首页> 美国卫生研究院文献>International Journal of Molecular Sciences >BrmiR828 Targets BrPAP1 BrMYB82 and BrTAS4 Involved in the Light Induced Anthocyanin Biosynthetic Pathway in Brassica rapa
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BrmiR828 Targets BrPAP1 BrMYB82 and BrTAS4 Involved in the Light Induced Anthocyanin Biosynthetic Pathway in Brassica rapa

机译:Brmir828 Targets Brap1Brmyb82和Brtas4涉及光线诱导的Brassica Rapa的花青素生物合成途径

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摘要

Comprehensive research in various plants shows that the metabolic pathway of anthocyanin biosynthesis is affected by environmental factors and regulated by microRNAs through post-transcriptional regulation. In seedlings of Brassica rapa Tsuda, the accumulation of anthocyanin is induced by light. However, the roles of BrmiR828 in the light-induced synthesis of anthocyanin in Brassica rapa remain to be explored. Here, a primary transcript of BrmiR828 was identified to be located on the chromosomes of the A03 sub-genome. Five candidate MYB family genes were predicted as targets of BrmiR828 in the database of Brassica rapa (BRAD, V1.1) by using psRNATarget. The transcript abundance of mature BrmiR828 was reduced in seedlings of Brassica rapa Tsuda under blue light irradiation comparing with dark treatment. However, Real-time PCR showed the transcript level of the five candidate targets, Bra004162, Bra022602, Bra001917, Bra029113, and Bra039763 was up-regulated when the seedlings exposed to blue or UV-A light. Trans-acting siRNA gene 4 (BrTAS4) was also identified to have a higher transcript level under blue and UV-A light irradiation than that in dark treatment. RNA ligase mediated 5′amplification of cDNA ends (RLM-5′ RACE) showed that BrmiR828 can splice the mRNA of Bra039763, Bra022602, and BrTAS4 on binding sites. Phylogenetic analysis of candidate BrMYBs targets along with MYBs from Arabidopsis thaliana showed that Bra039763, Bra004162, Bra001917, Bra029113, and Bra022602 are classified to the same group with AtMYB75, AtMYB114, AtMYB90, AtMYB113, and AtMYB82 which are involved in the anthocyanin biosynthetic pathway. As a result, light-induced down-regulation of BrmiR828 can target BrTAS4, BrPAP1 (Bra039763), MYB82 (Bra022602) to negatively regulate their transcript levels leading to the accumulation of MYB transcription factors that positively regulate anthocyanin biosynthesis in light-exposed seedlings of Brassica rapa.
机译:各种植物的综合研究表明,花青素生物合成的代谢途径受环境因素的影响,并通过转录后调节受到微小的影响。在Brassica Rapa Tsuda的幼苗中,通过光诱导花青素的积累。然而,Brmir828在芸苔属Rapa中的光诱导合成的Brashocyanin的作用仍然探讨。这里,鉴定了BRMIR828的主要转录物位于A03亚基因组的染色体上。使用Psrnatarget预测五个候选MYB系列基因作为Brassica Rapa(Brad,V1.1)数据库中Brmir828的目标。与黑暗处理相比,在Brassica Rapa Tsuda的幼苗中降低了成熟Brmir828的转录物丰度。然而,当幼苗暴露于蓝色或UV-A光时,实时PCR显示五个候选靶标的转录物水平,BRA004162,BRA004162,BRA022602,BRA001917,BRA029113和BRA039763。还鉴定反式作用siRNA Gene 4(BRTAS4),以在蓝色和UV-A光照射下具有比在黑暗处理中的更高的转录水平。 RNA连接酶介导的cDNA末端的5'缩小(RLM-5'竞争)显示BRMIR828可以在结合位点上接使BRA039763,BRA022602和BRTAS4的mRNA。候选BRMYBS靶向拟南芥的MyBS的系统发育分析表明,Bra039763,Bra004162,Bra001917,Bra029113和Bra022602分为与AtmyB75,AtmyB114,AtmyB90,AtmyB113和AtmyB82的分类为涉及花青素生物合成途径。结果,BRMIR828的光诱导的下调可以靶向BRTAS4,BRPAP1(BRA039763),MYB82(BRA022602),以负调节其转录水平,导致MYB转录因子积极调节阳性幼苗中的花青素生物合成的积累。芸苔属rapa。

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