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Biology subjects

Hussain, S. B.

Publications and source records attributed to Hussain, S. B..

2 recordsLinked to original sources

Mature Citrus Leaves Undergo Coordinated Photosynthetic Downregulation to Support Flush-Driven Carbon and Nitrogen Sink Demand

The source{square}sink attenuation hypothesis suggests that plants regulate carbon fixation in response to fluctuations in sink demands. Many evergreen trees exhibit flushing growth patterns, where new shoot development generates a strong, transient demand for both carbon and nitrogen that may influence the function of mature leaves. This study examined the source-sink attenuation hypothesis in the context of vegetative sink growth by investigating the photosynthetic capacity and nitrogen dynamics in mature citrus leaves across three stages of flush development. In contrast to expectations, photosynthesis declined as flush growth progressed. Early flush initiation induced stomatal limitation in mature leaves, whereas as sink demand from further shoot growth continued carboxylation capacity and Rubisco abundance declined, despite relatively stable total leaf nitrogen. These results suggest that mature leaves undergo selective protein retooling under prolonged sink demand, constraining CO{square} fixation while maintaining C export. Overall, this study revealed that under strong combined N and C sink demands, mature citrus leaves function primarily as regulated carbon conduits rather than dynamically upregulating photosynthesis, providing new insight into source-sink coordination in woody perennial species. HighlightCitrus flush growth shows that mature leaves suppress photosynthesis through stomatal and biochemical regulation while reallocating carbon and nitrogen to support new shoot development, challenging classic source-sink theory.

plant biology↗

Uncovering Carbohydrate Metabolism and Endogenous Hormone Regulation during Flush Phenology in Citrus Trees using Proteomics and Metabolomics

Rapid shoot growth (flushing) phenology is a fundamental developmental process in perennial woody plants such as citrus. In a separate study, we identified physiological shifts from photosynthesis to mobilization of nitrogen and carbohydrate to support new shoot growth. However, the underlying molecular and biochemical signals remain largely unknown. Here, we integrated proteomic and metabolomic analyses to investigate carbohydrate and hormone dynamics across three flush stages in Citrus sinensis: quiescent period (stage 1), new shoot initiation (stage 2), and full expansion (stage 3). Sucrose, maltose, and trehalose accumulated in apical leaves during early shoot initiation and declined during subsequent shoot expansion, indicating depletion of carbohydrate reserves and enhanced resource remobilization. These changes were accompanied by coordinated regulation of starch-metabolizing enzymes, including ADP-glucose pyrophosphorylase, -amylase, and isoamylase, supporting a transition from carbon storage to carbon export during active shoot growth. Indole-3-acetic acid increased continuously across stages, while trans-zeatin and gibberellin A{square} showed opposite trends in apical versus basal leaves before jointly increasing at stage 3. Hormone analysis revealed dynamic and coordinated signaling changes during flush development. Abscisic acid declined from stage 1 to 2, whereas jasmonoyl-isoleucine and salicylic acid increased from stage 2 to 3. Some hormone-responsive proteins, including Gretchen Hagen 3 and Gibberellin-insensitive dwarfing 1, exhibited expression patterns consistent with hormonal fluctuations. Together, these results support a stage-specific regulatory framework in which carbohydrate metabolism and hormone signaling are tightly coordinated to regulate rapid source-sink transitions during citrus flush development. HighlightWe reveal how carbohydrate metabolism and hormone signaling are spatiotemporally coordinated during citrus shoot growth phenology, and we develop an integrated metabolic-hormonal model that connects carbon allocation to developmental transitions.

plant biology↗