Companion cells with high florigen production express other small proteins and reveal a nitrogen-sensitive FT repressor

高成花素产量的伴胞表达其他小蛋白,并揭示了一种氮敏感的FT阻遏物。

阅读:2
作者:Hiroshi Takagi,Shogo Ito,Jae Sung Shim,Akane Kubota,Andrew K Hempton,Nayoung Lee,Takamasa Suzuki,Jared S Wong,Chansie Yang,Christine T Nolan,Kerry L Bubb,Cristina M Alexandre,Daisuke Kurihara,Yoshikatsu Sato,Yasuomi Tada,Takatoshi Kiba,Jose L Pruneda-Paz,Christine Quietsch,Josh T Cuperus,Takato Imaizumi

Abstract

The precise onset of flowering is crucial for successful reproduction. In longer days, the florigen gene FLOWERING LOCUS T (FT) is induced in specific leaf phloem companion cells in Arabidopsis. However, the molecular nature of these cells remains elusive. Here, we utilized bulk nuclei RNA-seq and single nuclei RNA (snRNA)-seq to investigate transcription in FT-expressing cells and other companion cells. Our bulk nuclei RNA-seq demonstrated that FT-expressing cells in cotyledons and true leaves showed differences in FT repressor gene expression. Within true leaves, our snRNA-seq analysis revealed that companion cells with high FT expression form a unique cluster. The cluster expresses other genes encoding small proteins, including the flowering and stem growth inducer FPF1-LIKE PROTEIN 1 (FLP1) and the anti-florigen BROTHER OF FT AND TFL1 (BFT). We also found that the promoters of FT and the genes co-expressed with FT in the cluster were enriched for the binding motif of NITRATE-INDUCIBLE GARP-TYPE TRANSCRIPTIONAL REPRESSOR 1 (NIGT1). Overexpression of NIGT1.2 and NIGT1.4 repressed FT and delayed flowering under nitrogen-rich conditions, implying the roles of NIGT1s as nitrogen-dependent FT repressors. Taken together, our results indicate that unique FT-expressing phloem cells may produce multiple systemic signals to regulate plant growth and development.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。