外源亚精胺对盐胁迫下甜菜生长及养分吸收的影响

为了探究外源亚精胺是否具有缓解甜菜盐害作用,采用霍兰营养液室内水培方法,测定了280mmol/L NaCl胁迫条件下,喷施0.25 mmol/L外源亚精胺后,耐盐‘T510’和盐敏感‘210’甜菜品系幼苗生长、生理及其体内N、P、K养分含量的变化情况。结果发现,盐胁迫下(Na处理),除MDA和P素含量升高外,两品系甜菜幼苗的叶片相对含水量、叶面积、叶绿素含量、幼苗生物量及N、K养分含量指标均明显降低;与Na处理比,喷施亚精胺的盐胁迫处理,除MDA和P素含量降低外,其它指标明显增加,两品系甜菜幼苗生长和养分吸收状况明显改善;外源亚精胺对耐盐‘T510’品系的调节作用大于‘210’品系。因此外源亚精胺能有效缓解盐胁迫对甜菜生长的伤害,对耐盐品系的调节效果更佳。     

华北平原地下水压采区冬小麦种植综合效应探讨

华北平原冬小麦-夏玉米一年两熟种植模式为维护国家粮食安全发挥了重要作用。但冬小麦生长期正处于华北平原降水较少的干旱季节,实现高产依赖于灌溉,是华北平原地下水超采的主导因素之一。随着国家地下水限采政策的实施,在地下水超采区如何稳定冬小麦的种植面积和产量是面临的一个重要问题。本文通过综述以往研究并结合典型地点田间试验结果,从冬小麦种植可减少休闲期土壤蒸发损失、具有的深根系系统可充分利用土壤储水、可利用微咸水替代淡水灌溉、通过限水灌溉发展优质麦生产、冬春形成覆盖层美化和防沙尘效应等方面论述了华北平原种植冬小麦的优势,提出华北平原冬小麦生产需要转变传统高耗水高产量理念,充分发挥冬小麦抗旱、耐盐能力强的特点,在不实施大规模压缩冬小麦种植面积条件下,通过冬小麦限水灌溉和微咸水利用满足对地下水压采需求,充分发挥华北平原冬小麦种植冬春防风沙、美化环境的生态功能,同时满足区域口粮安全的保障功能。     

不同温度下TMV侵染枯斑三生烟的LncRNA差异表达

【目的】 筛选不同温度下烟草花叶病毒（Tobacco mosaic virus,TMV）侵染后枯斑三生烟（Nicotiana tabacum var. Samsun NN）差异表达的长链非编码RNA（long non-coding RNA,lncRNA）,研究lncRNA在枯斑三生烟抗性反应中的作用。【方法】 N基因的温度敏感性使枯斑三生烟在25℃时具备对TMV的抗性、在31℃抗性丧失,在这两个温度条件下对枯斑三生烟接种TMV和磷酸盐缓冲盐水（phosphate buffered saline,PBS）,48 h后提取系统叶总RNA,构建链特异性文库后进行深度测序。对测序结果进行过滤后利用HTSeq将有效数据与近缘品种TN90（N. tabacum var. TN90）基因组比对,筛选得到lncRNA后利用FPKM法估计lncRNA的表达水平。通过edgeR筛选差异表达lncRNA（differentially expressed lncRNA,DElncRNA）,并利用qRT-PCR技术对这一结果进行验证。通过共定位及共表达分析预测DElncRNA的靶基因,通过参考基因组注释、GO和KEGG富集分析研究靶基因的功能。【结果】 4个处理共12个样本经lncRNA-seq各测得约8 000万条clean reads,共获得4 737条已知lncRNA、40 169条新lncRNA。其中64个lncRNA在不同温度条件下TMV侵染后存在差异表达,qRT-PCR测定结果显示这些lncRNA的测序正确率在80%左右,表明本研究所得测序数据具备较高的可信度。对DElncRNA进行靶基因预测,发现一些基因同时被25℃下调和31℃上调的DElncRNA靶向。靶基因注释功能丰富,主要参与植物抗病、激素和代谢等生理过程。部分可能与激素通路相关的lncRNA,在25℃下TMV侵染时呈现下调趋势,而在31℃下TMV侵染则呈现上调趋势。GO富集分析显示靶基因主要参与构成膜、囊泡等组分,具备钙、钾离子通道抑制剂活性等分子功能,使相应离子得以转运引发随后的反应,同时也参与发病、抗原加工和呈现、细胞分裂素代谢等生理过程。KEGG分析发现靶基因显著富集在植物激素信号转导通路,25℃下调和31℃上调的DElncRNA靶基因同时富集在激素信号传导、ABC运输蛋白、苯丙烷类生物合成等通路。【结论】 不同温度（25℃和31℃）条件下TMV侵染枯斑三生烟后,长链非编码RNA差异表达,DElncRNA通过作用于激素信号传导、物质转运等过程参与寄主系统获得性抗性反应。研究结果可为揭示植物系统获得性抗性中lncRNA的调控功能以及新型抗病毒技术开发提供依据。     

P0 protein of cotton leafroll dwarf virus-atypical isolate is a weak RNA silencing suppressor and the avirulence determinant that breaks the cotton Cbd gene-based resistance

Cotton blue disease (CBD) is the most important disease present in cotton crops in South America and cotton leafroll dwarf virus (CLRDV) is the causal agent. The disease has been controlled by sowing cotton varieties resistant to CLRDV. However, in the 2009/10 growing season, an outbreak due to an atypical CLRDV isolate (CLRDV-at) occurred in northwest Argentina. Although CLRDV and CLRDV-at genomes are very closely related, the symptoms they produce in cotton plants are quite different. P0 is the most divergent protein between the isolates and in CLRDV is a silencing suppressor protein. This work characterized the silencing suppressor activity of the P0 protein encoded by CLRDV-at (P0^CL-at) and evaluated its role in Cbd-resistance break in cotton plants. It was demonstrated that P0^CL-at, despite having a mutation in the consensus of the F-box-like motif, was able to suppress local RNA silencing, but displayed lower activity than P0^CL. P0^CL and P0^CL-at showed no differences in the interaction with Gossypium hirsutum SKP1 orthologue (GSK1) and Nicotiana benthamiana SKP1 and both P0 proteins triggered destabilization of ARGONAUTE1. However, when the ability to enhance PVX symptoms was evaluated, P0^CL-at was shown to be a weaker pathogenicity factor than P0^CL in N. benthamiana. Interestingly, trans-expressed P0^CL-at enabled CLRDV to systemically infect CBD-resistant plants, and a chimeric CLRDV-P0^CL-at infectious clone succeeded in establishing infection in CBD-resistant cotton varieties with symptoms resembling those produced by CLRDV-at. These results strongly suggest that P0^CL-at is the avirulence (Avr) determinant involved in breaking cotton Cbd gene-based resistance.     

Role of chlorogenic acid in endothelial dysfunction in db/db mice

AIM: To explore the effects of chlorogenic acid (CGA) on endothelial dysfunction in db/db mice and the possible mechanism. METHODS: Male db/db mice (n=12) were divided into control group and CGA group, with 6 mice in each group. The mice in CGA group were treated with diet containing 0.02% CGA, while the mice in control group were given normal diet only. The observation period was 12 weeks. Fasting blood glucose level, tail blood pressure and the body weight were analyzed each week. At the end of the 12th week, the mice were anesthetized and blood was taken from carotid artery. The plasma levels of heme oxygenase-1 (HO-1), catalase (CAT), NAD(P)H dehydrogenase quinone 1 (NQO1) and glutathione peroxidase-1 (GPx-1) were measured by ELISA. The mouse aortas were isolated, and the superoxide anion and nitric oxide (NO) levels were measured by DHE and DAF-2 DA staining, respectively. Wire Myograph System was used to detect the vasorelaxation of db/db mouse aorta. The protein levels of peroxisome proliferator-activated receptor α (PPARα), nuclear factor E2-related factor 2 (Nrf2), phosphorylated AMP-activated protein kinase (p-AMPK), phosphorylated endothelial NO synthase (p-eNOS), P22^phox and P47^phox were determined by Western blot. RESULTS: Dietary CGA decreased fasting blood glucose and body weight in db/db mice as compared with control group (P<0.01 or P<0.05). The plasma levels of HO-1, CAT, NQO1 and GPx-1 in CGA group were higher than those in control group (P<0.01 or P<0.05). Administration of CGA for 12 weeks attenuated superoxide anion level, increased NO level in the mouse endothelium and improved endothelium-dependent relaxation of the db/db mouse aorta. CGA also increased the protein levels of PPARα, Nrf2, p-AMPK and p-eNOS, and decreased P22^phox and P47^phox levels (P<0.01). CONCLUSION: Dietary CGA improves db/db mouse endothelium-dependent relaxation. This effect may be related to the increases in the levels of antioxidant molecules PPARα, Nrf2 and p-AMPK, and the up-regulation of antioxidant capacity, thus decreasing the oxidative stress, promoting eNOS phosphorylation, and increasing NO level.     

大豆PHD家族蛋白的全基因组鉴定及表达特征分析

PHD（Plant Homeodomain Finger）基因家族编码一类锌指转录因子,广泛参与植物的生长发育和逆境应答过程。通过全基因组鉴定获得了95个大豆PHD家族蛋白。通过共线性分析、进化树构建、基因结构和功能结构域鉴定、GO注释分析、不同组织间和非生物胁迫下表达分析等,获得了大豆PHD家族基因复制、家族进化、保守结构域及基因表达等信息。结果表明,大豆PHD基因在家族进化、基因结构和保守结构域上存在较大变异,可能参与Zn ²⁺结合、DNA结合及表观遗传调控等分子过程,参与调控植物生长发育和逆境应答。这些结果为进一步研究大豆PHD家族在生长发育和逆境应答中的生物学功能提供重要线索。     

NRF2 attenuates oxidative stress and lysosomal dysfunction in doxorubicin-induced H9C2 cells

AIM:To study the effect of nuclear factor E2-related factor 2 (NRF2) on oxidative stress injury and lysosomal dysfunction in doxorubicin (DOX)-induced rat myocardial H9C2 cells. METHODS:The H9C2 cells were treated with DOX. The expression of NRF2 at mRNA and protein levels was determined by real-time PCR and Western blot. The H9C2 cells stably over-expressing NRF2 were established by lentiviral infection. Real-time PCR and Western blot were used to identify the efficiency of over-expression. After DOX treatment, the cell viability was measured by CCK-8 assay, the activity of lactate dehydrogenase (LDH), superoxide dismutase (SOD), glutathione peroxidase (GSH-Px) and catalase (CAT), and the content of malondialdehyde (MDA) in the cell supernatant were detected. FITC-dextran was used to analyze lysosomal pH, and the protein expression of lysosomal-associated membrane protein 1 (LAMP1) and cathepsin B was determined by Western blot.RESULTS:The expression of NRF2 at mRNA and protein levels in DOX-treated H9C2 cells was significantly decreased (P<0.05). Over-expression of NRF2 significantly up-regulated the mRNA and protein expression of NRF2 in DOX-treated H9C2 cells (P<0.05). After DOX treatment, the cell viability was decreased, and LDH activity was increased. The activity of SOD, GSH-Px and CAT was decreased, and the content of MDA was increased (P<0.05). The lysosomal pH was increased, and the protein expression of LAMP1 and cathepsin B decreased (P<0.05). Over-expression of NRF2 increased the cell viability, decreased LDH activity, increased the activity of SOD, GSH-Px and CAT, and decreased the content of MDA in cell supernatant (P<0.05). Over-expression of NRF2 also decreased the lysosomal pH, and increased the protein expression of LAMP1 and cathepsin B (P<0.05). CONCLUSION:DOX inhibits the expression of NRF2 in the myocardial H9C2 cells. Over-expression of NRF2 attenuates oxidative stress and lysosomal dysfunction in the H9C2 cells induced by DOX.     

盐胁迫对膜荚黄芪种子萌发的影响

为了保护并开发膜荚黄芪,同时改良盐碱地,研究了3种不同盐（中性盐NaCl、碱性盐Na₂CO₃和复盐）对膜荚黄芪种子发芽率、发芽势、抗氧化酶活性、丙二醛含量、可溶性蛋白质含量和相对电导率的影响。结果表明,不同盐胁迫对膜荚黄芪种子的影响不同,随着盐浓度的增加,黄芪种子的发芽率和发芽势逐渐降低;低浓度的NaCl和复盐可提高抗氧化酶活性,Na₂CO₃处理随着其浓度增加对抗氧化酶活性的抑制作用增强;各处理均增大了丙二醛含量和相对电导率;NaCl和复盐处理降低了膜荚黄芪种子可溶性蛋白含量,Na₂CO₃处理的可溶性蛋白含量随盐浓度增加而增加,综合各项指标可得同等盐浓度条件下胁迫作用由强到弱为Na₂CO₃>NaCl>复盐。     

外源褪黑素和脱落酸对干旱胁迫下葡萄生理特性的影响

为了探讨褪黑素(MT)和脱落酸(ABA)两者混合施用对植物响应干旱胁迫的综合效应,以盆栽‘阳光玫瑰’葡萄为材料,通过根灌100μmol·L~(-1)的MT溶液和叶面喷施50μmol·L~(-1)的ABA溶液及二者组合处理,研究MT和ABA对干旱胁迫下葡萄生理特性的影响。结果表明,与干旱对照组(D_(ck))相比,MT处理导致葡萄叶片MDA、H_2O_2含量和相对电导率分别降低了14.42%、44.11%和21.26%,叶片相对含水量提高了1.12%,同时SOD和POD酶活性分别提高了14.00%和3.01%。这些均表明MT处理有效缓解了干旱胁迫对植株造成的损伤。50μmol·L~(-1 )的ABA处理组叶片MDA含量和相对电导率较干旱对照组提高了9.43%和17.25%,表明ABA处理没有缓解植株的胁迫状态。MT和ABA组合处理具有和MT处理类似的效果。结果表明,褪黑素可以通过减轻膜脂过氧化程度,增强抗氧化系统能力,从而缓解干旱胁迫对葡萄的氧化损伤,提高抗旱性;同时削弱ABA带来的负面效应。