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• Phytochrome-Interacting Factors (PIFs) are plant-specific basic helix-
loop-helix (bHLH)-type TFs whose regulatory roles have been widely
studied in arabidopsis (Castillon et al., 2007).
• PIF TFs regulate various biological processes in a red-light
phytochrome (phy)-dependent manner, including seed germination
(Oh et al., 2004), hypocotyl elongation (Nusinow et al., 2011),
flowering (Kumar et al., 2012), leaf senescence (Sakuraba et al.,
2014), Chl biosynthesis (Huq et al., 2004), and the biosynthesis or
signaling pathways of phytohormones, including gibberellic acid
(Feng et al., 2008), auxin (Franklin et al., 2011; Oh et al., 2014), and
brassinosteroids (Shahnejat-Bushehri et al., 2016).
• Six rice PIF TFs, termed OsPIF-Like11 (OsPIL11), OsPIL12, OsPIL13
(also termed OsPIL1), OsPIL14, OsPIL15, and OsPIL16, are considered
homologs of arabidopsis PIF TFs based on sequence similarity
(Nakamura et al., 2007).
• OsPIL15-overexpressing (OX) transgenic rice plants exhibit shorter
shoots and roots under dark conditions, indicating that OsPIL15 is
involved in growth of etiolated seedlings (Zhou et al., 2014), similar
to arabidopsis PIFs (Shin et al., 2009).
• Microarray analysis has shown that OsPIL1/OsPIL13 (hereafter
referred to as OsPIL1) is a stress-responsive gene (Maruyama et al.,
2012).
• Todaka et al. (2012) reported that overexpressing OsPIL1 promotes
internode elongation by increasing internode cell size, especially
under drought-stress conditions.
• In this study, we found that OsPIL1 is a key regulator of Chl
biosynthesis.
Results.pptx
Results.pptx
Results.pptx
Results.pptx
Results.pptx
Results.pptx
Results.pptx
Results.pptx
Results.pptx
Results.pptx
Results.pptx

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Results.pptx

  • 1.
  • 2. • Phytochrome-Interacting Factors (PIFs) are plant-specific basic helix- loop-helix (bHLH)-type TFs whose regulatory roles have been widely studied in arabidopsis (Castillon et al., 2007). • PIF TFs regulate various biological processes in a red-light phytochrome (phy)-dependent manner, including seed germination (Oh et al., 2004), hypocotyl elongation (Nusinow et al., 2011), flowering (Kumar et al., 2012), leaf senescence (Sakuraba et al., 2014), Chl biosynthesis (Huq et al., 2004), and the biosynthesis or signaling pathways of phytohormones, including gibberellic acid (Feng et al., 2008), auxin (Franklin et al., 2011; Oh et al., 2014), and brassinosteroids (Shahnejat-Bushehri et al., 2016). • Six rice PIF TFs, termed OsPIF-Like11 (OsPIL11), OsPIL12, OsPIL13 (also termed OsPIL1), OsPIL14, OsPIL15, and OsPIL16, are considered homologs of arabidopsis PIF TFs based on sequence similarity (Nakamura et al., 2007). • OsPIL15-overexpressing (OX) transgenic rice plants exhibit shorter shoots and roots under dark conditions, indicating that OsPIL15 is involved in growth of etiolated seedlings (Zhou et al., 2014), similar to arabidopsis PIFs (Shin et al., 2009). • Microarray analysis has shown that OsPIL1/OsPIL13 (hereafter referred to as OsPIL1) is a stress-responsive gene (Maruyama et al., 2012). • Todaka et al. (2012) reported that overexpressing OsPIL1 promotes internode elongation by increasing internode cell size, especially under drought-stress conditions. • In this study, we found that OsPIL1 is a key regulator of Chl biosynthesis.