This work was supported by the National Natural Science Foundation of China (Projects 31725004 31670276, 31461143001, and 31870237), the Pearl River S&T Nova Program of Guangzhou (201610010070), and the Major Project of China on New Varieties of GMO Cultivation (2018zx08011-01B to J.L.).*%blankline%*
The Supporting Information is available free of charge on the ACS Publications website at DOI: 10.1021/acs.jafc.9b04589 . Figure S1, Analysis of DEGs in the leaves and siliques; Figure S2, Comparison of microarray and qRT-PCR data; Figure S3, Expression profiling of transcription factors in transgenic Arabidopsis expressing CrBKT ; Figure S4, P5CS1 expression in the leaf and silique tissues of WT and CR5 plants; Figure S5, BKT-overexpressing transgenic plants were more tolerant to MV stress; Table S1, DEGs in astaxanthin pathway affected by CrBKT ; Table S2, DEGs of phytohormone-related pathway affected by CrBKT ; Table S3, DEGs of transcription factor affected by CrBKT ; and Table S4, List of primers used for qRT-PCR experiment ( PDF ) This work was supported by the National Natural Science Foundation of China (Projects 31725004, 31670276, 31461143001, and 31870237), the Pearl River S&T Nova Program of Guangzhou (201610010070), and the Major Project of China on New Varieties of GMO Cultivation (2018zx08011-01B to J.L.). The authors declare no competing financial interest.
