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. 2021 Sep 1;12:715487. doi: 10.3389/fpls.2021.715487

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Copyright © 2021 Li, Guo, Chen, Pan, Yang, Zhou, Wang 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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Quantitative real-time PCR (qRT-PCR) verification. (A) Relative expression levels of 12 selected DEGs between ethephon-treated and control plants. Error bars indicate the SEs. (B) Correlation analysis of RNA-seq log2 (fold change) and qRT-PCR log2 (fold change) of 12 selected genes: AD1-0960 (CmoCh09G010960.1), ETHYLENE INSENSITIVE 3 (EIN3)-3100 (CmoCh05G013100.1), EIN3-4690 (CmoCh09G004690.1), AUX-IAA-6330 (CmoCh10G006330.1), EIN3-2320 (CmoCh12G012320.1), AUX-22D-1500 (CmoCh15G011500.1), AUX-SAUR-7170 (CmoCh19G007170.1), ACO-640 (CmoCh02G000640.1), ACO-5880 (CmoCh03G005880.1), ACO-3260 (CmoCh07G003260.1), ACO-150 (CmoCh11G020150.1), and MK-3620 (CmoCh16G003620.1).