Summary: Yellowing/chlorophyll breakdown is a prominent phenomenon in leaf senescence, and is associated with the degradation of chlorophyll – protein complexes. From a rice mutant population generated by ionizing radiation, we isolated nyc4‐1, a stay‐green mutant with a defect in chlorophyll breakdown during leaf senescence. Using gene mapping, nyc4‐1 was found to be linked to two chromosomal regions. We extracted Os07g0558500 as a candidate for NYC4 via gene expression microarray analysis, and concluded from further evidence that disruption of the gene by a translocation‐related event causes the nyc4 phenotype. Os07g0558500 is thought to be the ortholog of THF1 in Arabidopsis thaliana. The thf1 mutant leaves show variegation in a light intensity‐dependent manner. Surprisingly, the F_v/F_m value remained high in nyc4‐1 during the dark incubation, suggesting that photosystem II retained its function. Western blot analysis revealed that, in nyc4‐1, the PSII core subunits D1 and D2 were significantly retained during leaf senescence in comparison with wild‐type and other non‐functional stay‐green mutants, including sgr‐2, a mutant of the key regulator of chlorophyll degradation SGR. The role of NYC4 in degradation of chlorophyll and chlorophyll – protein complexes during leaf senescence is discussed.

The cultivated chrysanthemum is the most important ornamental species in the genus Chrysanthemum. However, because it is predominantly hexaploid and additionally exhibits self-incompatibility, it harbors numerous functionally redundant genes and displays extremely high heterozygosity. As a result, its genomic architecture is highly complex, making it challenging to interpret data obtained from omics analyses such as RNA-seq. To provide a genetically tractable model, we previously developed Gojo-0, a self-compatible, pure line of the diploid wild species C. seticuspe. In this study, we established Gojo-1, an improved self-compatible pure line derived from Gojo-0 and its sibling lines, exhibiting enhanced viability and culture performance. Leveraging these traits, we performed CRISPR–Cas9 editing of the AGAMOUS orthologs and successfully isolated mutants with altered floral organ morphology, demonstrating the line’s suitability for functional genomics. Comparative genome analysis showed that, aside from chromosome 1, the Gojo-1 genome is highly similar to that of Gojo-0, whose complete sequence has been determined. Taken together, these features indicate that Gojo-1 will serve as a valuable resource for future omics-based studies and a broad range of additional research applications.