Analyses of Anthocyanin Biosynthesis Genes and Anthocyanin Accumulation in Arabidopsis Suspension-Cultured Cells Overexpressing <I>PAP1</I> Transcriptional Factor.

DOI
  • Takeda Migiwa
    The NEDO Team of Applied Plant Genomics, Kazusa DNA Res. Inst.
  • Sasaki Ryosuke
    The NEDO Team of Applied Plant Genomics, Kazusa DNA Res. Inst.
  • Suzuki Hideyuki
    The NEDO Team of Applied Plant Genomics, Kazusa DNA Res. Inst.
  • Sakurai Nozomu
    The NEDO Team of Applied Plant Genomics, Kazusa DNA Res. Inst.
  • Aoki Koh
    The NEDO Team of Applied Plant Genomics, Kazusa DNA Res. Inst.
  • Saito Kazuki
    The NEDO Team of Applied Plant Genomics, Kazusa DNA Res. Inst. Graduate School of Pharmaceutical Sciences, Chiba Univ.
  • Shibata Daisuke
    The NEDO Team of Applied Plant Genomics, Kazusa DNA Res. Inst.

Bibliographic Information

Other Title
  • <I>PAP1</I>形質転換培養細胞を用いたアントシアニン生合成関連遺伝子およびアントシアニン蓄積の解析

Abstract

Over-expression of the PAP1 gene, which encodes an MYB-like transcription factor in Arabidopsis thaliana, resulted in up-regulation of a set of genes that were assigned or putatively assigned for flavonoid biosynthesis and accumulation of cyanidin derivatives in leaves and roots (Tohge et al., Plant J. 42:218-235. 2005). In this study, we over-expressed the PAP1 gene under 35S CaMV promoter in Arabidopsis suspension-cultured cells and examined transcriptome and anthocyanin analyses of transgenic cell lines. Analysis with liquid chromatography-coupled mass spectrometry indicated that PAP1 over-expressing transgenic cell lines produced seven species of cyanin-derived anthocyanins, while no anthocyanins were detected in wild type cell lines. Mass fragmentation pattern analysis of these anthocyanin derivatives indicated that the major species among them had three glycosides and two acyl-moieties to the cyanin aglycone. The transcriptome analysis of the cells using DNA microarray chips indicated induction of anthocyanin biosynthesis genes.

Journal

Details 詳細情報について

  • CRID
    1390001205628851584
  • NII Article ID
    130006989200
  • DOI
    10.14841/jspp.2006.0.111.0
  • Data Source
    • JaLC
    • CiNii Articles
  • Abstract License Flag
    Disallowed

Report a problem

Back to top