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Identification and differential expression analysis of anthocyanin biosynthetic genes in root-skin color variants of radish (Raphanus sativus L.)

机译:萝卜根皮肤色素变种中花青素生物合成基因的鉴定及差异表达分析(Raphanus Sativus L.)

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Background Taproot skin color is a major trait for assessing the commercial and nutritional quality of radish, and red-skinned radish is confirmed to improve consumer's interest and health. However, little is known about the molecular mechanisms responsible for controlling the formation of red-skinned radish. Objective This study aimed to identify the differentially expressed anthocyanin biosynthetic genes between red- and white-skinned radishes and understand the molecular regulatory mechanism underlying red-skinned radish formation. Methods Based on the published complete genome sequence of radish, the digital gene expression profiles of Yangzhouyuanbai (YB, white-skinned) and Sading (SD, red-skinned) were analyzed using Illumina sequencing. Results A total of 3666 DEGs were identified in SD compared with YB. Interestingly, 46 genes encoded enzymes related to anthocyanin biosynthesis and 241 genes encoded transcription factors were identified. KEGG pathway analysis showed that the formation of red-skinned radish was mainly controlled by pelargonidin-derived anthocyanin biosynthetic pathway genes. This process included the upregulation of PAL, C4H, 4CL, CHS, CHI, F3H, DFR, LDOX, and UGT enzymes in SD. CHS genes were specifically expressed in SD, and it might be the key point for red pigment accumulation in red-skinned radish. Furthermore, MYB1/2/75, bHLH (TT8), and WD 40 showed higher expression in SD than in YB. Meanwhile, the corresponding low-abundance anthocyanin biosynthesis enzymes and upregulation of MYB4 might be the factors influencing the formation of white-skinned radish. Conclusion These findings provide new insights into the molecular mechanisms and regulatory network of anthocyanin biosynthesis in red-skinned radish.
机译:背景技术Taproot Skin Color是评估萝卜的商业和营养品质的主要特质,并确认红皮肤萝卜提高消费者的兴趣和健康。然而,关于负责控制红色皮肤萝卜形成的分子机制很少。目的本研究旨在鉴定红眼和白皮萝卜之间的差异表达的花青素生物合成基因,了解红皮萝卜形成的分子调节机制。使用Illumina测序分析了基于萝卜的发表完全基因组序列的方法,扬州源白(YB,白皮)和令人阵亡(SD,红皮肤)的数字基因表达谱。结果与YB相比,在SD中共鉴定了总共3666℃。有趣的是,鉴定了与花青素生物合成和241个基因相关的46个基因编码酶编码的转录因子。 Kegg途径分析表明,红色皮肤萝卜的形成主要由Pelargonidin衍生的花青素生物合成途径基因控制。该方法包括在SD中的PAL,C4H,4CL,CHS,CHI,F3H,DFR,LDOX和UGT酶的上调。 CHS基因在SD中特异性表达,并且它可能是红色皮肤萝卜红色颜料积累的关键点。此外,MyB1 / 2/75,BHLH(TT8)和WD 40在SD中显示出比YB更高的表达。同时,相应的低丰度花青素生物合成酶和MYB4的上调可能是影响白皮萝卜形成的因素。结论这些调查结果为红皮萝卜中的花青素生物合成的分子机制和监管网络提供了新的见解。

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