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. 2004 Apr;70(4):2437–2444. doi: 10.1128/AEM.70.4.2437-2444.2004

FIG. 1.

FIG. 1.

(A) Wild-type G. zeae MAT locus; (B) MAT locus deletion vector, pGzMAT-H, shown in the linear form that would result from digestion with SalI; (C) MAT locus in which the 9.6-kb region with the four MAT genes has been deleted and replaced by a 5.1-kb fragment carrying the hygB and pCR XL TOPO portions of pGzMAT-H; (D) MAT locus complementation vector pGzMAT-Gen. Numbered arrows indicate relative positions and orientations of PCR primers used in this study. The black bars in panels A and C and the white bars in panels A and D indicate the regions of DNA used to prepare the hybridization probe for Southern analysis of transformants carrying pGzMAT-Gen.