21The APETALA2/Ethylene Responsive Factor (AP2/ERF) gene family has been shown to play a 22 crucial role in plant growth and development, stress responses and secondary metabolite biosynthesis. 23 Nevertheless, little is known about the gene family in ginseng (Panax ginseng), an important traditional 24 medicinal herb in Asia and North America. Here, we report the systematic analysis of the gene family 25 present in ginseng using several transcriptomic databases. A total of 189 putative AP2/ERF genes, 26 defined as PgERF001 through PgERF189. The 93 PgERF genes that have the complete AP2 domain in 27 their open reading frames were classified into five subfamilies, DREB, ERF, AP2, RAV and Soloist. 28 The DREB subfamily and ERF subfamily were further clustered four and six groups, respectively, 29 compared to the 12 groups of these subfamilies found in Arabidopsis. Gene ontology categorized these 30 397 transcripts of the 189 PgERF genes into eight functional subcategories, suggesting their functional 31 differentiation and they have been especially enriched for the nucleic acid binding transcription factor 32 activity subcategory. The expression activity and networks of the 397 PgERF transcripts have 33 substantially diversified across tissues, developmental stages and genotypes. Then, the expression 34 change of six PgERF genes randomly selected from DREB subfamily, i.e., PgERF073, PgERF079, 35 PgERF110, PgERF115, PgERF120 and PgERF128 responding to cold stress suggesting that DREB 36 subfamily genes played an important role in cold resistance of ginseng. Finally, we studied the 37 responses of the PgERF genes to methyl jasmonate (MeJA). 288 (72.5%) of the 397 PgERF gene 38 transcripts responded to the MeJA treatment, with 136 up-regulated and 152 down-regulated, indicating 39 that most members of the PgERF gene family are responsive to MeJA. These results provide resources 40 and knowledge necessary for family-wide functional analysis of the PgERF genes in ginseng and 41 related species.42 3 44
Introduction
45Plants are subjected to numerous biotic and abiotic stresses all time through their growth and 46 development. Therefore, they have developed a variety of mechanisms by producing secondary 47 signaling molecules (e.g., ethylene and jasmonic acid) and response networks at the molecular, 48 biochemical and physiological levels to perceive the external signals from and response to the stresses 49 [1]. It has been documented that a large number of genes are involved in these processes [2]. Therefore, 50 it is important to decipher the regulatory mechanisms of the defense-related genes involved in the signal 51 transduction pathways and the plant responses to these stresses for enhanced and efficient plant genetic 52 improvement [3]. The APETALA2/Ethylene Responsive Factor (AP2/ERF) transcription factors have 53 been demonstrated to be one of the most important gene families actively functioning in plant response 54 to biotic and abiotic stresses by binding to cis-acting elements of downstream ta...