Inactivating Mutations in GT198 in Familial and Early-Onset Breast and Ovarian Cancers.

The human GT198 gene (gene symbol PSMC3IP) is located at chromosome 17q21, 470 kb proximal to BRCA1, a locus previously linked to breast and ovarian cancer predisposition. Its protein product (also known as TBPIP and Hop2) has been shown to regulate steroid hormone receptor-mediated gene activation and to stimulate homologous recombination in DNA repair. Here, we screened germline mutations in GT198 in familial and early-onset breast and ovarian cancer patients. We have identified 8 germline variants in a total of 212 index patients including reoccurring nonsense mutation c.310C>T (p.Q104X) and 5' UTR mutation c.-37A>T, each found in 2 unrelated families. Most identified index patients from cancer families had early onsets with a median age of 35 years. c.310C>T was absent in a total of 564 control individuals analyzed. GT198 gene amplification with an imbalanced mutant copy gain was identified in the blood DNA of one of the patients carrying c.310C>T. When tested, this truncating mutation abolished DNA damage-induced Rad51 foci formation. In addition, we have identified 15 somatic mutations in 2 tumors from 1 patient carrying germline mutation c.-37A>T. The presence of a somatic mutation on the wild-type allele showed that GT198 was biallelically mutated in the tumor. The somatic mutations identified near a splicing junction site caused defective alternative splicing and truncated the open reading frame. Therefore, distinct mutations may cause a similar consequence by truncating the full-length protein and inducing a loss of the wild type. Our study provides the first evidence of the presence of inactivating mutations in GT198 in familial and early-onset breast and ovarian cancer patients. Mutations in GT198, a gene regulating DNA repair, potentially contribute to an increased risk in familial breast and ovarian cancers.

[1]  Kari Stefansson,et al.  A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer , 2012, Nature Genetics.

[2]  Ayal B. Gussow,et al.  XX ovarian dysgenesis is caused by a PSMC3IP/HOP2 mutation that abolishes coactivation of estrogen-driven transcription. , 2011, American journal of human genetics.

[3]  Deborah Hughes,et al.  Germline mutations in RAD51D confer susceptibility to ovarian cancer , 2011, Nature Genetics.

[4]  C I Amos,et al.  Evolutionary evidence of the effect of rare variants on disease etiology , 2011, Clinical genetics.

[5]  Domenico Trombetta,et al.  Gene amplification as double minutes or homogeneously staining regions in solid tumors: origin and structure. , 2010, Genome research.

[6]  Marc Tischkowitz,et al.  RAD51C germline mutations in breast and ovarian cancer patients , 2010, Breast Cancer Research.

[7]  Dieter Niederacher,et al.  Germline mutations in breast and ovarian cancer pedigrees establish RAD51C as a human cancer susceptibility gene , 2010, Nature Genetics.

[8]  M. Mori,et al.  Tat-binding protein-1 (TBP-1), an ATPase of 19S regulatory particles of the 26S proteasome, enhances androgen receptor function in cooperation with TBP-1-interacting protein/Hop2. , 2009, Endocrinology.

[9]  K. Frazer,et al.  Common vs. rare allele hypotheses for complex diseases. , 2009, Current opinion in genetics & development.

[10]  J. Hopper,et al.  Are the so-called low penetrance breast cancer genes, ATM, BRIP1, PALB2 and CHEK2, high risk for women with strong family histories? , 2008, Breast Cancer Research.

[11]  R. Camerini-Otero,et al.  Hop2/Mnd1 acts on two critical steps in Dmc1-promoted homologous pairing. , 2007, Genes & development.

[12]  Katri Pylkäs,et al.  A recurrent mutation in PALB2 in Finnish cancer families , 2007, Nature.

[13]  S. Seal,et al.  PALB2, which encodes a BRCA2-interacting protein, is a breast cancer susceptibility gene , 2007, Nature Genetics.

[14]  A. Ashworth,et al.  The roles of BRCA1 and BRCA2 and associated proteins in the maintenance of genomic stability , 2006, Oncogene.

[15]  F. Couch,et al.  Control of BRCA2 cellular and clinical functions by a nuclear partner, PALB2. , 2006, Molecular cell.

[16]  Makoto Sato,et al.  Stimulation of DNA Strand Exchange by the Human TBPIP/Hop2-Mnd1 Complex* , 2006, Journal of Biological Chemistry.

[17]  Isaac Bentwich Prediction and validation of microRNAs and their targets , 2005, FEBS letters.

[18]  S. Mazoyer Genomic rearrangements in the BRCA1 and BRCA2 genes , 2005, Human mutation.

[19]  R. Camerini-Otero,et al.  The Hop2 and Mnd1 proteins act in concert with Rad51 and Dmc1 in meiotic recombination , 2005, Nature Structural &Molecular Biology.

[20]  R. Schmutzler,et al.  The rare ERBB2 variant Ile654Val is associated with an increased familial breast cancer risk , 2004 .

[21]  Makoto Sato,et al.  Positive Role of the Mammalian TBPIP/HOP2 Protein in DMC1-mediated Homologous Pairing* , 2004, Journal of Biological Chemistry.

[22]  R. Camerini-Otero,et al.  The Hop2 protein has a direct role in promoting interhomolog interactions during mouse meiosis. , 2003, Developmental cell.

[23]  B. Dutrillaux,et al.  Induction of multiple double-strand breaks within an hsr by meganucleaseI-SceI expression or fragile site activation leads to formation of double minutes and other chromosomal rearrangements , 2002, Oncogene.

[24]  R. Wooster,et al.  Breast cancer genetics: What we know and what we need , 2001, Nature Medicine.

[25]  M. King,et al.  Insights into the functions of BRCA1 and BRCA2. , 2000, Trends in genetics : TIG.

[26]  J Chang-Claude,et al.  Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium. , 1998, American journal of human genetics.

[27]  F. Toledo,et al.  Expression of Fragile Sites Triggers Intrachromosomal Mammalian Gene Amplification and Sets Boundaries to Early Amplicons , 1997, Cell.

[28]  J. Rommens,et al.  Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21. , 1995, Genomics.

[29]  K. Kinzler,et al.  Has the breast cancer gene been found? , 1994, Cell.

[30]  G. Lenoir,et al.  Familial breast-ovarian cancer locus on chromosome 17q12-q23 , 1991, The Lancet.

[31]  M. King,et al.  Linkage of early-onset familial breast cancer to chromosome 17q21. , 1990, Science.

[32]  W. Chin,et al.  Identification and Characterization of a Tissue-Specific Coactivator, GT198, That Interacts with the DNA-Binding Domains of Nuclear Receptors , 2022 .