TY - JOUR
T1 - Spatially and temporally restricted expression of PtrMYB021 regulates secondary cell wall formation in Arabidopsis
AU - Wang, Wei
AU - Li, Eryang
AU - Porth, Ilga
AU - Chen, Jin Gui
AU - Mansfield, Shawn D.
AU - Douglas, Carl J.
AU - Wang, Shucai
N1 - Publisher Copyright:
© 2016, Korean Society of Plant Biologists and Springer-Verlag Berlin Heidelberg.
PY - 2016/2/1
Y1 - 2016/2/1
N2 - 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.
AB - 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.
KW - Arabidopsis thaliana
KW - Populus trichocarpa
KW - PtrMYB021
KW - R2R3 MYB
KW - Secondary cell wall biosynthesis
KW - Transcription factor
UR - http://www.scopus.com/inward/record.url?scp=84957575143&partnerID=8YFLogxK
U2 - 10.1007/s12374-016-0438-0
DO - 10.1007/s12374-016-0438-0
M3 - Article
AN - SCOPUS:84957575143
SN - 1226-9239
VL - 59
SP - 16
EP - 23
JO - Journal of Plant Biology
JF - Journal of Plant Biology
IS - 1
ER -