摘要

The R1162 replication protein RepIB binds to a 20 bp DNA sequence, reiterated 3 and 1/2 times within the replicative origin of the plasmid, with a stoichiometry of 2 protein monomers: 1 direct repeat. Insertion and deletion mutations in the repIB gene were isolated, and the altered proteins encoded by several of these purified and characterized. Mutations in the amino-terminal coding region of the gene resulted in proteins that did not bind detectably to the direct repeat DNA. However, one of these proteins remained active for replication. Several of the non-binding proteins excluded R1162 from the cell. One of these interfered with binding by normal protein when co-purified from the cell, but not when the two proteins were separately purified and mixed. Taken together, our results indicate that RepIB forms a stable dimer by an interaction at a region within the protein distinct from the DNA-binding domain.

  • 出版日期1996-2-29