Early in short days 7 (ESD7) encodes the catalytic subunit of the DNA polymerase epsilon and is required for flowering repression through a mechanism involving epigenetic gene silencing

  1. del Olmo, I. 1
  2. López-González, L. 1
  3. Martín-Trillo, M.M. 2
  4. Martínez-Zapater, J.M. 2
  5. Piñeiro, M. 1
  6. Jarillo, J.A. 1
  1. 1 Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria
    info

    Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria

    Madrid, España

    ROR https://ror.org/011q66e29

  2. 2 Centro Nacional de Biotecnología
    info

    Centro Nacional de Biotecnología

    Madrid, España

    ROR https://ror.org/015w4v032

Revista:
Plant Journal

ISSN: 0960-7412

Año de publicación: 2010

Volumen: 61

Número: 4

Páginas: 623-636

Tipo: Artículo

DOI: 10.1111/J.1365-313X.2009.04093.X PMID: 19947980 SCOPUS: 2-s2.0-76449089255 GOOGLE SCHOLAR

Otras publicaciones en: Plant Journal

Resumen

We have characterized a mutation affecting the Arabidopsis EARLY IN SHORT DAYS 7 (ESD7) gene encoding the catalytic subunit of DNA polymerase epsilon (ε), AtPOL2a. The esd7-1 mutation causes early flowering independently of photoperiod, shortened inflorescence internodes and altered leaf and root development. esd7-1 is a hypomorphic allele whereas knockout alleles displayed an embryo-lethal phenotype. The esd7 early flowering phenotype requires functional FT and SOC1 proteins and might also be related to the misregulation of AG and AG-like gene expression found in esd7. Genes involved in the modulation of chromatin structural dynamics, such as LHP1/. TFL2 and EBS, which negatively regulate FT expression, were found to interact genetically with ESD7. In fact a molecular interaction between the carboxy terminus of ESD7 and TFL2 was demonstrated in vitro. Besides, fas2 mutations suppressed the esd7 early flowering phenotype and ICU2 was found to interact with ESD7. Discrete regions of the chromatin of FT and AG loci were enriched in activating epigenetic marks in the esd7-1 mutant. We concluded that ESD7 might be participating in processes involved in chromatin-mediated cellular memory. © 2009 The Authors. Journal compilation © 2009 Blackwell Publishing Ltd.