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首页> 外文期刊>Genetics and Molecular Research >Cloning and expression analysis of the 37-kDa laminin receptor precursor gene from Hyriopsis cumingii
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Cloning and expression analysis of the 37-kDa laminin receptor precursor gene from Hyriopsis cumingii

机译:三角帆蚌37-kDa层粘连蛋白受体前体基因的克隆与表达分析

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Hyriopsis cumingii is an economically important freshwater pearl mussel with high pearl quality that is endemic in China. Investigation of genes relevant to shell formation is important for increased pearl output. The substances that form mollusk shells are secreted by epithelial cells in the mantle, the proliferation of which influences secretion ability. This study focused on the proliferation-related 37-kDa laminin receptor precursor (37LRP) of H. cumingii. The full-length cDNA (1133 bp) encoding this 300-amino acid protein was cloned from the mantle. Quantitative fluorescence analysis showed that 37LRP expressed in eight tissues, with the highest expression observed in the liver, and its expression pattern in the mantle reflected shell repair. During repair, 37LRP expression was higher in the experimental shell repair group than that in the control group, exhibiting an initial increase followed by a decrease in expression, and returning to basal levels on completion of the repair. A similar trend was also observed with respect to immunity and cellular metabolism. Expression of the 37LRP protein in the experimental group was significantly higher than that in the control group at the first and second days after shell injury. After 4 days, 37LRP expression in the experimental group was lower than that in the control group. In situ hybridization revealed a strong positive signal corresponding to the 37LRP mRNA at the horny grooves of the mantle, evagination, and in epithelial cells of the velum, which implicated these areas in the repair and formation of the cuticle, prismatic layer, and nacre.
机译:三角帆蚌是一种经济上重要的淡水珍珠贻贝,具有较高的珍珠品质,在中国很普遍。与壳形成有关的基因的研究对于增加珍珠产量很重要。形成软体动物壳的物质由地幔中的上皮细胞分泌,其增殖会影响分泌能力。这项研究的重点是枯草芽孢杆菌与增殖相关的37 kDa层粘连蛋白受体前体(37LRP)。从地幔中克隆出编码这种300个氨基酸的蛋白质的全长cDNA(1133 bp)。定量荧光分析表明37LRP在八个组织中表达,在肝脏中观察到最高的表达,并且其在地幔中的表达模式反映了壳的修复。在修复过程中,实验性壳修复组的37LRP表达高于对照组,表现出最初的升高,随后表达降低,并在修复完成后恢复到基础水平。在免疫和细胞代谢方面也观察到类似趋势。在壳损伤后第一天和第二天,实验组中37LRP蛋白的表达显着高于对照组。 4天后,实验组37LRP表达低于对照组。原位杂交揭示了一个强阳性信号,对应于在外套膜的角质沟,外翻以及在膜的上皮细胞中的37LRP mRNA,这牵涉这些区域在表皮,棱柱层和珍珠质的修复和形成中。

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