“…Primers used for quantitative RT-PCR (qRT-PCR) of the Potri.001G188500, Potri.006G237700, Potri.018G044900, and Potri.T158300 are listed in Supplementary Table S3 . Analysis of expression levels of genes involved in cellulose biosynthesis pathways genes ( PtrCESA4 , PtrCESA7 , and PtrCESA8 ; Suzuki et al, 2006 ), xylan biosynthesis pathways genes ( PtrGT43A , PtrGT47C , and PtrGT8F ; Zhou et al, 2006 , 2007 ), lignin biosynthesis ( PtrPAL4 , PtrC4H1 , PtrC3H3 , Ptr4CL5 , PtrCCoAOMT3 , PtrCOMT2 , PtrCCR2 , PtrCAld5H2 , and PtrCAD1 ), PCD ( PtrXCP1 , PtrXCP2 , PtrRNS3 , and PtrBFN1 ; Hussey et al, 2013 ; Cubria-Radio and Nowack, 2019 ), and well-known wood-associated TFs ( PtrWND6A , PtrWND6B , PtrMYB2 , PtrMYB21 , PtrMYB157 , PtrMYB221 , PtrMYB28 , PtrMYB152 , PtrNAC105 , PtrMYB128 , PtrMYB52 , and PtrMYB54 ) in poplars ( Zhong et al, 2010a , 2011 ; Zhong and Ye, 2010 ; Hussey et al, 2013 ; Zhang et al, 2018b , 2020 ; Cubria-Radio and Nowack, 2019 ), were performed using qRT-PCR primers ( Supplementary Table S3 ). PtrActin was employed as internal controls, and the delta-delta CT method was used to quantify gene expression levels relative to PtrActin ( Taylor et al, 2019 ).…”