Resolving Cell Fate Decisions during Somatic Cell Reprogramming by Single-Cell RNA-Seq

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Zearalenone can relieve dextran sulfate sodium‐induced inflammatory reaction

In this study, we investigated the influence of zearalenone (ZEA) on the dextran sulfate sodium (DSS)‐induced colitis model both in vitro and in vivo. Our results show that the mRNA levels of IL‐1β, IL‐18, NLRP3, ASC, and caspase‐1 in the DSS+ZEA‐treated group are lower than those in either the DSS or ZEA group, and the protein expression trends are similar. Furthermore, colitis, which is characterized by body weight loss, stool consistency, and the presence of bloody feces, was significantly alleviated in the DSS+ZEA group when compared with that in the DSS group. In addition, histological analysis showed that inflammatory cell infiltration and tissue damage of the colon in the DSS+ZEA group were recovered compared with that in the DSS‐treated group. These results suggest that, instead of aggravating DSS‐induced colitis, ZEA relieves the inflammatory reaction in colon tissue, which may be related to its estrogenic activity.     

Microbial production of O-methylated flavanones from methylated phenylpropanoic acids in engineered Escherichia coli

Journal of Industrial Microbiology & Biotechnology - Methylated flavonoids possess improved bioactivities compared to their unmethylated counterparts. In this study, for the efficient...     

The influential factor of narcolepsy on quality of life: compared to obstructive sleep apnea with somnolence or insomnia

Sleep and Biological Rhythms - Narcoleptics tend to have a low quality of life (QoL). Few studies have compared QoL in narcolepsy against other sleep disorders. The purpose of this study was to...     

The Verticillium dahliae Sho1-MAPK pathway regulates melanin biosynthesis and is required for cotton infection

Verticillium dahliae is a soil-borne fungus that causes vascular wilt on numerous plants worldwide. The fungus survives in the soil for up to 14 years by producing melanized microsclerotia. The protective function of melanin in abiotic stresses is well documented. Here, we found that the V. dahliae tetraspan transmembrane protein VdSho1, a homolog of the Saccharomyces cerevisiae Sho1, acts as an osmosensor, and is required for plant penetration and melanin biosynthesis. The deletion mutant ΔSho1 was incubated on a cellophane membrane substrate that mimics the plant epidermis, revealing that the penetration of ΔSho1 strain was reduced compared to the wild-type strain. Furthermore, VdSho1 regulates melanin biosynthesis by a signalling mechanism requiring a kinase-kinase signalling module of Vst50-Vst11-Vst7. Strains, ΔVst50, ΔVst7 and ΔVst11 also displayed defective penetration and melanin production like the ΔSho1 strain. Defects in penetration and melanin production in ΔSho1 were restored by overexpression of Vst50, suggesting that Vst50 lies downstream of VdSho1 in the regulatory pathway governing penetration and melanin biosynthesis. Data analyses revealed that the transmembrane portion of VdSho1 was essential for both membrane penetration and melanin production. This study demonstrates that Vst50-Vst11-Vst7 module regulates VdSho1-mediated plant penetration and melanin production in V. dahliae, contributing to virulence.     

Reactive oxygen species‐mediated endoplasmic reticulum stress response induces apoptosis of Mycobacterium avium‐infected macrophages by activating regulated IRE1‐dependent decay pathway

Mycobacterium avium, a slow‐growing nontuberculous mycobacterium, causes fever, diarrhoea, loss of appetite, and weight loss in immunocompromised people. We have proposed that endoplasmic reticulum (ER) stress‐mediated apoptosis plays a critical role in removing intracellular mycobacteria. In the present study, we investigated the role of the regulated IRE1‐dependent decay (RIDD) pathway in macrophages during M. avium infection based on its role in the regulation of gene expression. The inositol‐requiring enzyme 1 (IRE1)/apoptosis signal‐regulating kinase 1 (ASK1)/c‐Jun N‐terminal kinase (JNK) signalling pathway was activated in macrophages after infection with M. avium. The expression of RIDD‐associated genes, such as Bloc1s1 and St3gal5, was decreased in M. avium‐infected macrophages. Interestingly, M. avium‐induced apoptosis was significantly suppressed by pretreatment with irestatin (inhibitor of IRE1α) and 4μ8c (RIDD blocker). Macrophages pretreated with N‐acetyl cysteine (NAC) showed decreased levels of reactive oxygen species (ROS), IRE1α, and apoptosis after M. avium infection. The expression of Bloc1s1 and St3gal5 was increased in NAC‐pretreated macrophages following infection with M. avium. Growth of M. avium was significantly increased in irestatin‐, 4μ8c‐, and NAC‐treated macrophages compared with the control. The data indicate that the ROS‐mediated ER stress response induces apoptosis of M. avium‐infected macrophages by activating IRE1α‐RIDD. Thus, activation of IRE1α suppresses the intracellular survival of M. avium in macrophages.     

A barley stripe mosaic virus-based guide RNA delivery system for targeted mutagenesis in wheat and maize

Plant RNA virus-based guide RNA (gRNA) delivery has substantial advantages compared to that of the conventional constitutive promoter-driven expression due to the rapid and robust amplification of gRNAs during virus replication and movement. To date, virus-induced genome editing tools have not been developed for wheat and maize. In this study, we engineered a barley stripe mosaic virus (BSMV)-based gRNA delivery system for clustered regularly interspaced short palindromic repeat (CRISPR)/Cas9-mediated targeted mutagenesis in wheat and maize. BSMV-based delivery of single gRNAs for targeted mutagenesis was first validated in Nicotiana benthamiana. To extend this work, we transformed wheat and maize with the Cas9 nuclease gene and selected the wheat TaGASR7 and maize ZmTMS5 genes as targets to assess the feasibility and efficiency of BSMV-mediated mutagenesis. Positive targeted mutagenesis of the TaGASR7 and ZmTMS5 genes was achieved for wheat and maize with efficiencies of up to 78% and 48%. Our results provide a useful tool for fast and efficient delivery of gRNAs into economically important crops.     

山东东营和烟台潮间带海草床食物网结构特征

为了探明海草床内主要生物类群间的营养关系以及食物网结构, 作者于2018年8月分别在东营黄河口潮间带和烟台西海岸潮间带海草床采集大型底栖生物样品, 采用δ ¹³C和δ ¹⁵N稳定同位素方法, 对生物样品的碳、氮同位素组成进行了测定和分析。结果表明: 东营海草床内生物的δ ¹³C、δ ¹⁵N值范围分别为-21.99‰至-12.13‰和5.23‰-11.05‰, 烟台海草床内生物的δ ¹³C、δ ¹⁵N值范围分别为-18.11‰至-14.06‰和6.60‰-10.22‰。东营海草床主要生物的营养级范围为2.00-3.85, 烟台海草床主要生物的营养级范围为2.00-3.15。根据δ ¹⁵N值计算所得的营养级图分析可知两区域海草床内初级消费者主要为滤食性双壳类和多毛类, 次级消费者为植食性或杂食性甲壳类,肉食性鱼类和腹足类。与近海海域大型底栖生物食物网相比, 海草床内底栖生物的营养级均值普遍较低。     

樟子松针叶化学成分研究

该研究以采自黑龙江省齐齐哈尔市的樟子松(Pinus sylvestris)针叶为对象,采用溶剂提取法对樟子松针叶中的化学成分进行提取,应用硅胶柱色谱、制备薄层色谱和高效液相色谱等现代色谱技术对提取浸膏中的化学成分进行分离和纯化,运用质谱,核磁(1H-NMR和13C-NMR)等波谱技术,鉴定了化合物结构,并对提取浸膏的抑菌活性进行了测试。结果表明:从樟子松针叶提取物中分离得到15个化合物,分别鉴定为松叶酸(1)、松叶酸甲酯(2)、18α-acetoxylabd-8(17)-en-15-oic acid (3)、4-eplimbricataloic acid (4)、15-乙基-18-松叶酸甲酯(5)、15-acetoxy-labda-8(17),13E-dien-18-al (6)、7β-羟基脱氢枞酸(7)、7α-羟基脱氢枞酸(8)、endo-peroxide (9)、α-杜松醇(10)、β-谷甾醇(11)、邻苯二甲酸二丁酯(12)、7R,11R-phytol (13)、正二十四烷醇(14)、N-octacosan7β-ol (15)。其中,化合物9,13,14和15为首次从该属植物中分离得到。抑菌活性结果表明,正己烷萃取浸膏在浓度为5~100 mg·mL~(-1)时对大肠杆菌和枯草芽孢菌的抑菌率分别为53%~71%和56%~70%,在浓度为50 mg·mL~(-1)和100 mg·mL~(-1)时对金黄色葡萄球菌的抑菌率分别为51%和69%。该研究课题进一步明确了樟子松针叶中的化学成分,为其活性测试及应用研究提供依据。     

毕赤酵母中tRNAPro CCG基因的表达及其作用效果

转运核糖核酸 (tRNA) 是蛋白质合成过程中重要参与成分之一,为了探索稀有密码子对应的tRNA (稀少tRNA) 丰度改变对外源基因表达量的影响,文中构建了毕赤酵母稀少tRNA基因与外源基因共表达体系。首先在GFP基因中添加由4个连续脯氨酸稀有密码子CCG组成的阻遏区,结果显示该GFP基因的表达量明显降低。然后将带有阻遏区的GFP基因和tRNAPro CCG基因顺次连接于pPIC9K载体上,在毕赤酵母GS115中共表达,结果使GFP表达量提高了4.9%;另将带有阻遏区的GFP基因和tRNAPro CCG基因分别连接于pPIC9K和pFLDα载体,在毕赤酵母GS115中共表达,GFP表达量最高提高了12.5%;应用同样方式将tRNAPro CCG基因与NFATc3T-GFP融合基因共表达,其表达量提高了21.3%。可见,tRNAPro CCG在毕赤酵母GS115中确为稀少tRNA,通过共表达tRNAPro CCG基因可显著提高带有连续该密码子的外源基因表达量,并且,文中构建的共表达体系将同样适用于其他稀少tRNA基因的筛选和验证。