RecQ Helicases: Conserved Guardians of Genomic Integrity

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RecQ Helicases : Conserved Guardians of Genomic Integrity. / Larsen, Nicolai Balle; Hickson, Ian D.

In: Advances in Experimental Medicine and Biology, Vol. 767, 2013, p. 161-84.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Larsen, NB & Hickson, ID 2013, 'RecQ Helicases: Conserved Guardians of Genomic Integrity', Advances in Experimental Medicine and Biology, vol. 767, pp. 161-84. https://doi.org/10.1007/978-1-4614-5037-5_8

APA

Larsen, N. B., & Hickson, I. D. (2013). RecQ Helicases: Conserved Guardians of Genomic Integrity. Advances in Experimental Medicine and Biology, 767, 161-84. https://doi.org/10.1007/978-1-4614-5037-5_8

Vancouver

Larsen NB, Hickson ID. RecQ Helicases: Conserved Guardians of Genomic Integrity. Advances in Experimental Medicine and Biology. 2013;767:161-84. https://doi.org/10.1007/978-1-4614-5037-5_8

Author

Larsen, Nicolai Balle ; Hickson, Ian D. / RecQ Helicases : Conserved Guardians of Genomic Integrity. In: Advances in Experimental Medicine and Biology. 2013 ; Vol. 767. pp. 161-84.

Bibtex

@article{fe469606394c4ec8b9ce3f7f05372fe9,
title = "RecQ Helicases: Conserved Guardians of Genomic Integrity",
abstract = "The RecQ family of DNA helicases is highly conserved throughout -evolution, and is important for the maintenance of genome stability. In humans, five RecQ family members have been identified: BLM, WRN, RECQ4, RECQ1 and RECQ5. Defects in three of these give rise to Bloom's syndrome (BLM), Werner's syndrome (WRN) and Rothmund-Thomson/RAPADILINO/Baller-Gerold (RECQ4) syndromes. These syndromes are characterised by cancer predisposition and/or premature ageing. In this review, we focus on the roles of BLM and its S. cerevisiae homologue, Sgs1, in genome maintenance. BLM/Sgs1 has been shown to play a critical role in homologous recombination at multiple steps, including end-resection, displacement loop formation, branch migration and double Holliday junction dissolution. In addition, recent evidence has revealed a role for BLM/Sgs1 in the stabilisation and repair of replication forks damaged during a perturbed S-phase. Finally BLM also plays a role in the suppression and/or resolution of ultra-fine anaphase DNA bridges that form between sister-chromatids during mitosis.",
author = "Larsen, {Nicolai Balle} and Hickson, {Ian D}",
year = "2013",
doi = "10.1007/978-1-4614-5037-5_8",
language = "English",
volume = "767",
pages = "161--84",
journal = "Advances in Experimental Medicine and Biology",
issn = "0065-2598",
publisher = "Springer",

}

RIS

TY - JOUR

T1 - RecQ Helicases

T2 - Conserved Guardians of Genomic Integrity

AU - Larsen, Nicolai Balle

AU - Hickson, Ian D

PY - 2013

Y1 - 2013

N2 - The RecQ family of DNA helicases is highly conserved throughout -evolution, and is important for the maintenance of genome stability. In humans, five RecQ family members have been identified: BLM, WRN, RECQ4, RECQ1 and RECQ5. Defects in three of these give rise to Bloom's syndrome (BLM), Werner's syndrome (WRN) and Rothmund-Thomson/RAPADILINO/Baller-Gerold (RECQ4) syndromes. These syndromes are characterised by cancer predisposition and/or premature ageing. In this review, we focus on the roles of BLM and its S. cerevisiae homologue, Sgs1, in genome maintenance. BLM/Sgs1 has been shown to play a critical role in homologous recombination at multiple steps, including end-resection, displacement loop formation, branch migration and double Holliday junction dissolution. In addition, recent evidence has revealed a role for BLM/Sgs1 in the stabilisation and repair of replication forks damaged during a perturbed S-phase. Finally BLM also plays a role in the suppression and/or resolution of ultra-fine anaphase DNA bridges that form between sister-chromatids during mitosis.

AB - The RecQ family of DNA helicases is highly conserved throughout -evolution, and is important for the maintenance of genome stability. In humans, five RecQ family members have been identified: BLM, WRN, RECQ4, RECQ1 and RECQ5. Defects in three of these give rise to Bloom's syndrome (BLM), Werner's syndrome (WRN) and Rothmund-Thomson/RAPADILINO/Baller-Gerold (RECQ4) syndromes. These syndromes are characterised by cancer predisposition and/or premature ageing. In this review, we focus on the roles of BLM and its S. cerevisiae homologue, Sgs1, in genome maintenance. BLM/Sgs1 has been shown to play a critical role in homologous recombination at multiple steps, including end-resection, displacement loop formation, branch migration and double Holliday junction dissolution. In addition, recent evidence has revealed a role for BLM/Sgs1 in the stabilisation and repair of replication forks damaged during a perturbed S-phase. Finally BLM also plays a role in the suppression and/or resolution of ultra-fine anaphase DNA bridges that form between sister-chromatids during mitosis.

U2 - 10.1007/978-1-4614-5037-5_8

DO - 10.1007/978-1-4614-5037-5_8

M3 - Journal article

C2 - 23161011

VL - 767

SP - 161

EP - 184

JO - Advances in Experimental Medicine and Biology

JF - Advances in Experimental Medicine and Biology

SN - 0065-2598

ER -

ID: 44689419