Dbf4-dependent kinase (DDK)-mediated proteolysis of CENP-A prevents mislocalization of CENP-A in Saccharomyces cerevisiae

Autor: Michael Weinreich, Lars Boeckmann, Richard Baker, Michael Costanzo, Anastasia Baryshnikova, Josefina Ocampo, Charles Boone, Levi Bursch, Chad L. Myers, Jessica R. Eisenstatt, David Clark, Munira A. Basrai, Valerie Garcia, Wei-Chun Au, Robert A. Sclafani
Jazyk: angličtina
Rok vydání: 2020
Předmět:
Zdroj: G3: Genes, Genomes, Genetics, Vol 10, Iss 6, Pp 2057-2068 (2020)
CONICET Digital (CONICET)
Consejo Nacional de Investigaciones Científicas y Técnicas
instacron:CONICET
Popis: The evolutionarily conserved centromeric histone H3 variant (Cse4 in budding yeast, CENP-A in humans) is essential for faithful chromosome segregation. Mislocalization of CENP-A to non-centromeric chromatin contributes to chromosomal instability (CIN) in yeast, fly, and human cells and CENP-A is highly expressed and mislocalized in cancers. Defining mechanisms that prevent mislocalization of CENP-A is an area of active investigation. Ubiquitin-mediated proteolysis of overexpressed Cse4 (GALCSE4)byE3 ubiquitin ligases such as Psh1 prevents mislocalization of Cse4, and psh1D strains display synthetic dosage lethality (SDL) with GALCSE4. We previously performed a genome-wide screen and identified five alleles of CDC7 and DBF4 that encode the Dbf4-dependent kinase (DDK) complex, which regulates DNA replication initiation, among the top twelve hits that displayed SDL with GALCSE4. We determined that cdc7-7 strains exhibit defects in ubiquitin-mediated proteolysis of Cse4 and show mislocalization of Cse4. Mutation of MCM5 (mcm5-bob1) bypasses the requirement of Cdc7 for replication initiation and rescues replication defects in a cdc7-7 strain. We determined that mcm5-bob1 does not rescue the SDL and defects in proteolysis of GALCSE4 in a cdc7-7 strain, suggesting a DNA replication-independent role for Cdc7 in Cse4 proteolysis. The SDL phenotype, defects in ubiquitin-mediated proteolysis, and the mislocalization pattern of Cse4 in a cdc7-7 psh1D strain were similar to that of cdc7-7 and psh1D strains, suggesting that Cdc7 regulates Cse4 in a pathway that overlaps with Psh1. Our results define a DNA replication initiation-independent role of DDK as a regulator of Psh1-mediated proteolysis of Cse4 to prevent mislocalization of Cse4. Fil: Eisenstatt, Jessica R.. National Institutes of Health; Estados Unidos Fil: Boeckmann, Lars. National Institutes of Health; Estados Unidos Fil: Au, Wei Chun. National Institutes of Health; Estados Unidos Fil: Garcia, Valerie. National Institutes of Health; Estados Unidos Fil: Bursch, Levi. National Institutes of Health; Estados Unidos Fil: Ocampo, Josefina. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Investigaciones en Ingeniería Genética y Biología Molecular "Dr. Héctor N. Torres"; Argentina. National Instituto of Child Health & Human Development; Estados Unidos Fil: Costanzo, Michael. National Institutes of Health; Estados Unidos. University of Toronto; Canadá Fil: Weinreich, Michael. Van Andel Research Institute; Estados Unidos Fil: Sclafani, Robert A.. University of Colorado; Estados Unidos Fil: Baryshnikova, Anastasia. University of Princeton; Estados Unidos Fil: Myers, Chad L.. University of Minnesota; Estados Unidos Fil: Boone, Charles. University of Toronto; Canadá. National Institutes of Health; Estados Unidos Fil: Clark, David J.. National Institutes of Health; Estados Unidos Fil: Baker, Richard. University of Massachusetts; Estados Unidos Fil: Basrai, Munira A.. National Institutes of Health; Estados Unidos
Databáze: OpenAIRE
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