The Stress-Repressive Zinc Finger (SRZ) family is a class of zinc finger proteins in plants that has been closely associated with plant growth, development, and stress responses. In this study, we conducted a genome-wide identification of the SRZ family members and identified 14 and 10 members in rice and Arabidopsis, respectively. We further characterized their phylogenetic relationships, gene structures, conserved motifs, promoter cis-elements, synteny, and spatiotemporal expression patterns. To investigate the functional role of this family in rice, we generated targeted mutants of OsSRZ1 using the CRISPR/Cas9 system. Phenotypic analysis revealed that srz1 knockout mutants exhibited significantly reduced plant height. Notably, the homozygous mutant srz1 completely failed in panicle exsertion from the flag leaf sheath, resulting in complete enclosure, whereas the heterozygous mutant srz1(h) exhibited only partial panicle exsertion. Further cytological observations revealed abnormal floral organ development and premature anther senescence in srz1, accompanied by a significant reduction in seed setting rate—srz1(h) set significantly fewer seeds, whereas srz1 exhibited complete sterility with a seed setting rate of 0%. Collectively, these findings suggest that members of the SRZ family may play important roles in rice growth and development. Our results demonstrate that OsSRZ1 is a critical regulator of plant height and panicle exsertion by regulating internode elongation, and that its disruption leads to premature anther programmed cell death (PCD) and consequent seed setting failure.

Vivipary adversely affects the production process of the cucumber seed industry and greatly limits the popularization of cucumber varieties. Identification of the cucumber seed vivipary phenotype and screening of vivipary-associated genes will provide important theoretical value and practical significance for solving this problem in agricultural production. In this study, cucumber near-isogenic lines with significant differences in vivipary traits (viviparous line F and non-viviparous line BF) were successfully screened and used to construct genetic populations. Bulk segregant analysis (BSA) and QTL-seq were performed to fine-map the major-effect quantitative trait locus associated with vivipary variation. Based on QTL and BSA analyses, CsaV3_3G044640 (designated CsCYP82D47), which encodes a cytochrome P450 family protein, was identified as a candidate gene associated with cucumber vivipary. CsCYP82D47 exhibits obvious tissue specificity and is highly expressed in leaves, sprouts, and seeds. However, no significant difference in CsCYP82D47 expression was detected between viviparous and non-viviparous cucumber materials. Further sequence analysis revealed multiple mutation sites in this gene between different genotypes. Specifically, the CYP82D47 protein in viviparous materials harbours one amino acid insertion (L63) and two missense mutations (M71L and S124L). In addition, the altered leucine residue distribution in viviparous cucumber may enlarge the substrate channel and enhance substrate catalytic efficiency, which may contribute to the vivipary phenotype. In summary, this study identifies a promising candidate gene potentially related to cucumber vivipary, which lays a foundation for further exploration of the molecular mechanism underlying cucumber vivipary and provides a potential genetic resource for cucumber molecular breeding.