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. 2013 Nov 1;14:25. doi: 10.1186/1471-2199-14-25

Table 4.

Transcripts at lower levels in stationary (high-toxin-producing) as compared to late-exponential (low-toxin-producing) phase in Pseudo-nitzschia multiseries ( Ps-n ) as determined by cDNA microarray analysis

 
 
Fold change a
 
Stationary versus late-exponential phase
Ps-n NR Identifier
JGI Ps-n Genome Hit
Non-axenic
Non-axenic
Axenic
Predicted gene product
  Scaffold:Start-End Expt. 1 Expt. 2 Expt.  
PSN0100
32:397085-398987
0.34 ± 0.01
0.33 ± 0.05
0.39 ± 0.01
Pyrophosphate-dependent phosphofructokinase (PFK)
PSN0060
133:16659-18505
0.20± 0.02
0.16 ± 0.03
0.44 ± 0.04
Predicted protein with signal or transit peptide
PSN0048
188:179178-180986
0.36± 0.08
0.25 ± 0.06
0.52 ± 0.05
Predicted protein with signal or transit peptide
PSN0080
461:123066-124152
0.32 ± 0.02
0.33 ± 0.03
0.57 ± 0.07
Predicted protein with mitochondrial transit peptide
135E4
1441:17433-18891
0.17 ± 0.00
0.19 ± 0.02
0.45 ± 0.02
Predicted protein
165G9
8:175639-176910
0.37 ± 0.02
0.37 ± 0.02
0.62 ± 0.04
Tetratricopeptide repeat protein
135H6b
214:78592-7971
0.41 ± 0.00
0.22 ± 0.02
0.59 ± 0.00
Fucoxanthin-chlorophyll a-c binding protein,
          chloroplastic (FCP)

aThe fold-change data presented are the average of all of the cDNA clones that were printed on the array for each transcript. The number of cDNA clones for each transcript was: PSN0100 (2), PSN0060 (5), PSN0048 (5), PSN0080 (3), 135E4 (1), 165G9 (1), 135H6 (1), and each clone was printed twice.

b135H6 was included as a gene of interest in RT-qPCR analysis, below, although it did not meet our fold-change cut-off for the original FDR microarray analysis (yet, all LFDRs were <10%). Please see Methods for statistical analysis, and Additional file 1 for FDR and LDFR data.