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Repression of flowering by the miR172 target SMZ

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Mathieu,  J
Department Molecular Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Yant,  LJ
Department Molecular Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Mürdter,  F
Department Molecular Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Küttner,  F
Department Molecular Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Schmid,  M
Department Molecular Biology, Max Planck Institute for Developmental Biology, Max Planck Society;

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Citation

Mathieu, J., Yant, L., Mürdter, F., Küttner, F., & Schmid, M. (2009). Repression of flowering by the miR172 target SMZ. PLoS Biology, 7(7): e1000148. doi:10.1371/journal.pbio.1000148.


Cite as: https://hdl.handle.net/21.11116/0000-000A-EDC1-1
Abstract
A small mobile protein, encoded by the FLOWERING LOCUS T (FT) locus, plays a central role in the control of flowering. FT is regulated positively by CONSTANS (CO), the output of the photoperiod pathway, and negatively by FLC, which integrates the effects of prolonged cold exposure. Here, we reveal the mechanisms of regulation by the microRNA miR172 target SCHLAFMUTZE (SMZ), a potent repressor of flowering. Whole-genome mapping of SMZ binding sites demonstrates not only direct regulation of FT, but also of many other flowering time regulators acting both upstream and downstream of FT, indicating an important role of miR172 and its targets in fine tuning the flowering response. A role for the miR172/SMZ module as a rheostat in flowering time is further supported by SMZ binding to several other genes encoding miR172 targets. Finally, we show that the action of SMZ is completely dependent on another floral repressor, FLM, providing the first direct connection between two important classes of flowering time regulators, AP2- and MADS-domain proteins.