A gain-of-function mutation in BnaIAA13 disrupts vascular tissue and lateral root development in Brassica napus.
Jinxiang GaoPei QinShan TangLiang GuoCheng DaiJing WenBin YiChaozhi MaJinxiong ShenTingdong FuJun ZouJinxing TuPublished in: Journal of experimental botany (2024)
Rapeseed (Brassica napus) is an important oilseed crop worldwide. Plant vascular tissues are responsible for material transport and provide mechanical support. The lateral roots (LRs) absorb sufficient water and nutrients. The genetic basis of vascular tissues and LRs development in rapeseed remains unknown. This study characterized an EMS-mutagenized rapeseed mutant, T16, which showed dwarf stature, reduced LRs, and leaf wilting. Scanning electron microscopy observations showed that the internode-cell shortened. Observations of the tissue sections revealed defects in the development of vascular bundles in the stems and petioles. Genetic analysis revealed that the phenotypes of T16 were controlled by a single semi-dominant nuclear gene. Map-based cloning and genetic complementarity confirmed that BnaA03.IAA13 is the functional gene, a G-to-A mutation in second exon changed the glycine at the 79th position to glutamic acid, disrupting the conserved degron motif VGWPP. Transcriptome analysis in roots and stems showed that auxin and cytokinin signaling pathways were disordered in T16. Evolutionary analysis showed that AUXIN/INDOLE-3-ACETIC ACID was conserved during plant evolution. The heterozygote of T16 significantly reduced the plant height while maintaining other agronomic traits. Our findings provide novel insights into the regulatory mechanisms of vascular tissues and LRs development, and provide a new germplasm resource for rapeseed breeding.
Keyphrases
- genome wide
- electron microscopy
- single cell
- gene expression
- copy number
- transcription factor
- dna methylation
- genome wide identification
- arabidopsis thaliana
- signaling pathway
- body mass index
- stem cells
- minimally invasive
- physical activity
- epithelial mesenchymal transition
- mesenchymal stem cells
- pi k akt
- cell proliferation
- cell therapy
- genome wide analysis
- cell wall