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. 2016 Sep 13;7:1367. doi: 10.3389/fpls.2016.01367

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Copyright © 2016 Lu, Zhang, Zheng, Zhu, Xu and Deng.

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) or licensor 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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Schematic representation of the CsLCYb1 promoter::GUS vectors construction. These constructs are based on the pCAMBIA1301 vector. LB, left border; 35S PolyA, Cauliflower Mosaic Virus 35S terminator; Hyg, hygromycin resistance gene; 35S P, Cauliflower Mosaic Virus 35S promoter; GUS, β-glucuronidase reporter gene; Nos PolyA, nopaline synthase terminator; RB, right border. Hollow arrows indicate the positions of the promoter insertion in the vectors. The promoters contain the full-length sequence (LP) and its five 5′ truncated fragments (LP1, LP2, LP3, LP4, and LP5). Numbers indicate the sequence length from the first base of the ATG.