Proteomics,Multiomics

Dataset Information

0

53BP1 cooperation with the REV7–shieldin complex underpins DNA structure-specific NHEJ


ABSTRACT: 53BP1 governs a specialized, context-specific branch of the classical non-homologous end joining DNA double-strand break repair pathway. Mice lacking 53bp1 (also known as Trp53bp1) are immunodeficient owing to a complete loss of immunoglobulin class-switch recombination, and reduced fidelity of long-range V(D)J recombination. The 53BP1-dependent pathway is also responsible for pathological joining events at dysfunctional telomeres, and its unrestricted activity in Brca1-deficient cellular and tumour models causes genomic instability and oncogenesis. Cells that lack core non-homologous end joining proteins are profoundly radiosensitive, unlike 53BP1-deficient cells, which suggests that 53BP1 and its co-factors act on specific DNA substrates. Here we show that 53BP1 cooperates with its downstream effector protein REV7 to promote non-homologous end joining during class-switch recombination, but REV7 is not required for 53BP1-dependent V(D)J recombination. We identify shieldin—a four-subunit putative single-stranded DNA-binding complex comprising REV7, c20orf196 (SHLD1), FAM35A (SHLD2) and FLJ26957 (SHLD3)— as the factor that explains this specificity. Shieldin is essential for REV7-dependent DNA end-protection and non-homologous end joining during class-switch recombination, and supports toxic non-homologous end joining in Brca1-deficient cells, yet is dispensable for REV7-dependent interstrand cross-link repair. The 53BP1 pathway therefore comprises distinct double-strand break repair activities within chromatin and single-stranded DNA compartments, which explains both the immunological differences between 53bp1- and Rev7- deficient mice and the context specificity of the pathway.

INSTRUMENT(S): Orbitrap Fusion Lumos

ORGANISM(S): Mus Musculus (mouse)

TISSUE(S): Lymphocyte Of B Lineage, Blood

DISEASE(S): Female Breast Cancer

SUBMITTER: Roman Fischer  

LAB HEAD: Roman Fischer

PROVIDER: PXD009650 | Pride | 2018-07-26

REPOSITORIES: Pride

altmetric image

Publications


53BP1 governs a specialized, context-specific branch of the classical non-homologous end joining DNA double-strand break repair pathway. Mice lacking 53bp1 (also known as Trp53bp1) are immunodeficient owing to a complete loss of immunoglobulin class-switch recombination<sup>1,2</sup>, and reduced fidelity of long-range V(D)J recombination<sup>3</sup>. The 53BP1-dependent pathway is also responsible for pathological joining events at dysfunctional telomeres<sup>4</sup>, and its unrestricted activ  ...[more]

Similar Datasets

2022-05-11 | GSE202567 | GEO
2022-02-04 | PXD031311 | Pride
2012-09-30 | E-GEOD-35698 | biostudies-arrayexpress
2019-10-22 | GSE133806 | GEO
2019-10-22 | GSE133805 | GEO
2018-05-31 | PXD009830 | Pride
2022-06-09 | PXD027727 | Pride
2018-01-08 | GSE106922 | GEO
2021-09-21 | PXD026912 | Pride
2012-09-30 | GSE35698 | GEO