The study demonstrates that the chromatin remodeler DDM1 is essential for biomass heterosis in Arabidopsis thaliana hybrids, as loss of DDM1 function leads to reduced rosette growth and extensive genotype‑specific transcriptomic and DNA methylation changes. Whole‑genome bisulfite sequencing revealed widespread hypomethylation in ddm1 mutants, while salicylic acid levels were found unrelated to heterosis, indicating that epigenetic divergence, rather than SA signaling, underpins hybrid vigor.

The study examined molecular responses in grapevine leaves with and without esca symptoms, using metabolite profiling, RNA‑seq and whole‑genome bisulfite sequencing. Metabolic and transcriptomic changes were confined to symptomatic leaves and linked to local DNA‑methylation alterations, while asymptomatic leaves showed distinct but overlapping methylation patterns, some present before symptoms, indicating potential epigenetic biomarkers for early disease detection.

The study identifies GyrB3 as a novel nuclear factor that interacts with histone deacetylases to regulate transposable element silencing in plants, acting as a suppressor of IBM1 deficiency–induced epigenetic defects. Loss of GyrB3 reduces DNA methylation and increases H3 acetylation at TEs, demonstrating the importance of histone deacetylation for genome stability.

The study examined gene expression, DNA methylation, and small RNA profiles in a Citrus hybrid (C. reticulata × C. australasica) using haplotype‑resolved subgenome assemblies, revealing allele‑specific expression and asymmetric CHH methylation that correlated with increased transcription and 24‑nt siRNA accumulation at promoters. This unconventional association suggests RNA‑directed DNA methylation (RdDM) can activate transcription in citrus fruit and provides a pipeline for epigenomic analysis of complex hybrids relevant to disease resistance breeding.

The study investigates the function of two GT47B arabinan arabinosyltransferases in the liverwort Marchantia polymorpha, generating loss‑of‑function and overexpression lines to assess cell wall composition. Using CoMPP, glycosyl linkage analysis, and LM6 immunolabelling, the authors found that MpARADL2 mutants have reduced 1,5‑L‑arabinan epitopes in elaters despite unchanged overall 5‑linked Araf levels, suggesting additional enzymes compensate in thallus tissue. Attempts to express and purify the enzymes in HEK293 cells failed, implying a clade‑specific solubility requirement and highlighting the need to identify interacting partners.

The study characterizes the composition and structure of cell wall glycans in eight tissue types of the liverwort Marchantia polymorpha, revealing both typical land‑plant features and unique traits such as abundant (1,5)-arabinan in sporophytes and low overall pectin levels. Comparative genomic analysis shows a diversified glycosyltransferase repertoire relative to Arabidopsis, and the authors created a Gateway‑compatible library of 93 M. polymorpha GTs to facilitate future functional studies.

The authors identified MpCAFA, a protein combining CAPS-like and FAP115-like domains, as a key factor for rapid ciliary swimming in the liverwort Marchantia polymorpha spermatozoids. Loss-of-function mutants displayed markedly reduced swimming speed despite normal axoneme structure, chemotaxis, and fertility, and these defects were rescued by a MpCAFA‑mCitrine fusion that localized along the entire cilium. Both the CAPS-like and FAP115-like regions are required for MpCAFA’s function and ciliary targeting, establishing it as a major ciliary protein and a marker for visualizing spermatozoid motility.

The study investigated meristem activation in the liverwort Marchantia polymorpha, revealing that simulated shade causes alternating inactivity of meristems. Transcriptomic comparison of active versus inactive meristems identified the cytochrome P450 monooxygenase MpCYP78E1 as an inhibitor of meristem activity and initiation, with loss- and gain-of-function mutants confirming its regulatory role in shoot branching architecture.

The study shows that the SnRK1 catalytic subunit KIN10 directs tissue-specific growth‑defense programs in Arabidopsis thaliana by reshaping transcriptomes. kin10 knockout mutants exhibit altered root transcription, reduced root growth, and weakened defense against Pseudomonas syringae, whereas KIN10 overexpression activates shoot defense pathways, increasing ROS and salicylic acid signaling at the cost of growth.

The study examines how the SnRK1 catalytic subunit KIN10 integrates carbon availability with root growth regulation in Arabidopsis thaliana. Loss of KIN10 reduces glucose‑induced inhibition of root elongation and triggers widespread transcriptional reprogramming of metabolic and hormonal pathways, notably affecting auxin and jasmonate signaling under sucrose supplementation. These findings highlight KIN10 as a central hub linking energy status to developmental and environmental cues in roots.