Nucleic Acids Research, 1990, Vol. 18, No. 16 4867-4876
© 1990
ENZYMOLOGY |
Further biochemical characterization of wheat DNA primase: possible functional implication of copurification with DNA polymerase A
Laboratoire de Biologie Moléculaire Végetale, IBCN-CNRS 1 rue Camille Saint Saëns, 33077, Bordeaux cedex, France
*To whom correspondence should be addressed
Received April 10, 1990. Revised July 27, 1990. Accepted July 27, 1990.
DNA primase has been partially purified from wheat germ. This enzyme, like DNA primases characterized from many procaryotic and eucaryotic sources, catalyses the synthesis of primers involved in DNA replication. However, the wheat enzyme differs from animal DNA primase in that it is found partially associated with a DNA polymerase which differs greatly from DNA polymerase a. Moreover, the only wheat DNA polymerase able to initiate on a natural or synthetic RNA primer is DNA polymerase A. In this report we describe in greater detail the chromatographic behaviour of wheat DNA primase and its copurification with DNA polymerase A. Some biochemical properties of wheat DNA primase such as pH optimum, Mn+2 or Mg+2 optima, and temperature optimum have been determined. The enzyme is strongly inhibited by KCI, cordycepine triphosphate and dATP, and to a lesser extent by cAMP and formycine triphosphate. The primase product reaction is resistant to DNAse digestion and sensitive to RNAse digestion. Primase catalyses primer synthesis on M13 ssDNA as template allowing E.coli DNA polymerase I to replicate the primed M13 single-stranded DNA leading to doublestranded M13 DNA (RF). M13 replication experiments were performed with wheat DNA polymerases A, B, Cl and CM purified in our laboratory. Only DNA polymerase A is able to recognize RNA-primed M13 ssDNA.