Department of Human and Molecular Genetics, Virginia Commonwealth University, School of Medicine, Richmond, Virginia.
J Cell Physiol. 2014 Dec;229(12):1952-62. doi: 10.1002/jcp.24645.
As a strategy to identify gene expression changes affected by human polynucleotide phosphorylase (hPNPase(old-35)), we performed gene expression analysis of HeLa cells in which hPNPase(old-35) was overexpressed. The observed changes were then compared to those of HO-1 melanoma cells in which hPNPase(old-35) was stably knocked down. Through this analysis, 90 transcripts, which positively or negatively correlated with hPNPase(old-35) expression, were identified. The majority of these genes were associated with cell communication, cell cycle, and chromosomal organization gene ontology categories. For a number of these genes, the positive or negative correlations with hPNPase(old-35) expression were consistent with transcriptional data extracted from the TCGA (The Cancer Genome Atlas) expression datasets for colon adenocarcinoma (COAD), skin cutaneous melanoma (SKCM), ovarian serous cyst adenocarcinoma (OV), and prostate adenocarcinoma (PRAD). Further analysis comparing the gene expression changes between Ad.hPNPase(old-35) infected HO-1 melanoma cells and HeLa cells overexpressing hPNPase(old-35) under the control of a doxycycline-inducible promoter, revealed global changes in genes involved in cell cycle and mitosis. Overall, this study provides further evidence that hPNPase(old-35) is associated with global changes in cell cycle-associated genes and identifies potential gene targets for future investigation.
作为一种鉴定受人类多核苷酸磷酸酶(hPNPase(old-35))影响的基因表达变化的策略,我们对 hPNPase(old-35)过表达的 HeLa 细胞进行了基因表达分析。然后将观察到的变化与 hPNPase(old-35)稳定敲低的 HO-1 黑素瘤细胞进行比较。通过这项分析,鉴定出了 90 个与 hPNPase(old-35)表达呈正相关或负相关的转录本。这些基因大多数与细胞通讯、细胞周期和染色体组织基因本体类别相关。对于其中的一些基因,与 hPNPase(old-35)表达的正相关或负相关与从 TCGA(癌症基因组图谱)表达数据集中提取的结肠腺癌(COAD)、皮肤黑色素瘤(SKCM)、卵巢浆液性囊腺癌(OV)和前列腺腺癌(PRAD)的转录数据一致。进一步比较 Ad.hPNPase(old-35)感染的 HO-1 黑素瘤细胞和在四环素诱导启动子控制下过表达 hPNPase(old-35)的 HeLa 细胞之间的基因表达变化的分析表明,细胞周期和有丝分裂相关基因发生了全局变化。总的来说,这项研究进一步证明了 hPNPase(old-35)与细胞周期相关基因的全局变化有关,并确定了未来研究的潜在基因靶点。