Defective replication initiation results in locus specific chromosome breakage and a ribosomal RNA deficiency in yeast

Autor: Bonita J. Brewer, Elizabeth X. Kwan, Thomas J. Pohl, M. K. Raghuraman, Joseph C. Sanchez, Haley M. Amemiya
Jazyk: angličtina
Rok vydání: 2017
Předmět:
0301 basic medicine
Cancer Research
Origin Recognition Complex
Synthesis Phase
Eukaryotic DNA replication
Yeast and Fungal Models
Cell Cycle Proteins
Pre-replication complex
Biochemistry
Electrophoretic Blotting
DNA replication factor CDT1
0302 clinical medicine
Cell Cycle and Cell Division
Genetics (clinical)
Growth Disorders
Gel Electrophoresis
Genetics
biology
Eukaryota
Chromosome Breakage
Patella
3. Good health
Nucleic acids
Ribosomal RNA
Experimental Organism Systems
Cell Processes
Research Article
DNA Replication
Cellular structures and organelles
Saccharomyces cerevisiae Proteins
lcsh:QH426-470
Micrognathism
Mutation
Missense

Molecular Probe Techniques
Saccharomyces cerevisiae
Origin of replication
Research and Analysis Methods
DNA
Ribosomal

03 medical and health sciences
Electrophoretic Techniques
Saccharomyces
Replication factor C
Model Organisms
Control of chromosome duplication
Humans
Amino Acid Sequence
Non-coding RNA
Molecular Biology Techniques
Molecular Biology
Ecology
Evolution
Behavior and Systematics

Congenital Microtia
Biology and life sciences
Organisms
Fungi
DNA
Cell Biology
Yeast
lcsh:Genetics
030104 developmental biology
Licensing factor
Genetic Loci
RNA
Ribosomal

biology.protein
Origin recognition complex
RNA
Ribosomes
Southern Blot
030217 neurology & neurosurgery
Zdroj: PLoS Genetics
PLoS Genetics, Vol 13, Iss 10, p e1007041 (2017)
ISSN: 1553-7404
1553-7390
Popis: A form of dwarfism known as Meier-Gorlin syndrome (MGS) is caused by recessive mutations in one of six different genes (ORC1, ORC4, ORC6, CDC6, CDT1, and MCM5). These genes encode components of the pre-replication complex, which assembles at origins of replication prior to S phase. Also, variants in two additional replication initiation genes have joined the list of causative mutations for MGS (Geminin and CDC45). The identity of the causative MGS genetic variants strongly suggests that some aspect of replication is amiss in MGS patients; however, little evidence has been obtained regarding what aspect of chromosome replication is faulty. Since the site of one of the missense mutations in the human ORC4 alleles is conserved between humans and yeast, we sought to determine in what way this single amino acid change affects the process of chromosome replication, by introducing the comparable mutation into yeast (orc4Y232C). We find that yeast cells with the orc4Y232C allele have a prolonged S-phase, due to compromised replication initiation at the ribosomal DNA (rDNA) locus located on chromosome XII. The inability to initiate replication at the rDNA locus results in chromosome breakage and a severely reduced rDNA copy number in the survivors, presumably helping to ensure complete replication of chromosome XII. Although reducing rDNA copy number may help ensure complete chromosome replication, orc4Y232C cells struggle to meet the high demand for ribosomal RNA synthesis. This finding provides additional evidence linking two essential cellular pathways—DNA replication and ribosome biogenesis.
Author summary The origin recognition complex (ORC) is essential for licensing replication origins during M/G1 for their firing in the subsequent S phase. Individuals with a rare form of dwarfism called Meier-Gorlin syndrome (MGS) have mutations in proteins required for origin activation, including various subunits of ORC. To better understand the molecular and cellular consequences of these mutations, we introduced an equivalent MGS mutation in ORC4 into yeast. We find that origin activity in the ribosomal DNA (rDNA) repeats is severely compromised in yeast that harbor the MGS allele. Consequently, cells that have reduced their rDNA copy number from ~150 to fewer than 30 copies overtake the culture. Although the loss of rDNA repeats helps ensure the complete replication of chromosome XII during S phase, cells with fewer rDNA repeats struggle to meet the high demand for ribosomal RNA.
Databáze: OpenAIRE