Abstract
GRAS transcription factors play important roles in plant growth, development, and abiotic and biotic stress responses. In this study, the genome-wide identification of the transcription factor family of Actinidia arguta was carried out including an analysis of the physical and chemical properties, phylogenetic development, gene structure, collinearity between genes, and protein interactions. A total of 88 GRAS genes were identified in the genome of Actinidia arguta with protein lengths of 103-510 aa, a molecular mass of 11,603.25-22,457.96 kDa, and isoelectric points in the hydrophilic range between 4.45 and 6.50 From these genes, 67 were located in the nucleus and 21 in the chloroplast. The identified genes were further divided into eight subfamilies: SCR, HAM, DELLA, PAT1, SHR, SCL4/7, and GIGR. Members of the same subfamily had similar gene structures and conserved motifs. Motif 5 was highly conserved in the GRAS family. On the chromosomes of LG3, LG15, LG22, LG24, LG26 and LG28, there was a large number of tandem duplications of GRAS genes, with 64 pairs of genes orthologous with Arabidopsis thaliana. The analysis of protein interactions found that there were interactive relationships between SCL28 in the DLT subfamily and SCL14 in the LISCL subfamily and between SCL13 in the PAT1 subfamily and proteins of the LAS subfamily. Interactions were also observed between the SCL30, SCL33, and HAM4 proteins in the LISCL subfamily. This study, therefore, provides a reference for mining and verification within the GRAS genes in the Actinidia arguta genome.