首页> 外文期刊>Molecular biology reports >Identification and transcript analysis of two glutamate decarboxylase genes, CsGAD1 and CsGAD2, reveal the strong relationship between CsGAD1 and citrate utilization in citrus fruit
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Identification and transcript analysis of two glutamate decarboxylase genes, CsGAD1 and CsGAD2, reveal the strong relationship between CsGAD1 and citrate utilization in citrus fruit

机译:两种谷氨酸脱羧酶基因CsGAD1和CsGAD2的鉴定和转录本分析揭示了CsGAD1与柑橘类水果中柠檬酸盐利用之间的密切关系。

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Glutamate decarboxylase (GAD, EC 4.1.1.15) has been suggested to be a key, regulatory point in the biosynthesis of gamma-aminobutyrate (GABA) and in the utilization of citric acid through GABA shunt pathway. In this study we discovered two GAD genes, named as CsGAD1 and CsGAD2, in citrus genome database and then successfully cloned. Both CsGAD1 and CsGAD2 have a putative pyridoxal 5-phosphate binding domain in the middle region and a putative calmodulin-binding domain at the carboxyl terminus. Gene structure analysis showed that much difference exists in the size of exons and introns or in cis-regulatory elements in promoter region between the two GAD genes. Gene expression indicated that CsGAD1 transcript was predominantly expressed in flower and CsGAD2 transcript was predominantly expressed in fruit juice sacs; in the ripening fruit, CsGAD1 transcript level was at least 2-time higher than CsGAD2 transcript level. Moreover, CsGAD1 transcript level was increased significantly along with the increase of GAD activity and accompanied by a significant decrease of titratable acid (TA), suggesting that it is CsGAD1 rather than CsGAD2 plays a role in the citric acid utilization during fruit ripening. In addition, injection of abscisic acid and foliar spray of K2SO4 significantly increased the TA content of Satsuma mandarin, and significantly decreased GAD activity as well as CsGAD1 transcript, further suggesting the important role of CsGAD1 in the citrate utilization of citrus fruit.
机译:谷氨酸脱羧酶(GAD,EC 4.1.1.15)被认为是生物合成γ-氨基丁酸酯(GABA)和通过GABA分流途径利用柠​​檬酸的关键调控点。在这项研究中,我们在柑橘基因组数据库中发现了两个GAD基因,分别名为CsGAD1和CsGAD2,然后成功克隆。 CsGAD1和CsGAD2均在中间区域具有一个假定的吡ido醛5-磷酸结合结构域,在羧基末端具有一个钙调蛋白结合结构域。基因结构分析表明,两个GAD基因之间的外显子和内含子大小或启动子区域的顺式调控元件存在很大差异。基因表达表明CsGAD1转录本主要在花中表达,而CsGAD2转录本主要在果汁囊中表达。在成熟果实中,CsGAD1转录水平比CsGAD2转录水平至少高2倍。此外,CsGAD1转录水平随GAD活性的增加而显着增加,并伴随着可滴定酸(TA)的显着降低,表明它是CsGAD1而不是CsGAD2在果实成熟期间的柠檬酸利用中起作用。此外,注射脱落酸和喷施K2SO4的叶面喷洒剂显着增加了萨摩柑的TA含量,并显着降低了GAD活性和CsGAD1转录本,进一步表明了CsGAD1在柑桔类柠檬酸盐利用中的重要作用。

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