期刊文献+
共找到7篇文章
< 1 >
每页显示 20 50 100
Preliminary Study on Geographical Distribution and Evolutionary Relationships Between Cultivated and Wild Adzuki Bean (Vigna angular is var. angularis and var. nipponensis) by AFLP Analysis 被引量:1
1
作者 ZONGXu-xiao DuncanVaughan +4 位作者 NorihikoTomooka AkitoKaga WANGXin-wang GUANJian-ping WANGShu-min 《Agricultural Sciences in China》 CAS CSCD 2003年第4期368-376,共9页
A set of representative 146 adzuki (Vigna angular is var. angularis, and var. nipponensis) germplasm from 6 Asian countries traditionally for adzuki bean production, together with an out group standard rice bean (Vign... A set of representative 146 adzuki (Vigna angular is var. angularis, and var. nipponensis) germplasm from 6 Asian countries traditionally for adzuki bean production, together with an out group standard rice bean (Vigna umbellata), were analyzed by AFLP methodology using 12 informative primer pairs. 313 unambiguous polymorphic bands were created. According to the dendrogram by cluster analysis based on AFLP banding, 143 of the accessions were distinct and revealed enough genetic diversity for identification and classification of accessions within Vigna angularis. A neighbor joining tree was generated using newly developed Innan's nucleotide diversity estimate from the AFLP data. From analysis, 7 distinct evolutionary groups, named as "Chinese cultivated", "Japanese cultivated", "Japanese complex-Korean cultivated", "Chinese wild", "China Taiwan wild", "Nepal-Bhutan cultivated" and "Hymalayan wild", were detected. Nucleotide diversity with geographical distribution of each group is discussed, regarding the evolutionary relationships between wild and cultivated adzuki beans. The preliminary results indicated that cultivated adzuki bean should be domesticated from at least 4 progenitors in at least 3 geographical origins. 展开更多
关键词 Adzuki bean (vigna angularis) AFLP Genetic diversity Geographical distribution Evolutionary relationships
下载PDF
小豆Dirigent基因家族鉴定及锈菌侵染对不同成员表达的影响 被引量:3
2
作者 柯希望 苑梦琦 +3 位作者 徐晓丹 殷丽华 郭永霞 左豫虎 《作物学报》 CAS CSCD 北大核心 2022年第11期2774-2785,共12页
为明确Dirigent (DIR)基因在小豆抗锈病中的作用,采用生物信息学方法,对小豆DIR基因家族(VaDIRs)进行了全基因组鉴定,结果发现小豆中共有33个DIR基因,其中29个成员分别定位在8条染色体上,系统进化分析表明,VaDIRs包括DIR-a、DIR-b/d、DI... 为明确Dirigent (DIR)基因在小豆抗锈病中的作用,采用生物信息学方法,对小豆DIR基因家族(VaDIRs)进行了全基因组鉴定,结果发现小豆中共有33个DIR基因,其中29个成员分别定位在8条染色体上,系统进化分析表明,VaDIRs包括DIR-a、DIR-b/d、DIR-e和DIR-f四个亚家族,对VaDIRs成员启动子区顺式作用元件的分析发现,VaDIRs启动子区均包含激素、病原体应答等元件。对小豆抗锈病品种接种后不同时间的转录组数据分析发现,差异表达基因中共有17个VaDIRs成员,其中6个于接种后24 h显著上调,2个于接种后24 h和48 h均高量表达。进一步应用qRT-PCR技术对上述8个基因在抗、感品种中应答锈菌侵染的表达分析表明,高抗品种中VaDIR14、VaDIR16和VaDIR33的表达量在锈菌侵染不同阶段均显著高于感病品种。上述结果表明,VaDIRs家族成员可作为正调节因子参与小豆对锈病的抗性。 展开更多
关键词 小豆(vigna angularis) 小豆锈病 豇豆单胞锈菌(Uromyces vignae) DIR基因 基因家族
下载PDF
The Sequence Variations of Intron-3 of the α-Amylase Gene in Adzuki Bean 被引量:2
3
作者 JINWen-lin YamaguchiHirofumi +1 位作者 IsigamiMatiko YasudaKentaro 《Agricultural Sciences in China》 CAS CSCD 2003年第10期1076-1082,共7页
This study describes variation of intron-3 of α-amylase gene from 156 breeds of adzuki beans using SSCP(single-strand conformation polymorphism)analysis. Based on α-amylase gene structure and sequence, A pair of P... This study describes variation of intron-3 of α-amylase gene from 156 breeds of adzuki beans using SSCP(single-strand conformation polymorphism)analysis. Based on α-amylase gene structure and sequence, A pair of PCR primers, F (CCTACATTCTAACACACCCT) and R (GCATATTGTGCCAGTACAAT) were designed to amplify intron-3 fragments of α-amylase gene. 14 variant types were detected, including 13, 9, 10, 4 variant types in the wild, weed, locally cultivated and modern brought-up adzuki beans respectively, 9, 8, 7 variant types of the wild adzuki beans from Japan, China and Korea respectively, and some other variant types in the local adzuki beans from China and Bhutan. 60% of subjects of cultivated races were found to be EE type in the experiment. In addition, sequence analysis of intron-3 of α-amylase gene from 8 variant types reveals the evolution process of various variant types in adzuki beans. 展开更多
关键词 Adzuki bean (vigna angularis) SSCP (single-strand conformation polymorphism) α- Amylase gene INTRON VARIATION
下载PDF
Construction of a high-density adzuki bean genetic map and evaluation of its utility based on a QTL analysis of seed size 被引量:1
4
作者 WANG Li-xia WANG Jie +7 位作者 LUO Gao-ling YUAN Xing-xing GONG Dan HU Liang-liang WANG Su-hua CHEN Hong-lin CHEN Xin CHENG Xu-zhen 《Journal of Integrative Agriculture》 SCIE CAS CSCD 2021年第7期1753-1761,共9页
Adzuki bean(Vigna angularis(Willd.)Ohwi&Ohashi)is an annual cultivated leguminous crop commonly grown in Asia and consumed worldwide.However,there has been limited research regarding adzuki bean genetics,which has... Adzuki bean(Vigna angularis(Willd.)Ohwi&Ohashi)is an annual cultivated leguminous crop commonly grown in Asia and consumed worldwide.However,there has been limited research regarding adzuki bean genetics,which has prevented the efficient application of genes during breeding.In the present study,we constructed a high-density genetic map based on whole genome re-sequencing technology and validated its utility by mining QTLs related to seed size.Moreover,we analyzed the sequences flanking insertions/deletions(In Dels)to develop a set of PCR-based markers useful for characterizing adzuki bean genetics.A total of 2904 markers were mapped to 11 linkage groups(LGs).The total length of the map was 1365.0 cM,with an average distance between markers of 0.47 cM.Among the LGs,the number of markers ranged from 208(LG7)to 397(LG1)and the total distance ranged from 97.4 cM(LG9)to 155.6 cM(LG1).Twelve QTLs related to seed size were identified using the constructed map.The two major QTLs in LG2 and LG9 explained 22.1 and 18.8%of the total phenotypic variation,respectively.Ten minor QTLs in LG4,LG5 and LG6 explained 3.0–10.4%of the total phenotypic variation.A total of 9718 primer pairs were designed based on the sequences flanking In Dels.Among the 200 selected primer pairs,75 revealed polymorphisms in 24 adzuki bean germplasms.The genetic map constructed in this study will be useful for screening genes related to other traits.Furthermore,the QTL analysis of seed size and the novel markers described herein may be relevant for future molecular investigations of adzuki bean and will be useful for exploiting the mechanisms underlying legume seed development. 展开更多
关键词 vigna angularis genetic map QTL seed size PCR-based marker development
下载PDF
小豆不定芽诱导及再生体系的建立 被引量:1
5
作者 林建辉 陆玉建 +3 位作者 张永磊 李震 朱丽晖 石东里 《湖北农业科学》 2019年第24期236-239,245,共5页
以小豆(Vigna angularis)下胚轴为外植体,分析影响小豆不定芽诱导及植株再生的因素,建立高效稳定的小豆离体再生体系。结果表明,小豆不定芽诱导最适培养基为MS+2.0 mg/L 6-BA;生根最适培养基为1/2MS+0.5 mg/L IBA。
关键词 小豆(vigna angularis) 胚轴 不定芽 生根 再生
下载PDF
小豆缺铁突变体分离群体叶色及产量性状分析
6
作者 晁兴晨 顾忠珺 +4 位作者 万平 杨凯 曹劲宏 赵波 李奕松 《分子植物育种》 CAS 北大核心 2024年第2期503-511,共9页
为了鉴定小豆铁吸收代谢突变体作图群体叶色性状的变异及其对产量的影响,本研究调查了‘河北801’(耐缺铁野生型)×FMY011(缺铁敏感突变体)和MY076(耐缺铁突变体)×GM352(缺铁敏感资源)的F_(2)分离群体的叶色分离情况,测定了叶... 为了鉴定小豆铁吸收代谢突变体作图群体叶色性状的变异及其对产量的影响,本研究调查了‘河北801’(耐缺铁野生型)×FMY011(缺铁敏感突变体)和MY076(耐缺铁突变体)×GM352(缺铁敏感资源)的F_(2)分离群体的叶色分离情况,测定了叶绿素SPAD值,并分析了其与单株产量及其他农艺性状的相关性。F_(2)群体分离出新叶黄化和正常单株,其叶绿素SPAD值差异极显著。相关性分析显示SPAD值与单株产量、单株荚数、百粒重呈极显著正相关,缺铁引起的新叶黄化会降低小豆产量。缺铁胁迫验证田间叶色分离表型,结果显示‘河北801’×FMY011群体的叶色表型与田间叶色分离符合度高,新叶黄化F_(2)单株的F_(2:3)家系全部黄化,新叶绿色F_(2)单株胁迫下其96.62%F_(2:3)家系表现正常绿叶或呈杂合叶色分离,3.38%新叶绿色F_(2)单株胁迫下其F_(2:3)家系新叶黄化,表型不符合。MY076×GM352分离群体,田间正常叶色与缺铁胁迫鉴定的叶色一致,但田间新叶黄化F_(2)单株胁迫下仅有36.07%的F_(2:3)家系仍新叶黄化,60.66%新叶黄化F_(2)单株胁迫下其F_(2:3)家系表现为杂合叶色分离,3.28%新叶黄化F_(2)单株胁迫下其F_(2:3)家系叶色正常表型不符合。本研究为进一步定位克隆小豆中铁吸收代谢相关基因和铁生物强化育种提供了基础材料。 展开更多
关键词 小豆(vigna angularis L.) 叶色分离群体 缺铁 相关分析
原文传递
小豆VaWRKY33基因克隆及其响应锈菌侵染的表达分析 被引量:3
7
作者 殷丽华 杨阳 +3 位作者 柯希望 崔素萍 张金鹏 左豫虎 《分子植物育种》 CAS CSCD 北大核心 2020年第22期7301-7308,共8页
为明确小豆VaWRKY33基因对抗锈病的作用,本研究以小豆基因组DNA为模板克隆了该基因全长。VaWRKY33的基因序列全长2 442 bp,包含4个内含子,编码区全长1 620 bp,编码539个氨基酸。VaWRKY33蛋白质相对分子质量为60.16 kD,理论等电点为7.66... 为明确小豆VaWRKY33基因对抗锈病的作用,本研究以小豆基因组DNA为模板克隆了该基因全长。VaWRKY33的基因序列全长2 442 bp,包含4个内含子,编码区全长1 620 bp,编码539个氨基酸。VaWRKY33蛋白质相对分子质量为60.16 kD,理论等电点为7.66,属于亲水性不稳定蛋白,有一个跨膜结构域,包含蛋白磷酸化位点85个。蛋白序列分析表明,VaWRKY33包含两个保守的WRKY结构域,锌指结构类型为C2H2型,属WRKY转录因子家族GroupⅠ亚家族。VaWRKY33启动子区分析发现,除核心作用元件外,主要包括光响应、逆境及组织特异性等三类顺式作用元件。基因表达分析表明,VaWRKY33在抗病品种‘庆红1号’(QH1)上于接种病菌12 h时开始显著上调,并在整个侵染过程中始终显著高于不接种对照;在感病品种‘宝清红’(BQH)上于接种病菌48~192 h时,VaWRKY33基因显著上调表达,但其响应时间较抗病品种明显滞后,推测VaWRKY33在病菌侵染早期的迅速响应在小豆抗锈菌侵入阶段发挥正调控作用。 展开更多
关键词 小豆(vigna angularis) 小豆锈病 豇豆单胞锈菌(Uromyces vignae) 转录因子
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部