Skip to main content
Article
Strand Exchange Protein 1 (Sep1) from Saccharomyces cerevisiae does not Promote Branch Migration in vitro
Journal of Biological Chemistry
  • Zhaoqing Zhang
  • Amanda M Simons, Framingham State University
  • Vidya P Prabhu
  • Junghuei Chen
Document Type
Article
Publication Date
2-27-1998
DOI
10.1074/jbc.273.9.4950
Version
Citation
Format
Other
Keywords
  • Sep1,
  • Saccharomyces cerevisiae strand exchange protein,
  • DNA
Subject Categories
Biology
Disciplines
Abstract
It has been shown in vitro that Saccharomyces cerevisiae strand exchange protein 1 (Sep1) promotes the transfer of one strand of a linear duplex DNA to a homologous single-stranded DNA circle. Sep1 also has an exonuclease active on DNA and RNA. By using exonuclease III-treated linear duplex DNA with various lengths of single-stranded tail as well as Ca2+ to inhibit the exonuclease activity of Sep1, we show that the processivity of exonuclease activity of Sep1 is greater than previously reported. The results in this work also demonstrate that the joint molecule between the linear duplex and single-stranded circle observed from the Sep1-promoted strand transfer reaction is just the pairing between the long single-stranded tail of the linear duplex DNA (generated by the exonuclease activity of Sep1) and the single-stranded circular DNA. When a synthetic Holliday junction was used as substrate, branch migration facilitated by Sep1 could not be detected. Finally, using electron microscopy no α-structure, a joint molecule with displaced single-stranded DNA tail that indicates branch migration could be observed. The results imply that Sep1 cannot promote branch migration in vitro. Further investigation is needed to determine the role of Sep1 in recombination in vivo.
Citation Information
Zhaoqing Zhang, Amanda M Simons, Vidya P Prabhu and Junghuei Chen. "Strand Exchange Protein 1 (Sep1) from Saccharomyces cerevisiae does not Promote Branch Migration in vitro" Journal of Biological Chemistry Vol. 273 (1998) p. 4950 - 4956
Available at: http://works.bepress.com/amanda_simons/6/