Et6 formed only a faint band that disappeared upon competition with 250-fold molar excess of cold probe (data not shown).
Analysis of 2,047 bp from the PbGP43 5′ flanking region In our laboratory, we had long been trying to clone an extended fragment of the 5′ intergenic region of the PbGP43 gene using different methods and Pb339 as reference isolate. Recently, we have finally managed to increase sequence information of this region to -2,047 bp (as detailed in Methods), which prompted us to search for length polymorphism in other isolates (Figures 4A). In order to do that, we compared PCR fragments amplified with P4 (forward) Akt inhibitor and GRN (reverse) primers (Figures 4B) and DNA template from 14 isolates (as coded in ). Note that amplicons from Pb2, Pb3, Pb4 and Pb5 had similar sizes of around 1,500 bp; amplicons from Pb9 and Pb17 were around
3,000 bp, while those from Pb6, Pb8, Pb10, Pb11, Pb14, Pb16 and Pb18 were similar to the original Pb339 fragment migrating at about 2,000 bp. Figure 4 Analysis of 2,047 bp upstream of the Pb GP43 ORF. A, Size comparison of the PbGP43 5′ flanking region from fourteen P. brasiliensis isolates. Ethidium bromide-stained agarose gel showing the amplicons LY333531 ic50 produced with P4 (forward) and GRN (reverse) primers using genomic DNA from the indicated isolates. M, molecular markers. B, schematic representation of the PbGP43 5′ flanking Ipatasertib molecular weight region from isolates Pb339/Pb18 and Pb3, where the positions of P4/GRN primers are shown. The repeated regions are boxed and start at the dark gray bar. The lighter-colored box indicates a 58-bp sequence (“”connector”", shown in C) that is absent in the upstream repeated region 1c and 1c/a/b. The sequences in the color-coded boxes can be found in the sites indicated in B by the correspondent colored arrow. D, sequence alignment of the Et12/Et23
Tryptophan synthase probes (-255 to -215 in 1a region) with the correspondent fragments in other regions from Pb3, Pb18 and Pb339, as indicated. The overlap between these probes is indicated, as well as one of the connector sequences (brown) boxed in C. We next sequenced the Pb3 shorter PCR product; at a similar time frame the P. brasiliensis genome from isolates Pb3, Pb18 and Pb01 was released http://www.broad.mit.edu/annotation/genome/paracoccidioides_brasiliensis/MultiHome.html. Therefore, we had a chance to compare our sequences with those analyzed by the Broad Institute and the results are summarized in Figure 4. We detected in Pb339 the presence of three consecutive repetitive regions: 1a (-652 to -156), 1b (-1159 to -653) and 1c (-1600 to -1158), which are about 500-bp long (Figure 4B). Two of the regions have initially been detected due to the difficulties to arrange the contigs generated through primer walking sequencing. A middle similar region has only been revealed very recently after further analysis of the data during preparation of this manuscript.