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. Author manuscript; available in PMC: 2007 Mar 1.
Published in final edited form as: J Mol Biol. 2006 Nov 3;366(1):53–66. doi: 10.1016/j.jmb.2006.10.09

TABLE 2.

Strains used to measure homeologous recombination using the HIS3::intron recombination assay

Strain Genotype Recombination substrates
SJR769 wild-type cβ2/cβ2: homologous substrates
SJR770 wild-type cβ2/cβ7: predicted to form 9% base-base mismatches
GCY615 wild-type cβ2/cβ2-ns: predicted to form four (1.3%) base-base mismatches
SJR767 wild-type cβ2/cβ2-1L: predicted to form four 1-nt loops
GCY559 wild-type cβ2/cβ2-4L: predicted to form four 4-nt loops
SJR768 wild-type cβ2/cβ2-12L: predicted to form two 12-nt loops
EAY1605 msh2Δ cβ2/cβ2
EAY1607 msh2Δ cβ2/cβ7
EAY1609 msh2Δ cβ2/cβ2-ns
EAY1611 msh2Δ cβ2/cβ2-1L
EAY1613 msh2Δ cβ2/cβ2-4L
EAY1615 msh2Δ cβ2/cβ2-12L
EAY1617 msh3Δ cβ2/cβ2
EAY1619 msh3Δ cβ2/cβ7
EAY1621 msh3Δ cβ2/cβ2-ns
EAY1623 msh3Δ cβ2/cβ2-1L
EAY1625 msh3Δ cβ2/cβ2-4L
EAY1627 msh3Δ cβ2/cβ2-12L
EAY1629 msh6Δ cβ2/cβ2
EAY1631 msh6Δ cβ2/cβ7
EAY1633 msh6Δ cβ2/cβ2-ns
EAY1635 msh6Δ cβ2/cβ2-1L
EAY1637 msh6Δ cβ2/cβ2-4L
EAY1639 msh6Δ cβ2/cβ2-12L
EAY1641 msh2Δ1 cβ2/cβ2
EAY1643 msh2Δ1 cβ2/cβ7
EAY1645 msh2Δ1 cβ2/cβ2-ns
EAY1647 msh2Δ1 cβ2/cβ2-1L
EAY1649 msh2Δ1 cβ2/cβ2-4L
EAY1651 msh2Δ1 cβ2/cβ2-12L
EAY1653 msh2Δ1 msh3Δ cβ2/cβ2
EAY1655 msh2Δ1 msh3Δ cβ2/cβ7
EAY1657 msh2Δ1 msh3Δ cβ2/cβ2-ns
EAY1659 msh2Δ1 msh3Δ cβ2/cβ2-1L
EAY1661 msh2Δ1 msh6Δ cβ2/cβ2
EAY1663 msh2Δ1 msh6Δ cβ2/cβ7
EAY1665 msh2Δ1 msh6Δ cβ2/cβ2-ns
EAY1667 msh2Δ1 msh6Δ cβ2/cβ2-1L

The SJR769, SJR770, SJR767, GCY559, GCY615 strains bearing the above recombination substrates are described.20 The mismatches predicted to form in heteroduplex DNA during genetic recombination are indicated for each substrate. Integration vectors used to make the indicated msh strains were: pEAI98 (msh2Δ::hisG-URA3-hisG), pEAI88 (msh3Δ::hisG-URA3-hisG), pEAI108 (msh6Δ::hisG-URA3-hisG), and pEAI244 (msh2Δ1::KanMX).16, 31 Note that the intact hisG-URA3-hisG cassette is present in these msh2Δ, msh3Δ and msh6Δ mutant derivatives.