Abstract

The human FANCM ATPase/translocase is involved in various cellular pathways including DNA damage repair, replication fork remodeling and R-loop resolution. Recently, reports from three independent laboratories have disclosed a previously unappreciated role for FANCM in telomerase-negative human cancer cells that maintain their telomeres through the Alternative Lengthening of Telomeres (ALT) pathway. In ALT cells, FANCM limits telomeric replication stress and damage, and, in turn, ALT activity by suppressing accumulation of telomeric R-loops and by regulating the action of the BLM helicase. As a consequence, FANCM inactivation leads to exaggerated ALT activity and ultimately cell death. The studies reviewed here not only unveil a novel function for human FANCM, but also point to this enzyme as a promising target for anti-ALT cancer therapy.

Highlights

  • The human FANCM ATPase/translocase is involved in various cellular pathways including DNA damage repair, replication fork remodeling and R-loop resolution

  • Fanconi anemia (FA) is a hereditary disorder characterized by bone marrow failure, hypersensitivity to agents inducing DNA interstrand crosslinks (ICLs), chromosomal abnormalities and, later in life, cancer

  • When a replication fork encounters an ICL, the FANCM-Fanconi Anemia core complex-Associated Protein 24 (FAAP24)-MHF1-MHF2 complex enhances the recruitment of the FA complex through interaction between FANCM MM1 and FANCF (Deans and West, 2009)

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Summary

ALTernative Functions for Human FANCM at Telomeres

Instituto de Medicina Molecular João Lobo Antunes (iMM), Faculdade de Medicina da Universidade de Lisboa, Lisbon, Portugal. The human FANCM ATPase/translocase is involved in various cellular pathways including DNA damage repair, replication fork remodeling and R-loop resolution. Reports from three independent laboratories have disclosed a previously unappreciated role for FANCM in telomerase-negative human cancer cells that maintain their telomeres through the Alternative Lengthening of Telomeres (ALT) pathway. Human FANConi anemia, complementation group M (FANCM) is a highly conserved protein with ATPase and DNA translocase activity, belonging to the Fanconi anemia (FA) core complex (Meetei et al, 2005). When a replication fork encounters an ICL, the FANCM-FAAP24-MHF1-MHF2 complex enhances the recruitment of the FA complex through interaction between FANCM MM1 and FANCF (Deans and West, 2009)

FANCM in Alternative Lengthening of Telomeres
ALTERNATIVE LENGTHENING OF TELOMERES
FANCM AND ALT
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