Identification of a topoisomerase I mutant, scsA1, as an extragenic suppressor of a mutation in scaANBS1, the apparent homolog of human nibrin in Aspergillus nidulans

Marcia R.Z.Kress Fagundes, Larissa Fernandes, Marcela Savoldi, Steven D. Harris, Maria H.S. Goldman, Gustavo H. Goldman

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

The Mre11-Rad50-Nbs1 protein complex has emerged as a central player in the human cellular DNA damage response, and recent observations suggest that these proteins are at least partially responsible for the linking of DNA damage detection to DNA repair and cell cycle checkpoint functions. Mutations in scaABS1, which encodes the apparent homolog of human nibrin in Aspergillus nidulans, inhibit growth in the presence of the antitopoisomerase I drug camptothecin. This article describes the selection and characterization of extragenic suppressors of the scaA1 mutation, with the aim of identifying other proteins that interfere with the pathway or complex in which the ScaA would normally be involved. Fifteen extragenic suppressors of the scaA1 mutation were isolated. The topoisomerase I gene can complement one of these suppressors. Synergistic interaction between the scaNBS1 and scsATOP1 genes in the presence of DNA-damaging agents was observed. Overexpression of topoisomerase I in the scaA1 mutant causes increased sensitivity to DNA-damaging agents. The scsATOP1 and the scaANBS1 gene products could functionally interact in pathways that either monitor or repair DNA double-strand breaks.

Original languageEnglish (US)
Pages (from-to)935-945
Number of pages11
JournalGenetics
Volume164
Issue number3
StatePublished - Jul 1 2003

Fingerprint

Genetic Suppression
Aspergillus nidulans
Type I DNA Topoisomerase
DNA Damage
Genes
Camptothecin
Proteins
Double-Stranded DNA Breaks
DNA
Cell Cycle Checkpoints
DNA Repair
Mutation
Growth
Pharmaceutical Preparations

ASJC Scopus subject areas

  • Genetics

Cite this

Fagundes, M. R. Z. K., Fernandes, L., Savoldi, M., Harris, S. D., Goldman, M. H. S., & Goldman, G. H. (2003). Identification of a topoisomerase I mutant, scsA1, as an extragenic suppressor of a mutation in scaANBS1, the apparent homolog of human nibrin in Aspergillus nidulans. Genetics, 164(3), 935-945.

Identification of a topoisomerase I mutant, scsA1, as an extragenic suppressor of a mutation in scaANBS1, the apparent homolog of human nibrin in Aspergillus nidulans. / Fagundes, Marcia R.Z.Kress; Fernandes, Larissa; Savoldi, Marcela; Harris, Steven D.; Goldman, Maria H.S.; Goldman, Gustavo H.

In: Genetics, Vol. 164, No. 3, 01.07.2003, p. 935-945.

Research output: Contribution to journalArticle

Fagundes, MRZK, Fernandes, L, Savoldi, M, Harris, SD, Goldman, MHS & Goldman, GH 2003, 'Identification of a topoisomerase I mutant, scsA1, as an extragenic suppressor of a mutation in scaANBS1, the apparent homolog of human nibrin in Aspergillus nidulans', Genetics, vol. 164, no. 3, pp. 935-945.
Fagundes, Marcia R.Z.Kress ; Fernandes, Larissa ; Savoldi, Marcela ; Harris, Steven D. ; Goldman, Maria H.S. ; Goldman, Gustavo H. / Identification of a topoisomerase I mutant, scsA1, as an extragenic suppressor of a mutation in scaANBS1, the apparent homolog of human nibrin in Aspergillus nidulans. In: Genetics. 2003 ; Vol. 164, No. 3. pp. 935-945.
@article{a0f20ee2905a46138da08cd9bbc52cda,
title = "Identification of a topoisomerase I mutant, scsA1, as an extragenic suppressor of a mutation in scaANBS1, the apparent homolog of human nibrin in Aspergillus nidulans",
abstract = "The Mre11-Rad50-Nbs1 protein complex has emerged as a central player in the human cellular DNA damage response, and recent observations suggest that these proteins are at least partially responsible for the linking of DNA damage detection to DNA repair and cell cycle checkpoint functions. Mutations in scaABS1, which encodes the apparent homolog of human nibrin in Aspergillus nidulans, inhibit growth in the presence of the antitopoisomerase I drug camptothecin. This article describes the selection and characterization of extragenic suppressors of the scaA1 mutation, with the aim of identifying other proteins that interfere with the pathway or complex in which the ScaA would normally be involved. Fifteen extragenic suppressors of the scaA1 mutation were isolated. The topoisomerase I gene can complement one of these suppressors. Synergistic interaction between the scaNBS1 and scsATOP1 genes in the presence of DNA-damaging agents was observed. Overexpression of topoisomerase I in the scaA1 mutant causes increased sensitivity to DNA-damaging agents. The scsATOP1 and the scaANBS1 gene products could functionally interact in pathways that either monitor or repair DNA double-strand breaks.",
author = "Fagundes, {Marcia R.Z.Kress} and Larissa Fernandes and Marcela Savoldi and Harris, {Steven D.} and Goldman, {Maria H.S.} and Goldman, {Gustavo H.}",
year = "2003",
month = "7",
day = "1",
language = "English (US)",
volume = "164",
pages = "935--945",
journal = "Genetics",
issn = "0016-6731",
publisher = "Genetics Society of America",
number = "3",

}

TY - JOUR

T1 - Identification of a topoisomerase I mutant, scsA1, as an extragenic suppressor of a mutation in scaANBS1, the apparent homolog of human nibrin in Aspergillus nidulans

AU - Fagundes, Marcia R.Z.Kress

AU - Fernandes, Larissa

AU - Savoldi, Marcela

AU - Harris, Steven D.

AU - Goldman, Maria H.S.

AU - Goldman, Gustavo H.

PY - 2003/7/1

Y1 - 2003/7/1

N2 - The Mre11-Rad50-Nbs1 protein complex has emerged as a central player in the human cellular DNA damage response, and recent observations suggest that these proteins are at least partially responsible for the linking of DNA damage detection to DNA repair and cell cycle checkpoint functions. Mutations in scaABS1, which encodes the apparent homolog of human nibrin in Aspergillus nidulans, inhibit growth in the presence of the antitopoisomerase I drug camptothecin. This article describes the selection and characterization of extragenic suppressors of the scaA1 mutation, with the aim of identifying other proteins that interfere with the pathway or complex in which the ScaA would normally be involved. Fifteen extragenic suppressors of the scaA1 mutation were isolated. The topoisomerase I gene can complement one of these suppressors. Synergistic interaction between the scaNBS1 and scsATOP1 genes in the presence of DNA-damaging agents was observed. Overexpression of topoisomerase I in the scaA1 mutant causes increased sensitivity to DNA-damaging agents. The scsATOP1 and the scaANBS1 gene products could functionally interact in pathways that either monitor or repair DNA double-strand breaks.

AB - The Mre11-Rad50-Nbs1 protein complex has emerged as a central player in the human cellular DNA damage response, and recent observations suggest that these proteins are at least partially responsible for the linking of DNA damage detection to DNA repair and cell cycle checkpoint functions. Mutations in scaABS1, which encodes the apparent homolog of human nibrin in Aspergillus nidulans, inhibit growth in the presence of the antitopoisomerase I drug camptothecin. This article describes the selection and characterization of extragenic suppressors of the scaA1 mutation, with the aim of identifying other proteins that interfere with the pathway or complex in which the ScaA would normally be involved. Fifteen extragenic suppressors of the scaA1 mutation were isolated. The topoisomerase I gene can complement one of these suppressors. Synergistic interaction between the scaNBS1 and scsATOP1 genes in the presence of DNA-damaging agents was observed. Overexpression of topoisomerase I in the scaA1 mutant causes increased sensitivity to DNA-damaging agents. The scsATOP1 and the scaANBS1 gene products could functionally interact in pathways that either monitor or repair DNA double-strand breaks.

UR - http://www.scopus.com/inward/record.url?scp=0042709609&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0042709609&partnerID=8YFLogxK

M3 - Article

C2 - 12871905

AN - SCOPUS:0042709609

VL - 164

SP - 935

EP - 945

JO - Genetics

JF - Genetics

SN - 0016-6731

IS - 3

ER -