Transcriptomic response to low salinity stress in gills of the Pacific white shrimp, Litopenaeus vannamei

被引:43
|
作者
Hu, Dongxu [1 ]
Pan, Luqing [1 ]
Zhao, Qun [1 ]
Ren, Qin [1 ]
机构
[1] Ocean Univ China, Key Lab Mariculture, Minist Educ, Qingdao 266003, Peoples R China
关键词
Digital gene expression; Salinity stress; Illumina sequencing; Litopenaeus vannamei; ACTIVATED PROTEIN-KINASES; SUBUNIT MESSENGER-RNA; PURPLE SHORE CRAB; OSMOTIC-STRESS; LONG-TERM; MACROBRACHIUM-OLFERSII; CALLINECTES-SAPIDUS; SIGNALING PATHWAYS; ADENYLATE-CYCLASE; ATPASE ACTIVITY;
D O I
10.1016/j.margen.2015.07.003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The Pacific white shrimp, Litopenaeus vannamei (L. vannamei), is one of the most farmed species. Salinity is an important environmental factor that affects its growth and distribution. However, the molecular mechanism of the shrimp in response to salinity stress remains largely unclear. High-throughput sequencing is a helpful tool to analyze the molecular response to salinity challenge in shrimp. In the present study, the transcriptomic responses of the gills in L. vannamei under low salinity stress were detected by Illumina's digital gene expression system. A total of 10,725,789 and 10,827,411 reads were generated from the non-changed and low salinity changed groups, respectively. 64,590 Unigenes with an average length of 764 bp were generated. Compared with the control, 585 genes were differentially expressed under low salinity. GO functional analysis and KEGG pathway analysis indicated some vital genes in response to the challenge. Ten genes related to osmoregulation and ambient salinity adaption were selected to validate the DGE results by RT-qPCR. This work provides valuable information to study the mechanism of salinity adaption in L. vannamei. Genes and pathways from the results will be beneficial to reveal the molecular basis of osmoregulation. It also gives an insight into the response to the salinity challenge in L. vannamei. (c) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:297 / 304
页数:8
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