• Title of article

    AtSERK1 expression precedes and coincides with early somatic embryogenesis in Arabidopsis thaliana

  • Author/Authors

    Salaj، نويسنده , , Jan and von Recklinghausen، نويسنده , , Iris R. and Hecht، نويسنده , , Valerie and de Vries، نويسنده , , Sacco C. and Schel، نويسنده , , Jan H.N. and van Lammeren، نويسنده , , André A.M.، نويسنده ,

  • Issue Information
    روزنامه با شماره پیاپی سال 2008
  • Pages
    6
  • From page
    709
  • To page
    714
  • Abstract
    The Arabidopsis thaliana primordia timing (pt) mutant was transformed with an AtSERK1::GUS construct. Liquid cultures of this line were used to study the relationship between somatic embryogenesis and the expression of SOMATIC EMBRYOGENESIS RECEPTOR-LIKE KINASE (AtSERK1) as a marker for cells competent to form embryos. In order to search for the expression of AtSERK1::GUS during early stages of somatic embryogenesis, histochemical as well as immunochemical approaches were used for the detection of β-glucuronidase (GUS). Four sites of AtSERK1 expression were found in the embryogenic cultures: in embryogenic callus, where primary somatic embryos developed; in the basal parts of primary somatic embryos; in the outer layers of cotyledons of primary somatic embryos where secondary embryos were formed; and in provascular and vascular strands of developing somatic embryos. The in vitro expression of AtSERK1::GUS coincides with embryogenic development up to the heart-shaped stage. Prior to the expression in embryos, AtSERK1 was expressed in single cells and small cell clusters, indicating that AtSERK1 indeed marks embryogenic competence. Its expression in (pro)vascular strands, suggests that embryogenic cells in tissue culture retain at least in part their original identity.
  • Keywords
    antibodies , AtSERK1 , Arabidopsis , SERK , somatic embryogenesis , Suspension culture , GUS
  • Journal title
    Plant Physiology and Biochemistry
  • Serial Year
    2008
  • Journal title
    Plant Physiology and Biochemistry
  • Record number

    2121909