synthesis, muscle development, new cuticle reconstruction, oxidation-reduction process and glycolytic process.
The data generated in this study is the first transcriptomic resource from the muscles of Chinese mitten crab, which would facilitate to characterize key molecular processes underlying crab muscle's growth and development during the molting cycles.
蜕皮是甲壳动物发育过程中的一个关键阶段,在此过程中,爪肌肉会经历周期性的萎缩和恢复。但是,这种蜕皮过程中特殊的肌肉重组机制尚未得到充分理解。
研究中国绒螯蟹(Eriocheir sinensis)蜕皮周期中爪肌肉重组的分子机制。
使用 Illumina 高通量测序技术对中国绒螯蟹三个蜕皮阶段(间蜕 C 期、预蜕 D 期和刚蜕 A-B 期)的整个爪肌肉转录组进行测序;使用生物信息学工具对拼接体进行从头组装、注释和功能评估。
共获得 129149 条 unigenes、128190 条 CDS、33770 个 SSRs 和大量 SNP 位点,A-B 期和 D 期与 C 期相比分别鉴定出 3700 个和 12771 个差异表达基因(DEGs)。A-B 期和 D 期与 C 期相比,鉴定出的 DEGs 分别富集到 746 和 1408 个 GO 术语(p≤0.05)。KEGG 通路分析表明,A-B 期和 D 期与 C 期相比,DEGs 分别显著富集到 14 个和 11 个通路(p≤0.05)。这些 DEGs 参与了动物生长和发育的几个关键生物学过程,如基因表达、蛋白质合成、肌肉发育、新表皮重建、氧化还原过程和糖酵解过程。
本研究提供的转录组数据是中国绒螯蟹肌肉的第一个转录组资源,有助于研究螃蟹肌肉在蜕皮周期中生长和发育的关键分子过程。