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. 2007 Dec 17;28(4):1393–1403. doi: 10.1128/MCB.01733-07

TABLE 2.

Observed synthetic interactions between SPN1 and specific gene products involved in RNAPII-mediated transcription

Protein category and deleted gene Change in phenotype under the following conditiona:
YPD
1 M NaCl 1 M sorbitol 4 mM H2O2 Ino YPGal YPEG 50 mM AT MPA
30°C 38°C 14°C
Subunits of Swi/Snf complex
    SNF2b Sup Sup N Sup Sup Sup Sup Sup Sup Sup Sup
    SNF5 N Sup N N N Sup Sup Sup Sup Sup Sup
    SNF6 N Sup N N N Sup Sup Sup Sup Sup Sup
Elongation factors
    DST1 N N N Ex Ex Ex N Ex Ex Ex Ex
    RTF1 N N N Ex Ex Ex N Ex Ex Ex Ex
    SPT4 SL SL SL SL SL SL SL SL SL SL SL
a

Deletion strains (as indicated) were combined with the K192N derivative of SPN1, and alterations in growth properties under 11 different conditions were assayed. N, no change in phenotype from that observed in either of the two parental strains (the knockout strain or the K192N strain); Ex, phenotype exacerbated in the double mutant strains; Sup, suppression of mutant phenotypes in the double mutant background; SL, synthetic lethality in the double mutant background.

b

Synthetic interactions between SNF2 and SPN1 were observed by mutating SPN1 in strain CMKy42 (15).