The common vetch (Vicia sativa L.) is a self-pollinated annual forage legume that is widely distributed worldwide. It has wide adaptability and high nutritional value and is commonly used as an important protein source for livestock feed. However, pod shattering seriously limits the yield of common vetch. To clarify the mechanism of pod shattering in common vetch, the pod walls of three shattering-resistant (SR) accessions (B65, B135, and B392) and three shattering-susceptible (SS) accessions (L33, L170, and L461) were selected for transcriptome sequencing. A total of 17,190 differentially expressed genes (DEGs) were identified in the pod wall of B135 and L461 common vetch at 5, 10, 15, 20, and 25 days after anthesis. Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis showed that “phenylpropanoid biosynthesis” was the most significantly enriched pathway, and 40 structural genes associated with lignin biosynthesis were identified and differentially expressed in B135 and L461 common vetch. We analysed the DEGs in the pod wall of three SR and three SS accessions at 15 days after anthesis, and most of the DEGs were consistent with the significant enrichment pathways identified in B135 and L461 common vetch. The total lignin content of SR accessions was significantly lower than the SS accessions. The present study lays a foundation for understanding the molecular regulatory mechanism of pod shattering related to lignin biosynthesis in common vetch and provides reference functional genes for breeders to further cultivate shattering-resistant common vetch varieties.

Alfalfa is the most widely cultivated perennial legume forage crop worldwide. Drought is one of the major environmental factors influencing alfalfa productivity. However, the molecular mechanisms underlying alfalfa responses to drought stress are still largely unknown. This study identified a drought-inducible gene of unknown function, designated as Medicago sativa DROUGHT-INDUCED UNKNOWN PROTEIN 1 (MsDIUP1). MsDIUP1 was localized to the nucleus, chloroplast, and plasma membranes. Overexpression of MsDIUP1 in Arabidopsis resulted in increased tolerance to drought, with higher seed germination, root length, fresh weight, and survival rate than in wild-type (WT) plants. Consistently, analysis of MsDIUP1 over-expression (OE) alfalfa plants revealed that MsDIUP1 also increased tolerance to drought stress, accompanied by physiological changes including reduced malondialdehyde (MDA) content and increased osmoprotectants accumulation (free proline and soluble sugar), relative to the WT. In contrast, disruption of MsDIUP1 expression by RNA interference (RNAi) in alfalfa resulted in a drought-hypersensitive phenotype, with a lower chlorophyll content, higher MDA content, and less osmoprotectants accumulation than that of the WT. Transcript profiling of alfalfa WT, OE, and RNAi plants during drought stress showed differential responses for genes involved in stress signaling, antioxidant defense, and osmotic adjustment. Taken together, these results reveal a positive role for MsDIUP1 in regulating drought tolerance.

As the second most abundant natural polymer, accounting for approximately 30% of the organic carbon in the biosphere, lignin plays an essential role in plant development. However, a high lignin content affects the nutritional quality of alfalfa (Medicago sativa L.), the most widely cultivated perennial legume forage crop. Histological analysis indicated that G-lignin and S-lignin were present in the stem, leaf, and petiole of alfalfa, and the deposition of lignin increased gradually in descending internodes. Neutral detergent fiber (NDF), acid detergent fiber (ADF), and acid detergent lignin (ADL) contents continually increased from the top to the bottom of the stem, and ADL content showed a similar trend in leaves. Alfalfa leaves and stems from five different nodes (1, 2, 4, 6, and 8) were used as materials to investigate molecular regulatory mechanisms in lignin synthesis by RNA sequencing. Respectively 8074 and 7752 differentially expressed genes (DEGs) were identified in leaves and stems, and 1694 DEGs were common to the two tissues. "Phenylpropanoid biosynthesis" was the most enriched pathway in both leaves and stems, and 134 key regulatory genes in lignin synthesis were identified by a weighted gene co-expression network analysis. The NAC family transcription factor MsNST1 gene was highly expressed in old leaf and stem tissues. The deposition pattern of G- and S-lignin differed among M. truncatula wild-type, nst1 mutants, and overexpression lines, and the transcription levels of lignin synthesis genes such as HCT, F5H, and COMT in these three materials also differed. These results suggest that MsNST1 affects lignin synthesis in alfalfa. These findings provide a genetic basis and abundant gene resources for further study of the molecular mechanisms of lignin synthesis, laying a foundation for low-lignin alfalfa breeding research.