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PbMYB120 Negatively Regulates Anthocyanin Accumulation in Pear

机译:PBMYB120负调节梨中的花青素积累

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Subgroup 4 R2R3 MYBs play vital roles in the regulation of anthocyanin biosynthesis. However, there is limited knowledge regarding the functions of MYB repressors in pear ( Pyrus × bretschneideri ). Here, PbMYB120 was identified as a potential regulator of anthocyanin biosynthesis. A phylogenetic analysis revealed that PbMYB120 was clustered into the FaMYB1-like clade of the subgroup 4 R2R3 MYBs. PbMYB120 was expressed higher in red peels than in green peels in five pear cultivars. PbMYB120 expression was positively correlated with anthocyanin accumulation. However, the transient overexpression of PbMYB120 led to the inhibition of anthocyanin accumulation and PbUFGT1 expression. Promoter binding and activation assays indicated that PbMYB120 binds to the promoter of PbUFGT1 and represses the promoter’s activity. Thus, the inhibition of anthocyanin accumulation by PbMYB120 may be correlated with the repression of PbUFGT1 . Furthermore, during anthocyanin induction, the expression levels of anthocyanin activators and PbMYB120 were upregulated. This study demonstrated that PbMYB120 was highly expressed in pear tissues having higher anthocyanin accumulations but acted as a repressor in the regulation of anthocyanin accumulation. PbMYB120 may work coordinately with anthocyanin activators and serve as a balancer of anthocyanin accumulation.
机译:亚组4 R2R3 MYBS在花青素生物合成的调节中发挥重要作用。然而,有关梨(Pyrus×Bretschneideri)的MYB阻遏物功能的知识有限。这里,PBMyB120被鉴定为花青素生物合成的潜在调节剂。系统发育分析表明,将PBMYB120聚集到亚组4R2R3 MOB的FamyB1样枝中。 PBMyB120在红色果皮中表达较高,而不是在五种梨品种中的绿皮中。 PBMYB120表达与花青素积极呈正相关。然而,PBMYB120的瞬态过度表达导致抑制花青素积累和PBUFGT1表达。启动子结合和活化测定表明,PBMYB120与PBUFGT1的启动子结合并抑制启动子的活性。因此,通过PBMYB120的抑制花青素积累可以与PBUFGT1的抑制相关。此外,在花青素诱导过程中,上调了花青素活化剂和PBMYB120的表达水平。本研究证明,PBMYB120在具有更高的花青素累积的梨组织中高度表达,但在调节花青素积累中的阻遏物。 PBMYB120可以与花青素活化剂协调,并用作花青素积累的平衡器。

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