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. 2021 Jun 25;12:695223. doi: 10.3389/fpls.2021.695223

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Copyright © 2021 Wang, Dai, Pang, Cheng, Huang, Li, Yan, Lu, Wei, Sederoff and Li.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Protein–protein interactions of BLH6a, BLH6b, and BLH2. (A) Yeast two hybridizations. BLH6a was fused with Gal4-binding domain (BD). BLH6b and BLH2 were fused with activation domain (AD). The resulting AD constructs (AD:BLH6b, AD:BLH2) and BD construct (BD:BLH6a) were co-transfected into a yeast cell, grown on the SD/-Leu-Trp medium (SD/-LT), and selected on the SD/-Ade-His-Leu-Trp medium (SD/-AHLT). (B) Luciferase complementation imaging (LCI) assays for the detection of the interactions between two proteins of BLH6a, BLH6b, and BLH, with one of them being fused to the N-terminal portion of LUC (nLUC), and the other being fused to the C-terminal portion of LUC (cLUC).