2011
DOI: 10.5511/plantbiotechnology.11.0823b
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Characterization and transgenic study of CONSTANS-LIKE8 (COL8) gene in Arabidopsis thaliana: expression of 35S:COL8 delays flowering under long-day conditions

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Cited by 40 publications
(23 citation statements)
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“…Previous studies have demonstrated that a functional B-box II domain is required for flower induction (Griffiths et al, 2003;Martin et al, 2004;Campoli et al, 2012). Interestingly, the overexpression of COL8, which is a COL TF with a single B-box domain, resulted in a phenotype with delayed flowering under LD conditions in Arabidopsis (Takase et al, 2011). Therefore, it seems that the absence of the B-box II domain in some COL TFs does not necessarily affect the regulation of flowering.…”
Section: Identification Of Six Bncol Tfs With a Full-length Orfmentioning
confidence: 91%
See 1 more Smart Citation
“…Previous studies have demonstrated that a functional B-box II domain is required for flower induction (Griffiths et al, 2003;Martin et al, 2004;Campoli et al, 2012). Interestingly, the overexpression of COL8, which is a COL TF with a single B-box domain, resulted in a phenotype with delayed flowering under LD conditions in Arabidopsis (Takase et al, 2011). Therefore, it seems that the absence of the B-box II domain in some COL TFs does not necessarily affect the regulation of flowering.…”
Section: Identification Of Six Bncol Tfs With a Full-length Orfmentioning
confidence: 91%
“…Seventeen members, including CO genes, were reported in Arabidopsis , whereas 16 COL TFs and 9 COL TFs were identified in rice and barley, respectively (Griffiths et al, 2003). Some COL members that were identified from Arabidopsis, rice, barley, and ryegrass have been characterized by their functions; the results revealed that most COL TFs either promoted or delayed flowering under LD or SD conditions (Yano et al, 2000;Suarez-Lopez et al, 2001;Martin et al, 2004;Cheng and Wang, 2005;Kim et al, 2008;Xue et al, 2008;Hassidim et al, 2009;Lee et al, 2010;Takase et al, 2011;Campoli et al, 2012;Kikuchi et al, 2012;Wu et al, 2013). These findings suggest that many COL family members have a conserved function in modulating flowering via the photoperiodic response.…”
Section: Introductionmentioning
confidence: 92%
“…The COL gene functions as a transcription factor in multiple growth and development pathways, and particularly in the photoperiod-mediated owering pathway. Some genes in this family have been found to play an important role in the light response-mediated regulation of owering [5,[17][18][19], with functions that differ between short-day (SD) and long-day (LD) conditions. For example, OsCOL10, OsCOL13 and OsCOL16 function as negative regulators of owering under both SD and LD condition in rice, while Hd1, a member of the COL gene family, promotes owering under SD and suppresses owering under LD [5,17,[20][21].…”
Section: Introductionmentioning
confidence: 99%
“…For example, OsCOL10, OsCOL13 and OsCOL16 function as negative regulators of owering under both SD and LD condition in rice, while Hd1, a member of the COL gene family, promotes owering under SD and suppresses owering under LD [5,17,[20][21]. In Arabidopsis, the overexpression of AtCOL3, AtCOL7 and AtCOL8 can delay owering time, while, in the contrast, the overexpression of the AtCOL5 gene promotes owering by enhancing the expression of FLOWERING LOCUS T (FT) [18][19][22][23]. Similar to their functions, the expression patterns also vary among the members of the COL gene family.…”
Section: Introductionmentioning
confidence: 99%
“…Among them, COL1 and COL2 have little effect on the flowering time, while COL3, COL4, and COL9 represent flowering repressors [27][28][29] . The overexpression of COL8 delays flowering under LDs, whereas COL5 promotes flowering 30,31 . Multiple CO/COL homologues have been identified in different species: 16 in rice, 9 in barley, 13 in sugar beet, and 28 in soybean [32][33][34][35] .…”
mentioning
confidence: 99%