植物病原真菌的菌核研究进展

真菌菌核是相关真菌在特殊环境下由营养体菌丝交织和聚集形成的具有抵御恶劣环境能力的休眠结构,在真菌生活史及病原真菌的病害循环中具有重要的生物学和生态学意义。许多引起严重植物病害的病原真菌能够形成菌核,这类真菌通过菌核度过逆境。菌核在适宜条件下萌发形成子囊盘和孢子或菌丝,造成植物的侵染。本文从形成菌核的真菌种类、生物学特性、黑色素及分子生物学等方面进行综述,旨在为深入研究真菌菌核及其在真菌学、植物病理学及药用真菌学等领域应用提供研究思路和参考依据。     

Molecular Mechanisms and Genetic Basis of Heavy Metal Tolerance/Hyperaccumulation in Plants

Phytoremediation has gained increased attention as a cost-effective method for the remediation of heavy metal-contaminated sites. Because some plants possess a range of potential mechanisms that may be involved in the detoxification of heavy metals, they manage to survive under metal stresses. High tolerance to heavy metal toxicity could rely either on reduced uptake or increased plant internal sequestration,which is manifested by an interaction between a genotype and its environment. The growing application of molecular genetic technologies has led to increased understanding of mechanisms of heavy metal tolerance/accumulation in plants and, subsequently, many transgenic plants with increased heavy metal resistance,as well as increased uptake of heavy metals, have been developed for the purpose of phytoremediation. In the present review, our major objective is to concisely evaluate the progress made so far in understanding the molecular/cellular mechanisms and genetic basis that control the uptake and detoxification of metals by plants.     

Silencing of Bcl-XL Expression in Human MGC-803 Gastric Cancer Cells by siRNA

To investigate the inhibitory effect of the Bcl-XL small interfering RNA(siRNA)on BcI-XLgene expression in the human gastric cancer cell line MGC-803,green fluorescent protein(GFP)siRNAwas constructed and transfected into MGC-803 ceils,together with GFP expression vector pTrace SV40.GFP expression levels were observed using fluorescence microscopy.Bcl-XL siRNA and negative siRNAwere then constructed and stably transfected into MGC-803 cells.RT-PCR and immunofluorescence wereused to detect the expression of Bcl-XL.Spontaneous apoptosis was detected by acridine orange(AO)andflow cytometry.Results were as follows:(1)48 h after GFP expression vector and GFP siRNA co-transfection,the expression level of GFP in the GFP siRNA group was much lower than the negative siRNA group,according to fluorescence microscopy results.The mRNA and protein levels of Bcl-XL in Bcl-XL siRNAstable transfectants were reduced to almost background level compared with negative siRNA transfectantsor untreated cells.(2)Changes in nucleus morphology was observed by AO staining nucleic and flowcytometry analysis,which showed that stable Bcl-XL siRNA transfectants have an increased spontaneousapoptosis (21.17%+1.26% vs.1.19%+0.18% and 1.56%+0.15% respectively,P<0.05 vs.negative siRNAor untreated control),siRNA targeting GFP or Bcl-XL genes can specifically suppress GFP or BcI-XLexpression in MGC-803 cells,and Bcl-XL siRNA can increase spontaneous apoptosis.Bcl-XL siRNA maybe a beneficial agent against human gastric adenocarcinoma.     

Zacopride selectively activates the Kir2.1 channel via a PKA signaling pathway in rat cardiomyocytes

We recently reported that zacopride is a selective inward rectifier potassium current (IK1 ) channel agonist, suppressing ventricular arrhythmias without affecting atrial arrhythmias. The present study aimed to investigate the unique pharmacological properties of zacopride. The whole-cell patch-clamp technique was used to study IK1 currents in rat atrial myocytes and Kir2.x currents in human embryonic kidney (HEK)-293 cells transfected with inward rectifier potassium channel (Kir)2.1, Kir2.2, Kir2.3, or mutated Kir2.1 (at phosphorylation site S425L). Western immunoblots were performed to estimate the relative protein expression levels of Kir2.x in rat atria and ventricles. Results showed that zacopride did not affect the IK1 and transmembrane potential of atrial myocytes. In HEK293 cells, zacopride increased Kir2.1 homomeric channels by 40.7%±9.7% at 50 mV, but did not affect Kir2.2 and Kir2.3 homomeric channels, and Kir2.1-Kir2.2, Kir2.1-Kir2.3 and Kir2.2-Kir2.3 heteromeric channels. Western immunoblots showed that similar levels of Kir2.3 protein were expressed in rat atria and ventricles, but atrial Kir2.1 protein level was only 25% of that measured in the ventricle. In addition, 5-hydroxytryptamine (5-HT) 3 receptor was undetectable, whereas 5-HT 4 receptor was weakly expressed in HEK293 cells. The Kir2.1-activating effect of zacopride in these cells was abolished by inhibition of protein kinase A (PKA), but not PKC or PKG. Furthermore, zacopride did not activate the mutant Kir2.1 channel in HEK293 cells but selectively activated the Kir2.1 homomeric channel via a PKA-dependent pathway, independent to that of the 5-HT receptor.     

南药巴戟天本草考证

巴戟天(Morinda officinalis)是我国传统四大南药之一。本文系统地梳理了中国历代本草及近现代文献对南药巴戟天的基原、产地变迁、加工炮制和品质评价等方面的记载。经考证,古今巴戟天基原植物差异很大,清末以前本草记载的巴戟天涉及基原植物有6科10属12种,通过比对本草文献中对巴戟天的有效生物学描述,可以明确古代巴戟天来源于葡萄科(Vitaceae)三叶崖爬藤(Tetrastigma hemsleynum Diels et Gilg)、百合科(Liliflorae)沿阶草(Ophiopogon bodinieri Levl.)及开口箭(Campylandra chinensis(Baker)M.N.Tamura et al.)3种;古代巴戟天产地与现代《中国药典》记载的品种产地差异大;炮制方法古今沿用,炮制品有盐巴戟天、制巴戟天和酒巴戟天;品质以条粗大而且呈连珠状、肉厚、色紫质软、内芯木部细、味微甜、无蛀虫、体干者为佳。通过本草考证,可厘清巴戟天古今之变,为巴戟天商品规格研制提供保障。     

Autophagy prevents autophagic cell death in Tetrahymena in response to oxidative stress

Autophagy is a major cellular pathway used to degrade long-lived proteins or organelles that may be damaged due to increased reactive oxygen species(ROS) generated by cellular stress. Autophagy typically enhances cell survival, but it may also act to promote cell death under certain conditions. The mechanism underlying this paradox, however, remains unclear. We showed that Tetrahymena cells exerted increased membranebound vacuoles characteristic of autophagy followed by autophagic cell death(referred to as cell death with autophagy) after exposure to hydrogen peroxide. Inhibition of autophagy by chloroquine or 3-methyladenine significantly augmented autophagic cell death induced by hydrogen peroxide. Blockage of the mitochondrial electron transport chain or starvation triggered activation of autophagy followed by cell death by inducing the production of ROS due to the loss of mitochondrial membrane potential. This indicated a regulatory role of mitochondrial ROS in programming autophagy and autophagic cell death in Tetrahymena. Importantly, suppression of autophagy enhanced autophagic cell death in Tetrahymena in response to elevated ROS production from starvation, and this was reversed by antioxidants. Therefore, our results suggest that autophagy was activated upon oxidative stress to prevent the initiation of autophagic cell death in Tetrahymena until the accumulation of ROS passed the point of no return, leading to delayed cell death in Tetrahymena.     

Erratum to: Coarse root spatial distribution determined using a ground-penetrating radar technique in a subtropical evergreen broad-leaved forest, China

Erratum to:Science China Life Sciences,November 2013 Vol.56 No.11:1038–1046doi:10.1007/s11427-013-4560-7The legend of Figure 1 should be as follows:Figure 1 Distribution map of 15 subplots at three types of habitats(ridge,slope and valley)     

长江口中华绒螯蟹放流亲蟹的繁殖力评估

在长江口中华绒螯蟹亲蟹生殖洄游期间, 通过研究中华绒螯蟹放流群体和自然群体繁殖力随壳宽的变化规律, 比较放流群体和自然群体繁殖力的差异, 从而评估人工增殖放流亲蟹的繁殖力。结果显示, 随着壳宽的增大, 中华绒螯蟹放流群体和自然群体的繁殖力都显著增加(P<0.05)。在相同壳宽范围内, 放流群体和自然群体的繁殖力之间没有显著差异(P>0.05)。回归分析显示, 放流群体繁殖力(F)与壳宽(CW)呈幂函数关系: F=3.979CW6.208(R2=0.822);自然群体F与CW呈幂函数关系: F=1.696CW6.636(R2=0.673)。协方差分析显示, 放流群体与自然群体F与CW的两条曲线在显著性为0.05时拟合较好。研究结果表明, 放流群体与自然群体的繁殖力与壳宽之间无显著性差异, 推断放流亲蟹能够适应长江口天然水域环境, 并与自然群体的繁殖力水平相当。     

用多重PCR检测上海地区汉族人群9个STR基因座的多态性

利用多重PCR和四色荧光（5－FAM,JOE,NED和ROX）自动化检测技术调查上海地区汉族人群D3S1358、vWA、FGA、D8S1179、D21S11、D18S51、D5S818、D13S317、D7S820等9个STR基因座多态性分布并计算 该9个基因座的的基因频率（Pi)、个体鉴别力（DP）、无偏倚期望杂合性（H）、多态性信息含量（PIC）和非父排除概率（PE）。结果显示：9个STR基因座的基因型分布符合Hardy-Weinberg平衡,9个STR基因座中FGA基因座的DP值最高为0.9584,D8S1179的H值最高为0.9403,D18S51的PIC值最高为0.8560,D18S51的PE值最高为0.7391,9个STR基因座累积个体鉴别力（CDP)为0.9999996,累积非父排除能力（CPE）为0.99991。9个STR基因座适合作为中国人群的遗传标志,用于人类学、遗传疾病基因连锁分析、法医学亲子鉴定和个体识别等研究领域。