Abstract

BRCA2 is an essential genome stability gene that has various functions in cells, including roles in homologous recombination, G2 checkpoint control, protection of stalled replication forks, and promotion of cellular resistance to numerous types of DNA damage. Heterozygous mutation of BRCA2 is associated with an increased risk of developing cancers of the breast, ovaries, pancreas, and other sites, thus BRCA2 acts as a classic tumor suppressor gene. However, understanding BRCA2 function as a tumor suppressor is severely limited by the fact that ~70% of the encoded protein has not been tested or assigned a function in the cellular DNA damage response. Remarkably, even the specific role(s) of many known domains in BRCA2 are not well characterized, predominantly because stable expression of the very large BRCA2 protein in cells, for experimental purposes, is challenging. Here, we review what is known about these domains and the assay systems that are available to study the cellular roles of BRCA2 domains in DNA damage responses. We also list criteria for better testing systems because, ultimately, functional assays for assessing the impact of germline and acquired mutations identified in genetic screens are important for guiding cancer prevention measures and for tailored cancer treatments.

Highlights

  • BRCA2 is an essential genome stability gene on chromosome 13 that has a key role in DNA repair mediated by homologous recombination (HR), both in response to DNA double-strand breaks (DSBs) and DNA interstrand crosslinks (ICLs) [1,2,3,4]

  • Despite its well-established identity as a tumor suppressor, much remains to be understood about BRCA2

  • Defining the roles of domains throughout BRCA2 will help in harnessing the abundant potential of genetic screens to guide the selection of cancer prevention measures and therapeutic options in individuals that harbor sequence variants/mutations in BRCA2

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Summary

Introduction

BRCA2 is an essential genome stability gene on chromosome 13 that has a key role in DNA repair mediated by homologous recombination (HR), both in response to DNA double-strand breaks (DSBs) and DNA interstrand crosslinks (ICLs) [1,2,3,4]. As part of its role in mediating HR and maintaining genome stability, the BRCA2 protein regulates the assembly of the RAD51 recombinase into a nucleoprotein filament with single-stranded DNA (ssDNA) following resection of DSBs [1,4]. In this manner, BRCA2 promotes strand invasion and the search for homologous DNA. What is known about the specific roles of different domains of BRCA2 in DNA damage responses, while limited, is examined (Section 4). We finish by considering how to better test the function(s) of different domains and how BRCA2 function is affected by patient-derived mutations (Section 5)

Known Domains within BRCA2
Systems Based upon Ectopic Expression of Mutants of Full-Length BRCA2
The Function of Different Domains of BRCA2 in DNA Damage Responses
Domain-by-Domain Look at Roles of BRCA2 in DNA Damage Responses
Checkpoint
Findings
Functional Relationships between Domains of BRCA2
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