Telomere length is regulated around an equilibrium set point. Telomeres shorten during replication and are lengthened by telomerase. Disruption of the length equilibrium leads to disease; thus, it is important to understand the mechanisms that regulate length at the molecular level. The prevailing protein-counting model for regulating telomerase access to elongate the telomere does not explain accumulating evidence of a role of DNA replication in telomere length regulation. Here I present an alternative model: the replication fork model that can explain how passage of a replication fork and regulation of origin firing affect telomere length.
CITATION STYLE
Greider, C. W. (2016). Regulating telomere length from the inside out: The replication fork model. Genes and Development, 30(13), 1483–1491. https://doi.org/10.1101/gad.280578.116
Mendeley helps you to discover research relevant for your work.