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. 2014 Jan;13(1):31–42. doi: 10.1128/EC.00202-13

TABLE 4.

Log2 fold regulation obtained from the microarray experiment of L. kluyveri genes related to pyrimidine metabolism in response to different sole nitrogen sourcesa

L. kluyveri name S. cerevisiae homolog Sequence ID Log2 fold regulation in response to:
Uracil Dihydrouracil Uridine Ammonia
URC1 None Contig145.1.A:821 9.703 4.158 10.131 −2.016
URC2 YDR520C Skluy_39.6.2:2 1.715 0.726 0.939 −0.418
URC3,5 DUR1,2 Skluy_36.1.5:5 5.264 1.554 4.326 −0.406
URC4 None Contig31.2.A:628 8.410 4.048 8.012 −0.501
URC6 FUR1 Skluy_1.3.12:12 5.465 4.622 4.502 0.080
PYD2 None Skluy_13.2.3:3 3.721 6.908 0.839 −0.078
PYD3 None Contig147.1.A:1027 3.590 9.015 2.798 −0.106
PYD4 UGA1 Skluy_29.2.17:17 0.585 1.213 −0.441 −0.941
URC8 YMR226C Skluy_76.1.28:28 3.819 4.984 4.161 −0.201
DAL4 DAL4 Skluy_54.3.14:14 4.280 0.986 3.090 0.107
DAL5 DAL5 Skluy_39.4.2:2 5.951 1.801 5.786 −0.121
DAL5 homolog DAL5 Skluy_40.3.7:7 −0.513 1.105 −1.614 −1.609
FUI1 FUI1 Skluy_32.2.16:16 5.728 2.406 6.070 −1.632
FUI1 homolog FUI1 SAKL0H03498gb NA NA NA NA
FUR4 FUR4 Skluy_182.1.2:2 3.890 5.903 2.406 −0.211
SAKL0A07480 Nonec Skluy_104.1.4:4 4.626 3.581 3.061 −1.632
DUR3 DUR3 Skluy_31.2.8:8 4.483 1.749 3.580 −0.351
a

Cells grown on single-nitrogen-source media were used, and the expression under the four conditions was compared to that in cells grown on media with proline as the nitrogen source. The log2 fold regulation was calculated by logarithmically normalizing the sample/reference ratio of the values recovered from the scanned arrays. NA, not applicable.

b

The oligonucleotide matching this gene could not be identified; therefore, its systematic name found in the Génolevures database was used.

c

Weakly similar to VBA2 (YBR293W).