期刊文献+
共找到5篇文章
< 1 >
每页显示 20 50 100
分子鉴定拟南芥myb26/mail sterile35突变体中表达下调基因At2g47500 被引量:1
1
作者 樊新萍 乔永胜 +1 位作者 牛西午 Zoe A Wilson 《华北农学报》 CSCD 北大核心 2014年第5期71-79,共9页
利用不可产生花粉的突变体作为研究花药和花粉发育的途径,以证实涉及花粉发育的基因及其在基因网络中的作用。研究结果表明,拟南芥中MYB26/MALE STERILE35(MS35)雄性不育基因会调控药室内壁次生加厚发育,影响其后的花药开裂,并可上调木... 利用不可产生花粉的突变体作为研究花药和花粉发育的途径,以证实涉及花粉发育的基因及其在基因网络中的作用。研究结果表明,拟南芥中MYB26/MALE STERILE35(MS35)雄性不育基因会调控药室内壁次生加厚发育,影响其后的花药开裂,并可上调木质素生物合成途径。而At2g47500基因是在芯片分析ms35/myb26突变体中涉及花粉发育表达下调的一个未被鉴定的基因。通过生物信息学分析发现,At2g47500基因是一个与微管发育有关的基因,在整个植株都表达,包括花发育阶段。利用拟南芥基因库筛选该基因中的T-DNA插入突变体,并通过PCR鉴定,得到插入位点在启动子和外显子的纯合突变体。通过表型分析和表达筛选发现,At2g47500突变并未对表现型产生影响,表明T-DNA插入位点在外显子的突变体基因并未在花药中表达;但转录表达分析认为,该基因在花粉里表达,并通过启动子:GUS表达结构得到进一步证实。35S启动子超量表达At2g47500,并未导致其在野生型植物中异位的过量表达;将其转入突变体中,基因表达量恢复,也未有表现差异。说明其对花粉发育的影响不明显。定量PCR分析微管发育其他相关基因,以及花发育中次生壁发育有关基因在突变体中的表达,At2g47500对花粉发育影响不明显。在突变体中,大部分基因也未因其缺失、表达受到明显影响。综上所述,该基因在花药发育中不受ms35/myb26的调控,发挥次要作用,受到主效基因的调控。 展开更多
关键词 At2g47500 ms35/myb26 分子鉴定 GUS表达 超量表达
在线阅读 下载PDF
拟南芥35S:MS606/myb26转基因植物的鉴定 被引量:6
2
作者 宋欣 赵淑清 《山西农业科学》 2017年第5期680-683,共4页
ms606是山西大学植物生殖发育实验室创制的雄性不育突变体,该突变体具有药室内壁次生加厚缺陷,导致花药不能开裂。而转录因子MYB26在药室内壁次生加厚过程中发挥着重要的调控作用。为了研究MS606和MYB26之间的关系,我们将35S:MS606融合... ms606是山西大学植物生殖发育实验室创制的雄性不育突变体,该突变体具有药室内壁次生加厚缺陷,导致花药不能开裂。而转录因子MYB26在药室内壁次生加厚过程中发挥着重要的调控作用。为了研究MS606和MYB26之间的关系,我们将35S:MS606融合基因在农杆菌介导下转化植物myb26/MYB26杂合体,通过潮霉素抗性筛选,结果获得T1转化植株;并通过在基因组水平的PCR检测和RNA水平的半定量RT-PCR检测,获得纯合的35S:MS606/myb26转基因植株。该材料的获得为深入研究MS606和MYB26基因在调控药室内壁次生加厚途径中的关系奠定了良好基础。 展开更多
关键词 拟南芥 转基因 MS606 myb26 基因表达
在线阅读 下载PDF
Domestication-related changes at PvMYB26 reduce pod shattering in common bean and shed light on the origins of agriculture in the Americas
3
作者 Burcu Celebioglu Jayanta Roy +6 位作者 Andrew Farmer Stephanie English Xingyao Yu Xiaosa Xu Phillip E.McClean Paul Gepts Travis A.Parker 《Molecular Plant》 2026年第2期313-327,共15页
Domestication imposed radical selection pressures on plants,transforming them into crops that support global populations today.In this study,we investigate the loss of seed dispersal via pod shattering during common b... Domestication imposed radical selection pressures on plants,transforming them into crops that support global populations today.In this study,we investigate the loss of seed dispersal via pod shattering during common bean(Phaseolus vulgaris L.)domestication.We identified PvMYB26 mutations in all three main gene pools of common bean,including an 8 kb deletion in Middle American lines eliminating the gene’s transcription start site and promoter,a frameshift/truncation deletion in the independently domesticated Andean population,and another frameshift/truncation insertion in the genetic background of the‘‘undomesticated’’debouckii population.Mutants with the 8 kb deletion express PvMYB26 at<1%of the level of wild types and produce 44%less pod lignin.RNA in situ hybridization and fluorescence microscopy showed that PvMYB26 is expressed in the lignified fiber layer of pods,while mutants showed no visible expression and a greatly reduced fiber layer.Sequencing of 327 accessions revealed that the mutation is nearly diagnostic for domestication status among Middle American common bean and identified a 125 kb hard selective sweep,indicating the gene’s importance in domestication.The main Andean frameshift mutation was found in 84.5%of Andean domesticates but 0%of wild lines,while the debouckii truncation was identified in six domesticated lines of race Peru,suggesting that a third proto-domestication of common bean may have occurred in Ecuador and/or northern Peru.Wild haplotypes most like Middle American domesticates were found in eastern Jalisco,Mexico,strongly suggesting west-central Mexico as the site of common bean domestication and the rise of agriculture in Middle America. 展开更多
关键词 plant domestication crop evolution Phaseolus vulgaris L. myb26 population genetics fruit dehiscence
原文传递
拟南芥amiR-RUS4 ms35雄性不育双突变体的构建、鉴定及表型分析
4
作者 董晶晶 赵淑清 《山西农业科学》 2016年第5期583-586,共4页
控制雄性育性是研究植物生殖和选择育种的一个重要目标。对雄性不育分子机制的深入理解将为控制雄性育性和杂种繁育提供有效途径。利用人工micro RNA技术对DUF647蛋白家族成员RUS4基因进行特异沉默,结果发现,ami R-RUS4植株败育,药室内... 控制雄性育性是研究植物生殖和选择育种的一个重要目标。对雄性不育分子机制的深入理解将为控制雄性育性和杂种繁育提供有效途径。利用人工micro RNA技术对DUF647蛋白家族成员RUS4基因进行特异沉默,结果发现,ami R-RUS4植株败育,药室内壁次生加厚异常,花药不开裂,表明RUS4与药室内壁的木质化有关。MS35/MYB26是木质素生物合成途径上游一个重要的激活因子,为了进一步了解RUS4和MYB26在调控花药药室内壁次生加厚过程中的作用,以ms35为母本、ami R-RUS4为父本进行人工杂交,得到杂交子2代(F2);并对杂交子2代(F2)的基因型、表型和基因表达进行了鉴定,结果获得一个纯合的ami R-RUS4 ms35双突变体,这为进一步分析RUS4和MS35在调控药室内壁次生加厚中的作用提供了宝贵的试验材料。 展开更多
关键词 拟南芥 雄性不育 RUS4 myb26
在线阅读 下载PDF
The regulatory mechanism of rapid lignification for timely anther dehiscence 被引量:1
5
作者 Jing-Shi Xue Yi-Feng Feng +7 位作者 Ming-Qi Zhang Qin-Lin Xu Ya-Min Xu Jun-Qin Shi Li-Fang Liu Xiao-Feng Wu Shui Wang Zhong-Nan Yang 《Journal of Integrative Plant Biology》 SCIE CAS CSCD 2024年第8期1788-1800,共13页
Anther dehiscence is a crucial event in plant reproduction,tightly regulated and dependent on the lignification of the anther endothecium.In this study,we investigated the rapid lignification process that ensures time... Anther dehiscence is a crucial event in plant reproduction,tightly regulated and dependent on the lignification of the anther endothecium.In this study,we investigated the rapid lignification process that ensures timely anther dehiscence in Arabidopsis.Our findings reveal that endothecium lignification can be divided into two distinct phases.During Phase Ⅰ,lignin precursors are synthesized without polymerization,while Phase Ⅱ involves simultaneous synthesis of lignin precursors and polymerization.The transcription factors MYB26,NST1/2,and ARF17 specifically regulate the pathway responsible for the synthesis and polymerization of lignin monomers in Phase Ⅱ.MYB26-NST1/2 is the key regulatory pathway responsible for endothecium lignification,while ARF17 facilitates this process by interacting with MYB26.Interestingly,our results demonstrate that the lignification of the endothecium,which occurs within approximately 26 h,is much faster than that of the vascular tissue.These findings provide valuable insights into the regulation mechanism of rapid lignification in the endothecium,which enables timely anther dehiscence and successful pollen release during plant reproduction. 展开更多
关键词 anther dehiscence ARF17 endothecium LIGNIN myb26 NST
原文传递
上一页 1 下一页 到第
使用帮助 返回顶部