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作 者:苗泽龙 黄亚龙 吕艳杰[1] 宁黔冀[1] MIAO Ze-long;HUANG Ya-long;LV Yan-jie;NING Qian-ji(College of Life Science, Henan Normal University, Xinxiang 453007 , Henan, Chin)
机构地区:[1]河南师范大学生命科学学院,河南新乡453007
出 处:《淡水渔业》2018年第3期19-24,共6页Freshwater Fisheries
基 金:河南省教育厅科学技术研究重点项目(14A240003);河南师范大学青年科学基金(5101049279089);天津市动植物抗性重点实验室开放基金(5201049160124)
摘 要:为探讨KK-42显著缩短日本沼虾(Macrobrachium nipponense)蜕皮周期的可能机制,本研究采用RACE技术首次从头胸甲中获得了一个含几丁质结合-4(chitin_bind_4)结构域的表皮蛋白(cuticle proteins,CPs)c DNA基因全长,命名为Mn CP-1。该序列全长604 bp,可编码122个氨基酸。氨基酸序列比对显示,Mn CP-1与普通黄道蟹(Cancer pagurus,P81576.1)相似性最高(61%)。系统进化分析发现,Mn CP-1与地中海实蝇(Ceratitis capitata)聚类为一支。Real-time PCR结果显示,头胸甲中Mn CP-1在蜕皮前期晚期(D3-4期)和蜕皮后期(A期)的表达量较高,而在蜕皮间期(C期)和蜕皮前期早期(D0-2期)的表达量较低。KK-42处理能显著上调C期和D0-2期Mn CP-1的表达,在处理后6、24和48 h,其mRNA表达水平较对照组高3倍以上。结果表明,头胸甲上皮细胞Mn CP-1的表达与蜕皮周期有关,KK-42可显著上调C期和D0-2期Mn CP-1的表达。In order to investigate the possible mechanism of KK -42 significant shortening the duration of molting cycle of Macrobrachium nippozwnse, a gene containing chitin bind 4 conserved domain called MnCP - 1 was firstly cloned in ear- apace from M. nippozwnse. The full length eDNA of MnCP - 1 was 604 bp and encoded a putative protein of 122 amino acid residues. Amino acid sequence alignment results showed that MnCP - 1 had the highest similarity of 61% with a cuticle pro- tein (CP)from Cancer pagurus. Phylogenetie analysis showed that a CP from Ceratitis capitata was the most closely related to MnCP - 1. The results of Real - time PCR showed MnCP - 1 mRNA expression levels were higher during late premolt stage (stage D3 4 ) and postmolt stage (stage A )while lower during intermolt stage (stage C )and early premolt stage (stage Do 2) in carapace. In addition, the expression levels during stage C and Do 2 were increased by more than 3 times compared with the control at 6, 24 and 48 h after KK - 42 treatment, respectively. Consequently, this research suggested that the expression of MnCP - 1 in epithelial cell from carapace was relevant to the molting cycle. Furthermore, KK -42 could significantly up - regulate the expression of MnCP - 1 during stage C and Do 2-
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