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Pathway · 4 proteins

Topology management

Gyrase, topoisomerases and reverse gyrase manage DNA topology.

How it works

  1. DNA gyrase, with an A and a B subunit (the B subunit also annotated as an ATP-hydrolysing topoisomerase), removes positive supercoils ahead of the fork at the cost of ATP.
  2. A type I topoisomerase relaxes supercoils without ATP, and a reverse gyrase introduces positive supercoils — the activity that stabilises duplex DNA at high temperature and is characteristic of thermophiles.
  3. In a hyperthermophile the reverse gyrase is not decoration: it addresses the same problem the growth temperature creates. The annotation names the enzymes; their relative contributions at 85 °C have not been measured here.

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
Type 2 topoisomerase subunit B5.6.2.2ATP-dependent breakage, passage and rejoining of double-stranded DNA.Mg(2+), Mn(2+), Ca(2+)792Step named
DNA topoisomerase 15.6.2.1ATP-independent breakage of single-stranded DNA, followed by passage and rejoining.Mg(2+)540Step named
Reverse gyrase 15.6.2.-ATP + H2O = ADP + phosphate + H(+)Zn(2+), Mg(2+)1146Step named
Type 2 topoisomerase subunit A5.6.2.2ATP-dependent breakage, passage and rejoining of double-stranded DNA.—769Step named

Origins

How could DNA be unwound and untangled before topoisomerases existed?

How it was discovered

  1. 1976Martin Gellert and colleagues discover DNA gyrase, which uses ATP to twist DNA and relieve the tension that copying creates.Brooker, Concepts of Genetics, PDF p. 264
Naturalistic proposal

The books searched describe topoisomerases only in present-day cells.

Design analysis

Unwinding DNA to copy it builds up twisting ahead of the fork; without gyrase the fork stops. After copying, circular daughter chromosomes are interlocked and must be cut apart and resealed by a topoisomerase. Four proteins in this pathway manage both problems.

From the books: Brooker, Concepts of Genetics, PDF p. 264; 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 · Joining and end processing · Recombination and restart · Chromosome preparation · Initiation and opening · Homologous recombination · Base excision repair · Cysteine and methionine metabolism · Not yet placed in a pathway