J. Barry et B. Alberts, A ROLE FOR 2 DNA HELICASES IN THE REPLICATION OF T4-BACTERIOPHAGE DNA, The Journal of biological chemistry, 269(52), 1994, pp. 33063-33068
The T4 bacteriophage gene 41 protein is the highly processive DNA heli
case of the T4 primosome, a central part of the protein machinery that
moves the T4 DNA replication fork. The T4 gene 59 protein accelerates
the loading of 41 protein onto DNA covered with 32 protein (the T4 si
ngle strand binding protein), and it makes the 41 protein DNA helicase
activity rapidly available to catalyze replication fork movement thro
ugh a DNA double helix (Barry, J., and Alberts, B. M. (1994) J. Biol.
Chem. 269, 33049-33062). With the aid of the 59 protein, we show that
the T4 primosome (the T4 gene 41 and 61 proteins) can move rapidly thr
ough a promoter-bound RNA polymerase molecule that would otherwise sto
p replication fork movement. A second, very different DNA helicase, th
e T4 dda protein, provides an alternative pathway for replication past
this DNA-bound RNA polymerase (Bedinger, P., Hochstrasser, M., Jongen
eel, C. V., and Alberts, B. M. (1983) Cell 34, 115-123). Combined with
other data, these in vitro experiments allow us to propose a model th
at explains why either the 59 protein or the dda protein, but not both
, are required to begin efficient DNA replication inside the T4 bacter
iophage-infected cell.