Functional analysis of genetic variants in the high-risk breast cancer susceptibility gene PALB2
Heterozygous carriers of germ-line loss-of-function variants in the DNA repair gene PALB2 are at a highly increased lifetime risk for developing breast cancer. While truncating variants in PALB2 are known to increase cancer risk, the interpretation of missense variants of uncertain significance (VUS...
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Veröffentlicht in: | Nature communications 2019-11, Vol.10 (1), p.5296-15, Article 5296 |
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Sprache: | eng |
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Zusammenfassung: | Heterozygous carriers of germ-line loss-of-function variants in the DNA repair gene
PALB2
are at a highly increased lifetime risk for developing breast cancer. While truncating variants in
PALB2
are known to increase cancer risk, the interpretation of missense variants of uncertain significance (VUS) is in its infancy. Here we describe the development of a relatively fast and easy cDNA-based system for the semi high-throughput functional analysis of 48 VUS in human
PALB2
. By assessing the ability of
PALB2
VUS to rescue the DNA repair and checkpoint defects in
Palb2
knockout mouse embryonic stem (mES) cells, we identify various VUS in
PALB2
that impair its function. Three VUS in the coiled-coil domain of PALB2 abrogate the interaction with BRCA1, whereas several VUS in the WD40 domain dramatically reduce protein stability. Thus, our functional assays identify damaging VUS in
PALB2
that may increase cancer risk.
PALB2 is an established breast cancer risk gene but the pathogenicity of many variants remains uncharacterised. Here, the authors present a cDNA-based system for the functional analysis of PALB2 variants of unknown significance. |
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ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-019-13194-2 |