Publication | Open Access
Human 75-kDa DNA-pairing Protein Is Identical to the Pro-oncoprotein TLS/FUS and Is Able to Promote D-loop Formation
168
Citations
44
References
1999
Year
GeneticsHpomp75/tls Require MgGenomic MechanismMolecular BiologyMolecular GeneticsProtein GeneticsPro-oncoprotein Tls/fusMulti-protein AssemblyHomologous Dna PairingD-loop FormationGenome InstabilityProtein FunctionHomologous RecombinationDna ReplicationChromosomal RearrangementCell BiologyChromatinNatural SciencesIs AbleRecombination DynamicMedicine
Homologous recombination plays a fundamental role in DNA double-strand break repair. Previously, we detected two mammalian nuclear proteins of 100 and 75 kDa (POMp100 and POMp75, respectively) that are able to promote homologous DNA pairing, a key step in homologous recombination. Here we describe the identification of human (h) POMp75 as the pro-oncoprotein TLS/FUS. hPOMp75/TLS binds both single- and double-stranded DNAs and mediates annealing of complementary DNA strands. More important, it promotes the uptake of a single-stranded oligonucleotide into a homologous superhelical DNA to form a D-loop. The formation of a D-loop is an essential step in DNA double-strand break repair through recombination. DNA annealing and D-loop formation catalyzed by hPOMp75/TLS require Mg(2+) and are ATP-independent. Interestingly, the oncogenic fusion form TLS-CHOP is not able to promote DNA pairing. These data suggest a possible role for hPOMp75/TLS in maintenance of genomic integrity.
| Year | Citations | |
|---|---|---|
Page 1
Page 1