Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The . gov means it’s official VSports app下载. Federal government websites often end in . gov or . mil. Before sharing sensitive information, make sure you’re on a federal government site. .

Https

The site is secure V体育官网. The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely. .

. 2013 Mar;13(3):153-9.
doi: 10.1038/nrc3459.

"V体育2025版" BAP1 and cancer

Affiliations

V体育ios版 - BAP1 and cancer

Michele Carbone et al. Nat Rev Cancer. 2013 Mar.

Abstract

BAP1 is a deubiquitylase that is found associated with multiprotein complexes that regulate key cellular pathways, including the cell cycle, cellular differentiation, cell death, gluconeogenesis and the DNA damage response (DDR). Recent findings indicate that germline BAP1 mutations cause a novel cancer syndrome that is characterized, at least in the affected families that have been studied so far, by the onset at an early age of benign melanocytic skin tumours with mutated BAP1, and later in life by a high incidence of mesothelioma, uveal melanoma, cutaneous melanoma and possibly additional cancers. VSports手机版.

PubMed Disclaimer

VSports - Figures

Figure 1a
Figure 1a. BAP1 protein partners
Putative BAP1 protein partners, identified by co-immunoprecipitation and/or affinity-capture mass spectrometry. Proteins forming the putative BAP1 core complex are shown in blue. Other putative BAP1 partners of hypothetical new complexes are shown in beige, , . Protein partners shown may vary in different cell types and under different conditions.
Figure 1b
Figure 1b. Possible mechanisms of BAP1 function
I) Epigenetic regulation of Polycomb target genes is achieved via the cooperation of multiple protein complexes. The signature of gene silencing mediated by PRC2 is the trimethylation of H3K27. PRC1 can be recruited to H3K27me3 sites and contributes to gene silencing via monoubiquitylation of H2AK119. The BAP1-ASXL1 complex (PR-DUB) has H2A-K119ub deubiquitylase activity opposite to PRC1. OGT contributes to the fine tuning of these epigenetic marks via O-GlcNacylation of PHCs. Hypothesis: PR-DUB might be recruited to Polycomb target genes because of the interaction between BAP1, HCF1 and OGT. II) BAP1 regulates gene transcription via association with other protein partners, e.g. HCF1 and YY1 or HCF1 and OGT. Other putative BAP1 partners are shown in grey. Hypothesis: BAP1, HCF1, YY1 and OGT might also be part of one large protein complex. III) BAP1-HCF1-OGT complex increases the stability of PGC-1α, regulating gluconeogenesis and possibly mitochondrial biogenesis. ASXL1/2, Additional sex combs like 1/2; BAP1, BRCA1-assiciated protein 1; BARD1, BRCA1-associated RING domain protein 1; BRCA1, breast cancer type 1 susceptibility protein; CBXs, mammalian chromobox protein homologues; EZHs, enhancer of zeste homologs; FOXK1/2, Forkhead box protein K1/2; HAT1, Histone acetyltransferase 1; HCF1, Host cell factor 1; KDM1B, lysine (K)-specific demethylase 1B; OGT, UDP-glucose-dependent O-glucosyltransferase; PCLs, Polycomb Like proteins; PGC-1α, Peroxisome proliferator-activated receptor gamma coactivator 1α; PHCs, Polyhomeotic-like proteins; PRC1, Polycomb repressive complex 1; PRC2, Polycomb repressive complex 2; PR-DUB, Polycomb repressive deubiquitinase; RING1, Really interesting new gene 1; RNF2, RING finger protein 2; YY1, Ying-Yang 1.
Figure 2
Figure 2. Schematic representation of BAP1 domains and locations of the reported BAP1 germline mutations
All the germline BAP1 mutations found in families with UVM and mesothelioma encode BAP1 proteins lacking the nuclear localization sequence. Most of them have an intact ubiquitin carboxyl-terminal hydrolase (UCH) domain, , , , , , , . Ba, BARD1 binding domain; H, HCF-1 binding domain; Br, BRCA1 binding domain; Y, YY1 binding domain; ULD, UCH37-like domain; NLS, nuclear localization signal; Red arrows, germline mutations.

References

    1. Carbone M, et al. A mesothelioma epidemic in Cappadocia: scientific developments and unexpected social outcomes. Nat Rev Cancer. 2007;7:147–54. - PubMed
    1. Carbone M, Yang H. Molecular pathways: targeting mechanisms of asbestos and erionite carcinogenesis in mesothelioma. Clin Cancer Res. 2012;18:598–604. - PMC - PubMed
    1. Carbone M, et al. Erionite exposure in North Dakota and Turkish villages with mesothelioma. Proc Natl Acad Sci U S A. 2011;108:13618–23. - PMC - PubMed
    1. Roushdy-Hammady I, Siegel J, Emri S, Testa JR, Carbone M. Genetic-susceptibility factor and malignant mesothelioma in the Cappadocian region of Turkey. Lancet. 2001;357:444–5. - PubMed
    1. Dogan AU, et al. Genetic predisposition to fiber carcinogenesis causes a mesothelioma epidemic in Turkey. Cancer Res. 2006;66:5063–8. - "V体育官网" PubMed

VSports注册入口 - Publication types