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. 2010 Nov 12;5(11):e15426. doi: 10.1371/journal.pone.0015426

Table 1. Genes required for surviving Spc110 cleavage.

Gene Role Synthetic Growth Defect in W303a
Mitosis
CTF19 Kinetochore
CIK1 b MT motor (kinesin-14 accessory) Yes
KAR3 b MT motor (kinesin-14) Yes
VIK1 b MT motor (kinesin-14 accessory) Yes
JNM1 b MT motor (dynactin complex) Yes
DYN3 b MT motor (dynein inter. light ch.) Yes
CLB2 mitotic cyclin
BFA1 mitotic exit
BUB3 mitotic spindle checkpoint
MAD1 b mitotic spindle checkpoint Yes
MAD3 mitotic spindle checkpoint
MAD2 b mitotic spindle checkpoint Yes
CTF18 sister chromatid cohesion
CTF8 sister chromatid cohesion
CHL1 sister chromatid cohesion
Protein Modification
RTS1 b PP2A B' subunit Yes
NCS2 b Urmylation Yes
PPM1 b PP2A methyltransferase No
UBC4 b Ubiquitination (E2) Yes
UBC7 Ubiquitination (E2)
Nuclear Pore
SAC3 b nuclear pore Yes
POM152 b nuclear pore Yes
NUP60 b nuclear pore Yes
Chromatin Remodeling
HTZ1 Histone
SIN3 Histone deacetylase
DOT1 b Histone methyltransferase No
EAF3 Histone acetyltransferase
VPS71 Part of Swi/Snf remodeling
mRNA Levels
LSM6 mRNA catabolism
NMD2 mRNA catabolism
SKI3 mRNA catabolism
LSM7 b mRNA catabolism No
SKI7 mRNA catabolism
UPF3 mRNA catabolism
PAT1 mRNA catabolism
PUS7 mRNA splicing
HCM1 b transcriptional activator Yes
Other
SLA1 Endocytosis
YOR052C Unknown (zinc-finger protein)

The top 36 candidates identified in the SGA screen are shown in this table. Deletion of each gene caused decreased growth in the presence of Spc110 cleavage with a p-value <2.17×10−3.

a

Each of these genes was deleted in the W303 genetic background and the synthetic growth defect verified.

b

Chosen for further study.