Interspecific cross‐hybrids of Nicotiana tabacum L. cv. (gla.) S ‘K326’ with Nicotiana alata          下载免费PDF全文

Jugou Liao  Jinran Dai  Shiyi Yang  Xiaoli Zhou  Longhui Ren  Zhuangzhuang Chen  Haili He  Suiyun Chen 《Plant Breeding》2017,136(3):427-435

In order to introduce the Tomato Spotted Wilt Virus (TSWV) resistance from Nicotiana alata into Nicotiana tabacum, a cytoplasmic male sterility (CMS) line of N. tabacum (N. tabacum L. cv. (gla.) S ‘K326’), was successfully crossed with N. alata. Despite a high DNA content variability, F₁ hybrids could be classified in two subgroups, a major one encompassing fertile hybrids morphologically similar to their tobacco maternal parent but TSWV sensitive, and a minor one displaying sterile hybrids showing an intermediate phenotype and TSWV resistant. In order to elucidate the unexpected fertility recovery of the fertile F₁ plants, some N. alata fertility restoration ppr genes were cloned and were shown to be differentially expressed between parental lineages as well as between both F₁ subgroups, suggesting that N. alata contains fertility restoring allele able to overcome the CMS of N. tabacum.  相似文献   

Investigation and genetic mapping of a Glomerella leaf spot resistance locus in apple          下载免费PDF全文

Yuanxia Liu  Jinhao Lan  Caihong Wang  Baohua Li  Jun Zhu  Chunxiao Liu  Hongyi Dai 《Plant Breeding》2017,136(1):119-125

Apple Glomerella leaf spot (GLS) is a severe fungal disease that damages apple leaves during the summer in China. Breeding new apple varieties that are resistant to the disease is considered the best way of controlling GLS. Fine mapping and tightly linked marker are critically essential for the preselection of resistant seedlings. In this study, a population of 207 F₁ individuals derived from a cross between ‘Golden Delicious’ and ‘Fuji’ was used to construct a fine simple sequence repeat (SSR)‐based genetic linkage map. The position of R_gls, a locus responsible for resistance to GLS, was identified on apple linkage group (LG) 15 using SSR markers CH05g05 and CH01d08, which was adapted from a published set of 300 SSR markers that were developed using the bulked segregant analysis (BSA) method. These two SSR markers flanked the gene, and its recombination rate was 8.7% and 23.2%, respectively. A total of 276 newly developed SSR markers around the target region and designed from the genome apple assembly contig of LG15 were screened. Only nine of these were determined to be linked to the R_gls locus. Thus, a total of 11 SSR markers were in linkage with R_gls, and mapped at distances ranging from 0.5 to 33.8 cM. The closest marker to the R_gls locus was S0405127, which showed a genetic distance of approximately 0.5 cM. The first mapping of the gene R_gls was constructed, and the locations of the 11 effective primers in the ‘Golden Delicious’ apple genome sequence were anchored. This result facilitates better understanding of the molecular mechanisms underlying the trait of resistance to GLS and could be used in improving the breeding efficiency of GLS‐resistant apple varieties.  相似文献   

棉花纤维中木质素的相对分子量     

胡文冉  范玲  李晓荣  谢丽霞  杨洋  李波  陈方圆 《作物学报》2017,43(6):940-944

分子量是聚合物的重要特性之一,木质素的分子量及其分布是研究苯丙烷类结构的反应、物理化学特性和评价其改性产物质量的内容之一。本研究以陆地棉TM-1成熟纤维为材料,分别利用酶解-温和酸解木质素法和二氧六环法提取棉纤维中木质素,结合凝胶渗透色谱法(gel permeation chromatography,GPC)调查和评价2种方法获得的棉纤维中木质素的相对分子量。结果表明,经二氧六环处理提取的棉花纤维中的木质素(dioxane lignin,DL)的重均分子量为2924g mol~(–1)、数均分子量2403 g mol~(–1),略高于由酶解-温和酸解处理提取的木质素(enzymatic hydrolysis-mild acidolysis lignin,EMAL)的重均分子量(2169 g mol~(–1))和数均分子量(1970 g mol~(–1)),EMAL的多分散系数稍低,说明木质素的均一性比DL高。表明EMAL法提取的木质素更适用于分析棉纤维中木质素的相对分子量。利用EMAL法分析棉纤维中木质素相对分子量表明,不同棉花品种的木质素重均分子量分布范围为938~2169 g mol~(–1),数均分子量分布范围为857~1970 g mol~(–1),多分散性系数在1.09~1.74间,均小于2。重均分子量与纤维马克隆值呈显著负相关,数均分子量与纤维长度呈显著负相关,与纤维马克隆值呈极显著负相关。  相似文献   

普通菜豆籽粒大小与形状的QTL定位   总被引：1，自引：0，他引：1  

耿庆河  王兰芬  武晶  王述民 《作物学报》2017,43(8):1149-1160

普通菜豆是世界上最重要的食用豆类作物之一,其籽粒大小和形状与产量及外观品质密切相关。本研究以来自安第斯基因库的大粒品种龙270709和来自中美基因库的小粒品种F5910配置杂交组合,获得的F2分离群体分别在哈尔滨大田与北京昌平温室种植,对百粒重、粒长、粒宽、粒厚、长宽比和长厚比6个籽粒性状进行了相关性分析和QTL定位。相关性分析表明,百粒重与粒长、粒宽、粒厚、长宽比、长厚比5个衡量籽粒大小和形状的性状均显著正相关。利用基于完备区间作图方法的Ici Mapping 4.1进行QTL定位,哈尔滨环境下定位到38个与百粒重、粒长、粒宽、粒厚、长宽比、长厚比相关的QTL,表型贡献率介于2.39%~17.37%之间,分布在除第1染色体外的其余10条染色体上;北京昌平环境下定位到21个上述性状的QTL,表型贡献率介于5.92%~22.53%之间,分布在第1、第3、第6、第7、第8、第9和第11染色体上。其中,百粒重QTLSW7与SW7’,SW6.1与SW6’,粒长QTLSL6.1与SL6.1’,粒厚QTLSH11与SH11’在2个环境下的标记区间重叠或者重合,SW7、SW6.1、SL6.1、SW6’和SL6.1’的表型贡献率在10%以上。  相似文献   

水稻紫鞘染色体片段代换系Z519的鉴定及PSH1候选基因分析     

周可  李燕  王世明  崔国庆  杨正林  何光华  凌英华  赵芳明 《作物学报》2017,43(7):974-982

花青素是广受人们喜爱的植物色素,在食品加工、杂种纯度鉴定中具有重要的作用。本研究鉴定了一个以日本晴为受体、优良紫鞘恢复系R225为供体亲本的紫鞘水稻染色体片段代换系Z519。Z519共含有16个代换片段,分布于除第10染色体外的其他11条染色体,平均长度为6.85 Mb。Z519在芽鞘3 mm时鞘尖呈现紫色,其后在叶鞘、叶缘、茎维管束和柱头等部位出现紫色线条,而日本晴各部位均为绿色。Z519叶鞘中花青素含量极显著高于日本晴,剑叶中没有显著差异。与受体日本晴相比,Z519的株高显著降低,千粒重、主穗总粒数和实粒数显著增加,有效穗数、主穗长和结实率无显著差异。进一步以日本晴与Z519杂交产生的F1和F2群体对紫鞘基因进行了遗传分析和分子定位。该紫鞘表型受显性单基因控制,位于第1染色体In Del标记L03和SSR标记L01之间37.8 kb的区域,被命名为PSH1。对该区间进行候选基因预测和测序,Z519在一个编码质体ATP/ADP转运蛋白的LOC_Os01g45910基因第一外显子的第238~252碱基的GTG重复区又多插入了GTG 3个碱基,导致增加了一个甘氨酸。q RT-PCR结果进一步表明其表达量在Z519中明显降低,初步确定LOC_Os01g45910是PSH1的候选基因。该研究为PSH1调控花青素的分子机制奠定了良好基础。  相似文献   

寄主诱导的基因沉默提高植物真菌病害抗性研究进展     

程伟  李和平  何水林  廖玉才 《作物学报》2017,43(8):1115-1121

寄主诱导的基因沉默(host-induced gene silencing,HIGS)以病原菌生长发育、产孢繁殖、侵染或致病过程中的关键基因作为靶点,在寄主植物中表达针对靶基因的RNAi构建体,在病原菌侵染植物的过程中,摄入相应的ds RNA或si RNA分子,通过识别、结合特异核苷酸序列,干扰病菌靶基因表达,从而抑制病菌侵染和扩展,使植物表现抗病。这项技术为培育基于病原菌特异序列的植物抗病性奠定了基础,显示了巨大的应用潜力。本文综述了利用HIGS技术提高植物真菌病抗性的最新研究进展,总结了国内外利用这项技术改良植物真菌病害抗性的主要策略、技术路线,展望了发展应用前景。  相似文献   

水稻颖花持续开放突变体sostenuto floret opening(sfo1)的鉴定与基因定位     

沈亚林  庄慧  陈欢  曾晓琴  李香凝  张君  郑昊  凌英华  李云峰 《作物学报》2017,43(8):1122-1127

水稻颖花开放是其生殖发育一个关键生理过程,对受精和随后种子发育具有重要影响。本文报道了一个与水稻颖花开放相关的突变体,来源于籼稻保持系西农1B的EMS(ethyl methane sulfonate)诱变群体。该突变体表现为开颖后浆片失水萎缩过程缓慢,内外稃持续开裂不闭合,暂命名为水稻颖花持续开放sostenuto floret opening 1(sfo1)突变体。遗传分析表明sfo1性状受1对隐性单基因控制,利用群体分离分析法(bulked segregation analysis,BSA)将SFO1基因定位在第5染色体SSR标记RM1054和IN/DEL标记ZTQ51之间,物理距离113 kb,含注释基因15个。本研究结果为SFO1基因的图位克隆和功能研究奠定了基础。  相似文献   

Effects of CENP-W down-regulation on human glioma U87 cells     

JI Qian-kun  LI Jian-bin  FAN Yang-hua  XU Bin  CHAI Yi  JI Chen-xing  ZHU Xin-gen 《园艺学报》2017,33(2):263-270

AIM: To study the effect of centromere protein W (CENP-W) down-regulation on human glioma U87 cells.METHODS: Small interfering RNA (siRNA) was used to inhibit the expression of CENP-W in the U87 cells. The interference effect of siRNA was evaluated by RT-qPCR and Western blot. The proliferation of the cells was analyzed by MTT assay, BrdU staining and colony formation experiment. Transwell chamber assay was used to detect the invasion ability of the cells. The cell migration ability was measured by a scratch test. The changes of the cell cycle distribution and apoptosis were analyzed by flow cytometry.RESULTS: The results of MTT assay, colony formation experiment and BrdU staining showed that the cell proliferation and colony formation abilities in experimental group were significantly lower than those in control group and negative control group. The results of Transwell and scratch experiments showed that the migration and invasion abilities in experimental group were weaker than those in blank control group and negative control group. The results of flow cytometry analysis showed that the cell cycle distribution in experimental group was arrested in G₀/G₁ phase. The percentage of apoptotic cells in experimental group was higher than that in control group (P<0.05).CONCLUSION: Down-regulation of CENP-W expression inhibits the proliferation, migration and invasion of human glioma cells and promotes the apoptosis of the cells, suggesting that CENP-W may be a potential target of gene therapy for human glioma.  相似文献   

Involvement of TLR4/NLRP3 inflammasome in contrast medium-induced inflammation and injury in renal tubular epithelial cells     

LIN Yan  LIN Jia-qiong  XIE Chu-li  GUAN Xiao-feng  TAN Xue-xian  HUANG Ze-na 《园艺学报》2017,33(12):2252-2258

AIM: To investigate whether Toll-like receptor 4 (TLR4) and Nod-like receptor protein 3 (NLRP3) inflammasome were involved in contrast medium (CM)-induced inflammation and injury in renal tubular epithelial cells. METHODS: Iopromide was used to injure NRK-52E cells in the study. The cell viability was measured by CCK-8 assay. The protein levels of TLR4, NLRP3, apoptosis-associated speckle-like protein (ASC), caspase-1 and cleaved caspase-3 were determined by Western blot. The releases of interleukin (IL)-1β and IL-18 were detected by ELISA. The apoptotic rate was evaluated by Hoechst staining, and mitochondrial membrane potential (MMP) was analyzed by JC-1 staining. siRNA was transfected into the NRK-52E cells to silence NLRP3 expression. RESULTS: CM decreased the viability of NRK-52E cells (P<0.05). CM also elevated the protein levels of cleaved caspase-3, TLR4, NLRP3, IL-1β and IL-18 (P<0.05). Silencing NLRP3 attenuated CM-induced releases of inflammatory cytokines. Moreover, treatment with TLR4 inhibitor TAK-242 or knockdown of NLRP3 by siRNA transfection both attenuated cell apoptosis and loss of MMP caused by CM. CONCLUSION: TLR4/NLRP3 inflammasome takes part in the pathogenesis of CM-induced acute kidney injury, and mediates CM-induced injury and inflammation in renal tubular epithelial cells.  相似文献   

Correlation between Mnk2 protein expression and prognosis of patients with esophageal squamous cell carcinoma     

ZENG Bo  FU Min-yi  FENG Yan-fen  HAN Xiang-qian  ZOU Da-wei  LUO Hong-he  LEI Yi-yan 《园艺学报》2017,33(10):1864-1868

AIM: To investigate the protein expression of mitogen-activated protein kinase-interacting kinase-2 (Mnk2) and its prognostic effect in the patients with resected esophageal squamous cell carcinoma (ESCC). METHODS: A total of 86 informative patients with surgically resected ESCC and 54 normal esophageal tissues were enrolled. Western blot and immunohistochemistry (IHC) were utilized to assess the protein expression of Mnk2, and its correlation with prognosis was statistically analyzed by the methods of Kaplan-Meier curve and Cox proportional hazard mode. RESULTS: The protein expression of Mnk2 was elevated in most of tumor tissues compared with the adjacent tissues. Clinicopathologic analysis showed that Mnk2 expression was significantly correlated with the TNM stage (P<0.05). Both disease-free survival (DFS) and overall survival (OS) of Mnk2 over-expression patients were shorter than those in Mnk2 negative expression group. Multivariate analysis confirmed that Mnk2 expression, as an independent and significant factor for both DFS and OS, predicted a poor prognosis of the patients with resected ESCC (P<0.05). CONCLUSION: The expression of Mnk2 was significantly related to the TNM stages, and might be a novel predictor for prognosis in ESCC.  相似文献