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Published May 15, 2011 | Published + Supplemental Material
Journal Article Open

Inviability of a DNA2 deletion mutant is due to the DNA damage checkpoint


Dna2 is a dual polarity exo/endonuclease, and 5' to 3' DNA helicase involved in Okazaki Fragment Processing (OFP) and Double-Strand Break (DSB) Repair. In yeast, DNA2 is an essential gene, as expected for a DNA replication protein. Suppression of the lethality of dna2Δ mutants has been found to occur by two mechanisms: overexpression of RAD27^(scFEN1), encoding a 5' to 3' exo/endo nuclease that processes Okazaki fragments (OFs) for ligation, or deletion of PIF1, a 5' to 3' helicase involved in mitochondrial recombination, telomerase inhibition and OFP. Mapping of a novel, spontaneously arising suppressor of dna2Δ now reveals that mutation of rad9 and double mutation of rad9 mrc1 can also suppress the lethality of dna2Δ mutants. Interaction of dna2Δ and DNA damage checkpoint mutations provides insight as to why dna2Δ is lethal but rad27Δ is not, even though evidence shows that Rad27^(ScFEN1) processes most of the Okazaki fragments, while Dna2 processes only a subset.

Additional Information

© 2011 Landes Bioscience. Submitted: 03/28/11; Accepted: 03/29/11. This work was supported by Public Health Service, NIGMS 078666 and Army Research Office (ARO) 09-1-0041.

Attached Files

Published - Budd2011p14038Cell_Cycle.pdf

Supplemental Material - BuddCC10-10-sup.pdf


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