Analysis of Human TACC3 in Cellular Responses to Polycyclic Aromatic Hydrocarbons

Very little is known about the etiology of ovarian cancer. However, studies have shown that occupational exposure to polycyclic aromatic hydrocarbons (PAHs) and tobacco smoking can increase ovarian cancer risk. Previously, we have determined that 100% of ovarian tumors show loss or aberrant subcellular localization of TACC3 (transforming acidic coiled coil 3) relative to the normal ovarian surface epithelium (OSE). In mice, a role for TACC3 in the cellular response to PAH has been defined. However, comparable studies for human TACC3 has not been performed. In this report, we show that specific knockdown of TACC3 in human ovarian cancer cells increases the basal level, and distorts the PAH-induced expression, of genes involved in metabolizing the procarcinogen PAH benzo[a]pyrene to its DNA damaging epoxide. In addition, we demonstrate that PAH stabilizes the TACC3 protein and induces the export of TACC3 and one of its binding partners, Ku70, from the nucleus. This parallels the subcellular distribution of TACC3 in those ovarian cancers that express TACC3. These data suggest that functional downregulation of TACC3 could aid tumor progression by altering cellular responses to chemical carcinogens and the DNA damage that they induce

TACC2 (transforming, acidic coiled-coil containing protein 2)

Review on TACC2, with data on DNA/RNA, on the protein encoded and where the gene is implicated

TACC3 (transforming, acidic coiled-coil containing protein 3)

Review on TACC3 (transforming, acidic coiled-coil containing protein 3), with data on DNA, on the protein encoded, and where the gene is implicated

Cloning and heterologous expression of bovine pyroglutamyl peptidase type-1 in Escherichia coli : purification , biochemical and kinetic characterisation

We describe the cloning, expression and purification of the bovine XM866409 form of pyroglutamyl-aminopeptidase I. The amino acid sequence, deduced from the nucleotide sequence, revealed that it consists of 209 amino acid residues and showed to have 98% homology with the human AJ278828 form of the enzyme. Three amino acid residues at positions 81, 205 and 208 were found to vary among the two sequences. The bovine enzyme was expressed in XL10-gold Esherichia coli cells. Immobilizied Ni-ion affinity chromatography was used to purify the expressed protein resulting in a yield of 3.3mg of PAP1 per litre culture. The purified enzyme had a specific activity of 1700 units/ml. SDS-PAGE produced a single band for bovine PAP1 with a molecular weight of ~23-24 kDa which is in good agreement with previously reported data on PAP1. Kinetic constants Km and Kcat were 59μΜ and 3.5s-1, respectively. It possessed an optimum pH between 9-9.5, a temperature of 37°C and showed an absolute requirement for a thiol-reducing agent (10mM DTT). EDTA didn’t prove to have an effect on enzyme activity. Competitive inhibition was seen with pyroglutamyl peptides pGlu-His-Pro-NH2 (TRH; Ki= 44.1 uM), pGlu-Ala- OH (Ki=141 uM) and pGlu-Val-OH (Ki=652.17)

Aberrations of TACC1 and TACC3 are associated with ovarian cancer

BACKGROUND: Dysregulation of the human Transforming Acidic Coiled Coil (TACC) genes is thought to be important in the development and progression of multiple myeloma, breast and gastric cancer. Recent, large-scale genomic analysis and Serial Analysis of Gene Expression data suggest that TACC1 and TACC3 may also be involved in the etiology of ovarian tumors from both familial and sporadic cases. Therefore, the aim of this study was to determine the occurrence of alterations of these TACCs in ovarian cancer. METHODS: Detection and scoring of TACC1 and TACC3 expression was performed by immunohistochemical analysis of the T-BO-1 tissue/tumor microarray slide from the Cooperative Human Tissue Network, Tissue Array Research Program (TARP) of the National Cancer Institute, National Institutes of Health, Bethesda, MD, USA. Tumors were categorized as either positive (greater than 10% of cells staining) or negative. Statistical analysis was performed using Fisher's exact test and p < 0.05 (single comparisons), and p < 0.02 (multiple comparisons) were considered to be significant. Transgenomics WAVE high performance liquid chromatography (dHPLC) was used to pre-screen the TACC3 gene in constitutional DNA from ovarian cancer patients and their unaffected relatives from 76 families from the Gilda Radner Familial Ovarian Cancer Registry. All variant patterns were then sequenced. RESULTS: This study demonstrated absence of at least one or both TACC proteins in 78.5% (51/65) of ovarian tumors tested, with TACC3 loss observed in 67.7% of tumors. The distribution pattern of expression of the two TACC proteins was different, with TACC3 loss being more common in serous papillary carcinoma compared with clear cell carcinomas, while TACC1 staining was less frequent in endometroid than in serous papillary tumor cores. In addition, we identified two constitutional mutations in the TACC3 gene in patients with ovarian cancer from the Gilda Radner Familial Ovarian Cancer Registry. These patients had previously tested negative for mutations in known ovarian cancer predisposing genes. CONCLUSION: When combined, our data suggest that aberrations of TACC genes, and TACC3 in particular, underlie a significant proportion of ovarian cancers. Thus, TACC3 could be a hitherto unknown endogenous factor that contributes to ovarian tumorigenesis