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HSF2BP Interacts with a Conserved Domain of BRCA2 and Is Required for Mouse Spermatogenesis

Authors :
Brandsma, Inger
Sato, Koichi
van Rossum-Fikkert, Sari E
van Vliet, Nicole
Sleddens, Esther
Reuter, Marcel
Odijk, Hanny
van den Tempel, Nathalie
Dekkers, Dick H W
Bezstarosti, Karel
Demmers, Jeroen A A
Maas, Alex
Lebbink, Joyce
Wyman, Claire
Essers, Jeroen
van Gent, Dik C
Baarends, Willy M
Knipscheer, Puck
Kanaar, Roland
Zelensky, Alex N
Brandsma, Inger
Sato, Koichi
van Rossum-Fikkert, Sari E
van Vliet, Nicole
Sleddens, Esther
Reuter, Marcel
Odijk, Hanny
van den Tempel, Nathalie
Dekkers, Dick H W
Bezstarosti, Karel
Demmers, Jeroen A A
Maas, Alex
Lebbink, Joyce
Wyman, Claire
Essers, Jeroen
van Gent, Dik C
Baarends, Willy M
Knipscheer, Puck
Kanaar, Roland
Zelensky, Alex N
Source :
Cell Reports vol.27 (2019) date: 2019-06-25 nr.13 p.3790-3798.e7 [ISSN 2211-1247]
Publication Year :
2019

Abstract

The tumor suppressor BRCA2 is essential for homologous recombination (HR), replication fork stability, and DNA interstrand crosslink repair in vertebrates. We identify HSF2BP, a protein previously described as testis specific and not characterized functionally, as an interactor of BRCA2 in mouse embryonic stem cells, where the 2 proteins form a constitutive complex. HSF2BP is transcribed in all cultured human cancer cell lines tested and elevated in some tumor samples. Inactivation of the mouse Hsf2bp gene results in male infertility due to a severe HR defect during spermatogenesis. The BRCA2-HSF2BP interaction is highly evolutionarily conserved and maps to armadillo repeats in HSF2BP and a 68-amino acid region between the BRC repeats and the DNA binding domain of human BRCA2 (Gly2270-Thr2337) encoded by exons 12 and 13. This region of BRCA2 does not harbor known cancer-associated missense mutations and may be involved in the reproductive rather than the tumor-suppressing function of BRCA2.

Details

Database :
OAIster
Journal :
Cell Reports vol.27 (2019) date: 2019-06-25 nr.13 p.3790-3798.e7 [ISSN 2211-1247]
Notes :
DOI: 10.1016/j.celrep.2019.05.096, Cell Reports vol.27 (2019) date: 2019-06-25 nr.13 p.3790-3798.e7 [ISSN 2211-1247], English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1139319025
Document Type :
Electronic Resource