%A Kim,Joonyup %A Yang,Jinyoung %A Yang,Ronghui %A Sicher,Richard C. %A Chang,Caren %A Tucker,Mark L. %D 2016 %J Frontiers in Plant Science %C %F %G English %K Transcription Factors,network,Abscission,Soybean,Organ polarity,cell fate,Glycine max %Q %R 10.3389/fpls.2016.00125 %W %L %M %P %7 %8 2016-February-17 %9 Original Research %+ Dr Joonyup Kim,Soybean Genomics and Improvement Laboratory, Agricultural Research Service, United States Department of Agriculture,Beltsville, MD, USA,joohnyup@gmail.com %+ Dr Joonyup Kim,Department of Cell Biology and Molecular Genetics, University of Maryland,College Park, MD, USA,joohnyup@gmail.com %+ Dr Mark L. Tucker,Soybean Genomics and Improvement Laboratory, Agricultural Research Service, United States Department of Agriculture,Beltsville, MD, USA,mark.tucker@ars.usda.gov %# %! Transcriptional networks underlying soybean abscission %* %< %T Transcriptome Analysis of Soybean Leaf Abscission Identifies Transcriptional Regulators of Organ Polarity and Cell Fate %U https://www.frontiersin.org/articles/10.3389/fpls.2016.00125 %V 7 %0 JOURNAL ARTICLE %@ 1664-462X %X Abscission, organ separation, is a developmental process that is modulated by endogenous and environmental factors. To better understand the molecular events underlying the progression of abscission in soybean, an agriculturally important legume, we performed RNA sequencing (RNA-seq) of RNA isolated from the leaf abscission zones (LAZ) and petioles (Non-AZ, NAZ) after treating stem/petiole explants with ethylene for 0, 12, 24, 48, and 72 h. As expected, expression of several families of cell wall modifying enzymes and many pathogenesis-related (PR) genes specifically increased in the LAZ as abscission progressed. Here, we focus on the 5,206 soybean genes we identified as encoding transcription factors (TFs). Of the 5,206 TFs, 1,088 were differentially up- or down-regulated more than eight-fold in the LAZ over time, and, within this group, 188 of the TFs were differentially regulated more than eight-fold in the LAZ relative to the NAZ. These 188 abscission-specific TFs include several TFs containing domains for homeobox, MYB, Zinc finger, bHLH, AP2, NAC, WRKY, YABBY, and auxin-related motifs. To discover the connectivity among the TFs and highlight developmental processes that support organ separation, the 188 abscission-specific TFs were then clustered based on a >four-fold up- or down-regulation in two consecutive time points (i.e., 0 and 12 h, 12 and 24 h, 24 and 48 h, or 48 and 72 h). By requiring a sustained change in expression over two consecutive time intervals and not just one or several time intervals, we could better tie changes in TFs to a particular process or phase of abscission. The greatest number of TFs clustered into the 0 and 12 h group. Transcriptional network analysis for these abscission-specific TFs indicated that most of these TFs are known as key determinants in the maintenance of organ polarity, lateral organ growth, and cell fate. The abscission-specific expression of these TFs prior to the onset of abscission and their functional properties as defined by studies in Arabidopsis indicate that these TFs are involved in defining the separation cells and initiation of separation within the AZ by balancing organ polarity, roles of plant hormones, and cell differentiation.