Fraxinus mandshurica (Manchurian ash) is an ecologically and economically valuable hardwood tree native to Northeast Asia, yet its genomic resources remain limited. We assembled its complete chloroplast (cp) genome (155,559 bp) using hybrid PacBio and Illumina sequencing and performed comparative, phylogenetic, and evolutionary analyses. The cp genome exhibits a typical quadripartite structure encoding 132 gene copies, comprising 114 unique genes (80 protein-coding, 30 tRNA, and 4 rRNA genes), with 18 genes duplicated in the inverted repeat (IR) regions. Simple sequence repeat analysis revealed dominance of mononucleotide A/T repeats. Phylogenetic analysis of 53 complete cp genomes strongly supported the monophyly of Oleaceae and resolved F. mandshurica as sister to the North American F. nigra, consistent with previously proposed Miocene intercontinental dispersal scenarios between East Asia and North America. Most protein-coding genes were under strong purifying selection (Ka/Ks << 1), whereas petB, rpl2, and several ndh genes showed elevated Ka/Ks values that are suggestive of altered selective constraint but are based on very few substitutions and are therefore not, on their own, evidence of positive selection. Nucleotide diversity (Pi) analysis identified 15 hypervariable intergenic spacers (mean Pi = 0.067), among which trnM-CAU-rps14, ndhJ-ndhK, and petL-petG represent promising candidate barcode regions requiring further validation. This study provides a high-quality, fully annotated cp genome of F. mandshurica and a valuable genomic resource for future phylogenetic, population genetic, and conservation studies of this important genus.
Wen-Xuan Liu, Jia-Wei Wu, Hao-Nan Zheng et al.· International Journal of Mol...· 0 citations
ABSTRACT MYB transcription factors play crucial roles in regulating plant growth and development, but the functions of the MYB‐related subfamily in woody plants remain poorly understood. In this study, we characterized PagMYBR028, an MYB‐related transcription factor from poplar ‘84 K’ ( Populus alba × Populus glandulosa), which was predominantly expressed in leaves and xylem. Compared with WT plants, PagMYBR028‐overexpressing transgenic poplar exhibited reduced leaf area and retarded secondary xylem development, whereas PagMYBR028‐RNAi lines displayed the opposite phenotypes. Further analysis revealed that PagMYBR028 interacts with PagMYBR005, a related regulator with overlapping functions in poplar development. Both proteins directly repress the expression of PagGRF12b, and their interaction enhances this transcriptional repression. In addition, overexpression of PagGRF12b promoted secondary cell wall deposition. Taken together, our results delineate a PagMYBR028‐PagMYBR005‐PagGRF12b module that coordinately regulates poplar growth and secondary wall development, providing new insights into the transcriptional network underlying wood formation and a theoretical basis for molecular breeding in trees.