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. 1999 May 25;96(11):6205–6210. doi: 10.1073/pnas.96.11.6205

Table 1.

Multicopy suppression analysis

Mutant Multicopy gene Temperature, °C
23 30 33 35 37
spc29-2 SPC29 +++ +++ +++ +++ +++
SPC42 +++ +++ +++
SPC110 +++ +++ +++
CDC31 +++ +++ +++ +++ +++
KAR1 +++ +++
control +++ +++ +++
spc29-3 SPC29 +++ +++ +++ +++ +++
SPC42 +++ +++
SPC110 +++ +
CDC31 +++ +++
KAR1 +++
control +++ +++
spc29-9 SPC29 +++ +++ +++ +++ +++
SPC42 +++ +
SPC110 +++ +
CDC31 +++ +++
KAR1 +++ +++
control +++ +++
spc42-9 SPC42 +++ +++ +++ +++ +++
SPC29 +++ +++ +++ +++
SPC110 +++ +++ +++ +++
control +++ +++ +++ +++
spc42-10 SPC42 +++ +++ +++ +++ +++
SPC29 +++ +++ +++ +++ +++
SPC110 +++ +++ +++
control +++ +++ +++
spc110-118 SPC110 +++ +++ +++ +++ +++
SPC29 +++ +++ +
CMDI +++ +++ +++ +++ +++
control +++ +++ +++ +
spc110-124 SPC110 +++ +++ +++ +++ +++
SPC29 +++ +++ +++
CMDI +++ +++ +++ +++ +++
control +++ +++ +++ +++

The conditional-lethal mutants spc29-2, spc29-3, spc29-9, spc42-9, spc42-10, spc110-118, and spc110-124 were transformed with either an empty 2-μm plasmid (control) or with a 2-μm plasmid carrying one of the indicated genes. Only KAR1 was on the centromere-based plasmid pRS315. Transformants were tested for growth at various temperatures. +++, good growth, +, reduced growth, −, no growth.