The DNA Replication Program Is Altered at the FMR1 Locus in Fragile X Embryonic Stem Cells

• Published in: Molecular cell Vol. 53; no. 1; pp. 19 - 31
• Main Authors: Gerhardt, Jeannine, Tomishima, Mark J., Zaninovic, Nikica, Colak, Dilek, Yan, Zi, Zhan, Qiansheng, Rosenwaks, Zev, Jaffrey, Samie R., Schildkraut, Carl L.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 09-01-2014
• Subjects: DNA Replication; Embryonic Development - genetics; Embryonic Stem Cells - metabolism; Embryonic Stem Cells - pathology; Fragile X Mental Retardation Protein - genetics; Fragile X Mental Retardation Protein - metabolism; Fragile X Syndrome - embryology; Fragile X Syndrome - genetics; Fragile X Syndrome - pathology; Genetic Loci; Humans; Trinucleotide Repeats
• ISSN: 1097-2765; 1097-4164
• DOI: 10.1016/j.molcel.2013.10.029

Fragile X syndrome (FXS) is caused by a CGG repeat expansion in the FMR1 gene that appears to occur during oogenesis and during early embryogenesis. One model proposes that repeat instability depends on the replication fork direction through the repeats such that (CNG)n hairpin-like structures form, causing DNA polymerase to stall and slip. Examining DNA replication fork progression on single DNA molecules at the endogenous FMR1 locus revealed that replication forks stall at CGG repeats in human cells. Furthermore, replication profiles of FXS human embryonic stem cells (hESCs) compared to nonaffected hESCs showed that fork direction through the repeats is altered at the FMR1 locus in FXS hESCs, such that predominantly the CCG strand serves as the lagging-strand template. This is due to the absence of replication initiation that would typically occur upstream of FMR1, suggesting that altered replication origin usage combined with fork stalling promotes repeat instability during early embryonic development.
•DNA replication program at the endogenous FMR1 locus is altered in FXS hESCs•Absence of detectable replication origins approximately 50 kb upstream of the repeats in FXS hESCs•DNA replication forks stall at the CGG/CCG repeats at the endogenous FMR1 locus•Differentiated FXS and nonaffected cells have a similar program at the examined FMR1