Rmi1 stimulates decatenation of double Holliday junctions during dissolution by Sgs1-Top3

Research output: Contribution to journal › Journal article › Research › peer-review

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Rmi1 stimulates decatenation of double Holliday junctions during dissolution by Sgs1-Top3. / Cejka, Petr; Plank, Jody L; Bachrati, Csanad Z; Hickson, Ian D; Kowalczykowski, Stephen C.

In: Nature Structural & Molecular Biology, Vol. 17, No. 11, 01.11.2010, p. 1377-82.

Research output: Contribution to journal › Journal article › Research › peer-review

Harvard

Cejka, P, Plank, JL, Bachrati, CZ, Hickson, ID & Kowalczykowski, SC 2010, 'Rmi1 stimulates decatenation of double Holliday junctions during dissolution by Sgs1-Top3', Nature Structural & Molecular Biology, vol. 17, no. 11, pp. 1377-82. https://doi.org/10.1038/nsmb.1919

APA

Cejka, P., Plank, J. L., Bachrati, C. Z., Hickson, I. D., & Kowalczykowski, S. C. (2010). Rmi1 stimulates decatenation of double Holliday junctions during dissolution by Sgs1-Top3. Nature Structural & Molecular Biology, 17(11), 1377-82. https://doi.org/10.1038/nsmb.1919

Vancouver

Cejka P, Plank JL, Bachrati CZ, Hickson ID, Kowalczykowski SC. Rmi1 stimulates decatenation of double Holliday junctions during dissolution by Sgs1-Top3. Nature Structural & Molecular Biology. 2010 Nov 1;17(11):1377-82. https://doi.org/10.1038/nsmb.1919

Author

Cejka, Petr ; Plank, Jody L ; Bachrati, Csanad Z ; Hickson, Ian D ; Kowalczykowski, Stephen C. / Rmi1 stimulates decatenation of double Holliday junctions during dissolution by Sgs1-Top3. In: Nature Structural & Molecular Biology. 2010 ; Vol. 17, No. 11. pp. 1377-82.

Bibtex

@article{fdb0f4a32f8a489db7223a324b329dfb,
title = "Rmi1 stimulates decatenation of double Holliday junctions during dissolution by Sgs1-Top3",
abstract = "A double Holliday junction (dHJ) is a central intermediate of homologous recombination that can be processed to yield crossover or non-crossover recombination products. To preserve genomic integrity, cells possess mechanisms to avoid crossing over. We show that Saccharomyces cerevisiae Sgs1 and Top3 proteins are sufficient to migrate and disentangle a dHJ to produce exclusively non-crossover recombination products, in a reaction termed {"}dissolution.{"} We show that Rmi1 stimulates dHJ dissolution at low Sgs1-Top3 protein concentrations, although it has no effect on the initial rate of Holliday junction (HJ) migration. Rmi1 serves to stimulate DNA decatenation, removing the last linkages between the repaired and template DNA molecules. Dissolution of a dHJ is a highly efficient and concerted alternative to nucleolytic resolution that prevents crossing over of chromosomes during recombinational DNA repair in mitotic cells and thereby contributes to genomic integrity.",
keywords = "DNA, Cruciform, DNA, Fungal, DNA-Binding Proteins, RecQ Helicases, Saccharomyces cerevisiae, Saccharomyces cerevisiae Proteins",
author = "Petr Cejka and Plank, {Jody L} and Bachrati, {Csanad Z} and Hickson, {Ian D} and Kowalczykowski, {Stephen C}",
year = "2010",
month = nov,
day = "1",
doi = "10.1038/nsmb.1919",
language = "English",
volume = "17",
pages = "1377--82",
journal = "Nature Structural and Molecular Biology",
issn = "1545-9993",
publisher = "nature publishing group",
number = "11",

}

RIS

TY - JOUR

T1 - Rmi1 stimulates decatenation of double Holliday junctions during dissolution by Sgs1-Top3

AU - Cejka, Petr

AU - Plank, Jody L

AU - Bachrati, Csanad Z

AU - Hickson, Ian D

AU - Kowalczykowski, Stephen C

PY - 2010/11/1

Y1 - 2010/11/1

N2 - A double Holliday junction (dHJ) is a central intermediate of homologous recombination that can be processed to yield crossover or non-crossover recombination products. To preserve genomic integrity, cells possess mechanisms to avoid crossing over. We show that Saccharomyces cerevisiae Sgs1 and Top3 proteins are sufficient to migrate and disentangle a dHJ to produce exclusively non-crossover recombination products, in a reaction termed "dissolution." We show that Rmi1 stimulates dHJ dissolution at low Sgs1-Top3 protein concentrations, although it has no effect on the initial rate of Holliday junction (HJ) migration. Rmi1 serves to stimulate DNA decatenation, removing the last linkages between the repaired and template DNA molecules. Dissolution of a dHJ is a highly efficient and concerted alternative to nucleolytic resolution that prevents crossing over of chromosomes during recombinational DNA repair in mitotic cells and thereby contributes to genomic integrity.

AB - A double Holliday junction (dHJ) is a central intermediate of homologous recombination that can be processed to yield crossover or non-crossover recombination products. To preserve genomic integrity, cells possess mechanisms to avoid crossing over. We show that Saccharomyces cerevisiae Sgs1 and Top3 proteins are sufficient to migrate and disentangle a dHJ to produce exclusively non-crossover recombination products, in a reaction termed "dissolution." We show that Rmi1 stimulates dHJ dissolution at low Sgs1-Top3 protein concentrations, although it has no effect on the initial rate of Holliday junction (HJ) migration. Rmi1 serves to stimulate DNA decatenation, removing the last linkages between the repaired and template DNA molecules. Dissolution of a dHJ is a highly efficient and concerted alternative to nucleolytic resolution that prevents crossing over of chromosomes during recombinational DNA repair in mitotic cells and thereby contributes to genomic integrity.

KW - DNA, Cruciform

KW - DNA, Fungal

KW - DNA-Binding Proteins

KW - RecQ Helicases

KW - Saccharomyces cerevisiae

KW - Saccharomyces cerevisiae Proteins

U2 - 10.1038/nsmb.1919

DO - 10.1038/nsmb.1919

M3 - Journal article

C2 - 20935631

VL - 17

SP - 1377

EP - 1382

JO - Nature Structural and Molecular Biology

JF - Nature Structural and Molecular Biology

SN - 1545-9993

IS - 11

ER -

ID: 33489825