Cultivar-Specific Transcriptional and Biochemical Responses of In Vivo-Grown Camellia sinensis Plants to Long-Term Nitrogen Deficiency

Nitrogen (N) availability strongly influences tea growth and the accumulation of quality-related metabolites, but long-term responses to withdrawal of external N can vary among cultivars. In this study, we characterized phenotypic, spectral, biochemical, and transcriptomic responses of four Camellia sinensis accessions—‘Kolkhida’, ‘Karatum’, and γ-irradiation-derived mutant forms #582 and #619—during two, four, or six months of complete withdrawal of exogenous NH4NO3 in greenhouse sand culture. Phenotypic, spectral, and biochemical measurements included all four accessions at all three time points; RNA-seq data were available for all four accessions were represented at four and six months, whereas two-month point were available only for ‘Kolkhida’ and ‘Karatum’. Nitrogen withdrawal decreased L-theanine and caffeine and generally increased simple and gallated catechins, consistent with a change in carbon/nitrogen balance towards phenolic metabolism. The four cultivars exhibited markedly distinct responses. ‘Karatum’ showed the optimum resilience, with minimal phenotypic alteration and a neutral transcriptional response, while #582 demonstrated a stronger stress-associated phenotype and metabolic response. Within the available RNA-seq comparisons, DEG counts were lower at four months than at six months, while the two-month datasets for ‘Kolkhida’ and ‘Karatum’ contained the largest DEG sets for those two cultivars, suggesting a phased acclimation process. CsELIP1, CsSRG1, CsHHO2/4, CsNRT2.4, and CsTAT2 were identified as potential candidate genes associated with nitrogen limitation, flavonoid regulation, and amino acid metabolism. Our findings show that N-deficiency reactions in tea are highly cultivar- and time-dependent, making single-time-point evaluations insufficient. We propose ‘Karatum’ as a promising candidate for further evaluation in low-nitrogen dose–response and field trials based on our combined biochemical and transcriptional findings.