Arsenic-induced promoter hypomethylation and over-expression of ERCC2 reduces DNA repair capacity in humans by non-disjunction of the ERCC2-Cdk7 complex

Somnath Paul, Nilanjana Banerjee, Aditi Chatterjee, Tanmoy J. Sau, Jayanta K. Das, Prafulla K. Mishra, Partha Chakrabarti, Arun Bandyopadhyay, Ashok K. Giri

Research output: Contribution to journalArticle

Abstract

Arsenic in drinking water is of critical concern in West Bengal, India, as it results in several physiological symptoms including dermatological lesions and cancers. Impairment of the DNA repair mechanism has been associated with arsenic-induced genetic damage as well as with several cancers. ERCC2 (Excision Repair Cross-Complementing rodent repair, complementation group 2), mediates DNA-repair by interacting with Cdk-activating kinase (CAK) complex, which helps in DNA proof-reading during transcription. Arsenic metabolism alters epigenetic regulation; we tried to elucidate the regulation of ERCC2 in arsenic-exposed humans. Water, urine, nails, hair and blood samples from one hundred and fifty seven exposed and eighty eight unexposed individuals were collected. Dose dependent validation was done in vitro using HepG2 and HEK-293. Arsenic content in the biological samples was higher in the exposed individuals compared with the content in unexposed individuals (p <0.001). Bisulfite-modified methylation specific PCR showed a significant (p <0.0001) hypomethylation of the ERCC2 promoter in the arsenic-exposed individuals. Densitometric analysis of immunoblots showed a nearly two-fold increase in expression of ERCC2 in exposed individuals, but there was an enhanced genotoxic insult as measured by micronuclei frequency. Immuno-precipitation and western blotting revealed an increased (p <0.001) association of Cdk7 with ERCC2 in highly arsenic exposed individuals. The decrease in CAK activity was determined by observing the intensity of Ser392 phosphorylation in p53, in vitro, which decreased with an increase in arsenic dose. Thus we infer that arsenic biotransformation leads to promoter hypomethylation of ERCC2, which in turn inhibits the normal functioning of the CAK-complex, thus affecting DNA-repair; this effect was highest among the arsenic exposed individuals with dermatological lesions.

Original languageEnglish (US)
Pages (from-to)864-873
Number of pages10
JournalMetallomics
Volume6
Issue number4
DOIs
StatePublished - 2014
Externally publishedYes

Fingerprint

Arsenic
DNA Repair
DNA
Repair
Nails
Phosphorylation
Methylation
Transcription
Biotransformation
Metabolism
Epigenomics
Potable water
Drinking Water
Hair
Reading
India
Rodentia
Neoplasms
Blood
Western Blotting

ASJC Scopus subject areas

  • Biomaterials
  • Metals and Alloys
  • Chemistry (miscellaneous)
  • Biochemistry
  • Biophysics

Cite this

Arsenic-induced promoter hypomethylation and over-expression of ERCC2 reduces DNA repair capacity in humans by non-disjunction of the ERCC2-Cdk7 complex. / Paul, Somnath; Banerjee, Nilanjana; Chatterjee, Aditi; Sau, Tanmoy J.; Das, Jayanta K.; Mishra, Prafulla K.; Chakrabarti, Partha; Bandyopadhyay, Arun; Giri, Ashok K.

In: Metallomics, Vol. 6, No. 4, 2014, p. 864-873.

Research output: Contribution to journalArticle

Paul, S, Banerjee, N, Chatterjee, A, Sau, TJ, Das, JK, Mishra, PK, Chakrabarti, P, Bandyopadhyay, A & Giri, AK 2014, 'Arsenic-induced promoter hypomethylation and over-expression of ERCC2 reduces DNA repair capacity in humans by non-disjunction of the ERCC2-Cdk7 complex', Metallomics, vol. 6, no. 4, pp. 864-873. https://doi.org/10.1039/c3mt00328k
Paul, Somnath ; Banerjee, Nilanjana ; Chatterjee, Aditi ; Sau, Tanmoy J. ; Das, Jayanta K. ; Mishra, Prafulla K. ; Chakrabarti, Partha ; Bandyopadhyay, Arun ; Giri, Ashok K. / Arsenic-induced promoter hypomethylation and over-expression of ERCC2 reduces DNA repair capacity in humans by non-disjunction of the ERCC2-Cdk7 complex. In: Metallomics. 2014 ; Vol. 6, No. 4. pp. 864-873.
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abstract = "Arsenic in drinking water is of critical concern in West Bengal, India, as it results in several physiological symptoms including dermatological lesions and cancers. Impairment of the DNA repair mechanism has been associated with arsenic-induced genetic damage as well as with several cancers. ERCC2 (Excision Repair Cross-Complementing rodent repair, complementation group 2), mediates DNA-repair by interacting with Cdk-activating kinase (CAK) complex, which helps in DNA proof-reading during transcription. Arsenic metabolism alters epigenetic regulation; we tried to elucidate the regulation of ERCC2 in arsenic-exposed humans. Water, urine, nails, hair and blood samples from one hundred and fifty seven exposed and eighty eight unexposed individuals were collected. Dose dependent validation was done in vitro using HepG2 and HEK-293. Arsenic content in the biological samples was higher in the exposed individuals compared with the content in unexposed individuals (p <0.001). Bisulfite-modified methylation specific PCR showed a significant (p <0.0001) hypomethylation of the ERCC2 promoter in the arsenic-exposed individuals. Densitometric analysis of immunoblots showed a nearly two-fold increase in expression of ERCC2 in exposed individuals, but there was an enhanced genotoxic insult as measured by micronuclei frequency. Immuno-precipitation and western blotting revealed an increased (p <0.001) association of Cdk7 with ERCC2 in highly arsenic exposed individuals. The decrease in CAK activity was determined by observing the intensity of Ser392 phosphorylation in p53, in vitro, which decreased with an increase in arsenic dose. Thus we infer that arsenic biotransformation leads to promoter hypomethylation of ERCC2, which in turn inhibits the normal functioning of the CAK-complex, thus affecting DNA-repair; this effect was highest among the arsenic exposed individuals with dermatological lesions.",
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AU - Das, Jayanta K.

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