DNA replication is undeniably important for life and as a consequence, cells have evolved mechanisms to monitor replication fidelity and to coordinate completion of replication with other cell cycle events. The goal of this project is to understand how cells choreograph the duplication of their chromosomes, and how defects in DNA replication may contribute to some recently discovered disorders in humans. Chromosome replication in eukaryotes is a process that involves the regulation of multiple initiation sites (origins) per chromosome. Origins show variation in timing-not all origins fire at the same time in S phase-and in efficiency-not all origins necessarily firing in every cell cycle. In addition, cells appea to maintain a backup set of origins (dormant origins) for use under special circumstances and these origins may differ in their basic control properties. Understanding how origin use is regulated is therefore critical for understanding how genome integrity is maintained. This notion is underscored by three recently described genetic disorders with links to replication defects: 1) Meier-Gorlin Syndrome with its point mutations in genes essential for origin licensing;2) a point mutation in a gene encoding part of the replicative helicase that is associated with breast cancer in mice and growth abnormalities in humans;and 3) human segmental triplications with an inverted central copy that can be explained by a replication fork error. Yeast is an ideal model organism for studying DNA replication because of its small chromosomes, well defined origin sequences, ease of altering chromosome structure, and exceptional systems for genetic and genomic analysis. This project will apply a combination of molecular, genetic and genomics approaches to: ? uncover modulators of origin efficiency and timing in yeast, to explore/investigate how orderly replication contributes to genome stability ? use point mutations in the yeast orthologs of genes involved in human disorders to understand the downstream consequences of defects in replication as they relate to human health and disease, and to identify genetic and chemical suppressors of the defects ? determine whether DNA replication errors are responsible for a particular class of inverted amplicons that can contribute to cancer progression and congenital copy number variants. This project will address outstanding questions regarding the biology of chromosome replication control: why do origins initiate replication at different times, what distinguishes origins in different temporal categories, what i the molecular basis for inefficient origins, and what defects in replication fork progression predispose chromosomal loci to inverted amplification? In addition, this work will give insight int human disorders resulting from errors in chromosome replication and could lead to diagnostic or therapeutic advances.
Brewer Errors in chromosomal DNA duplication are a major source of genomic instability and are associated with a number of human disorders including cancer and some developmental disorders. We propose to continue our investigations into the mechanisms that modulate the orderly progression of chromosome replication and a direct role that replication origins may play in leading to genome instability. This work will expand our understanding of the mechanisms regulating chromosome duplication and illuminate questions of importance to human health.
|Merrikh, Christopher N; Brewer, Bonita J; Merrikh, Houra (2015) The B. subtilis Accessory Helicase PcrA Facilitates DNA Replication through Transcription Units. PLoS Genet 11:e1005289|
|Brewer, Bonita J; Payen, Celia; Di Rienzi, Sara C et al. (2015) Origin-Dependent Inverted-Repeat Amplification: Tests of a Model for Inverted DNA Amplification. PLoS Genet 11:e1005699|
|Payen, Celia; Di Rienzi, Sara C; Ong, Giang T et al. (2014) The dynamics of diverse segmental amplifications in populations of Saccharomyces cerevisiae adapting to strong selection. G3 (Bethesda) 4:399-409|
|Peng, Jie; Raghuraman, M K; Feng, Wenyi (2014) Analysis of ssDNA gaps and DSBs in genetically unstable yeast cultures. Methods Mol Biol 1170:501-15|
|Hiraga, Shin-Ichiro; Alvino, Gina M; Chang, Fujung et al. (2014) Rif1 controls DNA replication by directing Protein Phosphatase 1 to reverse Cdc7-mediated phosphorylation of the MCM complex. Genes Dev 28:372-83|
|Peng, Jie; Raghuraman, M K; Feng, Wenyi (2014) Analysis of replication timing using synchronized budding yeast cultures. Methods Mol Biol 1170:477-99|
|Liachko, Ivan; Youngblood, Rachel A; Tsui, Kyle et al. (2014) GC-rich DNA elements enable replication origin activity in the methylotrophic yeast Pichia pastoris. PLoS Genet 10:e1004169|
|Kwan, Elizabeth X; Foss, Eric J; Tsuchiyama, Scott et al. (2013) A natural polymorphism in rDNA replication origins links origin activation with calorie restriction and lifespan. PLoS Genet 9:e1003329|
|Pohl, Thomas J; Kolor, Katherine; Fangman, Walton L et al. (2013) A DNA sequence element that advances replication origin activation time in Saccharomyces cerevisiae. G3 (Bethesda) 3:1955-63|
|Di Rienzi, Sara C; Lindstrom, Kimberly C; Mann, Tobias et al. (2012) Maintaining replication origins in the face of genomic change. Genome Res 22:1940-52|
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