Comparative Transcriptome Analysis Reveals the Mechanisms Underlying Differential Seed Vigor in Two Contrasting Peanut Genotypes

• Published in: Agriculture (Basel) Vol. 12; no. 9; p. 1355
• Main Authors: Li, Shengyu, Zeng, Jiali, Zheng, Zhao, Zhou, Qi, Chen, Shaona, Zheng, Yixiong, Wan, Xiaorong, Yang, Bin
• Format: Journal Article
• Language: English
• Published: Basel MDPI AG 01.09.2022
• Subjects: Abscisic acid; Arabinogalactan; Cell walls; Cellulose; Comparative analysis; Cultivars; DEGs; DNA binding proteins; Dormancy; Gene expression; Gene regulation; Genes; Genotypes; Germination; Homology; Hormones; Oxidation; Oxidative stress; peanut; Peanuts; Physiological effects; Polygalacturonase; Regulatory mechanisms (biology); Scavenging; Seed germination; seed vigor; Seeds; Signal transduction; Signaling; Transcription factors; transcriptome; Transcriptomes; Vigor; China; Beijing China; United States > US
• ISSN: 2077-0472; 2077-0472
• DOI: 10.3390/agriculture12091355

Seed vigor is an important agronomic trait, and wide variation exists among peanut accessions. However, the detailed regulatory mechanisms underlying differences in seed vigor between varieties are not known in peanut yet. Here, we performed a comparative transcriptome analysis of germinating seeds in two contrasting peanut accessions, namely A86 (high-vigor variety) and A279 (low-vigor variety). A total of 583 and 860 differentially expressed genes (DEGs) were identified at two imbibition stages between A86 and A279, respectively. Pathway enrichment tests highlighted the cell wall remodeling-, hormone signaling-, transcriptional regulation-, and oxidative stress-related DEGs, which may explain to a certain extent the difference in seed vigor between the two cultivars. Among them, the largest number of cell wall remodeling-related DEGs were extensions followed by cellulose synthases, fasciclin-like arabinogalactan proteins, polygalacturonases, expansins, and pectinesterases and the hormone signaling-related DEGs belonged mainly to the auxin and ethylene signaling pathway. The majority of transcriptional regulation-related DEGs were MYB, FAR1, and bHLH transcription factors, and the oxidative stress-related DEGs were mainly peroxidases. Further physiological analyses indicated that differences in seed vigor between A86 and A279 may be associated with differences in the ROS-scavenging abilities mediated by peroxidases. Moreover, we identified 16 DEGs homologous to known Arabidopsis regulators of seed dormancy and germination, suggesting that these DEGs would play similar functional roles during peanut seed germination. Our results not only provide important insights into the difference in seed vigor between varieties, but offer candidate genes that are worth investigating in future studies.