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RT-PCR Expression analysis of ACC oxidase gene and ACC synthase gene in melon leaf in field condition.

RT-PCR Expression analysis of ACC oxidase gene and ACC synthase gene in melon leaf in field condition.
RT-PCR 田间条件下甜瓜叶片 ACC 氧化酶基因和 ACC 合酶基因的表达分析
批准号:
08660041
负责人:
FURUKAWA Hajime
金额:
$0.9万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
1996
资助国家:
日本
项目状态:
已结题
起止时间:
1996 至 1997

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中文摘要
翻译
研究了大田条件下ME-ACS1和CM-ACO1基因在不同基因表达诱导剂诱导下的表达模式。(1)与甜瓜GAPDH基因相比,甜瓜肌动蛋白基因是有用的内参基因。(2)RT-PCR结果表明,在田间条件下,这两个基因的表达都受到伤害、IAA和乙烯的诱导。(3)这两个基因都受到热激胁迫(38゚C)的诱导,在10min内表达达到最大,在1h达到最大值,直到6h。(4)热激1h后,甜瓜平台恢复到25゚C,(5)在叶片衰老过程中,ME-ACS1mRNA水平不变,而CM-ACO1mRNA水平逐渐降低。
英文摘要
We investigated the expression pattem of the ME-ACS 1 and CM-ACO 1 genes in the response to various inducers of gene expression in field condition.(1) The melon actin gene is useful internal standard, compare with the melon GAPDH gene..(2) Results of RT-PCR showed that the expression of both genes were induced by wounding, IAA,Ethylene in field condition.(3) Both genes were induced by heat shock stress (38゚C) with in 10 min, expression reaching a maximum at 1 hr.and decreasing until 6 h.(4) After heat shock for 1h.melon plats were returned to 25゚C,ME-ACS 1 mRNA level gradually decreased, but level of CM-ACO 1 mRNA rewired high for 6 h.(5) ME-ACS 1 mRNA level was constant during leaf senescence, but CM-ACO 1 mRNA level was gradually decreased.
期刊论文(9)
专著(0)
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会议论文
古川一: "PCRによるメロンのACC合成酵素遺伝子の増幅" 園芸学会雑誌. 65別2. 288-289 (1996)
Hajime Furukawa:“通过PCR扩增甜瓜ACC合酶基因”日本园艺学会杂志65 Betsu 2. 288-289 (1996)。
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通讯作者:
Hajime FURUKAWA: "RT-PCR expression analysis of ACC synthasegene and ACC oxidase gene in melon leaf" Plat Cell Physiol.3S S4ppl.117-117 (1997)
Hajime FURUKAWA:“甜瓜叶中 ACC 合成酶基因和 ACC 氧化酶基因的 RT-PCR 表达分析”Plat Cell Physiol.3S S4ppl.117-117 (1997)
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Hajime FURUKAWA: "Tne melon polyubiguitin gene is inducel by HEat Shock" J.Japan.Soc.Hort.Sci.67S4ppl.1. 144-144 (1998)
Hajime FURUKAWA:“热休克诱导甜瓜多聚泛素基因”J.Japan.Soc.Hort.Sci.67S4ppl.1。
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