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桑树绿枝扦插生根过程中乙烯合成相关基因aco和sams的表达分析 被引量:5
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作者 聂浩 焦锋 +3 位作者 张晓峰 李小玉 唐壮 程嘉翎 《蚕业科学》 CAS CSCD 北大核心 2013年第4期633-637,共5页
植物内源乙烯对愈伤组织的诱导、增殖,不定芽、不定根的形成以及体细胞胚的诱导等过程都会产生重要的影响。利用荧光定量PCR技术检测诱导桑树绿枝插穗基部皮层生根过程中与乙烯合成相关的1-氨基-羧酸环丙烷氧化酶基因aco和S-腺苷-L-蛋... 植物内源乙烯对愈伤组织的诱导、增殖,不定芽、不定根的形成以及体细胞胚的诱导等过程都会产生重要的影响。利用荧光定量PCR技术检测诱导桑树绿枝插穗基部皮层生根过程中与乙烯合成相关的1-氨基-羧酸环丙烷氧化酶基因aco和S-腺苷-L-蛋氨酸合成酶基因sams的转录水平变化。结果表明插穗生根发育过程中aco和sams均表现为表达下调,其中生根率低的未诱导对照组插穗中这2个基因的转录水平均表现出先小幅下降后升高的变化特点,而生根率高的诱导组插穗中这2个基因则表现为持续低水平转录,尤其在插穗生根发育后期,2个基因在2个试验组插穗中的转录水平变化呈现近乎相反的变化特点。研究结果初步说明,乙烯合成相关基因aco和sams的mRNA转录水平与桑树绿枝插穗的生根率呈现负相关性。 展开更多
关键词 桑树 扦插 生根率 内源乙烯 1-氨基-羧酸环丙烷氧化酶基因 S-腺苷-L-蛋氨酸合成酶基因 实时荧光定量PCR
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斑茅ACO基因(aco)的克隆及其在水分胁迫下的表达(英文) 被引量:5
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作者 张积森 李伟 +3 位作者 阮妙鸿 阙友雄 陈如凯 张木清 《热带作物学报》 CSCD 2007年第2期60-68,共9页
利用RT-PCR技术,首次克隆了斑茅1-氨基环丙烷-1-羧酸氧化酶基因序列.该片段长度为1123bp的片段,包括1个编码322个氨基酸的完整开放读码框,包括具有与异青霉素合成酶功能区类似的氧化功能PcbC区,和1个Fe2+和CO2活性中心。应用实时荧光PC... 利用RT-PCR技术,首次克隆了斑茅1-氨基环丙烷-1-羧酸氧化酶基因序列.该片段长度为1123bp的片段,包括1个编码322个氨基酸的完整开放读码框,包括具有与异青霉素合成酶功能区类似的氧化功能PcbC区,和1个Fe2+和CO2活性中心。应用实时荧光PCR技术分析了1-氨基环丙烷-1-羧酸氧化酶基因在聚乙二醇胁迫下4个时段的表达。结果表明,聚乙二醇胁迫2h时,该基因在叶片明显上调表达,4h后的表达趋向平缓。本研究为1-氨基环丙烷-1-羧酸氧化酶基因进一步用于基因工程研究奠定基础,同时也初步揭示1-氨基环丙烷-1-羧酸氧化酶基因的表达与水分胁迫相互关系,为探讨乙烯对水分胁迫响应的分子机制提供了初步依据。 展开更多
关键词 斑茅 1-氨基环丙烷-1-羧酸氧化酶基因(aco基因 aco) RT-PCR 实时荧光定量PCR 聚乙二醇胁迫
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外源ABA和乙烯利胁迫下斑茅ACO基因表达的实时PCR分析 被引量:3
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作者 郭春芳 张积森 +1 位作者 张木清 陈如凯 《中国农学通报》 CSCD 2008年第2期48-52,共5页
研究了外源ABA和乙烯利胁迫处理对斑茅1-氨基环丙烷-1-羧酸氧化酶基因(ACO基因)表达情况的影响。在项目组克隆斑茅ACO基因的基础上,应用实时荧光PCR技术分析斑茅ACO基因在A-BA、乙烯利胁迫下的表达。结果表明,斑茅ACO基因在ABA的胁迫下,... 研究了外源ABA和乙烯利胁迫处理对斑茅1-氨基环丙烷-1-羧酸氧化酶基因(ACO基因)表达情况的影响。在项目组克隆斑茅ACO基因的基础上,应用实时荧光PCR技术分析斑茅ACO基因在A-BA、乙烯利胁迫下的表达。结果表明,斑茅ACO基因在ABA的胁迫下,在3h有微弱上调表达,而6h时明显抑制,其后表达趋向平缓;在乙烯利的胁迫下,ACO基因在前期受抑制,其后呈明显上调表达,在24h后ACO基因的表达趋向平缓。斑茅ACO基因的表达受乙烯利诱导,而不受外源ABA诱导。 展开更多
关键词 斑茅 1-氨基环丙烷-1-羧酸氧化酶基因(aco基因) 脱落酸 乙烯利 实时荧光PCR
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大蒜内参基因筛选及AsACO基因对盐胁迫和促生菌的响应分析 被引量:1
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作者 王启璋 张祥林 +1 位作者 韩睿 田洁 《南方农业学报》 CAS CSCD 北大核心 2022年第12期3297-3306,共10页
【目的】筛选大蒜在盐胁迫下的稳定内参基因,并分析1-氨基环丙烷-1-羧酸氧化酶基因(AsACO)对盐胁迫和促生菌的响应表达特性,为深入探究促生菌的促生机制及大蒜对盐胁迫的响应机制研究提供理论参考。【方法】以乐都紫皮大蒜为试材,采用... 【目的】筛选大蒜在盐胁迫下的稳定内参基因,并分析1-氨基环丙烷-1-羧酸氧化酶基因(AsACO)对盐胁迫和促生菌的响应表达特性,为深入探究促生菌的促生机制及大蒜对盐胁迫的响应机制研究提供理论参考。【方法】以乐都紫皮大蒜为试材,采用实时荧光定量PCR(qRT-PCR)检测5个内参基因ACT、UBC、HIS3、18S rRNA、TUB在盐胁迫下的表达稳定性,结合GeNorm、NormFinder和BestKeeper筛选出最稳定的内参基因,并分析恶臭假单胞菌UW4对盐胁迫下AsACO基因表达的影响。【结果】5个候选内参基因引物的特异性强、无引物二聚体。GeNorm分析得出候选内参基因稳定性排名为18S rRNA=TUB>HIS3>UBC>ACT,NormFinder分析得出内参基因稳定性排名为18S rRNA>HIS3>TUB>UBC>ACT,BestKeeper分析得出内参基因稳定性排名为UBC>HIS3>18S rRNA>TUB>ACT,最终以几何平均数综合分析得出18S rRNA为最稳定的内参基因。以18S rRNA为内参基因,检测出AsACO基因表达具有明显的组织特异性,在叶片中的相对表达量明显高于根。整个处理过程中,盐胁迫明显诱导AsACO基因在不同处理时间及不同组织中表达上调,根和叶片中AsACO基因的相对表达量分别在2 d和12 h时达最高,较正常培养(CK)分别显著升高124.43%和238.34%(P<0.05,下同),与盐胁迫处理相比,盐胁迫+浇施恶臭假单胞菌UW4处理显著降低AsACO基因在不同处理时间根和叶片中的相对表达量,其中在2 d和12 h时降幅较大,分别降低了112.08%和343.34%。【结论】18S rRNA是盐胁迫下大蒜中最稳定的内参基因。盐胁迫可诱导大蒜根和叶片中AsACO基因的上调表达,从而间接促进ACO和乙烯水平升高,加速由乙烯调控的细胞衰老,甚至死亡,但盐胁迫下恶臭假单胞UW4具有抑制AsACO基因表达的作用,以减少ACO和乙烯的合成,从而延缓大蒜细胞衰老,提高逆境耐受性。 展开更多
关键词 大蒜 盐胁迫 内参基因 1-氨基环丙烷-1-羧酸氧化酶(aco) 恶臭假单胞菌UW4
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Functional mechanism study of the allelochemical myrigalone A identifies a group of ultrapotent inhibitors of ethylene biosynthesis in plants
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作者 George Heslop-Harrison Kazumi Nakabayashi +7 位作者 Ana Espinosa-Ruiz Francesca Robertson Robert Baines Christopher R.L.Thompson Katrin Hermann David Alabadí Gerhard Leubner-Metzger Robin S.B.Williams 《Plant Communications》 SCIE CSCD 2024年第6期246-262,共17页
Allelochemicals represent a class of natural products released by plants as root,leaf,and fruit exudates that interfere with the growth and survival of neighboring plants.Understanding how allelochemicals function to ... Allelochemicals represent a class of natural products released by plants as root,leaf,and fruit exudates that interfere with the growth and survival of neighboring plants.Understanding how allelochemicals function to regulate plant responses may provide valuable new approaches to better control plant function.One such allelochemical,Myrigalone A(MyA)produced by Myrica gale,inhibits seed germination and seedling growth through an unknown mechanism.Here,we investigate MyA using the tractable modelDictyostelium discoideum and reveal that its activity depends on the conserved homolog of the plant ethylenesynthesis protein 1-aminocyclopropane-1-carboxylic acid oxidase(ACO).Furthermore,in silico modeling predicts the direct binding of MyA to ACO within the catalytic pocket.In D.discoideum,ablation of ACO mimics the MyA-dependent developmental delay,which is partially restored by exogenous ethylene,and MyA reduces ethylene production.In Arabidopsis thaliana,MyA treatment delays seed germination,and this effect is rescued by exogenous ethylene.It also mimics the effect of established ACO inhibitors on root and hypocotyl extension,blocks ethylenedependent root hair production,and reduces ethylene production.Finally,in silico binding analyses identify a rangeof highlypotentethylene inhibitorsthatblock ethylene-dependent responseand reduce ethyleneproduction in Arabidopsis.Thus,we demonstrate a molecular mechanism by which the allelochemical MyA reduces ethylene biosynthesis and identify a range of ultrapotent inhibitors of ethylene-regulated responses. 展开更多
关键词 1-aminocyclopropane-1-carboxylic acid ACC ACC oxidase aco ALLELOCHEMICALS ethylene synthesis inhibitors structure-activity relationship
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Exogenous ethylene influences flower opening of cut roses (Rosa hybrida) by regulating the genes encoding ethylene biosynthesis enzymes 被引量:22
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作者 MA Nan1, CAI Lei1, LU Wangjin2, TAN Hui1 & GAO Junping1 1. Department of Ornamental Horticulture and Landscape Architecture, China Agricultural University, Beijing 100094, China 2. Department of Horticulture, South China Agricultural University, Guangzhou 510642,China 《Science China(Life Sciences)》 SCIE CAS 2005年第5期434-444,共11页
The purpose of this paper is to investigate the differential responses of flower opening to ethylene in two cut rose cultivars, ‘Samantha’, whose opening process is promoted, and ‘Kardinal’, whose opening process ... The purpose of this paper is to investigate the differential responses of flower opening to ethylene in two cut rose cultivars, ‘Samantha’, whose opening process is promoted, and ‘Kardinal’, whose opening process is inhibited by ethylene. Ethylene production and 1- aminocyclopropane-1-carboxylate (ACC) synthase and oxidase activities were determined first. After ethylene treatment, ethylene production, ACC synthase (ACS) and ACC oxidase (ACO) activities in petals increased and peaked at the earlier stage (stage 3) in ‘Samantha’, and they were much more dramatically enhanced and peaked at the later stage (stage 4) in ‘Kardinal’ than control during vasing. cDNA fragments of three Rh-ACSs and one Rh- ACO genes were cloned and designated as Rh-ACS1, Rh-ACS2, Rh-ACS3 and Rh-ACO1 respectively. Northern blotting analysis revealed that, among three genes of ACS, ethylene-in- duced expression patterns of Rh-ACS3 gene corresponded to ACS activity and ethylene production in both cultivars. A more dramatic accumulation of Rh-ACS3 mRNA was induced by ethylene in ‘Kardinal’ than that of ‘Samantha’. As an ethylene action inhibitor, STS at concentration of 0.2 mmol/L generally inhib-ited the expression of Rh-ACSs and Rh-ACO in both cultivars, although it induced the expression of Rh-ACS3 transiently in ‘Kardinal’. Our results suggests that ‘Kardinal’ is more sensitive to ethylene than ‘Samantha’; and the changes of Rh-ACS3 expression caused by ethylene might be related to the acceleration of flower opening in ‘Samantha’ and the inhibition in ‘Kardinal’. Additional results indicated that three Rh-ACSs genes were differentially associated with flower opening and senescence as well as wounding. 展开更多
关键词 cut ROSE (Rosa hybrida) FLOWER opening ethylene 1-aminocyclopropane-1-carboxylic acid (ACC) ACC SYNTHASE (ACS) ACC oxidase (aco) gene expression.
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