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MYB transcription factor PdMYB118 directly interacts with bHLH transcription factor PdTT8 to regulate wound-induced anthocyanin biosynthesis in poplar

机译:MYB转录因子PdMYB118直接与bHLH转录因子PdTT8相互作用调节伤口诱导的杨树花色苷生物合成

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摘要

Wound induced accumulation of anthocyanins in the leaves of transgenic plants overexpressing . Wound prompts anthocyanin biosynthesis in the leaves of transgenic plants. The leaves of WT and transgenic plantlets cultured on MS medium were cut into pieces and transferred onto MS medium for 2 days. Images in the third row were the higher magnification of the framed area of the images in the secondary row. Scale bars for the images in the first and secondary rows stand for 1 cm and in the third row stand for 1 mm. Accumulated anthocyanin biosynthesis in the wounded leaves of transgenic plants grown in greenhouse. Matured leaves were cut into leaf discs and transferred onto MS medium for 2 days. The black arrows indicate the red speckles. Scale bar = 0.5 cm. Anthocyanin extracted from the wounded leaf discs in (b). Scale bar = 0.5 cm. Relative content of anthocyanins extracted from the leaves in (b). Control, before wound induction; Wound, after wound induction on MS medium for 2 days; WT, leaves of wild type Shanxin Yang plants; L2 and L7, leaves of transgenic plants overexpressing ; WT-W, wounded leaves of wild type plant; L2-W and L7-W, wounded leaves of transgenic plants (Lines L2 and L7). Values are means and standard deviations of three biological replicates (  = 3). ** and ***, significant differences in comparison to WT, L2 and L7 at  P
机译:伤口诱导花青素在过表达转基因植物叶片中的积累。伤口促使转基因植物叶片中的花色苷生物合成。将在MS培养基上培养的WT和转基因苗的叶子切成片,并转移到MS培养基上2天。第三行中的图像是第二行中图像的边框区域的较高放大倍率。第一行和第二行中图像的比例尺为1 cm,第三行中图像的比例尺为1 mm。在温室中生长的转基因植物受伤的叶子中积累的花色苷生物合成。将成熟的叶子切成叶盘并转移到MS培养基上2天。黑色箭头表示红色斑点。比例尺= 0.5 cm。从(b)中从受伤的叶片上提取的花色苷。比例尺= 0.5 cm。 (b)中从叶片中提取的花色苷的相对含量。诱导伤口前进行控制;在MS培养基上诱导伤口2天后伤口; WT,野生型山西杨植物的叶子; L2和L7,过表达转基因植物的叶子; WT-W,野生型植物的叶片受伤; L2-W和L7-W,转基因植物的受伤叶子(品系L2和L7)。值是三个生物学重复的平均值和标准差((= 3)。 **和***,在P时与WT,L2和L7相比有显着差异

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