SUMMARY Drought is an environmental factor that can severely influence plant development and distribution, and greatly affect the yield and economic value of crops. We characterized CmBBX19, a BBX family subgroup IV member gene, from the transcriptome database of Chrysanthemum morifolium in response to drought stress. Drought stress and ABA treatments downregulated the expression of CmBBX19. We generated CmBBX19‐overexpressing (CmBBX19‐OX) lines and CmBBX19‐suppressing lines (CmBBX19‐RNAi), and found that suppressed expression of CmBBX19 led to enhanced drought tolerance compared with the wild‐type (WT) controls, while CmBBX19‐OX lines exhibited reduced drought tolerance. Downstream gene analysis showed that CmBBX19 modulates drought tolerance mainly through inducing changes in the expression of ABA‐dependent pathway genes, including protective protein, redox balance and cell wall biogenesis genes, such as responsive to ABA 18, peroxidase 12, and cellulose synthase‐like protein G2. Moreover, CmBBX19 was shown to interact with CmABF3, a master ABA signaling component, to suppress expression of these downstream genes. We conclude that BBX19‐ABF3 module functions in the regulation of drought tolerance of chrysanthemum through an ABA‐dependent pathway.

Developmental transitions in plants require adequate carbon resources, and organ abscission often occurs due to competition for carbohydrates/assimilates. Physiological studies have indicated that organ abscission may be activated by sucrose deprivation; however, an underlying regulatory mechanism that links sucrose transport to organ shedding has yet to be identified. Here, we report that transport of sucrose and the phytohormone auxin to petals through the phloem of the abscission zone (AZ) decreases during petal abscission in rose (Rosa hybrida), and that auxin regulates sucrose transport into the petals. Expression of the sucrose transporter RhSUC2 decreased in the AZ during rose petal abscission. Similarly, silencing of RhSUC2 reduced the sucrose content in the petals and promotes petal abscission. We established that the auxin signaling protein RhARF7 binds to the promoter of RhSUC2, and that silencing of RhARF7 reduces petal sucrose contents and promotes petal abscission. Overexpression of RhSUC2 in the petal AZ restored accelerated petal abscission caused by RhARF7 silencing. Moreover, treatment of rose petals with auxin and sucrose delayed ethylene-induced abscission, while silencing of RhARF7 and RhSUC2 accelerated ethylene-induced petal abscission. Our results demonstrate that auxin modulates sucrose transport during petal abscission, and that this process is regulated by a RhARF7-RhSUC2 module in the AZ.

SUMMARY Chrysanthemum (Chrysanthemum morifolium) is well known as a photoperiod‐sensitive flowering plant. However, it has also evolved into a temperature‐sensitive ecotype. Low temperature can promote the floral transition of the temperature‐sensitive ecotype, but little is known about the underlying molecular mechanisms. Here, we identified MADS AFFECTING FLOWERING 2 (CmMAF2), a putative MADS‐box gene, which induces floral transition in response to low temperatures independent of day length conditions in this ecotype. CmMAF2 was shown to bind to the promoter of the GA biosynthesis gene CmGA20ox1 and to directly regulate the biosynthesis of bioactive GA1 and GA4. The elevated bioactive GA levels activated LEAFY (CmLFY) expression, ultimately initiating floral transition. In addition, CmMAF2 expression in response to low temperatures was directly activated by CmC3H1, a CCCH‐type zinc‐finger protein upstream. In summary, our results reveal that the CmC3H1–CmMAF2 module regulates flowering time in response to low temperatures by regulating GA biosynthesis in the temperature‐sensitive chrysanthemum ecotype.

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