Short and narrow flag leaf1, a GATA zinc finger domain-containing protein, regulates flag leaf size in rice (Oryza sativa)
文献类型: 外文期刊
作者: He, Peilong 1 ; Wang, Xiaowen 1 ; Zhang, Xiaobo 1 ; Jiang, Yudong 2 ; Tian, Weijiang 1 ; Zhang, Xiaoqiong 1 ; Li, Yang 1 ;
作者机构: 1.Southwest Univ, Acad Agr Sci, Rice Res Inst, Key Lab Applicat & Safety Control Genet Modified, Chongqing, Peoples R China
2.Sichuan Acad Agr Sci, Inst Rice & Sorghum, Key Lab Southwest Rice Biol & Genet Breeding, Deyang, Peoples R China
关键词: Rice (Oryza sativa); Alternative splicing; Short and narrow leaf; Map-based cloning; GATA zinc finger domain
期刊名称:BMC PLANT BIOLOGY ( 影响因子:4.215; 五年影响因子:4.96 )
ISSN: 1471-2229
年卷期: 2018 年 18 卷
页码:
收录情况: SCI
摘要: BackgroundThe 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.ResultsIn 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.ConclusionsWe 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.
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