Intein-Mediated Protein trans-Splicing of the Recombinant Streptavidin on Magnetosomes

Molecular Biology - When expressing streptavidin recombinant polypeptide on magnetosomes (called bacterial magnetic nanoparticles, or BMPs), the presence of endogenous bacterial biotin might be...     

Genetic Analysis of Human Adenovirus Type 7 Strains Circulating in Different Parts of China

To investigate the molecular epidemiology and genetic variation of human adenovirus type 7(HAdV-7) in children with acute respiratory infections(ARI) in China. HAdV-7-positive respiratory samples collected from children with ARI in Beijing, Shijiazhuang, Wenzhou and Guangzhou from 2014–2018 were selected for gene amplification and sequence analysis. Fifty-seven HAdV-7 clinical strains with hexon, penton base and fiber gene sequences were obtained. Meanwhile17 strains were selected randomly from different cities for whole genome sequencing. Phylogenetic and variation analyses were performed based on the obtained sequences, HAdV-7 prototype strain Gomen(AY594255), vaccine strains(AY495969 and AY594256) and representative sequences of strains. The phylogenetic trees constructed based on whole genome sequences, major capsid protein genes(hexon, penton base and fiber) and the early genes(E1, E2, E3 and E4) were not completely consistent. The HAdV-7 strains obtained in this study always clustered with most of the circulating strains worldwide from the 1980 s to the present. Compared with the HAdV-7 prototype strain Gomen(AY594255), some amino acid mutations in loop1 and loop2 of hexon and the RGD loop region of the penton base gene were observed. Recombination analysis showed that partial regions of 55 k Da protein and 100 kDa hexon-assembly associated protein genes among all HAdV-7 strains in this study were from HAdV-16 and HAdV-3, respectively. Our study demonstrated the molecular evolution characteristics of HAdV-7 strains circulating in China and provided basic reference data for the prevention, control and vaccine development of HAdV-7.     

罗氏沼虾MrLc3a基因cDNA的克隆及在副溶血弧菌胁迫下的表达分析

虾类和果蝇同属节肢动物.果蝇的相关研究表明自噬与免疫关系密切,而虾类自噬机制研究鲜少.微管相关蛋白1轻链3 (microtubule-associated protein 1 light chain 3,Lc3)与自噬基因Atg8同源,其与自噬体的形成密切相关,是自噬活性的标志分子.本研究利用RACE技术克隆了罗氏沼虾的MrLc3a基因的全长cDNA,用RT-qPCR检测了该基因在罗氏沼虾主要组织中的表达量;并研究了正常和副溶血弧菌感染两种情况下MrLc3a基因和免疫基因Relish的表达变化情况,为其在病害防御方面的应用提供了前期数据.试验结果表明:MrLc3a基因全长653 bp,其中包括195 bp的5'-UTR、378 bp的ORF开放阅读框和80 bp的3'-UTR,共编码126个氨基酸;序列比对结果显示,其编码的氨基酸序列和南美白对虾Lc3a编码的氨基酸序列具有较高的同源性,并在系统发育树上聚为一支;RT-qPCR结果显示,MrLc3a基因在罗氏沼虾各个组织均有表达,其中在脑、鳃、胃中的表达量较高,在肝胰腺和性腺中的表达量较少;副溶血弧菌感染罗氏沼虾后显著影响了MrLc3a和Relish基因在罗氏沼虾肝胰腺组织中的转录情况,MrLc3a和Relish基因随时间变化都呈现出先上升后下降的趋势,表明MrLc3a基因通过参与细胞自噬过程而参与了免疫反应.     

Sustained expression of MCP-1 induced low wall shear stress loading in conjunction with turbulent flow on endothelial cells of intracranial aneurysm

Shear stress was reported to regulate the expression of AC007362, but its underlying mechanisms remain to be explored. In this study, to isolate endothelial cells of blood vessels, unruptured and ruptured intracranial aneurysm (IA) tissues were collected from IA patients. Subsequently, quantitative real-time PCR (qRT-PCR), Western blot and luciferase assay were performed to investigate the relationships between AC007362, miRNAs-493 and monocyte chemoattractant protein-1 (MCP-1) in human umbilical vein endothelial cells (HUVECs) exposed to shear stress. Reduced representation bisulphite sequencing (RRBS) was performed to assess the level of DNA methylation in AC007362 promoter. Accordingly, AC007362 and MCP-1 were significantly up-regulated while miR-493 was significantly down-regulated in HUVECs exposed to shear stress. AC007362 could suppress the miR-493 expression and elevate the MCP-1 expression, and miR-493 was shown to respectively target AC007362 and MCP-1. Moreover, shear stress in HUVECs led to the down-regulated DNA methyltransferase 1 (DNMT1), as well as the decreased DNA methylation level of AC007362 promoter. Similar results were also observed in ruptured IA tissues when compared with unruptured IA tissues. In conclusion, this study presented a deep insight into the operation of the regulatory network of AC007362, miR-493 and MCP-1 upon shear stress. Under shear stress, the expression of AC007362 was enhanced by the inhibited promoter DNA methylation, while the expression of MCP-1 was enhanced by sponging the expression of miR-493.     

Poly(ADP-ribose) polymerase inhibitor PJ34 protects against UVA-induced oxidative damage in corneal endothelium

Apoptosis - Fuchs endothelial corneal dystrophy (FECD) is one of the main causes for corneal endothelial blindness, which is characterized by the progressive decline of corneal endothelial cells....     

不同放牧强度对赛罕乌拉草原蜘蛛多样性的影响

蜘蛛作为草原生态系统中的主要消费者, 对维系草原生物多样性和生态系统功能具有重大意义。放牧是人类利用草原最普遍的方式, 了解放牧对蜘蛛多样性的影响具有重要生态学意义。本研究调查了内蒙古赛罕乌拉草原上5个不同放牧强度样地中的蜘蛛多样性, 通过单因素方差分析(one-way analysis of variance)比较各样地中的蜘蛛多样性, 非度量多维标度分析(non-metric multidimensional scale, NMDS)和相似性分析(analysis of similarities, ANOSIM)比较各样地间的蜘蛛物种组成相似性, 再结合相关性分析探讨了植被高度对蜘蛛多样性的影响。结果表明: 重度放牧强度样地的蜘蛛多样性显著低于其他未放牧及轻度放牧样地; 具体到常见科上, 放牧强度对织网型的园蛛物种数和个体数影响显著, 而对游猎型的狼蛛、跳蛛却不明显; 织网型蜘蛛主要受植被结构影响, 而游猎型蜘蛛更可能受潜在猎物可得性的影响。NMDS分析表明不同放牧强度下, 蜘蛛类群的物种组成呈现明显的梯度变化, 放牧强度越低, 物种组成和未放牧样地越相近。相关性分析表明草原植被高度与蜘蛛多样性总体上呈正相关关系, 即植被高度越高, 蜘蛛多样性越高。其中依靠植物构建蛛网的园蛛科和在植物上层伏击猎物的蟹蛛科、逍遥蛛科等与植被高度显著相关。这说明植物资源及其空间异质性可能对草原蜘蛛多样性起着主导作用。因此, 降低放牧强度有助于保护草原蜘蛛群落的多样性, 特别有利于织网型蜘蛛。     

国家公园陆地自然生态系统完整性与原真性评价方法探索: 以钱江源国家公园体制试点为例

中国建立国家公园的目的是保护自然生态系统的完整性和原真性, 促进生物多样性保护。国家公园的完整性和原真性评价是国家公园的布局规划、边界范围确定以及功能区划等研究的前提条件。为了评估国家公园自然生态系统完整性和原真性状态, 本文基于陆地自然生态系统的结构和功能, 通过指标筛选、专家咨询、指标量化和建立综合评价模型, 构建了陆地自然生态系统完整性与原真性的评价指标体系及其量化评价方法。该评价方法包括5个自然生态系统完整性指标、5个自然生态系统原真性指标和2个综合评价指标。以浙江省钱江源国家公园体制试点为例, 本文初步评估了其生态系统完整性与原真性状态, 并对评价结果进行了分级。按照本研究的评价方法, 钱江源国家公园体制试点的自然生态系统完整性评价结果为52.83%, 评价等级为较差; 自然生态系统原真性评价结果为87.06%, 评价等级为好。钱江源国家公园体制试点有待关注和提升的指标有保护区域完整性指数(27.00%)和旗舰种适宜生境完整性指数(53.04%)。最后, 本文结合研究区域评价结果对生态系统完整性和原真性领域应关注的问题进行了讨论。该自然生态系统完整性和原真性评价方法可提供一种评价指标覆盖较全面、数据易获取, 且评价结果易被决策者和管理者理解的评价思路。     

The Relationship Between Insulin Resistance and CpG Island Methylation of LMNA Gene in Polycystic Ovary Syndrome

We sought to investigate the relationship between the changes of CpG island methylation status of LMNA gene and insulin resistance in polycystic ovary syndrome (PCOS) patients. The genome-wide methylation microarray screening was done in three PCOS cases of insulin resistance and one case of a normal woman. The PCOS insulin resistance-related genes were identified as indicated by the results of gene chip screening. Then, 24 cases of insulin-resistant PCOS patients and 24 cases of normal individuals were studied to identify the effects of the candidate genes using genome-wide study of DNA from the peripheral blood analyzed by MassARRAY^®EpiTYPER? DNA methylation analysis technique. We found that the methylation status of CpG island in the promoter area of LMNA gene was changed. The 20 CG sites in CpG island of LMNA gene were examined using case control experiment among which 12 CpG sites differed significantly (P < 0.05) between two groups while the remaining eight CpG sites differed non-significantly. We, therefore, concluded that the changes in the hypermethylation status of CpG island of LMNA gene were related to the insulin resistance in PCOS patients, indicating that this gene may be involved in the regulation of PCOS-associated insulin resistance.