4.7 Article

GmFULc Is Induced by Short Days in Soybean and May Accelerate Flowering in Transgenic Arabidopsis thaliana

Journal

Publisher

MDPI
DOI: 10.3390/ijms221910333

Keywords

soybean; GmFULc; photoperiod; flowering time; TPL

Funding

  1. National Natural Science Foundation of China [32072086, 31771820]
  2. Heilongjiang Province Natural Science Foundation [ZD2020C002]

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This study investigated the role of GmFULc in regulating flowering time in Arabidopsis and found that it inhibits the transcriptional activity of TPL, leading to the up-regulation of FT, SOC1, and LFY genes for promoting early flowering. GmFULc's involvement in the molecular mechanism of flowering regulation highlights its importance in plant development.
Flowering is an important developmental process from vegetative to reproductive growth in plant; thus, it is necessary to analyze the genes involved in the regulation of flowering time. The MADS-box transcription factor family exists widely in plants and plays an important role in the regulation of flowering time. However, the molecular mechanism of GmFULc involved in the regulation of plant flowering is not very clear. In this study, GmFULc protein had a typical MADS domain and it was a member of MADS-box transcription factor family. The expression analysis revealed that GmFULc was induced by short days (SD) and regulated by the circadian clock. Compared to wild type (WT), overexpression of GmFULc in transgenic Arabidopsis caused significantly earlier flowering time, while ful mutants flowered later, and overexpression of GmFULc rescued the late-flowering phenotype of ful mutants. ChIP-seq of GmFULc binding sites identified potential direct targets, including TOPLESS (TPL), and it inhibited the transcriptional activity of TPL. In addition, the transcription levels of FLOWERING LOCUS T (FT), SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1 (SOC1) and LEAFY (LFY) in the downstream of TPL were increased in GmFULc- overexpression Arabidopsis, suggesting that the early flowering phenotype was associated with up-regulation of these genes. Our results suggested that GmFULc inhibited the transcriptional activity of TPL and induced expression of FT, SOC1 and LFY to promote flowering.

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