TY - JOUR
T1 - Faithful chromosome transmission requires Spt4p, a putative regulator of chromatin structure in Saccharomyces cerevisiae
AU - Basrai, Munira A.
AU - Kingsbury, Jeffrey
AU - Koshland, Douglas
AU - Spencer, Forrest
AU - Hieter, Philip
PY - 1996
Y1 - 1996
N2 - A chromosome transmission fidelity (ctf) mutant, s138, of Saccharomyces cerevisiae was identified by its centromere (CEN) transcriptional readthrough phenotype, suggesting perturbed kinetochore integrity in vivo. The gene complementing the s138 mutation was found to be identical to the S. cerevisiae SPT4 gene. The s138 mutation is a missense mutation in the second of four conserved cysteine residues positioned similarly to those of zinc finger proteins, and we henceforth refer to the mutation as spt4-138. Both spt4-138 and spt4Δ strains missegregate a chromosome fragment at the permissive temperature, are temperature sensitive for growth at 37°C, and upon a shift to the nonpermissive temperature show an accumulation of large budded cells, each with a nucleus. Previous studies suggest that Spt4p functions in a complex with Spt5p and Spt6p, and we determined that spt6-140 also causes missegregation of a chromosome fragment. Double mutants carrying spt4Δ2:: HIS3 and kinetochore mutation ndc10-42 or ctf13-30 show a synthetic conditional phenotype. Both spt4-138 and spt4Δ strains exhibit synergistic chromosome instability in combination with CEN DNA mutations and show in vitro defects in microtubule binding to minichromosomes. These results indicate that Spt4p plays a role in chromosome segregation. The results of in vivo genetic interactions with mutations in kinetochore proteins and CEN DNA and of in vitro biochemical assays suggest that Spt4p is important for kinetochure function.
AB - A chromosome transmission fidelity (ctf) mutant, s138, of Saccharomyces cerevisiae was identified by its centromere (CEN) transcriptional readthrough phenotype, suggesting perturbed kinetochore integrity in vivo. The gene complementing the s138 mutation was found to be identical to the S. cerevisiae SPT4 gene. The s138 mutation is a missense mutation in the second of four conserved cysteine residues positioned similarly to those of zinc finger proteins, and we henceforth refer to the mutation as spt4-138. Both spt4-138 and spt4Δ strains missegregate a chromosome fragment at the permissive temperature, are temperature sensitive for growth at 37°C, and upon a shift to the nonpermissive temperature show an accumulation of large budded cells, each with a nucleus. Previous studies suggest that Spt4p functions in a complex with Spt5p and Spt6p, and we determined that spt6-140 also causes missegregation of a chromosome fragment. Double mutants carrying spt4Δ2:: HIS3 and kinetochore mutation ndc10-42 or ctf13-30 show a synthetic conditional phenotype. Both spt4-138 and spt4Δ strains exhibit synergistic chromosome instability in combination with CEN DNA mutations and show in vitro defects in microtubule binding to minichromosomes. These results indicate that Spt4p plays a role in chromosome segregation. The results of in vivo genetic interactions with mutations in kinetochore proteins and CEN DNA and of in vitro biochemical assays suggest that Spt4p is important for kinetochure function.
UR - http://www.scopus.com/inward/record.url?scp=0029905349&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0029905349&partnerID=8YFLogxK
U2 - 10.1128/MCB.16.6.2838
DO - 10.1128/MCB.16.6.2838
M3 - Article
C2 - 8649393
AN - SCOPUS:0029905349
SN - 0270-7306
VL - 16
SP - 2838
EP - 2847
JO - Molecular and cellular biology
JF - Molecular and cellular biology
IS - 6
ER -