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791.
792.
家蚕Bmyan基因的克隆表达和作为microRNA 7靶基因的验证 总被引:2,自引:0,他引:2
microRNAs(miRNAs)是一类长约22 nt的非编码RNA,通过与其靶基因3′端非翻译区(3′-UTR)的结合来调节各项生命活动。克隆表达家蚕Bmyan基因,验证其是否是bmo-miR-7的靶基因对于深入研究家蚕变态发育机制有重要意义。基于同源性检索和PCR扩增,克隆了家蚕Bmyan基因CDS全长,编码476个氨基酸。序列分析表明,家蚕YAN蛋白的氨基酸序列保守,含SAM-PNT和ETs结构域。芯片数据、RT-PCR和定量PCR的检测结果表明,Bmyan在五龄3 d的家蚕头部、体壁、卵巢中高量表达,在其余组织中低量表达或不表达。在幼虫期,Bmyan表达水平相对较低,但在上蔟期和蛹期前4 d高量表达。通过3′RACE克隆了Bmyan基因的3′-UTR。RNAhybrid在线软件预测了其3'-UTR上bmo-miR-7的两个靶位点。构建了含有Bmyan基因3′-UTR和荧光素酶报告基因的转染载体,将该载体与bmo-miR-7的mimics序列共转染到家蚕胚胎细胞系BmE中,通过测定荧光素酶的活性,证明了Bmyan基因是bmo-miR-7的靶基因。本研究为进一步揭示bmo-miR-7和Bmyan在家蚕体内的生物学功能奠定了基础。 相似文献
793.
Varsha Singh Jianbo Yang Boyoung Cha Tiane-e Chen Rafiquel Sarker Jianyi Yin Leela Rani Avula Ming Tse Mark Donowitz 《Molecular biology of the cell》2015,26(11):2030-2043
Sorting nexin 27 (SNX27) contains a PDZ domain that is phylogenetically related to the PDZ domains of the NHERF proteins. Studies on nonepithelial cells have shown that this protein is located in endosomes, where it regulates trafficking of cargo proteins in a PDZ domain–dependent manner. However, the role of SNX27 in trafficking of cargo proteins in epithelial cells has not been adequately explored. Here we show that SNX27 directly interacts with NHE3 (C-terminus) primarily through the SNX27 PDZ domain. A combination of knockdown and reconstitution experiments with wild type and a PDZ domain mutant (GYGF → GAGA) of SNX27 demonstrate that the PDZ domain of SNX27 is required to maintain basal NHE3 activity and surface expression of NHE3 in polarized epithelial cells. Biotinylation-based recycling and degradation studies in intestinal epithelial cells show that SNX27 is required for the exocytosis (not endocytosis) of NHE3 from early endosome to plasma membrane. SNX27 is also required to regulate the retention of NHE3 on the plasma membrane. The findings of the present study extend our understanding of PDZ-mediated recycling of cargo proteins from endosome to plasma membrane in epithelial cells. 相似文献
794.
795.
796.
A new distinctive species of the rare Oriental goniacerine genus Awas Löbl, Awas
gigas
sp. n., is described and illustrated, based on three males and fourteen females taken at the Daoyao Shan Natural Reserve in the southern Chinese province of Guangxi. All specimens were collected from colonies of the ant genus Pachycondyla F. Smith nesting in decomposing woods. 相似文献
797.
Xiangguo Wang Pengfei Lin Yanlong Yin Jinhua Zhou Lanjie Lei Xudong Zhou Yaping Jin Aihua Wang 《Cell stress & chaperones》2015,20(3):399-409
Brucella, which is regarded as an intracellular pathogen responsible for a zoonotic disease called brucellosis, survives and proliferates within several types of phagocytic and non-phagocytic cells. Brucella infects not only their preferred hosts but also other domestic and wild animal species, inducing abortion and infertility. Therefore, the interaction between uterine cells and Brucella is important for understanding the pathogenesis of this disease. In this study, we describe the Brucella suis vaccine strain S2 (B.suis.S2) infection and replication in the immortalized caprine endometrial epithelial cell line hTERT-EECs and the induced cellular and molecular response modulation in vitro. We found that B.suis S2 was able to infect and replicate to high titers and inhibit the proliferation of EECs and induce non-apoptotic pathways, as determined by B.suis.S2 detection using MTT and acridine orange/ethidium bromide (AO/EB) staining and flow cytometry. We explored the evidence of non-apoptotic pathways using real-time quantitative RT-PCR and by western blot analysis. Finally, we discovered the over-expression of GRP78, ATF4, ATF6, PERK, eIF2α, CHOP, and cytochrome c (Cyt-c) but not IRE1, xbp-1, and caspase-3 in B.suis.S2 (HK)-attacked and B.suis.S2-infected cells, suggesting that the molecular mechanism of ER stress sensor activation by B.suis.S2 is basically concomitant with that by B.suis.S2 (HK) and that ER stress, especially the PERK pathway, plays an important role in the process of B.suis.S2 infecting EEC, which may, in part, explain the role of the uterus in the pathogenesis of B.suis.S2.
Electronic supplementary material
The online version of this article (doi:10.1007/s12192-014-0564-x) contains supplementary material, which is available to authorized users. 相似文献798.
799.
Protein kinase FgSch9 serves as a mediator of the target of rapamycin and high osmolarity glycerol pathways and regulates multiple stress responses and secondary metabolism in Fusarium graminearum 下载免费PDF全文
Qin Gu Chengqi Zhang Fangwei Yu Yanni Yin Won‐Bo Shim Zhonghua Ma 《Environmental microbiology》2015,17(8):2661-2676
Saccharomyces cerevisiae protein kinase Sch9 is one of the downstream effectors of the target of rapamycin (TOR) complex 1 and plays multiple roles in stress resistance, longevity and nutrient sensing. However, the functions of Sch9 orthologs in filamentous fungi, particularly in pathogenic species, have not been characterized to date. Here, we investigated biological and genetic functions of FgSch9 in Fusarium graminearum. The FgSCH9 deletion mutant (ΔFgSch9) was defective in aerial hyphal growth, hyphal branching and conidial germination. The mutant exhibited increased sensitivity to osmotic and oxidative stresses, cell wall‐damaging agents, and to rapamycin, while showing increased thermal tolerance. We identified FgMaf1 as one of the FgSch9‐interacting proteins that plays an important role in regulating mycotoxin biosynthesis and virulence of F. graminearum. Co‐immunoprecipitation and affinity capture‐mass spectrometry assays showed that FgSch9 also interacts with FgTor and FgHog1. More importantly, both ΔFgSch9 and FgHog1 null mutant (ΔFgHog1) exhibited increased sensitivity to osmotic and oxidative stresses. This defect was more severe in the FgSch9/FgHog1 double mutant. Taken together, we propose that FgSch9 serves as a mediator of the TOR and high osmolarity glycerol pathways, and regulates vegetative differentiation, multiple stress responses and secondary metabolism in F. graminearum. 相似文献
800.