Searching journal content for articles similar to Kunnev et al. 25 (4): 558.

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  1. ...are accompanied by replication checkpoint activation, a delayed cell cycle, and increased lethality in checkpoint-compromised embryos. Our comprehensive analysis of DNA replication in C. elegans reveals the genomic location of replication origins and the dynamics of their firing, and uncovers a role of H3...
  2. ...to this work. ↵ Present addresses: 2 Mercyhurst University, Department of Biology, Erie, PA 16546, USA; 3 Institute for Molecular Medicine, University of Southern Denmark, 5000 Odense C, Denmark. Abstract Nascent strand sequencing (NS-seq) is used to discover DNA replication origins...
  3. ...; Schwaiger et al. 2009). The process of DNA replication has been studied extensively. Replication origins are licensed during mitosis and early G1, with the binding of ORC (origin recognition complex) and the subsequent recruitment of the minichromosome maintenance (MCM) complex (part of the replicative DNA...
  4. ...-capped extremities composed of sequences originating from more internal genomic regions were associated with high DNA methylation, suggesting that de novo heterochromatin formation contributes to the restoration of chromosome end stability in C. reinhardtii. The diversity of alternative strategies present...
  5. ...as a primer for DNA synthesis (Liu and Malkova 2022). Following initiation of replication, unidirectional migration of a replication bubble may occur over hundreds of kilobases, followed by DNA repair (Liu and Malkova 2022). In centromere repeat arrays, there may be multiple locations to which the invading...
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  6. ..., for the identification of mutations that suppress the growth deficiency imposed by excessive initiations from the Escherichia coli origin of replication, oriC . The E. coli chromosome, like the majority of bacterial chromosomes, is circular, and DNA replication is initiated by assembling two replication complexes...
  7. ..., telomerase-added DNA repeats (Greider and Blackburn 1989; Zakian 1989, 1996; Blackburn 1991) counteract the “end-replication problem” that otherwise erodes unique DNA sequence at chromosome termini (Watson 1972). However, telomeres of select fungi (Starnes et al. 2012), algae (Higashiyama et al. 1997), moths...
  8. .... Results SUMO1 and SUMO2 are widely distributed over the in proliferating human fibroblasts To profile sumoylated proteins on the of proliferating primary cells, we performed chromatin immunoprecipitation coupled toDNA sequencing (ChIP-seq) inWI38 human fibroblasts using antibodies specific for SUMO1...
  9. ...formation in C. albicans, we propose a model shown in Figure 8D. The presence of neocentromere hotspots within the centromere proximal regions indicates that the nature of DNA sequences such as structural motifs or replication origins may play an important role in the assembly of CENPA on centromeres...
  10. ....200604072 ↵Aparicio OM, Weinstein DM, Bell SP. 1997. Components and dynamics of DNA replication complexes in S. cerevisiae: redistribution of MCM proteins and Cdc45p during S phase. Cell 91: 59–69. doi:10.1016/S0092-8674(01)80009-X ↵Aragon AD, Rodriguez AL, Meirelles O, Roy S, Davidson GS, Tapia PH, Allen C...
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