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Identification of an SCPL Gene Controlling Anthocyanin Acylation in Carrot (Daucus carota L.) Root

机译:鉴定红萝卜(Daucus Carota L.)根中花青素酰化的SCPL基因

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摘要

Anthocyanins are natural health promoting pigments that can be produced in large quantities in some purple carrot cultivars. Decoration patterns of anthocyanins, such as acylation, can greatly influence their stability and biological properties and use in the food industry as nutraceuticals and natural colorants. Despite recent advances made toward understanding the genetic control of anthocyanin accumulation in purple carrot, the genetic mechanism controlling acylation of anthocyanin in carrot root have not been studied yet. In the present study, we performed fine mapping combined with gene expression analyses (RNA-Seq and RT-qPCR) to identify the genetic factor conditioning the accumulation of non-acylated (Cy3XGG) versus acylated (Cy3XFGG and Cy3XSGG) cyanidin derivatives, in three carrot populations. Segregation and mapping analysis pointed to a single gene with dominant effect controlling anthocyanin acylation in the root, located in a 576kb region containing 29 predicted genes. Orthologous and phylogenetic analyses enabled the identification of a cluster of three SCPL-acyltransferases coding genes within this region. Comparative transcriptome analysis indicated that only one of these three genes, DcSCPL1, was always expressed in association with anthocyanin pigmentation in the root and was co-expressed with DcMYB7, a gene known to activate anthocyanin biosynthetic genes in carrot. DcSCPL1 sequence analysis, in root tissue containing a low level of acylated anthocyanins, demonstrated the presence of an insertion causing an abnormal splicing of the 3rd exon during mRNA editing, likely resulting in the production of a non-functional acyltransferase and explaining the reduced acylation phenotype. This study provides strong linkage-mapping and functional evidences for the candidacy of DcSCPL1 as a primary regulator of anthocyanin acylation in carrot storage root.
机译:花青素是天然健康促进颜料,可以在一些紫色胡萝卜品种中大量生产。花青素的装饰模式,如酰化,可以极大地影响它们的稳定性和生物学性质,并在食品工业中使用作为营养保健品和自然着色剂。尽管最近对理解紫色胡萝卜中的花青素积累的遗传控制进行了进展,但尚未研究控制红萝卜根中花青素的酰化的遗传机制。在本研究中,我们对基因表达分析(RNA-SEQ和RT-QPCR)进行了精细的映射,以鉴定遗传因子调节非酰化(Cy3xGG)的积累与酰化(Cy3xFGG和Cy3XSGG)Cyanidin衍生物,三个胡萝卜群体。分离和映射分析指向具有控制含有29个预测基因的576KB区域中的偏离效果的单个基因。正交和系统发育分析使得能够鉴定该区域内的三种SCPL-酰基转移酶的组簇。对比转录组分析表明,只有这三种基因中的一种DCSCPL1,总是与根部中的花青素色素沉着结合,并用DCMYB7共表达,该基因已知在胡萝卜中激活花青素生物合成基因。 DCSCPL1序列分析,含有低水平的酰化花青素的根组织中,证明了在mRNA编辑期间的第3次外显子的插入的存在,可能导致产生非功能性酰基转移酶并解释减少的酰化表型。 。本研究为DCSCPL1作为红萝卜储存根的花青素酰化的初级调节剂提供了强烈的联系 - 映射和功能证据。

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