外源ABA在衰老康乃馨雌蕊中触发乙烯的作用:ABA含量的变化及ABA生物合成和作用基因的表达

Yoshihiro Nomura, T. Harada, S. Morita, S. Kubota, M. Koshioka, H. Yamaguchi, K. Tanase, M. Yagi, T. Onozaki, S. Satoh
{"title":"外源ABA在衰老康乃馨雌蕊中触发乙烯的作用:ABA含量的变化及ABA生物合成和作用基因的表达","authors":"Yoshihiro Nomura, T. Harada, S. Morita, S. Kubota, M. Koshioka, H. Yamaguchi, K. Tanase, M. Yagi, T. Onozaki, S. Satoh","doi":"10.2503/JJSHS1.82.242","DOIUrl":null,"url":null,"abstract":"In senescing carnation ( Dianthus caryophyllus L.) flowers, ethylene production begins in the gynoecium, and the resulting ethylene acts on petals, inducing autocatalytic ethylene production. We investigated the role of abscisic acid (ABA) in ethylene production in the gynoecium of flowers. First, cDNAs of major genes involved in ABA biosynthesis and signaling were cloned from carnation flower tissues. Then, changes in ABA content and gene expression of ABA biosynthesis and signaling in the ovary were examined using three cultivars, ‘Light Pink Barbara (LPB)’ and ‘Excerea’, whose cut flowers produce ethylene during senescence and have an ordinary vase-life of about one week, and ‘Miracle Rouge’, whose cut flowers produce no detectable ethylene during senescence and have a vase-life of about three weeks. ABA content in the ovary was 530–710 pmol·g − 1 fresh weight (FW) from Os 2 (early opening stage) to Os 6 (end of opening stage) in ‘LPB’, and at 200–380 pmol·g − 1 FW in ‘Excerea’ at the same stages; but 930 pmol·g − 1 FW at Ss 1 (early senescence stage). The ABA content remained at 70– 160 pmol·g − 1 FW in ‘Miracle Rouge’. The changes in ABA content were in parallel with the transcript levels of DcNCED1 (carnation gene for 9-cis -epoxycarotenoid dioxygenase). DcPYR1 (ABA receptor gene) transcript was 0.004–0.007 relative expression level (r.e.l.) in ‘LPB’ ovary at Os 1–Os 3, and 0.028 r.e.l. at Ss 1 (beginning of senescence stage). In ‘Excerea’ ovary, DcPYR1 transcript was 0.025–0.037 r.e.l. during flower opening and higher at Ss 1. By contrast, DcPYR1 transcript remained at 0.002–0.006 r.e.l. in ‘Miracle Rouge’ ovary during flower opening and senescence. The transcripts of DcACS1 , the key gene for ethylene biosynthesis, were detected at Ss 1 in ‘LPB’, and at Ss 2 in ‘Excerea’, but not in ‘Miracle Rouge’ throughout flower opening and senescence stages. These findings suggest that ABA plays a causal role in inducing the expression of the DcACS1 gene in the gynoecium, leading to ethylene biosynthesis, and that both the ABA content and DcPYR1 expression must be above putative threshold levels for ABA to exert its action.","PeriodicalId":17343,"journal":{"name":"Journal of The Japanese Society for Horticultural Science","volume":"82 1","pages":"242-254"},"PeriodicalIF":0.0000,"publicationDate":"2013-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"6","resultStr":"{\"title\":\"Role of ABA in Triggering Ethylene Production in the Gynoecium of Senescing Carnation Flowers: Changes in ABA Content and Expression of Genes for ABA Biosynthesis and Action\",\"authors\":\"Yoshihiro Nomura, T. Harada, S. Morita, S. Kubota, M. Koshioka, H. Yamaguchi, K. Tanase, M. Yagi, T. Onozaki, S. Satoh\",\"doi\":\"10.2503/JJSHS1.82.242\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"In senescing carnation ( Dianthus caryophyllus L.) flowers, ethylene production begins in the gynoecium, and the resulting ethylene acts on petals, inducing autocatalytic ethylene production. We investigated the role of abscisic acid (ABA) in ethylene production in the gynoecium of flowers. First, cDNAs of major genes involved in ABA biosynthesis and signaling were cloned from carnation flower tissues. Then, changes in ABA content and gene expression of ABA biosynthesis and signaling in the ovary were examined using three cultivars, ‘Light Pink Barbara (LPB)’ and ‘Excerea’, whose cut flowers produce ethylene during senescence and have an ordinary vase-life of about one week, and ‘Miracle Rouge’, whose cut flowers produce no detectable ethylene during senescence and have a vase-life of about three weeks. ABA content in the ovary was 530–710 pmol·g − 1 fresh weight (FW) from Os 2 (early opening stage) to Os 6 (end of opening stage) in ‘LPB’, and at 200–380 pmol·g − 1 FW in ‘Excerea’ at the same stages; but 930 pmol·g − 1 FW at Ss 1 (early senescence stage). The ABA content remained at 70– 160 pmol·g − 1 FW in ‘Miracle Rouge’. The changes in ABA content were in parallel with the transcript levels of DcNCED1 (carnation gene for 9-cis -epoxycarotenoid dioxygenase). DcPYR1 (ABA receptor gene) transcript was 0.004–0.007 relative expression level (r.e.l.) in ‘LPB’ ovary at Os 1–Os 3, and 0.028 r.e.l. at Ss 1 (beginning of senescence stage). In ‘Excerea’ ovary, DcPYR1 transcript was 0.025–0.037 r.e.l. during flower opening and higher at Ss 1. By contrast, DcPYR1 transcript remained at 0.002–0.006 r.e.l. in ‘Miracle Rouge’ ovary during flower opening and senescence. The transcripts of DcACS1 , the key gene for ethylene biosynthesis, were detected at Ss 1 in ‘LPB’, and at Ss 2 in ‘Excerea’, but not in ‘Miracle Rouge’ throughout flower opening and senescence stages. These findings suggest that ABA plays a causal role in inducing the expression of the DcACS1 gene in the gynoecium, leading to ethylene biosynthesis, and that both the ABA content and DcPYR1 expression must be above putative threshold levels for ABA to exert its action.\",\"PeriodicalId\":17343,\"journal\":{\"name\":\"Journal of The Japanese Society for Horticultural Science\",\"volume\":\"82 1\",\"pages\":\"242-254\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2013-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"6\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of The Japanese Society for Horticultural Science\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2503/JJSHS1.82.242\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of The Japanese Society for Horticultural Science","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2503/JJSHS1.82.242","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 6

摘要

在衰老的康乃馨(Dianthus caryophyllus L.)花中,乙烯的产生始于雌蕊,产生的乙烯作用于花瓣,诱导自催化乙烯的产生。我们研究了脱落酸(ABA)在花雌蕊乙烯生产中的作用。首先,从康乃馨花组织中克隆了ABA生物合成和信号转导的主要基因cdna。然后,研究了三个品种的ABA含量的变化以及卵巢中ABA生物合成和信号传导的基因表达,' Light Pink Barbara (LPB) '和' Excerea ',其切花在衰老过程中产生乙烯,花瓶寿命约为一周;' Miracle Rouge ',其切花在衰老过程中不产生可检测到的乙烯,花瓶寿命约为三周。‘LPB’植株2期(开放前期)至6期(开放末期)子房ABA含量为530 ~ 710 pmol·g−1鲜重(FW),‘Excerea’植株同一时期子房ABA含量为200 ~ 380 pmol·g−1 FW;ss1(衰老早期)为930 pmol·g−1 FW。‘奇迹胭脂’的ABA含量保持在70 ~ 160 pmol·g−1 FW。ABA含量的变化与康乃馨9-顺式-环氧类胡萝卜素双加氧酶基因DcNCED1的转录水平一致。dpyr1 (ABA受体基因)转录本在“LPB”子房1 ~ 3期的相对表达量为0.004 ~ 0.007,在第1期(衰老初期)的相对表达量为0.028。在‘Excerea’子房中,DcPYR1转录本在花期为0.025 ~ 0.037 rell,在第1期较高。相比之下,“奇迹胭脂”子房在开花和衰老过程中,DcPYR1转录本保持在0.002 ~ 0.006 r.e.l。乙烯生物合成的关键基因DcACS1的转录本在‘LPB’和‘Excerea’的s1位点和s2位点都检测到了,而在‘Miracle Rouge’的整个开花和衰老阶段都没有检测到。这些结果表明,ABA在雌蕊中诱导DcACS1基因的表达,导致乙烯的生物合成,ABA含量和DcPYR1的表达都必须高于假定的阈值水平,ABA才能发挥作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Role of ABA in Triggering Ethylene Production in the Gynoecium of Senescing Carnation Flowers: Changes in ABA Content and Expression of Genes for ABA Biosynthesis and Action
In senescing carnation ( Dianthus caryophyllus L.) flowers, ethylene production begins in the gynoecium, and the resulting ethylene acts on petals, inducing autocatalytic ethylene production. We investigated the role of abscisic acid (ABA) in ethylene production in the gynoecium of flowers. First, cDNAs of major genes involved in ABA biosynthesis and signaling were cloned from carnation flower tissues. Then, changes in ABA content and gene expression of ABA biosynthesis and signaling in the ovary were examined using three cultivars, ‘Light Pink Barbara (LPB)’ and ‘Excerea’, whose cut flowers produce ethylene during senescence and have an ordinary vase-life of about one week, and ‘Miracle Rouge’, whose cut flowers produce no detectable ethylene during senescence and have a vase-life of about three weeks. ABA content in the ovary was 530–710 pmol·g − 1 fresh weight (FW) from Os 2 (early opening stage) to Os 6 (end of opening stage) in ‘LPB’, and at 200–380 pmol·g − 1 FW in ‘Excerea’ at the same stages; but 930 pmol·g − 1 FW at Ss 1 (early senescence stage). The ABA content remained at 70– 160 pmol·g − 1 FW in ‘Miracle Rouge’. The changes in ABA content were in parallel with the transcript levels of DcNCED1 (carnation gene for 9-cis -epoxycarotenoid dioxygenase). DcPYR1 (ABA receptor gene) transcript was 0.004–0.007 relative expression level (r.e.l.) in ‘LPB’ ovary at Os 1–Os 3, and 0.028 r.e.l. at Ss 1 (beginning of senescence stage). In ‘Excerea’ ovary, DcPYR1 transcript was 0.025–0.037 r.e.l. during flower opening and higher at Ss 1. By contrast, DcPYR1 transcript remained at 0.002–0.006 r.e.l. in ‘Miracle Rouge’ ovary during flower opening and senescence. The transcripts of DcACS1 , the key gene for ethylene biosynthesis, were detected at Ss 1 in ‘LPB’, and at Ss 2 in ‘Excerea’, but not in ‘Miracle Rouge’ throughout flower opening and senescence stages. These findings suggest that ABA plays a causal role in inducing the expression of the DcACS1 gene in the gynoecium, leading to ethylene biosynthesis, and that both the ABA content and DcPYR1 expression must be above putative threshold levels for ABA to exert its action.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
审稿时长
>36 weeks
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信