Strand exchange reaction in vitro and DNA-dependent ATPase activity of recombinant LIM15/DMC1 and RAD51 proteins from Coprinus cinereus

We previously cloned recA-homolog genes from a basidiomycete, Coprinus cine reus, and obtained the recombinant proteins (Nara et at, Mot Gen, Genet. 26 2, 781-789, 1999, see Ref, 1; Nara and Sakaguchi, Biochem, Biophys. Res. Co mmun. 275, 97-102, 2000, see Ref, 2), The primary purpose of the present st udy was to characterize the biochemical properties of the recombinant LIM15 /DMC1 (CoLIM15) and RAD51 (CoRAD51) proteins. We purified the recombinant p roteins, and their molecular masses were 37 and 35 kDa, respectively. Both enzymes showed DNA-dependent ATPase activity and ATP-dependent strand excha nge reaction in vitro. CoRad51 was a five- to sixfold stronger DNA-dependen t ATPase and showed greater dependency on single-stranded DNA than CoLim15, In meiosis, both enzymes were highly accumulated in the meiotic tissue at leptotene and zygotene stages at which the homologous chromosomes pair, but disappeared just before the pachytene stage at which they recombine, From these and the previously reported results, we discuss here the relationship s between the enzymes and meiosis, (C) 2001 Academic Press.