Adenomatous polyposis coli interacts with flap endonuclease 1 to block its nuclear entry and function

Aruna S. Jaiswal; Melissa L. Armas; Tadahide Izumi; Phyllis R. Strauss; Satya Narayan

doi:10.1593/neo.12680

Adenomatous polyposis coli interacts with flap endonuclease 1 to block its nuclear entry and function

Aruna S. Jaiswal
, Melissa L. Armas
, Tadahide Izumi
, Phyllis R. Strauss
, Satya Narayan

Toxicology and Cancer Biology

Producción científica: Article › revisión exhaustiva

10 Citas (Scopus)

Resumen

In previous studies, we found that adenomatous polyposis coli (APC) blocks the base excision repair (BER) pathway by interacting with 5′-flap endonuclease 1 (Fen1). In this study, we identify the molecular features that contribute to the formation and/or stabilization of the APC/Fen1 complex that determines the extent of BER inhibition, and the subsequent accumulation of DNA damage creates mutagenic lesions leading to transformation susceptibility. We show here that APC binds to the nuclear localization sequence of Fen1 (Lys³⁶⁵Lys³⁶⁶Lys³⁶⁷), which prevents entry of Fen1 into the nucleus and participation in Pol-β-directed long-patch BER. We also show that levels of the APC/Fen1 complex are higher in breast tumors than in the surrounding normal tissues. These studies demonstrate a novel role for APC in the suppression of Fen1 activity in the BER pathway and a new biomarker profile to be explored to identify individuals who may be susceptible to the development of mammary and other tumors.

Idioma original	English
Páginas (desde-hasta)	495-508
Número de páginas	14
Publicación	Neoplasia (United States)
Volumen	14
N.º	6
DOI	https://doi.org/10.1593/neo.12680
Estado	Published - jun 2012

Nota bibliográfica

Funding Information:
Abbreviations: APC, adenomatous polyposis coli; DRI domain, DNA repair inhibitory domain; Fen1, flap endonuclease 1; LP-BER, long-patch base excision repair; NLS, nuclear localization signal; Pol-β, DNA polymerase β Address all correspondence to: Satya Narayan, PhD, Department of Anatomy and Cell Biology, Basic Science Bldg, Room B1-016, PO Box 100235, University of Florida, Gainesville, FL 32610. E-mail: [email protected] 1Financial support for these studies was provided by grants from the National Institutes of Health (R01-CA097031 and R01-CA100247 to S.N. and RO1-CA98664 to T.I.) and Flight Attendant Medical Research Institute, Miami, FL (CIA-072088) to S.N. The authors declare no potential conflicts of interest with respect to the authorship and/or publication of this article. 2These authors equally contributed to this study. Received 12 April 2012; Revised 4 May 2012; Accepted 7 May 2012 Copyright © 2012 Neoplasia Press, Inc. All rights reserved 1522-8002/12/$25.00 DOI 10.1593/neo.12680

Financiación

Abbreviations: APC, adenomatous polyposis coli; DRI domain, DNA repair inhibitory domain; Fen1, flap endonuclease 1; LP-BER, long-patch base excision repair; NLS, nuclear localization signal; Pol-β, DNA polymerase β Address all correspondence to: Satya Narayan, PhD, Department of Anatomy and Cell Biology, Basic Science Bldg, Room B1-016, PO Box 100235, University of Florida, Gainesville, FL 32610. E-mail: [email protected] 1Financial support for these studies was provided by grants from the National Institutes of Health (R01-CA097031 and R01-CA100247 to S.N. and RO1-CA98664 to T.I.) and Flight Attendant Medical Research Institute, Miami, FL (CIA-072088) to S.N. The authors declare no potential conflicts of interest with respect to the authorship and/or publication of this article. 2These authors equally contributed to this study. Received 12 April 2012; Revised 4 May 2012; Accepted 7 May 2012 Copyright © 2012 Neoplasia Press, Inc. All rights reserved 1522-8002/12/$25.00 DOI 10.1593/neo.12680

Financiadores	Número del financiador
National Institutes of Health (NIH)	R01-CA100247, RO1-CA98664, CIA-072088
National Institutes of Health (NIH)
National Childhood Cancer Registry – National Cancer Institute	R01CA097031
National Childhood Cancer Registry – National Cancer Institute

ODS de las Naciones Unidas

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Good health and well being

ASJC Scopus subject areas

Cancer Research

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abstract = "In previous studies, we found that adenomatous polyposis coli (APC) blocks the base excision repair (BER) pathway by interacting with 5′-flap endonuclease 1 (Fen1). In this study, we identify the molecular features that contribute to the formation and/or stabilization of the APC/Fen1 complex that determines the extent of BER inhibition, and the subsequent accumulation of DNA damage creates mutagenic lesions leading to transformation susceptibility. We show here that APC binds to the nuclear localization sequence of Fen1 (Lys365Lys366Lys367), which prevents entry of Fen1 into the nucleus and participation in Pol-β-directed long-patch BER. We also show that levels of the APC/Fen1 complex are higher in breast tumors than in the surrounding normal tissues. These studies demonstrate a novel role for APC in the suppression of Fen1 activity in the BER pathway and a new biomarker profile to be explored to identify individuals who may be susceptible to the development of mammary and other tumors.",

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AU - Izumi, Tadahide

AU - Strauss, Phyllis R.

AU - Narayan, Satya

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N2 - In previous studies, we found that adenomatous polyposis coli (APC) blocks the base excision repair (BER) pathway by interacting with 5′-flap endonuclease 1 (Fen1). In this study, we identify the molecular features that contribute to the formation and/or stabilization of the APC/Fen1 complex that determines the extent of BER inhibition, and the subsequent accumulation of DNA damage creates mutagenic lesions leading to transformation susceptibility. We show here that APC binds to the nuclear localization sequence of Fen1 (Lys365Lys366Lys367), which prevents entry of Fen1 into the nucleus and participation in Pol-β-directed long-patch BER. We also show that levels of the APC/Fen1 complex are higher in breast tumors than in the surrounding normal tissues. These studies demonstrate a novel role for APC in the suppression of Fen1 activity in the BER pathway and a new biomarker profile to be explored to identify individuals who may be susceptible to the development of mammary and other tumors.

AB - In previous studies, we found that adenomatous polyposis coli (APC) blocks the base excision repair (BER) pathway by interacting with 5′-flap endonuclease 1 (Fen1). In this study, we identify the molecular features that contribute to the formation and/or stabilization of the APC/Fen1 complex that determines the extent of BER inhibition, and the subsequent accumulation of DNA damage creates mutagenic lesions leading to transformation susceptibility. We show here that APC binds to the nuclear localization sequence of Fen1 (Lys365Lys366Lys367), which prevents entry of Fen1 into the nucleus and participation in Pol-β-directed long-patch BER. We also show that levels of the APC/Fen1 complex are higher in breast tumors than in the surrounding normal tissues. These studies demonstrate a novel role for APC in the suppression of Fen1 activity in the BER pathway and a new biomarker profile to be explored to identify individuals who may be susceptible to the development of mammary and other tumors.

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ER -

Adenomatous polyposis coli interacts with flap endonuclease 1 to block its nuclear entry and function

Resumen

Nota bibliográfica

Financiación

ODS de las Naciones Unidas

ASJC Scopus subject areas

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