A Self-Replicating Linear DNA
journal contributionposted on 25.03.2020, 20:29 authored by Pei Sheng Liew, Tze Hao Tan, Yin Cheng Wong, Edmund Ui Hang Sim, Choon Weng Lee, Kumaran Narayanan
TelN and tos are a unique DNA linearization unit isolated from bacteriophage N15. While being transferable, the TelN cleaving-rejoining activities remained stable to function on tos in both bacterial and mammalian environments. However, TelN contribution in linear plasmid replication in mammalian cells remains unknown. Herein, we investigated the association of TelN in linear tos-containing DNA (tos-DNA) replication in mammalian cells. Additionally, the mammalian origin of replication (ori) that is well-known to initiate the replication event of plasmid vectors was also studied. In doing so, we identified that both TelN and mammalian initiation sites were essential for the replication of linear tos-DNA, determined by using methylation sensitive DpnI/MboI digestion and polymerase chain reaction (PCR) amplification approaches. Furthermore, we engineered the linear tos-DNA to be able to retain in mammalian cells using S/MAR technology. The resulting S/MAR containing tos-DNA was robust for at least 15 days, with (1) continuous tos-DNA replication, (2) correct splicing of gene transcripts, and (3) stable exogenous gene expression that was statistically comparable to the endogenous gene expression level. Understanding the activities of TelN and tos in mammalian cells can potentially provide insights for adapting this simple DNA linearization unit in developing novel genetic engineering tools, especially to the eukaryotic telomere/telomerase study.
Read the peer-reviewed publication
15 daysPCRpolymerase chain reactionSelf-Replicating Linear DNA TelNplasmid replicationTelN contributionDNA linearization unitplasmid vectorsgene transcriptsamplification approachesreplication eventexogenous gene expressionengineering toolsTelN cleaving-rejoining activitiesbacteriophage N 15.gene expression levelinitiation sitesDNA replication