S-RNase complexes and pollen rejection

J Exp Bot. 2003 Jan;54(380):123-30. doi: 10.1093/jxb/erg045.

Abstract

Biochemical interactions between the pollen and the pistil allow plants fine control over fertilization. S-RNase-based pollen rejection is among the most widespread and best understood of these interactions. At least three plant families have S-RNase-based self-incompatibility (SI) systems, and S-RNases have also been implicated in interspecific pollen rejection. Although S-RNases determine the specificity of SI, other genes are required for the pollen rejection system to function. Progress is being made toward identifying these non-S-RNase factors. HT-protein, first identified as a non-S-RNase factor that was required for SI in Nicotiana alata, has now been implicated in other species as well. In addition, several pistil proteins bind to S-RNase in vitro. One hypothesis is that S-RNase forms a complex with these proteins in vivo that is the active form of S-RNase in pollen rejection.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Review

MeSH terms

  • Amino Acid Sequence
  • Fertility / physiology
  • Flowers / physiology
  • Glycoproteins / metabolism
  • Molecular Sequence Data
  • Plant Proteins / genetics
  • Plant Proteins / metabolism
  • Pollen / physiology*
  • Ribonucleases / metabolism*
  • Sequence Homology, Amino Acid
  • Substrate Specificity

Substances

  • Glycoproteins
  • HT protein, Nicotiana alata
  • Plant Proteins
  • self-incompatibility glycoprotein, Nicotiana
  • Ribonucleases
  • ribonuclease S