基于形态数据的大白菜核心种质构建方法的研究

 以国家蔬菜种质资源中期库收集保存的1 651份大白菜种质为试材,按照大白菜分类系统和生态型,采用分层分组法,将所有种质分为6组。基于43个形态性状的数据,比较了4种组内取样比例法、6种总体取样规模和2种取样方法在构建大白菜核心种质中的作用和效果。结果表明：组内以多样性比例法更能使各组的取样份数或比例趋于平衡,并较好地保持原始收集品的变异度。当总体取样规模为15%时,多样性比例法所构建的核心种质的遗传多样性指数达到最大,表型保留比例亦能达到98％左右;而当总体取样规模增加到20%以上时,虽然表型保留比例接近100％,但核心种质遗传多样性指数迅速降低。因此,认为15%总体取样规模较为合适。在一定的组内取样比例法和总体取样规模下,聚类取样构建的核心种质的遗传多样性指数（I）、表型保留比例（RPR）和变异系数（CV）均比随机取样的高。根据获得的优化方案最终在表型水平建立了包含248份种质的中国大白菜核心种质。     

茉莉花ISSR-PCR反应体系的建立

以茉莉花为材料,研究了PCR反应体系的主要成分及退火温度对茉莉花ISSR扩增结果的影响.结果表明:在20μL的反应体中,Mg2 的用量为1.2～1.6 mmol/L,dNTPs 浓度为0.15 mmol/L,引物的浓度为0.5μmol/L,Taq DNA 聚合酶的用量为1U,模板DNA的用量为40～70 ng,在48～50℃的退火温度下40个循环,能得到清晰、多态性高的ISSR带谱.     

聊红国槐谷胱甘肽过氧化物酶活性测定的研究

用直接测定法测定聊红国槐、国槐、龙爪槐、黄金槐样品谷胱甘肽过氧化物酶活性,其中以聊红国槐最高、龙爪槐活性最低.同时探讨了不同条件下的聊红国槐谷胱甘肽过氧化酶的活性高低,这一结果为今后研究该酶在国槐上的应用奠定了试验基础,为研究乔木树种中的GSH-Px活性情况提供理论依据.     

江西大富生态农业观光园总体规划

通过对大富生态农业观光园的指导思想、规划目标、功能分区、绿化配置诸方面,对其总体规划进行了介绍,力求将景观元素与农业生产相结合,使园区建设集观光、旅游、休闲、教育、生产、示范于一体.     

不同因素对贺兰山丁香愈伤组织诱导的影响

利用正交实验设计研究4种因素(6-BA、NAA、2,4-D、外植体)对贺兰山丁香愈伤组织诱导的影响,筛选出最佳的愈伤组织诱导条件为MS 6-BA 0.5 mg/L 2,4-D 0.1 mg/L,其中6-BA的浓度和外植体类型对贺兰山丁香种苗的出愈率有极显著影响(P=0.01).同时发现子叶和胚轴均可作为外植体材料,且以胚轴为外植体在最佳诱导条件下出愈率高达93.3%.     

优良观赏果树榅桲的推广应用

榅桲的栽培具有悠久的历史,它具有较强的耐寒、耐旱、耐盐碱能力,适于我国北方大多数城市栽培;其树姿、叶片、花和果实均具有较高的观赏价值,是较好的观赏树种;同时,榅桲又具有很高的经济价值,是优良的果树.因此,在我国北方,榅桲具有很高的推广价值.     

昆山市蔬菜市场准入工作的做法和思考

根据昆山市蔬菜市场供应与准入的主要做法。针对性地提出了包括加强环节管理、完善监管网络、做好准出准入衔接等方面的蔬菜市场安全准入工作的对策建议。     

杨梅雌、雄种质遗传关系的RAPD和ISSR分析

为获得与主栽的杨梅品种遗传基础相近的杨梅雄株,文章采用了22个多态的RAPD引物和7个多态的ISSR引物,对浙江杨梅的栽培品种东魁、荸荠种、晚稻杨梅、丁岙梅和早色等10个雌株与17个雄株种质资源间的遗传关系进行了研究。结果表明,不同杨梅产地收集的这17个杨梅雄株种质资源中,雄株与品种间的遗传关系呈规律性,即同一产区的地方品种与当地的雄株间遗传相似程度最高,而同一地区不同雄株与当地主栽品种间的遗传相似程度也有不同。通过UPGMA法进行聚类分析,上述5个杨梅主栽品种分别获得了与其亲缘关系相对接近的雄株,成对遗传相似系数最高为0.958,最低为0.878。     

Calreticulin promotes migration and invasion of nasopharyngeal carcinoma cells by inducing cell EMT

AIM:To observe the expression of calreticulin (CRT) in nasopharyngeal carcinoma tissues, analyze the significance of clinical pathology and the influence on epithelial-mesencymal transition (EMT) of CNE2 cells. METHODS:The expression of calreticulin was detected by immunohistochemistry in 52 nasopharyngeal carcinoma and 57 nasopharyngeal benign tissues, and the significance of clinical pathology was evaluated. The calreticulin gene-specific small interfering RNA was constructed, and then was transfected into the NPC cell line CNE2 using the cationic liposome method. The effect of CRT on the morphological changes of the CNE2 cells was observed under light microscope. The effect of CRT on the cell migration and invasion abilities of the CNE2 cells was detected by Transwell migration and invasion assays. The expression of EMT-related proteins E-cadherin, vimentin, transforming growth factor (TGF)-β and matrix metalloproteinase (MMP)-9 in the CNE2 cells was determined by Western blot. RESULTS:The positive expression rate of CRT in the benign lesion tissues was 19.29% (11/57), which was significantly increased in the nasopharyngeal carcinoma tissues as 82.69% (43/52). The expression rate of CRT was positively correlated with the stage of nasopharyngeal carcinoma and lymph node metastasis (P<0.05). Knockdown of CRT expression made the CNE2 cells showing a spindle shape to a flat, cobblestone-like epithelial state change, arranged more compact, and the migration and invasion abilities were significantly decreased (P<0.05). Knockdown of CRT expression resulted in significant increase in the protein expression of E-cadhe-rin, and the decreases in the protein expression of vimentin, TGF-β and MMP-9 in the CNE2 cells (P<0.05). CONCLUSION:Calreticulin expression in nasopharyngeal carcinoma is significantly higher and positively correlated with nasopharyngeal carcinoma stage and lymph node metastasis. Calreticulin promotes cell migration and invasion of nasopharyngeal carcinoma CNE2 cells by inducing EMT.     

High expression level of TAL1 gene in newly diagnosed acute myeloid leukemia

AIM: To investigate the characteristic of T-cell acute lymphocytic leukemia 1 (TAL1) gene expression in acute myeloid leukemia (AML) cell lines and in primary AML cells from de novo AML patients with different subtypes. METHODS: Real-time PCR was used to determine the expression of TAL1 mRNA in acute leukemia cell lines (Jurkat, CCRF-CEM, HL-60 and NB4 cell lines) and peripheral blood mononuclear cells from 47 newly diagnosed AML patients. Twelve healthy individuals were served as healthy control group. RESULTS: A significantly increased level in TAL1 mRNA was found in AML cell lines (HL-60 and NB4), T-cell acute lymphacytic leukemia (T-ALL) cell lines (Jurkat, CCRF-CEM) and primary AML cells compared with the healthy controls. Over-expression of TAL1 was found in all detected AML subtypes, the highest level of TAL-1 mRNA was found in AML-M1 and AML-M5 subtype (P<0.05). CONCLUSION: High expression of TAL1 in AML might influence the differentiation and proliferation of myeloid cells, further investigation needs to confirm whether it would be as a biomarker for pathogenesis of AML.