Dissecting the Regulatory Network of Maize Phase Change in <i>ZmEPC1</i> Mutant by Transcriptome Analysis.
Xiaoqi LiWeiya LiNa LiRunmiao TianFeiyan QiJuan MengYajuan JiangChenhui WangYongqiang ChenZhanyong GuoJihua TangZhanhui ZhangPublished in: Genes (2022)
The developmental phase changes of maize are closely associated with the life span, environmental adaption, plant height, and disease resistance of the plant and eventually determines the grain yield and quality of maize. A natural mutant, <i>Early Phase Change 1</i> (<i>ZmEPC1</i>), was selected from the inbred line KN5585. Compared with the wild type plant, the <i>ZmEPC1</i> mutant exhibits deceased plant stature, accelerated developmental stages, and decreased leaf size. Through the transcriptome sequencing analysis of leaf samples at flowering stage, a total of 4583 differentially expressed genes (DEGs) were screened between the mutant and wild type, including 2914 down-regulated genes and 1669 up-regulated genes. The GO enrichment and KEGG enrichment analysis revealed that the DEGs were mainly involved in hormone response, hormone signal transduction, autophagy, JA response and signal response, photosynthesis, biotic/abiotic stress, and circadian rhythms. The RT-qPCR results revealed that the most tested DEGs display consistent expression alterations between V5 and FT stages. However, several genes showed opposite expression alterations. Strikingly, most of the JA biosynthesis and signaling pathway-related genes displayed diametrically expression alterations between V5 and FT stages. miR156, a key regulator of plant phase transition, exhibited significant down-regulated expression at V5 and FT stages. The expression of two miR156 target genes were both significantly different between mutants and wild type. In conclusion, <i>ZmEPC1</i> was identified to be mainly involved in the regulation of JA-mediated signaling pathways and hormone response and signaling, which is possible to confer developmental phase change through miR156-<i>SPLs</i> pathway.
Keyphrases
- wild type
- poor prognosis
- long non coding rna
- signaling pathway
- genome wide
- transcription factor
- cell proliferation
- genome wide identification
- single cell
- binding protein
- bioinformatics analysis
- body mass index
- gene expression
- oxidative stress
- dna methylation
- endoplasmic reticulum stress
- heat stress
- risk assessment
- data analysis
- kidney transplantation