两种变应性接触性皮炎动物模型的建立及比较

目的比较两种动物作为变应性接触性皮炎（allergic contact dermatitis,ACD）模型各自的优势,为实际应用中恰当选择动物模型提供依据。方法利用二硝基氯苯（dinitrochlorobenzene,DNCB）作为致敏剂,以腹部致敏、背部激发的方法分别建立豚鼠（连续激发4次）和小鼠（1次激发）两种ACD动物模型,并以丙酮作为对照。激发后0～96h,对激发部位进行动态分级。激发后96h,H-E染色观察激发部位皮肤病理变化,并计算脾指数和胸腺指数。结果动态评分结果显示：豚鼠激发后72h红斑程度最强,临床分级以3级为主,并于72～96h保持不变;小鼠激发后24h红斑程度最强,临床分级以4级为主,48h后红斑程度减轻。病理结果显示：两种模型激发部位皮肤内均有大量炎症细胞浸润。脾指数和胸腺指数计算结果显示：两种动物模型的脾指数和胸腺指数均较对照组明显增加（P〈0．05）。结论通过上述方法分别成功建立了豚鼠和小鼠ACD动物模型。豚鼠红斑程度较弱,且出现较晚,持续时间较长;小鼠红斑程度较强,出现较早,持续时间较短。     

High-throughput Binary Vectors for Plant Gene Function Analysis

A series of high-throughput binary cloning vectors were constructed to facilitate gene function analysis in higher plants. This vector series consists of plasmids designed for plant expression, promoter analysis, gene silencing, and green fluorescent protein fusions for protein localization. These vectors provide for high-throughput and efficient cloning utilizing sites for λ phage integrase/excisionase. In addition, unique restriction sites are incorporated in a multiple cloning site and enable promoter replacement. The entire vector series are available with complete sequence information and detailed annotations and are freely distributed to the scientific community for non-commercial uses.     

草莓开花期发生霜害的温度

用人工霜箱对草莓(Fragaria ananassa)叶片和花托进行模拟春霜实验。结果表明草莓叶片有忍耐胞间结冰的能力, 最低叶温-6.4 ℃以上, 结冰持续90分钟以内的叶片解冻后还能存活。花托不能忍耐胞间结冰, 是通过保持过冷却状态以回避结冰伤害。花托温度越低, 发生霜害的累积百分率越大, 半开花的花托温度降到-5.4 ℃时累计有50%发生结冰而造成霜害。盛开的花及鲜重大的花发生霜害的温度较高。     

EGCG防治神经退行性疾病的作用机制

表没食子儿茶素没食子酸酯（epigallocatechin-3-gallate,EGCG）是绿茶多酚成分中的一种主要组分,参与了神经细胞生长与凋亡的调控,研究发现其机制可能与抗氧化损伤和影响MAPK．PKC和PI-3K／Akt等细胞内信号转导通路相关。因此,探讨EGCG的神经保护作用及其机制,将为应用EGCG防治帕金森氏症、阿尔茨海默病等中枢神经系统退行性疾病的基础与临床研究提供理论依据。     

Functional gene-mining for salt-tolerance genes with the power of Arabidopsis

Here we report on a functional gene-mining method developed to isolate stress tolerance genes without any prior knowledge of the genome or genetic mapping of the source germplasms. The feasibility of this approach was demonstrated by isolating novel salt stress tolerance genes from salt cress (Thellungiella halophila), an extremophile that is adapted to a harsh saline environment and a close relative of the model plant Arabidopsis thaliana. This gene-mining method is based on the expression of salt cress cDNA libraries in Arabidopsis. A cDNA expression library of the source germplasm, salt cress, was constructed and used to transform Arabidopsis via Agrobacterium-mediated gene transfer. A transgenic seed library consisting of >125,000 independent lines was generated and screened for salt-tolerant lines via a high-throughput genetic screen. A number of salt-tolerant lines were isolated, and the salt cress cDNAs were identified by PCR amplification and sequencing. Among the genes isolated, several novel small protein-encoding genes were discovered. The homologs of these genes in Arabidopsis have not been experimentally analyzed, and their functions remain unknown. The function of two genes isolated by this method, ST6-66 and ST225, and their Arabidopsis homologs, were investigated in Arabidopsis using gain- and loss-of-function analyses, and their importance in salt tolerance was demonstrated. Thus, our functional gene-mining method was validated by these results. Our method should be applicable for the functional mining of stress tolerance genes from various germplasms. Future improvements of the method are also discussed.     

Methanol/sorbitol co-feeding induction enhanced porcine interferon-α production by P. pastoris associated with energy metabolism shift

The production of porcine interferon-α (pIFN-α) by Pichia pastoris was largely enhanced when adopting sorbitol/methanol co-feeding induction strategy at 30 °C in a 10-L fermentor. Analysis of energy regeneration pattern and carbon metabolism revealed that major energy metabolism energizing pIFN-α synthesis shifted from formaldehyde dissimilatory energy metabolism pathway to TCA cycle under the methanol/sorbitol co-feeding induction strategy. The sorbitol/methanol co-feeding induction strategy weakened formaldehyde dissimilatory pathway and repressed the accumulation of toxic metabolite-formaldehyde, reduced theoretical oxygen consumption rate and oxygen supply requirement, and increased energy/methanol utilization efficiency so that more methanol could be effectively used for pIFN-α synthesis. As a result, pIFN-α antiviral activity reached a highest level of 1.8 × 10(7) IU/mL which was about 10- to 200-folds of those obtained under pure methanol induction at 20 and 30 °C, respectively.     

基因谱系示踪揭示Tbx18+祖细胞的多分化潜能

为探讨Tbx18+祖细胞在小鼠生长发育过程中的多分化潜能及分化的组织类型,本工作建立了Tbx18：Cre/Rosa26RLacZ谱系示踪小鼠.该示踪小鼠基于Cre/LoxP系统,能够准确及有效地示踪Tbx18+祖细胞的分化命运,通过整体胚胎及组织X-gal染色,检测分析报告基因LacZ在其中的表达情况.结果显示,在Tbx18：Cre/Rosa26RLacZ双杂合小鼠胚胎发育早期,报告基因LacZ主要在脊柱、四肢及心外膜表达|而在胚胎发育晚期则分别表达于皮肤、毛囊、肾脏、输尿管、膀胱、睾丸、输精管、椎间盘、肋软骨、心耳、心肌、冠状动脉.结果阐明,Tbx18+祖细胞在小鼠生长发育过程中具有强大的多器官及组织分化潜能,包括分化形成表皮系统,泌尿生殖系统,骨骼系统,心血管系统,并在其生长发育中发挥重要作用.     

内生真菌感染对禾草宿主生境土壤特性和微生物群落的影响

以羊草(Leymus chinensis)-内生真菌共生体为研究对象, 分别在野外样地和室内盆栽两种实验条件下研究了内生真菌感染对土壤特性和微生物群落结构的影响。结果显示：在处理时间较长并伴随有枯落物分解的羊草样地中, 内生真菌感染促进了土壤氮(N)的积累, 提高了30天培养时间内土壤初始碳(C)矿化速率和前3天土壤矿化量和土壤矿化总量; 而在处理时间较短且没有地上枯落物分解的盆栽羊草中, 内生真菌感染对土壤的C、N含量及C矿化均无显著影响。无论是野外样地还是室内盆栽实验, 内生真菌感染均未引起土壤微生物磷脂脂肪酸种类的变化, 但内生真菌感染均有提高土壤微生物生物量的趋势, 内生真菌显著增加了盆栽羊草土壤中细菌、革兰氏阴性细菌、真菌磷脂脂肪酸含量和磷脂脂肪酸总量, 增加了羊草样地土壤中革兰氏阳性细菌和放线菌的磷脂脂肪酸含量。总体看来, 内生真菌感染能够改变土壤N积累和C矿化率, 并且改变土壤中微生物群落的结构, 这有助于进一步认识内生真菌与羊草之间的共生关系及其在生态系统C、N循环中所起的作用。     

山矾科中原氏山矾复合体的叶形态特征及分类意义

该研究在形态学观察以及统计学分析的基础上,深入研究了山矾科中原氏山矾复合体的叶片形态学结构。结果表明:叶片质地在整个复合体中可分为革质、纸质2种类型,叶片大小变异幅度较大,除中原氏山矾(Symplocos kawakamii)、棱角山矾(S.tetragona)、蒙自山矾(S.henryi)均与其他种差异显著外,其余种均属于连续过度,叶片分形可以初步区分该复合体植物。该研究结果为中原氏山矾复合体的进一步研究提供了依据,对复合体的分类处理具有一定的分类学意义。     

土壤杆菌氧调控基因fnrN突变株发酵性能及基于RNA-Seq的基因表达

【目的】研究Crp家族转录调节因子fnr N突变对土壤杆菌ATCC 31749发酵性能和基因表达的影响。【方法】利用三亲结合法将构建的自杀式质粒p JQ-fnr N-kan导入土壤杆菌ATCC31749中,从而获得fnr N基因突变株(Δfnr N);分析Δfnr N的发酵特性;基于RNA-Seq对产胶期土壤杆菌ATCC 31749野生菌和Δfnr N差异表达基因进行分析。【结果】fnr N的突变使土壤杆菌合成热凝胶能力下降了22.0%,转录组分析发现在Δfnr N中186个基因表达发生显著性变化(|log2(|fold change|)|≥1且q≤0.001),其中65%的基因表达上调。热凝胶合成的关键基因crd ASC的表达受到不同程度的抑制,fnr N的突变使编码σ因子的ecf R和编码生物膜合成调节因子的sin R显著下调;Δfnr N菌中与细胞色素有关基因cyd AB、cy2、fix NOPQ的转录水平下调2-13倍。【结论】fnr N通过调控ecf R和sin R的表达调控热凝胶合成,通过调控fix NOPQ等基因的表达参与氧信号调控,该研究有助于丰富对土壤杆菌氧调控系统的认识。