BRCA1 is a nuclear polypeptide to suppress familial breast and ovarian cancers. Accumulated evidence suggests that BRCA1 participates in DNA damage response. However, the molecular mechanisms by which BRCA1 participates in DNA damage response remain elusive. Recently, we have identified two new BRCA1 partners, RAP80 and CCDC98. Both RAP80 and CCDC98 associate with BRCA1 BRCT domain and participate in DNA damage response. Functionally, RAP80 and CCDC98 facilitate BRCA1's translocation to DNA damage sites. To search for the signals that recruit this BRCA1 complex to the DNA damage lesions, we have found that BRCA1-associated protein RAP80 recognizes ubiquitinated histone H2A and H2B. And both histone H2A and H2B are further ubiquitinated following DNA damage. In addition, we have identified two biallelic missense mutations and one truncation mutation of RAP80 gene in breast and ovarian cancer cells, suggesting that RAP80 could be another breast and ovarian tumors suppressor in BRCA1-dependent pathway. Thus, we hypothesize that recognition of ubiquitinated histone by RAP80 is the molecular basis that loads BRCA1 to DNA damage sites, which regulates proper DNA damage response, protects genomic integrity and prevents breast and ovarian tumor development. We propose following experiments to examine our hypothesis.
Aim1 : To examine the molecular mechanism by which RAP80 and CCDC98 target BRCA1 to DNA damage lesions.
Aim2 : To examine the functional defects of RAP80 mutations in BRCA1-dependent DNA damage response.
Aim3 : To examine the role of RAP80 in tumor prevention. In summary, studies outlined here will not only reveal the molecular mechanism by which BRCA1 participates in DNA damage response, but also identify the functional partners of BRCA1 in tumor suppression.
Accumulated evidence suggests that BRCA1 protects genomic integrity in response to DNA double strand breaks. Here, we have identified two BRCA1 partners, CCDC98 and RAP80, which participate in DNA damage response. In this proposal, we plan to not only dissect the molecular mechanism of this BRCA1 complex in DNA damage response, but also examine the role of this complex in tumorigenesis in vivo.
|Chen, Qian; Kassab, Muzaffer Ahmad; Dantzer, Françoise et al. (2018) PARP2 mediates branched poly ADP-ribosylation in response to DNA damage. Nat Commun 9:3233|
|Wang, Jiaxu; Yuan, Zenglin; Cui, Yaqi et al. (2018) Molecular basis for the inhibition of the methyl-lysine binding function of 53BP1 by TIRR. Nat Commun 9:2689|
|Wang, Mengxi; Yuan, Zenglin; Xie, Rong et al. (2018) Structure-function analyses reveal the mechanism of the ARH3-dependent hydrolysis of ADP-ribosylation. J Biol Chem 293:14470-14480|
|Liu, Yidan; Zhang, Bin; Meng, Xiaoyu et al. (2017) UHRF2 regulates local 5-methylcytosine and suppresses spontaneous seizures. Epigenetics 12:551-560|
|Li, Mo; Chen, Qian; Ma, Teng et al. (2017) Targeting reactive nitrogen species suppresses hereditary pancreatic cancer. Proc Natl Acad Sci U S A 114:7106-7111|
|Liu, Chao; Vyas, Aditi; Kassab, Muzaffer A et al. (2017) The role of poly ADP-ribosylation in the first wave of DNA damage response. Nucleic Acids Res 45:8129-8141|
|Han, Deqiang; Chen, Qian; Shi, Jiazhong et al. (2017) CTCF participates in DNA damage response via poly(ADP-ribosyl)ation. Sci Rep 7:43530|
|Li, Mo; Chen, Qian; Yu, Xiaochun (2017) Chemopreventive Effects of ROS Targeting in a Murine Model of BRCA1-Deficient Breast Cancer. Cancer Res 77:448-458|
|Evans, Joseph R; Zhao, Shuang G; Chang, S Laura et al. (2016) Patient-Level DNA Damage and Repair Pathway Profiles and Prognosis After Prostatectomy for High-Risk Prostate Cancer. JAMA Oncol 2:471-80|
|Yu, Xiaochun (2016) A special issue on the DNA damage response and genomic instability. Acta Biochim Biophys Sin (Shanghai) 48:593|
Showing the most recent 10 out of 54 publications