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Mechanism of stimulation of DNA binding of the transcription factors by human apurinic/apyrimidinic endonuclease 1, APE1. / Bazlekowa-Karaban, Milena; Prorok, Paulina; Baconnais, Sonia et al.

In: DNA Repair, Vol. 82, 102698, 01.10.2019, p. 102698.

Research output: Contribution to journalArticlepeer-review

Harvard

Bazlekowa-Karaban, M, Prorok, P, Baconnais, S, Taipakova, S, Akishev, Z, Zembrzuska, D, Popov, AV, Endutkin, AV, Groisman, R, Ishchenko, AA, Matkarimov, BT, Bissenbaev, A, Le Cam, E, Zharkov, DO, Tudek, B & Saparbaev, M 2019, 'Mechanism of stimulation of DNA binding of the transcription factors by human apurinic/apyrimidinic endonuclease 1, APE1', DNA Repair, vol. 82, 102698, pp. 102698. https://doi.org/10.1016/j.dnarep.2019.102698

APA

Bazlekowa-Karaban, M., Prorok, P., Baconnais, S., Taipakova, S., Akishev, Z., Zembrzuska, D., Popov, A. V., Endutkin, A. V., Groisman, R., Ishchenko, A. A., Matkarimov, B. T., Bissenbaev, A., Le Cam, E., Zharkov, D. O., Tudek, B., & Saparbaev, M. (2019). Mechanism of stimulation of DNA binding of the transcription factors by human apurinic/apyrimidinic endonuclease 1, APE1. DNA Repair, 82, 102698. [102698]. https://doi.org/10.1016/j.dnarep.2019.102698

Vancouver

Bazlekowa-Karaban M, Prorok P, Baconnais S, Taipakova S, Akishev Z, Zembrzuska D et al. Mechanism of stimulation of DNA binding of the transcription factors by human apurinic/apyrimidinic endonuclease 1, APE1. DNA Repair. 2019 Oct 1;82:102698. 102698. Epub 2019 Aug 31. doi: 10.1016/j.dnarep.2019.102698

Author

Bazlekowa-Karaban, Milena ; Prorok, Paulina ; Baconnais, Sonia et al. / Mechanism of stimulation of DNA binding of the transcription factors by human apurinic/apyrimidinic endonuclease 1, APE1. In: DNA Repair. 2019 ; Vol. 82. pp. 102698.

BibTeX

@article{9d7c376592ec4da9add56bc8dc544d37,
title = "Mechanism of stimulation of DNA binding of the transcription factors by human apurinic/apyrimidinic endonuclease 1, APE1",
abstract = "Aerobic respiration generates reactive oxygen species (ROS), which can damage nucleic acids, proteins and lipids. A number of transcription factors (TFs) contain redox-sensitive cysteine residues at their DNA-binding sites, hence ROS-induced thiol oxidation strongly inhibits their recognition of the cognate DNA sequences. Major human apurinic/apyrimidinic (AP) endonuclease 1 (APE1/APEX1/HAP-1), referred also as a redox factor 1 (Ref-1), stimulates the DNA binding activities of the oxidized TFs such as AP-1 and NF-κB. Also, APE1 participates in the base excision repair (BER) and nucleotide incision repair (NIR) pathways to remove oxidative DNA base damage. At present, the molecular mechanism underlying the TF-stimulating/redox function of APE1 and its biological role remains disputed. Here, we provide evidence that, instead of direct cysteine reduction in TFs by APE1, APE1-catalyzed NIR and TF-stimulating activities may be based on transient cooperative binding of APE1 to DNA and induction of conformational changes in the helix. The structure of DNA duplex strongly influences NIR and TF-stimulating activities. Homologous plant AP endonucleases lacking conserved cysteine residues stimulate DNA binding of the p50 subunit of NF-κB. APE1 acts synergistically with low-molecular-weight reducing agents on TFs. Finally, APE1 stimulates DNA binding of the redox-insensitive p50-C62S mutant protein. Electron microscopy imaging of APE1 complexes with DNA revealed preferential polymerization of APE1 on the gapped and intrinsically curved DNA duplexes. Molecular modeling offers a structural explanation how full-length APE1 can oligomerize on DNA. In conclusion, we propose that DNA-directed APE1 oligomerization can be regarded as a substitute for diffusion of APE1 along the DNA contour to probe for anisotropic flexibility. APE1 oligomers exacerbate pre-existing distortions in DNA and enable both NIR activity and DNA binding by TFs regardless of their oxidation state.",
keywords = "AP endonuclease, Base excision repair, Nucleotide incision repair, Oxidative damage, Redox regulation, Transcription factors, TERMINAL DOMAIN, BASE EXCISION, P50 SUBUNIT, APURINIC ENDONUCLEASE, LYSINE RESIDUES, REDOX REGULATION, GENE-EXPRESSION, ANISOTROPIC NETWORK MODEL, NF-KAPPA-B, WEB SERVER",
author = "Milena Bazlekowa-Karaban and Paulina Prorok and Sonia Baconnais and Sabira Taipakova and Zhiger Akishev and Dominika Zembrzuska and Popov, {Alexander V.} and Endutkin, {Anton V.} and Regina Groisman and Ishchenko, {Alexander A.} and Matkarimov, {Bakhyt T.} and Amangeldy Bissenbaev and {Le Cam}, Eric and Zharkov, {Dmitry O.} and Barbara Tudek and Murat Saparbaev",
note = "Publisher Copyright: {\textcopyright} 2019 Elsevier B.V.",
year = "2019",
month = oct,
day = "1",
doi = "10.1016/j.dnarep.2019.102698",
language = "English",
volume = "82",
pages = "102698",
journal = "DNA Repair",
issn = "1568-7864",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Mechanism of stimulation of DNA binding of the transcription factors by human apurinic/apyrimidinic endonuclease 1, APE1

AU - Bazlekowa-Karaban, Milena

AU - Prorok, Paulina

AU - Baconnais, Sonia

AU - Taipakova, Sabira

AU - Akishev, Zhiger

AU - Zembrzuska, Dominika

AU - Popov, Alexander V.

AU - Endutkin, Anton V.

AU - Groisman, Regina

AU - Ishchenko, Alexander A.

AU - Matkarimov, Bakhyt T.

AU - Bissenbaev, Amangeldy

AU - Le Cam, Eric

AU - Zharkov, Dmitry O.

AU - Tudek, Barbara

AU - Saparbaev, Murat

N1 - Publisher Copyright: © 2019 Elsevier B.V.

PY - 2019/10/1

Y1 - 2019/10/1

N2 - Aerobic respiration generates reactive oxygen species (ROS), which can damage nucleic acids, proteins and lipids. A number of transcription factors (TFs) contain redox-sensitive cysteine residues at their DNA-binding sites, hence ROS-induced thiol oxidation strongly inhibits their recognition of the cognate DNA sequences. Major human apurinic/apyrimidinic (AP) endonuclease 1 (APE1/APEX1/HAP-1), referred also as a redox factor 1 (Ref-1), stimulates the DNA binding activities of the oxidized TFs such as AP-1 and NF-κB. Also, APE1 participates in the base excision repair (BER) and nucleotide incision repair (NIR) pathways to remove oxidative DNA base damage. At present, the molecular mechanism underlying the TF-stimulating/redox function of APE1 and its biological role remains disputed. Here, we provide evidence that, instead of direct cysteine reduction in TFs by APE1, APE1-catalyzed NIR and TF-stimulating activities may be based on transient cooperative binding of APE1 to DNA and induction of conformational changes in the helix. The structure of DNA duplex strongly influences NIR and TF-stimulating activities. Homologous plant AP endonucleases lacking conserved cysteine residues stimulate DNA binding of the p50 subunit of NF-κB. APE1 acts synergistically with low-molecular-weight reducing agents on TFs. Finally, APE1 stimulates DNA binding of the redox-insensitive p50-C62S mutant protein. Electron microscopy imaging of APE1 complexes with DNA revealed preferential polymerization of APE1 on the gapped and intrinsically curved DNA duplexes. Molecular modeling offers a structural explanation how full-length APE1 can oligomerize on DNA. In conclusion, we propose that DNA-directed APE1 oligomerization can be regarded as a substitute for diffusion of APE1 along the DNA contour to probe for anisotropic flexibility. APE1 oligomers exacerbate pre-existing distortions in DNA and enable both NIR activity and DNA binding by TFs regardless of their oxidation state.

AB - Aerobic respiration generates reactive oxygen species (ROS), which can damage nucleic acids, proteins and lipids. A number of transcription factors (TFs) contain redox-sensitive cysteine residues at their DNA-binding sites, hence ROS-induced thiol oxidation strongly inhibits their recognition of the cognate DNA sequences. Major human apurinic/apyrimidinic (AP) endonuclease 1 (APE1/APEX1/HAP-1), referred also as a redox factor 1 (Ref-1), stimulates the DNA binding activities of the oxidized TFs such as AP-1 and NF-κB. Also, APE1 participates in the base excision repair (BER) and nucleotide incision repair (NIR) pathways to remove oxidative DNA base damage. At present, the molecular mechanism underlying the TF-stimulating/redox function of APE1 and its biological role remains disputed. Here, we provide evidence that, instead of direct cysteine reduction in TFs by APE1, APE1-catalyzed NIR and TF-stimulating activities may be based on transient cooperative binding of APE1 to DNA and induction of conformational changes in the helix. The structure of DNA duplex strongly influences NIR and TF-stimulating activities. Homologous plant AP endonucleases lacking conserved cysteine residues stimulate DNA binding of the p50 subunit of NF-κB. APE1 acts synergistically with low-molecular-weight reducing agents on TFs. Finally, APE1 stimulates DNA binding of the redox-insensitive p50-C62S mutant protein. Electron microscopy imaging of APE1 complexes with DNA revealed preferential polymerization of APE1 on the gapped and intrinsically curved DNA duplexes. Molecular modeling offers a structural explanation how full-length APE1 can oligomerize on DNA. In conclusion, we propose that DNA-directed APE1 oligomerization can be regarded as a substitute for diffusion of APE1 along the DNA contour to probe for anisotropic flexibility. APE1 oligomers exacerbate pre-existing distortions in DNA and enable both NIR activity and DNA binding by TFs regardless of their oxidation state.

KW - AP endonuclease

KW - Base excision repair

KW - Nucleotide incision repair

KW - Oxidative damage

KW - Redox regulation

KW - Transcription factors

KW - TERMINAL DOMAIN

KW - BASE EXCISION

KW - P50 SUBUNIT

KW - APURINIC ENDONUCLEASE

KW - LYSINE RESIDUES

KW - REDOX REGULATION

KW - GENE-EXPRESSION

KW - ANISOTROPIC NETWORK MODEL

KW - NF-KAPPA-B

KW - WEB SERVER

UR - http://www.scopus.com/inward/record.url?scp=85071902129&partnerID=8YFLogxK

U2 - 10.1016/j.dnarep.2019.102698

DO - 10.1016/j.dnarep.2019.102698

M3 - Article

C2 - 31518879

AN - SCOPUS:85071902129

VL - 82

SP - 102698

JO - DNA Repair

JF - DNA Repair

SN - 1568-7864

M1 - 102698

ER -

ID: 21467500