The study examined how DNA methylation influences cold stress priming in Arabidopsis thaliana, revealing that primed plants exhibit distinct gene expression and methylation patterns compared to non-primed plants. DNA methylation mutants, especially met1 lacking CG methylation, showed altered cold memory and misregulation of the CBF gene cluster, indicating that methylation ensures transcriptional precision during stress recall.

The authors used a bottom‑up thermodynamic modelling framework to investigate how plants decode calcium signals, starting from Ca2+ binding to EF‑hand proteins and extending to higher‑order decoding modules. They identified six universal Ca2+-decoding modules that can explain variations in calcium sensitivity among kinases and provide a theoretical basis for interpreting calcium signal amplitude and frequency in plant cells.

The study systematically identified heterosis-associated genes and metabolites in rice, functionally validated three genes influencing seedling length, and integrated these molecules into network modules to explain heterosis variance. Predominant additive and partially dominant inheritance patterns were linked to parental genomic variants and were shown to affect 17 agronomic traits in rice, as well as yield heterosis in maize and biomass heterosis in Arabidopsis. The work highlights the quantitative contribution of transcriptomic and metabolomic variation, especially in phenylpropanoid biosynthesis, to hybrid vigor.

The study evaluated two approaches for defining heterotic groups in bitter gourd (Momordica charantia L.) by comparing traditional morphological clustering with a breeding value-based method (HSGCA). Using a half‑diallel of 11 inbred lines to produce 55 F1 hybrids, HSGCA clustering into three groups more reliably predicted heterosis, especially in inter‑group crosses, than K‑means clustering of morphological traits. These results support HSGCA as a superior tool for efficient hybrid breeding in bitter gourd.

The study evaluated morphological, physiological, and yield traits of eight sweet pepper (Capsicum annuum) hybrids compared to two check varieties, assessing standard heterosis and identifying superior hybrids. Field and lab experiments using RCBD and CRD designs with three replications revealed significant trait variation, and statistical analyses (Pearson correlation and PCA) highlighted key associations for breeding.

Using genome‑wide association studies in Arabidopsis thaliana, the authors identified the chromatin‑associated protein CDCA7 as a trans‑regulator that specifically controls CG methylation (mCG) and TE silencing. CDCA7 and its paralog CDCA7β bind the remodeler DDM1, modulating its activity without broadly affecting non‑CG methylation or histone variant deposition, and natural variation in CDCA7 regulatory sequences correlates with local ecological adaptation.

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 generated high‑quality genome assemblies for 12 indica and japonica rice accessions and demonstrated that structural variants (SVs) are abundant and strongly associated with heterosis across 17 agronomic traits. Correlation analyses revealed that SV count between parental lines predicts hybrid performance, and functional validation of SVs in S5‑ORF5 and OsBZR1 confirmed their contributions to seed setting rate and yield heterosis, supporting an overdominance model for inter‑subspecific hybrid vigor.

The study shows that silencing of NOR2 rRNA genes in Arabidopsis thaliana depends primarily on CHH-context cytosine methylation, particularly mediated by CMT2 and the chromatin remodeler DDM1, rather than CG or CHG methylation. Comparative promoter analysis revealed a prevalence of CHH sites in plant rDNA promoters, explaining why CHH methylation mutants disrupt NOR2 silencing more strongly, while NOR2 loci are hyper‑methylated and more condensed than NOR4.