2003
DOI: 10.1038/nature01549
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Adaptation of photoperiodic control pathways produces short-day flowering in rice

Abstract: The photoperiodic control of flowering is one of the important developmental processes of plants because it is directly related to successful reproduction. Although the molecular genetic analysis of Arabidopsis thaliana, a long-day (LD) plant, has provided models to explain the control of flowering time in this species, very little is known about its molecular mechanisms for short-day (SD) plants. Here we show how the photoperiodic control of flowering is regulated in rice, a SD plant. Overexpression of OsGI, … Show more

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Cited by 676 publications
(653 citation statements)
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“…These genes are regulated by vernalization and by active alleles of VRN1, consistent with the idea that these genes are downstream targets of the VRN1 gene (see Introduction). SOC1-like and CONSTANS-like genes, which regulate the reproductive development of rice 38,39 , were also identified as direct targets of VRN1. FT1 was identified as a direct binding target of VRN1 and also shows altered expression during early development in the early flowering VRN1-HA transgenic plants (Figs 2 and 4).…”
Section: Discussionmentioning
confidence: 99%
“…These genes are regulated by vernalization and by active alleles of VRN1, consistent with the idea that these genes are downstream targets of the VRN1 gene (see Introduction). SOC1-like and CONSTANS-like genes, which regulate the reproductive development of rice 38,39 , were also identified as direct targets of VRN1. FT1 was identified as a direct binding target of VRN1 and also shows altered expression during early development in the early flowering VRN1-HA transgenic plants (Figs 2 and 4).…”
Section: Discussionmentioning
confidence: 99%
“…Photoperiodic flowering has been explained by the coincidence of CONSTANS (CO) diurnal expression rhythm and external light signals in both SD and LD model annuals, rice (Oryza sativa) and Arabidopsis (Arabidopsis thaliana), respectively (Suárez-López et al, 2001;Hayama et al, 2003). In both species, CO controls flowering through the CETS (for CEN, TFL1, and FT) family protein FLOWERING LOCUS T (FT), which is thought to be a universal flowering signal (Suárez-López et al, 2001;Hayama et al, 2003;Komiya et al, 2009;Turnbull, 2011).…”
mentioning
confidence: 99%
“…In both species, CO controls flowering through the CETS (for CEN, TFL1, and FT) family protein FLOWERING LOCUS T (FT), which is thought to be a universal flowering signal (Suárez-López et al, 2001;Hayama et al, 2003;Komiya et al, 2009;Turnbull, 2011). In the LD plant Arabidopsis, CO protein accumulates in the leaf phloem companion cells and activates FT expression only in LDs when the light period coincides with the CO expression peak in the late afternoon Valverde et al, 2004;Corbesier et al, 2007).…”
mentioning
confidence: 99%
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“…4a). The expression levels of OsLFL1 as negative regulators of Ehd1 (Peng et al 2007) and Hd1 as a negative regulator of Hd3a/RFT1 (Yano et al 2000;Hayama et al 2003) under LD conditions were not altered significantly in Ubi1::OsNF-YC2:GFP, Ubi1::OsNF-YC4:GFP, and Ubi1::OsNF-YC6:GFP plants ( Supplementary Figs. S4, S5, S6).…”
Section: Osnf-yc Proteins Are Ld-specific Flowering Regulatorsmentioning
confidence: 99%