DNA聚合酶α在正常和转化人成纤维细胞中的差异表达

Vinod K. Srivastava , Matthew D. Schroeder , Susan D. Miller , David L. Busbee
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引用次数: 2

摘要

研究了DNA聚合酶α (pol α)在人成纤维细胞系WI38(胎儿肺)和GM3529(66岁供体皮肤)及其类人猿病毒40 (SV40)大肿瘤抗原(TAg)转化的结合体2RA和2-1中的表达。sv40转换和pSV3。neo (sv40衍生质粒)转化细胞表达TAg,这是一种正常亲本细胞系不表达的病毒编码蛋白。Northern blot杂交研究表明,与正常细胞相比,转化细胞中pol α mRNA的回收率增加。核运行试验证实,这种增加与pol α mRNA转录增加相关。Northern blot分析也显示转化细胞中翻译活性pol α mRNA的不稳定性增加。结果表明,TAg除了其dsDNA结合、pol α结合、视网膜母细胞瘤蛋白结合和解旋酶活性外,可能直接或间接地参与了胎儿和老年供体来源转化成纤维细胞中pol α mRNA转录水平的稳态调控。
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Differential expression of DNA polymerase α in normal and transformed human fibroblasts

The expression of DNA polymerase α (pol α) was studied in human fibroblast lines WI38 (fetal lung) and GM3529 (skin, established from a 66 yr old donor), and their Simian virus 40 (SV40) large tumor antigen (TAg)-transformed corollaries, 2RA and 2-1 respectively. Both SV40-transformed and pSV3.neo (SV40-derived plasmid)-transformed cells express TAg, a virally encoded protein not expressed by the normal parent cell lines. Northern blot hybridization studies showed increased recovery of pol α mRNA from transformed cells compared with normal cells. This increase was correlated with increased pol α mRNA transcription as determined by nuclear run-on assays. Northern blot analyses also showed an increase in the instability of translationally active pol α mRNA in transformed cells. The results suggest that TAg, in addition to its dsDNA binding, pol α binding, retinoblastoma protein binding and helicase activities, may be involved either directly or indirectly in regulation of the steady state mRNA levels of pol α at the transcriptional level in both fetal and aged donor-derived transformed fibroblasts.

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Publisher's note Editorial An accessory protein enhances both DNA binding and activity of DNA polymerase α isolated from normal, but not transformed, human fibroblasts Differences in the spectrum of spontaneous mutations in the hprt gene between tumor cells of the microsatellite mutator phenotype Spermatid micronucleus analysis of aging effects in hamsters
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