Open AccessRat liver DNA ligases
Author(s) -
ELDER Rhoderick H.,
MONTECUCCO Alessandra,
CIARROCCHI Giovanni,
ROSSIGNOL JeanMichel
Publication year - 1992
Publication title -
european journal of biochemistry
Language(s) - English
Resource type - Journals
eISSN - 1432-1033
pISSN - 0014-2956
DOI - 10.1111/j.1432-1033.1992.tb19826.x
Subject(s) - dna ligase , dna ligases , ligase chain reaction , dna clamp , biology , dna , dna polymerase mu , in vitro recombination , ubiquitin ligase , microbiology and biotechnology , biochemistry , circular bacterial chromosome , dna replication , ubiquitin , molecular cloning , complementary dna , polymerase chain reaction , gene , reverse transcriptase , multiplex polymerase chain reaction
A novel form of rat liver DNA ligase (molecular mass 100 kDa) can be differentiated from DNA ligase I by several biochemical parameters. It is a more heat‐labile enzyme and unable to join bluntended DNA, even in the presence of poly(ethylene glycol) concentrations which stimulate such joining by DNA ligase I and T4 DNA ligase. It also lacks the AMP‐dependent nicking/closing reaction, which is a property of all other DNA ligases tested so far, including DNA ligase I from rat liver. Both rat liver DNA ligases were inhibited by deoxyadenosinetriphosphate, however this inhibition was competitive with respect to ATP, for DNA ligase I ( K i 22 μM) and non‐competitive for the 100‐kDa DNA ligase ( K i 170 μM). These results support the idea that, when compared with other DNA ligases, the novel form of DNA ligase has a unique AMP‐binding site, may have an absolute requirement for single‐strand breaks and, furthermore, may have an altered reaction mechanism to that which is conserved from bacteriophage to mammalian DNA ligase I.