Institute of Biomedical Nutrition, Hungkuang University, Sha-Lu, Taichung 43302, Taiwan, ROC.
Fish Shellfish Immunol. 2013 Nov;35(5):1613-23. doi: 10.1016/j.fsi.2013.09.002. Epub 2013 Sep 12.
Complementary (c)DNA encoding transglutaminaseII (TGII) messenger (m)RNA of white shrimp, Litopenaeus vannamei, was cloned from haemocytes by a reverse-transcription polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends (RACE) using oligonucleotide primers based on the TG sequence of the horseshoe crab, Tachypleus tridentatus (accession no.: BAA02134), tiger shrimp, Penaeus monodon (AAV49005; AAO33455), kuruma shrimp, Marsupenaeus japonicus (BAD36808) and Pacifastacus leniusculus (AAK69205) TG. The 2405-bp cDNA contained an open reading frame (ORF) of 2292 bp, a 31-bp 5'-untranslated region (UTR), and an 82-bp 3'-UTR containing a poly A tail. The molecular mass of the deduced amino acid (aa) sequence (764 aa) was 85.9 kDa with an estimated pI of 5.32. The L. vannamei TGII (abbreviated LvTGII) contains a typical TG-like homologue, two putative integrin binding motif (RGD and KGD), and five calcium-binding sites; three catalytic triad is present as in arthropod TG. Sequence comparison and phylogenetic analysis revealed that shrimp TG can be separated into two groups, STGI and STGII, and LvTGII is more closely related to STGII than to STGI. LvTGII mRNA was detected in all tested tissues of L. vannamei, and was highly expressed in haemocytes. The haemocytes of L. vannamei injected with Vibrio alginolyticus showed a significant increase of LvTGI and LvTGII mRNA expression at 6 h followed by a notable decrease at 24 h in LvTGI and a continually increase in LvTGII indicating a complementary effect, which implied that both LvTGs involved in the immune response of shrimp, and LvTGII was more important in the later defense response. The gene silencing of LvTGII in shrimp significantly decreased LvTGII expression and TG activity of haemocytes, and significantly increased clotting time of haemolymph, suggests that the cloned LvTGII is a clotting enzyme involved in haemolymph coagulation of L. vannamei. In conclusion, the cloned LvTGII is a clotting enzyme involved in coagulation of haemolymp and immune response of white shrimp, L. vannamei.
凡纳滨对虾转谷氨酰胺酶 II(TGII)信使(m)RNA 的 cDNA 是通过逆转录聚合酶链反应(RT-PCR)和基于鲎 TG 序列(登录号:BAA02134)的寡核苷酸引物从血细胞中克隆出来的快速扩增 cDNA 末端(RACE),马蹄蟹,三疣梭子蟹(AAV49005; AAO33455),日本对虾(BAD36808)和太平洋螯龙虾(AAK69205)TG。2405bp 的 cDNA 包含一个 2292bp 的开放阅读框(ORF),一个 31bp 的 5'-非翻译区(UTR)和一个包含多聚 A 尾巴的 82bp 3'-UTR。推导的氨基酸(aa)序列(764aa)的分子量为 85.9kDa,估计 pI 为 5.32。凡纳滨对虾 TGII(缩写为 LvTGII)含有一个典型的 TG 同源物,两个假定的整合素结合基序(RGD 和 KGD)和五个钙结合位点; 三个催化三联体如在节肢动物 TG 中存在。序列比较和系统发育分析表明,虾 TG 可分为两组,STGI 和 STGII,LvTGII 与 STGII 的关系比与 STGI 的关系更密切。LvTGII mRNA 在凡纳滨对虾的所有检测组织中均有表达,并在血细胞中高度表达。凡纳滨对虾血细胞注射溶藻弧菌后,LvTGI 和 LvTGII mRNA 表达在 6 小时显著增加,24 小时 LvTGI 显著下降,LvTGII 持续增加表明存在互补效应,这表明两种 LvTGs 都参与了虾的免疫反应,LvTGII 在后期防御反应中更为重要。LvTGII 在虾中的基因沉默显著降低了血细胞中 LvTGII 的表达和 TG 活性,显著增加了血淋巴的凝固时间,表明克隆的 LvTGII 是一种参与凡纳滨对虾血淋巴凝固的凝血酶。总之,克隆的 LvTGII 是一种参与凡纳滨对虾血淋巴凝固和免疫反应的凝血酶。