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Evolutionarily conserved enzyme play key role in DNA replication

Date:
September 12, 2016
Source:
Umea University
Summary:
Genome-wide studies of fission yeast (Schizosaccharomyces pombe) suggest that the evolutionary conserved enzyme Pfh1 helicase facilitates DNA synthesis by tracking along with the replication apparatus, promoting intact DNA synthesis at hard-to-replicate sites and consequently suppressing DNA damage.
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Genome-wide studies of fission yeast (Schizosaccharomyces pombe) suggest that the evolutionary conserved enzyme Pfh1 helicase facilitates DNA synthesis by tracking along with the replication apparatus, promoting intact DNA synthesis at hard-to-replicate sites and consequently suppressing DNA damage. The findings are published in PLOS Genetics.

Genome organization similarities of fission yeast and humans suggest that human DNA replication likely also need such helicases at hard-to-replicate sites. According to the new findings, human PIF1 is a top nominee for this task.

"Using genome-wide analyses, we show that the Pfh1 DNA helicase promotes fork progression and suppresses DNA damage at regions called 'hard-to-replicate' sites," says Nasim Sabouri, researcher at the Department of Medical Biochemistry and Biophysics at Umeå University and co-author of the study. "Hard-to replicate sites exists naturally in all genomes investigated. These natural impediments slow fork movement if they are not removed and may cause DNA breakage and genome instability, one of the hallmarks of cancer. Pfh1 possesses the unique ability to promote fork progression through these natural impediments."

Together with her graduate student, as well as researchers from Princeton and Vanderbilt universities, Nasim Sabouri used genome-wide studies and mass spectrometry to study DNA replication mechanisms in fission yeast.

The findings also reveal that Pfh1 interacts with many components of the replication machinery. Pfh1 helicase occupy many common regions genome-wide with one of the main polymerases involved in DNA replication. These are not only hard-to-replicate sites, but also sites where replication is not Pfh1-dependent. This prevalence suggests that Pfh1 is in close proximity of the replication apparatus during DNA synthesis and promotes fork progression when necessary.

"Because human cells also contain these hard-to-replicate regions, they also likely require replicative accessory DNA helicases to facilitate replication and suppress DNA damage at these sites. We believe that hPIF1 is a good candidate for this role, as Pfh1 and hPIF1 both belong to the Pif1 family helicases," says Nasim Sabouri.


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Materials provided by Umea University. Note: Content may be edited for style and length.


Journal Reference:

  1. Karin R. McDonald, Amanda J. Guise, Parham Pourbozorgi-Langroudi, Ileana M. Cristea, Virginia A. Zakian, John A. Capra, Nasim Sabouri. Pfh1 Is an Accessory Replicative Helicase that Interacts with the Replisome to Facilitate Fork Progression and Preserve Genome Integrity. PLOS Genetics, 2016; 12 (9): e1006238 DOI: 10.1371/journal.pgen.1006238

Cite This Page:

Umea University. "Evolutionarily conserved enzyme play key role in DNA replication." ScienceDaily. ScienceDaily, 12 September 2016. <www.sciencedaily.com/releases/2016/09/160912111907.htm>.
Umea University. (2016, September 12). Evolutionarily conserved enzyme play key role in DNA replication. ScienceDaily. Retrieved May 23, 2017 from www.sciencedaily.com/releases/2016/09/160912111907.htm
Umea University. "Evolutionarily conserved enzyme play key role in DNA replication." ScienceDaily. www.sciencedaily.com/releases/2016/09/160912111907.htm (accessed May 23, 2017).

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