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论文题目: |
WRKY53 integrates classic brassinosteroid signaling and the mitogen-activated protein kinase pathway to regulate rice architecture and seed size |
英文论文题目: |
WRKY53 integrates classic brassinosteroid signaling and the mitogen-activated protein kinase pathway to regulate rice architecture and seed size |
第一作者: |
Tian, Xiaojie |
英文第一作者: |
Tian, Xiaojie |
联系作者: |
卜庆云 |
英文联系作者: |
Q. Y. Bu |
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发表年度: |
2021 |
卷: |
33 |
期: |
8 |
页码: |
2753-2775 |
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英文摘要: |
In rice (Oryza sativa) and other plants, plant architecture and seed size are closely related to yield. Brassinosteroid (BR) signaling and the mitogen-activated protein kinase (MAPK) pathway (MAPK kinase kinase 10 [MAPKKK10]-MAPK kinase 4 [MAPKK4]-MAPK6) are two major regulatory pathways that control rice architecture and seed size. However, their possible relationship and crosstalk remain elusive. Here, we show that WRKY53 mediated the crosstalk between BR signaling and the MAPK pathway. Biochemical and genetic assays demonstrated that glycogen synthase kinase-2 (GSK2) phosphorylates WRKY53 and lowers its stability, indicating that WRKY53 is a substrate of GSK2 in BR signaling. WRKY53 interacted with BRASSINAZOLE-RESISTANT 1(BZR1); they function synergistically to regulate BR-related developmental processes. We also provide genetic evidence showing that WRKY53 functions in a common pathway with the MAPKKK10-MAPKK4-MAPK6 cascade in leaf angle and seed size control, suggesting that WRKY53 is a direct substrate of this pathway. Moreover, GSK2 phosphorylated MAPKK4 to suppress MAPK6 activity, suggesting that GSK2-mediated BR signaling might also regulated MAPK pathway. Together, our results revealed a critical role for WRKY53 and uncovered sophisticated levels of interplay between BR signaling and the MAPK pathway in regulating rice architecture and seed size. |
刊物名称: |
Plant Cell |
英文刊物名称: |
Plant Cell |
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参与作者: |
X. J. Tian, M. L. He, E. Y. Mei, B. W. Zhang, J. Q. Tang, M. Xu, J. L. Liu, X. F. Li, Z. Y. Wang, W. Q. Tang, Q. J. Guan and Q. Y. Bu |
英文参与作者: |
X. J. Tian, M. L. He, E. Y. Mei, B. W. Zhang, J. Q. Tang, M. Xu, J. L. Liu, X. F. Li, Z. Y. Wang, W. Q. Tang, Q. J. Guan and Q. Y. Bu |
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