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Molecular and Cellular Biology, February 2004, p. 1351-1364, Vol. 24, No. 3
0270-7306/04/$08.00+0     DOI: 10.1128/MCB.24.3.1351-1364.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Microhomology-Dependent End Joining and Repair of Transposon-Induced DNA Hairpins by Host Factors in Saccharomyces cerevisiae

Jianhua Yu,1,{dagger} Kelly Marshall,1 Miyuki Yamaguchi,2 James E. Haber,2 and Clifford F. Weil1*

Department of Agronomy, Purdue University, West Lafayette, Indiana 47907-1150,1 Rosenstiel Cancer Center and Department of Biology, Brandeis University, Waltham, Massachusetts 02454-91102

Received 11 September 2003/ Returned for modification 15 October 2003/ Accepted 31 October 2003

The maize, cut-and-paste transposon Ac/Ds is mobile in Saccharomyces cerevisiae, and DNA sequences of repair products provide strong genetic evidence that hairpin intermediates form in host DNA during this transposition, similar to those formed for V(D)J coding joints in vertebrates. Both DNA strands must be broken for Ac/Ds to excise, suggesting that double-strand break (DSB) repair pathways should be involved in repair of excision sites. In the absence of homologous template, as expected, Ac excisions are repaired by nonhomologous end joining (NHEJ) that can involve microhomologies close to the broken ends. However, unlike repair of endonuclease-induced DSBs, repair of Ac excisions in the presence of homologous template occurs by gene conversion only about half the time, the remainder being NHEJ events. Analysis of transposition in mutant yeast suggests roles for the Mre11/Rad50 complex, SAE2, NEJ1, and the Ku complex in repair of excision sites. Separation-of-function alleles of MRE11 suggest that its endonuclease function is more important in this repair than either its exonuclease or Rad50-binding properties. In addition, the interstrand cross-link repair gene PSO2 plays a role in end joining hairpin ends that is not seen in repair of linearized plasmids and may be involved in positioning transposase cleavage at the transposon ends.

* Corresponding author. Mailing address: Department of Agronomy, 1150 Lilly Hall, Purdue University, West Lafayette, IN 47907-1150. Phone: (765) 496-1917. Fax: (765) 496-2926. E-mail: cweil{at}purdue.edu.

{dagger} Present address: Department of Molecular Virology, Immunology, and Medical Genetics, College of Medicine and Public Health, Ohio State University, Columbus, OH 43210.

Molecular and Cellular Biology, February 2004, p. 1351-1364, Vol. 24, No. 3
0022-538X/04/$08.00+0     DOI: 10.1128/MCB.24.3.1351-1364.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.



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