Supplemental material

Files in this Data Supplement:

• Supplemental file 1 - Figure legends for Fig. S5, S6, S8, and S9.
  Word document, 29K.
• Supplemental file 2 - Genotypes of the Candida albicans strains used in this paper.
  Word document, 78K.
• Supplemental file 3 - Table of the oligo sequences used in this paper.
  Word document, 73K.
• Supplemental file 4 - Methods used for isolating NORE-associated proteins from C. albicans whole-cell extract and methods used in preparing samples for tandem mass spectrometry.
  Word document, 34K.
• Supplemental file 5 - Figure displaying relative positions of the linker scanning mutations Msub1 to Msub16 used to analyze the YHB1 regulatory region at −481 to −352 from the start codon and the results of β-galactosidase assays on strains with these mutations.
  TIFF document, 9.7MB.
• Supplemental file 6 - Figure displaying sequences and positions of the linker scanning mutations Msub14 to Msub31 used to analyze the YHB1 regulatory region close to the NORE and the results of β-galactosidase assays on strains with these mutations. (This is an expanded version of Fig. 1 in the paper.)
  TIFF document, 22MB.
• Supplemental file 7 - Table showing results for DTASelect filtering of mass spectrometry data on the SDS-PAGE gel bands containing NORE-associated proteins.
  Word document, 590K.
• Supplemental file 8 - Figure showing sensitivity of C. albicans ssu1Δ/ssu1Δ mutant strains to sulfite stress.
  JPG document, 41K.
• Supplemental file 9 - Figure showing RT-PCR results of effects of DETA NONOate on SSU1 expression in wild-type and cta4Δ/cta4Δ C. albicans strains.
  Word document, 53K.