Mutations of the SLX4 gene in Fanconi anemia

Yonghwan Kim, Francis P. Lach, Rohini Desetty, Helmut Hanenberg, Arleen D. Auerbach, Agata Smogorzewska

Research output: Contribution to journalArticle

233 Citations (Scopus)

Abstract

Fanconi anemia is a rare recessive disorder characterized by genome instability, congenital malformations, progressive bone marrow failure and predisposition to hematologic malignancies and solid tumors. At the cellular level, hypersensitivity to DNA interstrand crosslinks is the defining feature in Fanconi anemia. Mutations in thirteen distinct Fanconi anemia genes have been shown to interfere with the DNA-replicationg-dependent repair of lesions involving crosslinked DNA at stalled replication forks. Depletion of SLX4, which interacts with multiple nucleases and has been recently identified as a Holliday junction resolvase, results in increased sensitivity of the cells to DNA crosslinking agents. Here we report the identification of biallelic SLX4 mutations in two individuals with typical clinical features of Fanconi anemia and show that the cellular defects in these individuals' cells are complemented by wildtype SLX4, demonstrating that biallelic mutations in SLX4 (renamed here as FANCP) cause a new subtype of Fanconi anemia, Fanconi anemia-P.

Original languageEnglish
Pages (from-to)142-146
Number of pages5
JournalNature Genetics
Volume43
Issue number2
DOIs
StatePublished - Feb 2011

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Fanconi Anemia
Mutation
Genes
DNA
Holliday Junction Resolvases
Genomic Instability
Hematologic Neoplasms
Hypersensitivity
Bone Marrow
Neoplasms

ASJC Scopus subject areas

  • Genetics

Cite this

Kim, Y., Lach, F. P., Desetty, R., Hanenberg, H., Auerbach, A. D., & Smogorzewska, A. (2011). Mutations of the SLX4 gene in Fanconi anemia. Nature Genetics, 43(2), 142-146. https://doi.org/10.1038/ng.750

Mutations of the SLX4 gene in Fanconi anemia. / Kim, Yonghwan; Lach, Francis P.; Desetty, Rohini; Hanenberg, Helmut; Auerbach, Arleen D.; Smogorzewska, Agata.

In: Nature Genetics, Vol. 43, No. 2, 02.2011, p. 142-146.

Research output: Contribution to journalArticle

Kim, Y, Lach, FP, Desetty, R, Hanenberg, H, Auerbach, AD & Smogorzewska, A 2011, 'Mutations of the SLX4 gene in Fanconi anemia', Nature Genetics, vol. 43, no. 2, pp. 142-146. https://doi.org/10.1038/ng.750
Kim Y, Lach FP, Desetty R, Hanenberg H, Auerbach AD, Smogorzewska A. Mutations of the SLX4 gene in Fanconi anemia. Nature Genetics. 2011 Feb;43(2):142-146. https://doi.org/10.1038/ng.750
Kim, Yonghwan ; Lach, Francis P. ; Desetty, Rohini ; Hanenberg, Helmut ; Auerbach, Arleen D. ; Smogorzewska, Agata. / Mutations of the SLX4 gene in Fanconi anemia. In: Nature Genetics. 2011 ; Vol. 43, No. 2. pp. 142-146.
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