Moso bamboo (Phyllostachys edulis (Carriere) J. Houzeau), native to China, is one of the most economically and ecologically important bamboo species. Since the economic interests and the strong clonality, it has been widely cultivated in southern China, which inevitably reduces the natural stands and leads to gene loss in this species. In this study, three natural populations of Moso bamboo distributed in Anhui, Guangxi, and Zhejiang province, were used to analyze the correlation between phenotypic traits, cell structure, and material properties from the perspective of phenotypic, genetic, and environmental. Among those traits and properties, fiber width was correlated with wall thickness at breast height and average nodes length under branch positively. Leaf length was correlated positively with fiber lumen diameter and parenchyma lumen diameter. Furthermore, it showed a very close correlation between moisture content, bending strength, modulus of elasticity, and diameter at breast height, clear height, and leaf length. The lumen diameter of fiber cell wall thickness is positively correlated with bending strength and modulus of elasticity. Density is positively correlated with parenchyma cell wall thickness. The experimental design is relatively detailed and representative, and the workload is huge. This study reflects the research objectives with scientific and rational experiments and data. This study will analyze the differences of various indicators from the perspective of genetic to build a bridge between micro-structure and macro-structure for rational utilization of the whole area of Moso bamboo resources in China.

As a woody plant, peony (Paeonia suffruticosa) has a long growth cycle and inefficient traditional breeding techniques. There is an urgent need in peony molecular breeding to establish an efficient and stable in vitro regeneration and genetic transformation system, in order to overcome the recalcitrant characteristics of peony regeneration and shorten the breeding cycle. The development of plant somatic embryos is an important way to establish an efficient and stable in vitro regeneration and genetic transformation system. Plant-specific WUSCHEL-related homeobox (WOX) family transcription factors play important roles in plant development, from embryogenesis to lateral organ development. Therefore, in this research, four PoWOX genes of “Fengdan” (Paeonia ostii) were cloned from the peony genome and transcriptome data of preliminary peony somatic embryos. The sequence characteristics and evolutionary relationships of the PoWOX genes were analyzed. It was demonstrated that the four PoWOX genes, named PoWOX1, PoWOX4, PoWOX11, and PoWOX13, belonged to three branches of the WOX gene family. Their expression patterns were analyzed at different stages of development and in different tissues of peony seedlings. The expression localization of the PoWOX genes was determined to be the nucleus via subcellular localization assay. Finally, the interaction protein of the PoWOX genes was identified via yeast two-hybrid assay combined with bimolecular fluorescence complementation assay. It was shown that PoWOX1 and PoWOX13 proteins could form homodimers by themselves, and PoWOX11 interacted with PoWOX1 and PoWOX13 to form heterodimers. Peony stem cell activity may be regulated from PoWOX1 and PoWOX13 by forming dimers and moving to peony stem cells through plasmodesmata. Additionally, PoWOX11–PoWOX1 and PoWOX11–PoWOX13 may play important regulatory functions in promoting the proliferation of stem cells and maintaining the homeostasis of stem cells in the SAM of peony stems. Exploring the critical genes and regulatory factors in the development of the peony somatic embryo is beneficial not only to understand the molecular and regulatory mechanisms of peony somatic embryo development but also to achieve directed breeding and improvements in efficiency through genetic engineering breeding technology to accelerate the fundamental process of molecular breeding in peony.

Narcissus tazetta var. chinensis M.Roem. (Chinese Narcissus) is a traditional and famous flower in China, and its corona shows a transition from green to yellow with the opening of flowers, which is of great ornamental value. To investigate the molecular mechanism of the corona color-forming in the Chinese Narcissus, in this study, a MYB gene was screened from the transcriptome of the corona by bioinformatics analysis methods, named NtMYB9. The expression level of the NtMYB9 gene was significantly higher in the corona than in the tepal, filament, ovary and leaf, and reached the highest level at the fourth period of complete coloration of the corona. The full-length sequence of the NtMYB9 coding region was cloned using the corona cDNA as a template. Sequence analysis revealed that NtMYB9 protein contained R2 and R3 domains, phylogenetic tree analysis showed that the NtMYB9 protein was most closely related to flavonol activators. Subcellular localization showed that NtMYB9 was localized in the nucleus. The overexpression of NtMYB9 gene into tobacco leaves and the expression level of seven enzyme genes related to the flavonoid biosynthesis pathway were significantly up-regulated. The transient transformation of Petunia × hybrida (Petunia) and Phalaenopsis aphrodite (Phalaenopsis) significantly revealed that the NtMYB9 gene could turn flowers yellow. These results suggest that the NtMYB9 gene is involved in the positive regulation of flavonoid biosynthesis in the Chinese Narcissus and may promote the synthesis of flavonols. In conclusion, these findings provide a valuable resource for further studies on the regulatory mechanism of the flavonoid biosynthesis pathway, and they are also beneficial to the molecular breeding of Chinese Narcissus.