Genome-Wide Exploration of the Ethylene-Responsive Element-Binding Factor Gene Family in Sweet Cherry (Prunus avium L.): Preliminarily Unveiling Insights into Normal Development and Fruit Cracking

Author:

Wang Yanbo1,Du Xiaoyun12ORCID,Liu Minxiao12,Li Yanju12,Shang Zhong1,Zhao Lingling12,Yu Xiaoli12,Zhang Shuo12,Li Peng12ORCID,Liu Jie1,Wang Yilin1,Liu Yunfen3,Zhao Jun4,Bi Zuolin4,Zhang Xu1,Liu Xueqing12

Affiliation:

1. Yantai Academy of Agricultural Sciences, Yantai 265500, China

2. Key Laboratory of Apple Germplasm Innovation and Quality Control, Yantai 265500, China

3. Fushan Agricultural Technology Extension Center, Yantai 265500, China

4. Tibet Autonomous Region Academy of Forestry Sciences, Lhasa 850032, China

Abstract

The ERF subfamily, a significant part of the APETALA2/ethylene-responsive element-binding factor (AP2/ERF) transcription family, plays a crucial role in plant growth, development, and stress responses. Despite its importance, research on this gene family in sweet cherry (Prunus avium L.) is limited. This study identified and analyzed the sweet cherry ERF subfamily in terms of classification, physicochemical properties, structural characteristics, chromosome distribution, gene replication and collinearity, Cis-acting elements, and potential protein interactions. Preliminary investigations of transcription during fruit cracking and normal development were also conducted. Fifty ERFs (PatiERF1~50) were identified, distributed unevenly across eight chromosomes and classified into ten groups with nineteen conserved motifs. Collinearity analysis with other plant species revealed homology, with the highest number of ERF orthologous genes found in apple (Malus domestica L.). Cis-acting elements, particularly abscisic acid response factor, were abundant in PatiERF promoters. Weighted gene co-expression network analysis (WGCNA) and quantitative real-time PCR (RT-qPCR) analysis indicated the involvement of PatiERFs in sweet cherry fruit development and cracking, and nine and four significant candidates related to these processes were speculated, respectively. Furthermore, four other classes of transcription factors (TFs), namely MYB, GRAS, BHLH, and BZIP, as well as 23 structure genes, were predicted to have co-expression and interaction relationships with PatiERFs during fruit development. This suggests their potential synergistic regulation with ERFs in the cherry fruit development process. Our study represents the first comprehensive genome-wide analysis of the ERF subfamily in sweet cherry, laying a crucial foundation for a deeper understanding of the molecular mechanisms correlated with fruit growth, development, and cracking mediated by ERF genes.

Funder

Key R&D Projects in Tibet Autonomous Region

CARS

Publisher

MDPI AG

Reference79 articles.

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