香蕉果实的1个14-3-3蛋白同源基因的克隆及序列分析(简报)

根据在香蕉果实抑制缩减文库中获得的1个14-3-3蛋白基因片段,采用PCR和RACE相结合的方法从香蕉(Musa acuminate L.AAA group cv.Brazilian)cDNA文库中筛选到其全长cDNA序列.序列测定和Blastx比对分析结果表明,该cDNA全长1 037 bp,含有1个完整的阅读框,其编码区编码261个氨基酸残基,具有植物14-3-3蛋白基因的保守结构域,并与其他植物来源的14-3-3蛋白具有很高的同源性,将其命名为Ma-14-3-36(Musa acuminate 14-3-3).采用遗传进化系统发育树的分析结果表明,Ma-14-3-36与来源于单子叶植物的多数14-3-3蛋白基因序列在同一个进化枝上.采用RT-PCR对其在香蕉果实发育不同时期的表达进行分析结果表明,在香蕉果实发育的不同时期差异表达,推测其可能在果实的发育中起作用.     

灌浆期高温对小麦光合产物运转的影响

以扬素５号为材料,用＾１４Ｃ示踪方法,利用多探头活体测量仪,测定了小麦灌浆期在３０℃和４０℃高温条件下对剑叶＾１４Ｃ－同化产物运转的影响。结果表明,高温使剑叶光合同化效率降低,叶片光合产物输出动态发生紊乱,抑制了籽粒中光合产物的累积,最终对千粒重影响显。     

嫁接促活剂对黄瓜嫁接苗愈伤过程、~(32)P和~(14)C的吸收和运转的影响

^32P和^14C示踪试验结果表明,嫁接促活剂可使砧木吸收^32P的量比对照增加1倍,使砧木吸收的^32P运到接穗或使接穗同化的^14C到砧木比对照提早2d,并且明显提高了^32P和^14C的输出量及比例,明显促进接口愈伤组织的形成和维管束的连接,提高了嫁接成活率。     

Stabilization mechanisms of organic matter in four temperate soils: Development and application of a conceptual model

Based on recent findings in the literature, we developed a process‐oriented conceptual model that integrates all three process groups of organic matter (OM) stabilization in soils namely (1) selective preservation of recalcitrant compounds, (2) spatial inaccessibility to decomposer organisms, and (3) interactions of OM with minerals and metal ions. The model concept relates the diverse stabilization mechanisms to active, intermediate, and passive pools. The formation of the passive pool is regarded as hierarchical structured co‐action of various processes that are active under specific pedogenetic conditions. To evaluate the model, we used data of pool sizes and turnover times of soil OM fractions from horizons of two acid forest and two agricultural soils. Selective preservation of recalcitrant compounds is relevant in the active pool and particularly in soil horizons with high C contents. Biogenic aggregation preserves OM in the intermediate pool and is limited to topsoil horizons. Spatial inaccessibility due to the occlusion of OM in clay microstructures and due to the formation of hydrophobic surfaces stabilizes OM in the passive pool. If present, charcoal contributes to the passive pool mainly in topsoil horizons. The importance of organo‐mineral interactions for OM stabilization in the passive pool is well‐known and increases with soil depth. Hydrophobicity is particularly relevant in acid soils and in soils with considerable inputs of charcoal. We conclude that the stabilization potentials of soils are site‐ and horizon‐specific. Furthermore, management affects key stabilization mechanisms. Tillage increases the importance of organo‐mineral interactions for OM stabilization, and in Ap horizons with high microbial activity and C turnover, organo‐mineral interactions can contribute to OM stabilization in the intermediate pool. The application of our model showed that we need a better understanding of processes causing spatial inaccessibility of OM to decomposers in the passive pool.     

大肠癌中HSP27、p14^ARF和caspase-3蛋白的表达及意义

目的：探讨HSP27、p14^ARF和caspase-3蛋白在大肠癌中的表达及其与大肠癌I临床病理特征的关系。方法：利用sP法检测大肠癌48例和大肠腺瘤10例以及正常大肠黏膜组织15例中HSP27、p14^ARF和caspase-3蛋白的表达。结果：大肠癌组织中HSP27、p14^ARF和caspase-3蛋白阳性表达率分别为79．2％、58．4％和66．7％,大肠腺瘤组织中分别为40．0％、70．0％和100．0％,正常大肠黏膜组织中分别为33．3％、80．0％和93．3％。p14^ARF和caspase-3蛋白的表达在高、中分化癌组的表达率分别为64．1％、74．4％,明显高于低分化组22．2％、33．3％（Pd0．05）。结论：HSP27、p14^ARF和caspase-3与大肠癌的发生有关,可作为大肠癌临床评价肿瘤生物学行为的指标。     

USP14 regulates H2O2 induced oxidative stress in H9c2 cells

AIM:To evaluate the effect of inhibiting ubiquitin-specific protease 14(USPl4) activity on oxidative stress induced by H₂O₂ of H9c2 cells.METHODS:The H9c2 cells were incubated with H₂O₂ at 25 μmol/L for 2 h to establish the oxidative stress injury model.The cells were divided into control group,H₂O₂ group,IU1 group (25 μmol/L or 50 μmol/L) and IU1+H₂O₂ group.The H9c2 cells activity was measured by MTS assay.The level of intracellular reactive oxygen species (ROS) and cell survival rate were analyzed by flow cytometry assay.The changes of the mitogen-activated protein kinase (MAPK) family related proteins were detected by Western blot.RESULTS:Compared with control group,the cell activity and the viability rate in H₂O₂ group were decreased (P<0.05),while the intracellular ROS,the protein levels of Bax/Bcl-2,P53,p-ERK1/2,p-JNK and p-P38 were increased (P<0.05).Compared with H₂O₂ group,the cell activity and the viability rate of the H9c2 cells in IU1+H₂O₂ group were increased (P<0.05),while the intracellular ROS,the protein levels of Bax/Bcl-2,P53,p-ERK1/2,p-JNK and p-P38 were decreased (P<0.05).CONCLUSION:Inhibition of USPl4 activity reduces the oxidative stress injury of the H9c2 cells.The mechanism may be related to inhibition of the MAPK signaling and down-regulation of apoptosis related proteins.     

土壤中红霉素结合残留在菜心中生物有效性研究

为探究土壤环境中红霉素污染的生物风险,本试验采用¹⁴C示踪技术,选取广东菜心为代表,研究红霉素结合残留的释放、转化及生物有效性,并探讨添加外源有机肥(如鸡粪、活性淤泥)对该过程的影响。结果表明,土壤中红霉素结合残留随着时间推移逐渐释放,在培养45 d时下降至引入量的59.83%,其中15.00%转化为可提态残留;植物根系的吸收和扰动能促进红霉素结合残留的释放和转化(P <0.05);土壤中的红霉素结合残留能够被广东菜心根部吸收并转运至可食部分,转运系数为0.34,表明红霉素结合残留在菜心体内不易向上运输;放射性自显影图片显示,被植物吸收的¹⁴C-红霉素及其放射性衍生物主要集中在叶片和根部;外源添加有机肥(鸡粪和活性淤泥)处理,一方面可抑制结合残留的释放,增加富啡酸中红霉素结合残留的含量(P<0.05),导致土壤中红霉素污染更持久,另一方面可促进植物对土壤中红霉素残留的吸收;腐殖质分级结果显示,红霉素结合残留主要集中在富啡酸中(87.92%~97.21%),并随着时间推移不断释放。本研究结果为科学评价红霉素的生态安全提供了理论支持。     

TRANSPORTATION AND DISTRIBUTION OF 14C-RESERVES ON DIFFERENT GENOTYPE WHEAT VARIETIES AFTER ANTHESIS

利用14CO₂对不同持绿性状的小麦品种进行花前示踪标记,研究持绿小麦的14C-储备物在花后的转运与分配规律。结果表明,小麦花前标记的14C-储备物在开花时80%～90%已储存于茎杆和颖壳中,仅有约10%～20%残留在叶片中;开花后这些储备物都向籽粒转运,成熟时籽粒中14C分配率约为20%～40%,茎杆与颖壳中含有约60%～80%,极少量残留在叶片中。持绿型小麦YM66的14C-储备物从叶片和茎杆中输出的快,成熟时籽粒含有40%的14C-储备物,这样比率高于对照品种XY22 和早衰品种WM6的14C-储备物。     

基于14C同化物运转和分配对黄柏剥皮的再生机理

以14C为示踪剂,用14CO2+CO2法对2年生黄柏进行半株标记,在主干上环状剥去韧皮部,以塑料薄膜包裹,燃烧法制样、液体闪烁测量法测14C活度。结果表明,未剥皮黄柏韧皮部的14C同化物运输速率为52.0cm/h,3h左右同化物从树冠运输到根系,树冠不同部位的功能叶14C同化物分配为:中部功能叶>上部功能叶>下部功能叶;剥皮后,同化物分配规律改变为:上部功能叶>中部功能叶>下部功能叶;剥皮第15天在新生韧皮部、剥口下方的树皮及根系中检测到14C同化物,表明新生韧皮部的生理功能得到恢复。     

香蕉14-3-3蛋白基因Ma-14-3-3d的克隆及序列分析(英文)

[Objective] The aim of the study is to clone and analyze the gene encoding 14-3-3 protein from banana. [Method] Combined with PCR amplification, RACE (rapid amplification of cDNA ends) technique was employed to clone 14-3-3 gene from banana; then the amplified sequence was sequenced and homologically analyzed. [Result] A new cDNA homologous with 14-3-3 protein genes were obtained by RT-PCR and RACE ( rapid amplification of cDNA ends ) approaches. The full length of this cDNA was 866 bp encoding 197 amino acids. Alignment of deduced amino acid sequence with those from other plants revealed that the cDNA shared high homology with 14-3-3 protein genes from other plants, and was designated as Musa acuminata 14-3-3 gene (Ma-14-3-3d). Phylogenetic analysis reveals that Ma-14-3-3d has closer genetic relationship with those from monocotyledon species than those from other species. [Conclusion] Ma-14-3-3d belongs to the same lineage of 14-3-3 from monocotyledon.