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Regulation of Flowering Time in Rice

机译:水稻开花时间的调控

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Rice flowers after a lengthy vegetative growth. During the vegetative growth period flowering is inhibited by several independent pathways. Whereas Grain number, plant height, and heading date 7 (Ghd7), Heading date 1 (Hd1), Heading date 5 (Hd5), Heading date 6 (Hd6), and Heading date 16 (Hd16) preferentially function to delay flowering under long day conditions, Oryza sativa Phytochrome B (OsPhyB), Oryza sativa CONSTANS-like 4 (OsCOL4), SUPERNUMERARY BRACT (SNB) and Oryza sativa INDETERMINATE SPIKELET 1 (OsIDS1) independently inhibit flowering regardless of day length. After sufficient vegetative growth, flowering signals are produced in the leaves due to reduced expression of the inhibitors. In addition, Hd1 becomes a flowering promoter when the day length becomes shorter. Long-day specific activators OsMADS50 and OsDof12, and a constitutive activators Oryza sativa INDETERMINATE 1 (OsId1), Early heading date 4 (Ehd4), and miR172, are accumulated in the leaves when plants are grown sufficiently. Several circadian clock genes are also involved in floral transition, including Oryza sativa GIGANTEA (OsGI), Heading date 2 (Hd2), and Heading date 17 (Hd17). Floral transition is also controlled by photoreceptors and chromatin remodeling factors. Most of the upstream signals are transferred to Early heading date 1 (Ehd1) that is a positive regulator of Heading data 3a (Hd3a) and Rice FT 1 (RFT1), which are transferred to the shoot apical meristem to induce the reproductive transition.
机译:水稻在长期营养生长后开花。在营养生长期中,开花受到多种独立途径的抑制。粒数,株高和抽穗期7(Ghd7),抽穗期1(Hd1),抽穗期5(Hd5),抽穗期6(Hd6)和抽穗期16(Hd16)优先用于延迟长时间开花在日间条件下,稻米植物色素B(OsPhyB),稻米CONSTANS-like 4(OsCOL4),超高BRACT(SNB)和稻米不确定性小穗1(OsIDS1)均能独立抑制开花,无论白天如何。在足够的营养生长后,由于抑制剂表达降低,在叶片中产生开花信号。另外,当日长度变短时,Hd1成为开花促进剂。当植物充分生长时,长日特异性激活因子OsMADS50和OsDof12以及组成型激活因子稻不定稻1(OsId1),早抽穗日期4(Ehd4)和miR172会累积在叶片中。一些昼夜节律时钟基因也参与花期转换,包括水稻(Osza sativa GIGANTEA)(OsGI),抽穗期2(Hd2)和抽穗期17(Hd17)。花的过渡也受感光器和染色质重塑因子控制。大多数上游信号被转移到早期抽穗日期1(Ehd1),这是抽穗数据3a(Hd3a)和Rice FT 1(RFT1)的正调节剂,它们被转移到茎尖分生组织以诱导生殖过渡。

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