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Spatially and temporally restricted expression of PtrMYB021 regulates secondary cell wall formation in Arabidopsis

机译:PtrMYB021的时空限制表达调节拟南芥中次生细胞壁的形成

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Among the R2R3 MYB transcription factors that involve in the regulation of secondary cell wall formation in Arabidopsis, MYB46 alone is sufficient to induce the entire secondary cell wall biosynthesis program. PtrMYB021, the poplar homolog of MYB46, has been reported to regulate secondary cell wall formation when expressed in Arabidopsis. We report here that spatially and temporally restricted expression of PtrMYB021 is critical for its function in regulating secondary cell wall formation. By using quantitative RT-PCR, we found that PtrMYB021 was expressed primarily in xylem tissues. When expressed in Arabidopsis under the control of PtrCesA8, but not the 35S promoter, PtrMYB021 increased secondary cell wall thickness, which is likely caused by increased lignification as well as changes in cell wall carbohydrate composition. In consistent with this, elevated expression of lignin and cellulose biosynthetic genes were observed in the transgenic plants. When expressed in Arabidopsis protoplasts as fusion proteins to the Gal4 DNA binding domain, PtrMYB021 activated the reporter gene Gal4-GUS. In summary, our results suggest that PtrMYB021 is a transcriptional activator, and spatially and temporally restricted expression of PtrMYB021 in Arabidopsis regulates secondary cell wall formation by activating a subset of secondary cell wall biosynthesis genes.
机译:在拟南芥中参与调节次生细胞壁形成的R2R3 MYB转录因子中,仅MYB46足以诱导整个二次细胞壁生物合成程序。据报道,MYB46的杨树同源物PtrMYB021在拟南芥中表达时可调节次生细胞壁的形成。我们在这里报告,PtrMYB021的时空限制表达对其调节次级细胞壁形成的功能至关重要。通过使用定量RT-PCR,我们发现PtrMYB021主要在木质部组织中表达。当在PtrCesA8而不是35S启动子的控制下在拟南芥中表达时,PtrMYB021增加了次生细胞壁的厚度,这可能是由于木质化的增加以及细胞壁碳水化合物组成的变化所致。与此一致,在转基因植物中观察到木质素和纤维素生物合成基因的表达升高。当在拟南芥原生质体中表达为Gal4 DNA结合域的融合蛋白时,PtrMYB021激活了报告基因Gal4-GUS。总之,我们的结果表明PtrMYB021是转录激活因子,拟南芥中PtrMYB021的时空限制表达通过激活次级细胞壁生物合成基因的一个子集来调节次级细胞壁的形成。

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