苹果新品种‘红光3号’

‘红光3号’是由‘国光’苹果选育出的芽变新品种。植株生长健壮,抗逆性强,果实性状优异。果实扁圆形,单果质量120 g,果面着条红,着色度85%,果实可溶性固形物含量17.94%,可滴定酸含量0.93%,口感酸甜适口。在河北张承地区果实10月初成熟,丰产稳产,平均产量22.5 t · hm-2。     

Genetic Analysis and Mapping of TWH Gene in Rice Twisted Hull Mutant

A mutant with twisted hulls was found in a breeding population of rice (Oryza sativa L.). The mutant shows less grain weight and inferior grain quality in addition to twisted hulls. Genetic analysis indicated that the phenotype of mutant was controlled by a single recessive gene (temporarily designated as TWH). To map the TWH gene, an F2 population was generated by crossing the twh mutant to R725, an indica rice variety with normal hulls. For bulked segregant analysis, the bulk of mutant plants was prepared by mixing equal amount of plant tissue from 10 twisted-hull plants and the bulk of normal plants was obtained by pooling equal amount tissue of 10 normal-hull plants. Two hundred and seven pairs of simple sequence repeat (SSR) primers, which are distributed on 12 rice chromosomes, were used for polymorphism analysis of the parents and the two bulks. The TWH locus was initially mapped close to the SSR marker RM526 on chromosome 2. Therefore, further mapping was performed using 50 pairs of SSR primers around the marker RM526. The TWH was delimited between the SSR markers RM14128 and RM208 on the long arm of chromosome 2 at the genetic distances of 1.4 cM and 2.7 cM, respectively. These results provide the foundation for further fine mapping, cloning and functional analysis of the TWH gene.     

鸡冠花新品种‘彩虹鸡冠花’

‘彩虹鸡冠花’是从‘早水鸡冠花’航天诱变的种子后代中选育出的新品种。株高33.37 cm,冠幅25.23 cm,花序枝8.75条,穗状花序鸡冠状,出冠整齐一致,花冠排列平整,冠长8.17 cm,冠宽4.95 cm,冠色紫红,花期长,达74 d以上。群体整齐性好,适合夏季露地栽培。     

SIRT1 promotes autophagy of pancreatic cancer cells induced by hypoxia via regulating FOXO1/RAB7 signaling pathway

AIM: To investigate the effect of SIRT1 on the autophagy of pancreatic cancer cells under hypoxia condition, and to analyze the underlying mechanism of regulating FOXO1/RAB7 signaling pathway. METHODS: Western blot and immunofluorescence methods were used to determine the expression of SIRT1 in the pancreatic cancer cells. The small interfering RNA targeting SIRT1 and SIRT1 over-expression plasmid were transfected into the pancreatic cancer Panc-1 cells. Confocal microscopy was used to detect the LC3 expression. Western blot was used to analyze the protein levels of LC3, p62 and FOXO1/RAB7 signaling pathway-related molecules. Co-immunoprecipitation was used to detected the protein interaction between SIRT1 and FOXO1. RESULTS: The expression level of SIRT1 in the nucleus of Panc-1 cells was increased under hypoxia condition. Compared with negative control under hypoxia condition, knock-down of SIRT1 expression attenuated the autophagy flux in the pancreatic cancer Panc-1 cells (P<0.05). Over-expression of SIRT1 increased the protein levels of FOXO1 and RAB7. On the contrary, knock-down of SIRT1 expression inhibited the protein levels of FOXO1 and RAB7. The protein interaction between SIRT1 and FOXO1 in the pancreatic cancer cells was observed. CONCLUSION: SIRT1 in pancreatic cancer Panc-1 cells under hypoxia condition is over-expressed in the nucleus. Down-regulation of SIRT1 inhibits autophagy and its mechanism may be related to FOXO1/RAB7 signaling pathway.     

藏绵羊KLF7基因表达特征分析及其过表达对前脂肪细胞增殖分化的影响

【目的】分析藏绵羊Krüppel样因子7(Krüppel-like factor 7,KLF7)基因表达特征,研究过表达该基因对前脂肪细胞增殖及分化的影响。【方法】从藏绵羊脂肪组织中分离前脂肪细胞进行培养及成脂诱导,应用实时荧光定量PCR技术检测KLF7基因在藏绵羊7个组织(大脑、皮下脂肪、肾脏、背最长肌、瘤胃、睾丸和回肠)和前脂肪细胞不同分化阶段(第0、2、4和8天)的mRNA相对表达水平;应用RT-PCR方法从藏绵羊脂肪组织中扩增KLF7基因CDS区序列,并将其连接到pcDNA3.1(+)真核表达载体获得pcDNA3.1-KLF7过表达质粒,转染前脂肪细胞;应用实时荧光定量PCR方法检测脂肪细胞增殖及分化标志基因mRNA表达水平;采用EdU和CCK-8方法分别检测过表达KLF7基因对EdU阳性细胞数和细胞活力的影响;采用油红O染色检测过表达KLF7基因后脂肪细胞脂滴生成量。【结果】KLF7基因在藏绵羊7个组织中均有表达,其中在大脑中的表达量最高,其次为皮下脂肪和肾脏,均显著高于其他组织(P<0.05);诱导分化第2、4和8天脂肪细胞mRNA表达量均显著高于分化前(P＜0.05),且分化第2天表达量最高;pcDNA3.1-KLF7过表达质粒转染前脂肪细胞2 d后显著或极显著抑制增殖标志基因CDK4、CyclinB1和CyclinD1的表达水平(P＜0.05;P＜0.01),极显著降低细胞活力及EdU阳性细胞数量(P＜0.01);pcDNA3.1-KLF7过表达质粒转染前脂肪细胞,诱导分化8 d后,脂肪细胞分化标志基因PPARγ、Glut4和ELOVL6的mRNA相对表达水平显著或极显著下调(P＜0.05;P＜0.01),且脂质沉积极显著减少(P＜0.01),表明过表达KLF7基因可抑制藏绵羊前脂肪细胞增殖及分化。【结论】KLF7基因在藏绵羊多个组织中广泛表达,且大脑、皮下脂肪、肾脏中表达量较高;诱导分化后脂肪细胞表达量显著高于分化前,且分化第2天表达量最高;过表达KLF7基因可抑制藏绵羊前脂肪细胞的增殖及分化。试验结果为阐明藏绵羊脂肪沉积的分子调控机制提供了基础数据。     

植物生长调节剂对马铃薯叶片生理代谢及产量品质的影响

大田栽培条件下,以马铃薯克新13为材料,叶面喷施植物生长调节剂2-N,N-二乙氨基乙基己酸酯(Diethyl aminoethyl hexanoate,简称DTA-6)、缩节安(Mepiquat chloride,简称DPC)以及烯效唑(Uniconazole,简称S3307),研究植物生长调节剂对马铃薯叶片生理代谢及产量、品质形成的影响。结果表明:在马铃薯块茎膨大期喷施植物生长调节剂,均显著增加了单薯重、淀粉产量和鲜薯产量,其中,以DTA-6调控效果为最佳,单薯重、淀粉产量、鲜薯产量和淀粉含量比CK分别增加了10.40%、40.26%、26.56%和11.32%,块茎还原糖含量比CK降低了20%。此外,调节剂处理均提高了马铃薯叶片叶绿素含量、净光合速率、蒸腾速率和细胞间隙CO_2浓度,加快了叶片的光合作用,各指标与产量之间呈正相关。随着时间的推移,各处理的叶片淀粉和蔗糖含量呈先降低后升高的变化趋势,淀粉酶活性呈降低的变化趋势,调节剂对叶片蔗糖转化酶活性的调控效果呈不同规律的变化。总体而言,调节剂均提高了马铃薯产量,改善了块茎品质,其中DTA-6处理效果最佳。     

皱纹盘鲍人工育苗的初步研究

为探讨近三十年来我国皱纹盘鲍养殖模式对群体遗传结构产生的影响,利用线粒体细胞色素C氧化酶亚基 (COⅠ)基因和细胞色素b (Cytb)基因分析了定殖漳州的群体、大连培育蓬莱越冬群体、荣成培育福建越冬群体及长山列岛 (砣矶岛、大钦岛、南隍城岛)皱纹盘鲍群体的遗传多样性与群体遗传结构。结果显示,在259个个体730 bp的COⅠ序列片段中检测到48个变异位点和30个单倍型,6个群体的单倍型多样性为0.586~0.897,核苷酸多样性为0.0056~0.0081。259个个体730 bp的Cytb序列片段中检测到59个变异位点和32个单倍型,6个群体的单倍型多样性为0.605~0.909,核苷酸多样性为0.0077~0.0120。基于COⅠ和Cytb基因的群体间F_st值以及AMOVA结果表明,绝大部分群体之间存在显著的遗传分化,并且遗传变异主要来源于群体内。现行的皱纹盘鲍北鲍南养模式加强了不同群体之间的基因交流,使不同遗传背景的种群二次接触,导致皱纹盘鲍6个群体均具有较高的单倍型多样性和核苷酸多样性;而各养殖群体中的不同选育条件则可能是造成显著遗传分化的重要原因。本研究对分属南北沿海的6个皱纹盘鲍群体的遗传评估将为我国皱纹盘鲍资源的合理利用以及养殖模式对遗传结构的影响提供科学依据。

     

沙质草地植物群落及土壤质地对补播和翻耕措施的响应

选取3个翻耕模式(深翻、浅翻及免耕),以未补播的原生沙质草地为对照(CK),分析不同模式下禾-豆混播草地土壤颗粒组成、植物群落结构特征及数量特征,研究退化沙质草地土壤质地及植物群落对翻耕和补播措施的响应。结果表明:深翻、浅翻、免耕及CK对应的草地群落物种丰富度分别为9、9、5种和8种,机械扰动和补播牧草降低了游击型克隆植物的繁殖与扩展能力,提高了补播牧草在群落中的优势度,深翻处理下多年生禾本科及豆科牧草优势度最为明显,翻耕及补播后草地植物群落物种多样性和均匀度明显增大,生态优势度与物种多样性变化趋势正好相反,其中浅翻处理下补播草地群落物种多样性和均匀度最高,游击型克隆植物提高了原生草地生态优势度;补播草地群落地上生物量大小表现为:深翻(348.39 g·m~(-2))浅翻(285.77 g·m~(-2))免耕(242.08 g·m~(-2))CK(141.83 g·m~(-2)),且与原生草地存在极显著性差异(P0.01);补播草地土壤颗粒组成主要以50~250μm的细沙粒为主,深翻、浅翻及补播牧草显著提高了0~20 cm土层土壤黏粉粒含量和土壤颗粒体积分形维数(P0.01),土壤质地改善效果明显,土壤整体稳定性明显提高。     

转基因动物研究进展

转基因动物是现代生物技术中一个极其重要的研究领域，目前已经有转基因小鼠、兔、绵羊、山羊、猪、牛、鸡和鱼等多种转基因动物问世。本文综述了转基因动物的制作方法、转基因动物的应用研究以及所取得的重要成就，并指出了转基因动物存在的主要问题，展望了其发展前景。     

Study on Synergistic Effect of VA5 Immunopotentiator on Pigeon NDV Inactivated Vaccine

This study was designed to evaluate the synergistic effect of VA5 immunopotentiator on pigeon ND4416 inactivated vaccine.160 healthy pigeons were randomly divided into four groups,including ND4416 strain inactivated vaccine group (NDV group),ND4416 strain inactivated vaccine and immunopotentiator (VA5) mixed group (NDV+VA5 group),La Sota inactivated vaccine group (La Sota group) and normal saline as the control group (C group),to assess their vaccine efficacy against virulent pigeon NDV by serological analysis and animal testing.Pigeons sera were collected at different time points after immunization and measured the HI antibody titer of each group.The results showed that VA5 immunopotentiator significantly improved the serum antibody level of pigeons immunized with pigeon Newcastle disease inactivated vaccine (P<0.05).In addition,comparative test of spleen lymphocyte transformation was conducted at various time points after immunization.The results indicated that VA5 effectively stimulated the lymphocyte transformation of immune pigeon.Pigeons in each groups were challenged with ND4416 strain at the 30th,90th and 180th d after immunization.The results presented that the NDV+VA5 group had 100% protection rate and higher than La Sota group.The duration of immunization test showed that the antibody titer of NDV+VA5 group reached peak 11.20log₂ at the 21st d,remained 7.50log₂ at 180th d,and the protection rate remained 100% at 180th d.It indicated that VA5 immunopotentiator sustained the immune duration of pigeon NDV vaccine up to 180 d.Moreover,the in vitro detoxification test results suggested that VA5 immunopotentiator reduced the in vitro detoxification cycle of pigeons after challenge.Overall,this study suggested VA5 immunopotentiator could significantly improve the immune efficacy of pigeon Newcastle disease inactivated vaccine,which provided a basis for further enhancing the efficacy of Newcastle disease vaccine,as well increased experimental data for the application of immunopotentiators.