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Bra031539-3eR1

E1. Bra031539-OC_MF1. Bra031539-R2. Bra031539-F3. E2. Bra031539-OC_MR1. Bra031539-R3. Bra031539-F4. E3. E4. E5. Bra031539_TeF1. E6. Bra031539-R4. Bra031539_TeF2. E7. Bra031539_TeR1. E8. E9. Bra031539_TeF3. Bra031539_TeR2. Bra031539-3eF1. E10. E11. Bra031539_TeF4.

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Bra031539-3eR1

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  1. E1 Bra031539-OC_MF1 Bra031539-R2 Bra031539-F3 E2 Bra031539-OC_MR1 Bra031539-R3 Bra031539-F4 E3 E4 E5 Bra031539_TeF1 E6 Bra031539-R4 Bra031539_TeF2 E7 Bra031539_TeR1 E8 E9 Bra031539_TeF3 Bra031539_TeR2 Bra031539-3eF1 E10 E11 Bra031539_TeF4 Bra031539_TeR3 E12 E13 Bra031539_TeF5 Bra031539-3eR1 Bra031539_TeR4 Bra031539-3eR1(OC) EX040997 Supplementary fig. 1.Sequence comparison of BrCRTISO1 from OC and YE cultivars. Genomic sequence of BrCRTISO1 was determined by nucleotide sequencing and assembly of DNA fragments amplified by primers depicted by blue arrows (Supplementary table 1). Red and green boxes indicate exons (E1 to E13) predicted based on BRAD information and 3’terminal region identical to EST sequence (accession no. EX040997), respectively. Some primers and their site were not shown because sequences at the both ends were trimmed. The start codon and stop codon are marked by red rectangles. The alignment was generated using ClustalW (http://www.genome.jp/tools/clustalw/) and GeneDoc software.

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