Key Laboratory of Sustainable Development of Marine Fisheries, Ministry of Agriculture, P.R.China, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, 266071, China.
Laboratory for Marine Fisheries and Aquaculture, Qingdao National Laboratory for Marine Science and Technology, No. 1 Wenhai Road, Aoshanwei Town, Jimo, Qingdao, China.
Cell Stress Chaperones. 2019 May;24(3):517-525. doi: 10.1007/s12192-019-00980-6. Epub 2019 Feb 14.
The crustacean hyperglycemic hormone (CHH) gene of Portunus trituberculatus (Pt-CHH) consists of four exons and three introns spanning 3849 bp in size and generating two mature mRNA, Pt-CHH1, and Pt-CHH2. The primary gene transcript produces a cDNA encoding for the putative Pt-CHH2 from exons 1, 2, 3, and 4 and an alternative transcript encodes for a putative Pt-CHH1 peptide from exons 1, 2, and 4. A promoter fragment of about 3 kb was obtained by genomic walking. The tissue-specific expression pattern is examined by reverse transcriptase chain reaction, and the results show that Pt-CHH1 is detected in the eyestalk, brain, muscle, and blood. However, Pt-CHH2 is detected in the ganglia thoracalis and gill. The results indicate that the expression of Pt-CHH2 in the gill might suggest a potential role in osmoregulation. The Pt-CHH transcript level in the gill increases when the crab is exposed to low salinity. The injection of dsRNA for Pt-CHH causes a significant reduction in Pt-CHH2 transcript level and the activity of Na/K-ATPase, and carbonic anhydrase (CA) show a serious decrease. In conclusion, this study provides molecular evidence to support the osmoregulatory function of Pt-CHH2.
三疣梭子蟹(Portunus trituberculatus)的甲壳质激素(CHH)基因(Pt-CHH)由 4 个外显子和 3 个内含子组成,大小为 3849bp,可产生两种成熟的 mRNA,Pt-CHH1 和 Pt-CHH2。初级基因转录物从外显子 1、2、3 和 4 编码推测的 Pt-CHH2 的 cDNA,而替代转录物从外显子 1、2 和 4 编码推测的 Pt-CHH1 肽。通过基因组步移获得了约 3kb 的启动子片段。通过逆转录链反应检查组织特异性表达模式,结果表明 Pt-CHH1 存在于眼柄、脑、肌肉和血液中。然而,Pt-CHH2 存在于胸神经节和鳃中。结果表明,Pt-CHH2 在鳃中的表达可能暗示其在渗透压调节中的潜在作用。当螃蟹暴露在低盐度环境中时,鳃中的 Pt-CHH 转录本水平增加。注射 Pt-CHH 的 dsRNA 会导致 Pt-CHH2 转录本水平和 Na/K-ATPase 活性显著降低,碳酸酐酶(CA)活性严重下降。总之,本研究为 Pt-CHH2 的渗透压调节功能提供了分子证据。