Chang Zhong-Wen, Chang Chin-Chyuan
Department of Aquaculture, National Pingtung University of Science and Technology, Pingtung 91201, Taiwan, ROC.
Fish Shellfish Immunol. 2015 Oct;46(2):753-64. doi: 10.1016/j.fsi.2015.08.016. Epub 2015 Aug 20.
Complementary (c)DNA encoding a receptor for activated protein kinase C1 (RACK1) messenger (m)RNA of the white shrimp Litopenaeus vannamei, designated LvRACK1, consisted a 1136-bp cDNA containing an open reading frame (ORF) of 954 bp, a 111-bp 5'-untranslated region (UTR), and a 71-bp 3'-UTR, which is a 36 kDa cytosolic protein, belonging to the Trp-Asp40 (WD40) family of proteins, characterized by containing seven highly conserved Trp-Asp40 (WD40) internal repeats, and a poly A tail. The WD repeat of LvRACK1 can be predicted to form a seven-bladed propeller structure with each WD repeat composed of four antiparallel β-sheets. The WD40 domains have been implicated in protein-protein interactions. A comparison of amino acid sequences showed that LvRACK1 was closely related to arthropods RACK1. LvRACK1 cDNA was synthesized in all tested tissues detected with real-time PCR including haemocytes, hepatopancreas, gills, muscles, subcuticular epithelium, intestines, abdominal nervous ganglia, thoracic nervous ganglia, lymphoid organ, stomach, heart, and antennal gland, especially in subcuticular epithelium and gill. LvRACK1 mRNA transcription in haemocytes of L. vannamei injected with Vibrio alginolyticus decreased. The depletion of LvRACK1 of haemocytes in L. vannamei received its dsRNA revealed the increased respiratory bursts per haemocyte, superoxide dismutase (SOD), activity, glutathione peroxidase (GPx) activity, and clotting time, but showed the decreased total haemocyte count (THC), hyaline cells (HCs), phagocytic activity, and transglutaminase (TG) activity. LvRACK1 silenced shrimp showed the upregulated gene expressions of cyMnSOD, mtMnSOD, peroxinectin (PE), and TGI, and showed the downregulated α2-macroglobulin (α2-M), clottable protein (CP), lysozyme, and crustin gene expressions. It is therefore concluded that LvRACK1 is involved in immune defense and signaling transduction in haemocytes of L. vannamei infected with V. alginolyticus.
凡纳滨对虾中编码活化蛋白激酶C1受体(RACK1)信使核糖核酸(mRNA)的互补(c)DNA,命名为LvRACK1,其cDNA由1136个碱基对组成,包含一个954个碱基对的开放阅读框(ORF)、一个111个碱基对的5'非翻译区(UTR)和一个71个碱基对的3'UTR,它是一种36千道尔顿的胞质蛋白,属于色氨酸-天冬氨酸40(WD40)蛋白家族,其特征是含有七个高度保守的色氨酸-天冬氨酸40(WD40)内部重复序列以及一个聚腺苷酸尾。LvRACK1的WD重复序列可预测形成一个七叶螺旋桨结构,每个WD重复序列由四个反平行β折叠组成。WD40结构域参与蛋白质-蛋白质相互作用。氨基酸序列比较表明,LvRACK1与节肢动物的RACK1密切相关。通过实时PCR在所有测试组织中均检测到LvRACK1 cDNA的合成,这些组织包括血细胞、肝胰腺、鳃、肌肉、皮下上皮、肠道、腹神经节、胸神经节、淋巴器官、胃、心脏和触角腺,尤其是在皮下上皮和鳃中。注射溶藻弧菌后凡纳滨对虾血细胞中LvRACK1 mRNA转录减少。对接受双链RNA处理的凡纳滨对虾血细胞中LvRACK1进行敲减后发现,每个血细胞的呼吸爆发、超氧化物歧化酶(SOD)活性、谷胱甘肽过氧化物酶(GPx)活性和凝血时间增加,但血细胞总数(THC)、透明细胞(HCs)、吞噬活性和转谷氨酰胺酶(TG)活性降低。LvRACK1沉默的对虾显示出胞质锰超氧化物歧化酶(cyMnSOD)、线粒体锰超氧化物歧化酶(mtMnSOD)、过氧化物酶(PE)和转谷氨酰胺酶I(TGI)基因表达上调,而α2巨球蛋白(α2-M)、可凝蛋白(CP)、溶菌酶和甲壳素基因表达下调。因此得出结论,LvRACK1参与溶藻弧菌感染的凡纳滨对虾血细胞的免疫防御和信号转导。