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Pathway · 1 proteins

Initiation and opening

DnaA, helicase and primase support replication initiation and fork formation.

How it works

  1. DnaA binds the replication origin and opens the duplex at an AT-rich region; the reaction needs ATP and is controlled by the nucleotide state of DnaA itself.
  2. A replicative helicase is loaded onto the opened strand and unwinds the duplex, while DNA primase makes the short RNA primers that a DNA polymerase requires to start.
  3. This module is the assembly step: helicase and primase stay at the fork as it moves. The factors are listed here; the loading order is established in model bacteria and was not re-measured for VF5.

Grouped by the atlas’s curated pathway map. The table order is not a proven reaction order.

Its proteins

ProteinECReaction (UniProt)Metal or clusterAmino acidsCertainty
Replicative DNA helicase5.6.2.3ATP + H2O = ADP + phosphate + H(+)Mg(2+)468Step named

Also part of this pathway

These proteins are described under another pathway, but also take part here.

ProteinECReaction (UniProt)Metal or clusterAmino acidsCertainty
Chromosomal replication initiator protein DnaAHome: Chromosome preparation——Mg(2+), ssDNA399Step named
DNA primaseHome: DNA replication2.7.7.101ssDNA + n NTP = ssDNA/pppN(pN)n-1 hybrid + (n-1) diphosphate.Mg(2+), Zn(2+)498Step named

Origins

How does copying begin at the right place, once per cycle?

Naturalistic proposal

Koonin calls the origin of replication and translation the core of the origin-of-life problem, and notes that the chemistry before life lies outside biology.

Design analysis

Copying starts only where an initiator protein recognises the origin sequence and opens the helix there, after which the helicase is loaded. Starting once, and only once, per cell cycle keeps every daughter cell with one full copy.

From the books: Koonin, The Logic of Chance, PDF p. 226; Rana, The Cell's Design, ch. 11.

The wider question for this part of the cell: origins for copying and repairing the genome.

Sources

Other pathways in this group: DNA damage repair · DNA synthesis · Topology management · Joining and end processing · Recombination and restart · Chromosome preparation · Homologous recombination · Base excision repair · Cysteine and methionine metabolism · Not yet placed in a pathway