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Short and narrow flag leaf1, a GATA zinc finger domain-containing protein, regulates flag leaf size in rice ( Oryza sativa )

机译:短窄的旗叶1,含Gata锌手指结构域的蛋白质,调节水稻的旗叶大小(Oryza sativa)

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The flag leaf of rice (Oryza sativa L.) is an important determinant of plant type characteristics and grain yield. Identification of flag leaf mutants of rice is crucial to elucidate the molecular mechanism of flag-leaf development, and for exploitation of rice germplasm resources. In this study, we describe a mutant designated short and narrow flag leaf 1 (snfl1). Histological analysis showed that the length of epidermal cells and number of longitudinal veins were decreased in the flag leaf of the snfl1 mutant. Map-based cloning indicated that a member of the GATA family of transcription factors is a candidate gene for SNFL1. A single-nucleotide transition at the last base in the single intron of snfl1 led to variation in alternative splicing and early termination of translation. Complemented transgenic plants harbouring the candidate SNFL1 gene rescued the snfl1 mutant. Analysis of RT-PCR and the SNFL1 promoter by means of a GUS fusion expression assay showed that abundance of SNFL1 transcripts was higher in the culm, leaf sheath, and root. Expression of the SNFL1-GFP fusion protein in rice protoplasts showed that SNFL1 was localized in nucleus. We conclude that SNFL1 is an important regulator of leaf development, the identification of which might have important implications for future research on GATA transcription factors.
机译:稻草叶(Oryza sativa L.)是植物型特性和籽粒产量的重要决定因素。鉴定水稻标志叶片突变体是至关重要的,阐明旗叶发育的分子机制,以及剥削水稻种质资源的剥削。在这项研究中,我们描述了突变体指定的短窄旗叶1(SNFL1)。组织学分析表明,SnFl1突变体的旗叶中,表皮细胞的长度和纵向脉冲数减少。基于地图的克隆表明,Gata的转录因子的成员是SnFl1的候选基因。在SNFL1的单个内含子中的最后一个基座的单核苷酸过渡导致替代剪接和翻译早期终止的变化。含有候选SnFl1基因的补充转基因植物拯救了SnFl1突变体。通过GUS融合表达测定的RT-PCR和SnFl1启动子的分析表明,秆,叶片和根部的SnFl1转录物的丰度高。 SNFL1-GFP融合蛋白在水稻原生质体中的表达表明,SNFL1局部化核。我们得出结论,SNFL1是叶发育的重要调节因素,其鉴定可能对未来对GATA转录因子的研究有重要影响。

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