Regulatory mechanisms of miR171d-SCL6 module in the rooting process of Acer rubrum L.

Autor: Li H; College of Landscape Architecture, Beijing University of Agriculture, Beijing, 102206, China.; Beijing Laboratory of Urban and Rural Ecological Environment, Beijing, 102206, China., Yu J; College of Landscape Architecture, Beijing University of Agriculture, Beijing, 102206, China.; Beijing Laboratory of Urban and Rural Ecological Environment, Beijing, 102206, China., Qin J; College of Landscape Architecture, Beijing University of Agriculture, Beijing, 102206, China., Zhao H; College of Landscape Architecture, Beijing University of Agriculture, Beijing, 102206, China.; Beijing Laboratory of Urban and Rural Ecological Environment, Beijing, 102206, China., Zhang K; College of Landscape Architecture, Beijing University of Agriculture, Beijing, 102206, China. kezhong.zhang@bua.edu.cn.; Beijing Laboratory of Urban and Rural Ecological Environment, Beijing, 102206, China. kezhong.zhang@bua.edu.cn., Ge W; College of Landscape Architecture, Beijing University of Agriculture, Beijing, 102206, China. wei.ge@bua.edu.cn.; Beijing Laboratory of Urban and Rural Ecological Environment, Beijing, 102206, China. wei.ge@bua.edu.cn.
Jazyk: angličtina
Zdroj: Planta [Planta] 2024 Sep 28; Vol. 260 (5), pp. 109. Date of Electronic Publication: 2024 Sep 28.
DOI: 10.1007/s00425-024-04539-3
Abstrakt: Main Conclusion: MiR171d and SCL6 are induced by the plant hormone auxin. MiR171d negatively regulates the expression of SCL6, thereby regulating the growth and development of plant adventitious roots. Under natural conditions, it is difficult to induce rooting in the process of propagating Acer rubrum L. via branches, which seriously limits its wide application in landscaping construction. In this study, the expression of Ar-miR171d was downregulated and the expression of ArSCL6 was upregulated after 300 mg/L indole-3-butyric acid (IBA) treatment. The transient interaction of Ar-miR171d and ArSCL6 in tobacco cells further confirmed their cleavage activity. Transgenic function verification confirmed that OE-Ar-miR171d inhibited adventitious root (AR) development, while OE-ArSCL6 promoted AR development. Tissue-specific expression verification of the ArSCL6 promoter demonstrated that it was specifically expressed in the plant root and leaf organs. Subcellular localization and transcriptional activation assays revealed that both ArSCL6 and ArbHLH089 were located in the nucleus and exhibited transcriptional activation activity. The interaction between the two was verified by bimolecular fluorescence complementarity (BIFC) experiments. These results help elucidate the regulatory mechanisms of the Ar-miR171d-ArSCL6 module during the propagation of A. rubrum and provide a molecular basis for the rooting of branches.
(© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.)
Databáze: MEDLINE
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