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首页> 外文期刊>Stem cells and development >All the Tested Human Somatic Cells Express Both Oct4A and Its Pseudogenes but Express Oct4A at Much Lower Levels Compared with Its Pseudogenes and Human Embryonic Stem Cells
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All the Tested Human Somatic Cells Express Both Oct4A and Its Pseudogenes but Express Oct4A at Much Lower Levels Compared with Its Pseudogenes and Human Embryonic Stem Cells

机译:所有测试的人类体细胞均表达Oct4A及其假基因,但与其伪基因和人类胚胎干细胞相比,其Oct4A的表达水平要低得多

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摘要

Oct4 pseudogenes and isoforms seriously confuse the detection of the pluripotency-associated Oct4A expression in somatic cells, which in many cases was not accurately determined. This confusion has recently been discussed, but the wrong conclusions have continuously been made. Most studies failed to detect the expression of Oct4 pseudogenes and isoforms in somatic cells but detected only Oct4A, for which the detection signals incorrectly came from its pseudogenes and isoforms. Some studies detected the expression of only Oct4 pseudogenes in somatic cells but failed to detect Oct4A. The other studies failed to detect the expression of any Oct4 genes. Oct4A is more homologous to its pseudogenes than its isoforms, and it is much more difficult to distinguish Oct4A from its pseudogenes, so this study focused on them. In this study, the strict experimental procedures were followed. Three pairs of Oct4A-specific polymerase chain reaction (PCR) primers were carefully designed and tested by sequencing reverse transcription-polymerase chain reaction (RT-PCR) clones, which showed that only one of them was truly specific to Oct4A. RT-PCR was also performed with the primers amplifying both Oct4A and its pseudogenes, and several hundreds of PCR clones from each cell type were sequenced to reliably distinguish the low-abundant Oct4A from its high-abundant pseudogenes. Western blot, immunocytochemistry, and flow cytometric analyses were performed with three Oct4 antibodies to confirm the results of Oct4 mRNA expression. This study undoubtedly made the correct conclusions about Oct4 expression in human somatic cells and showed that all the tested human somatic cells expressed both Oct4A and its pseudogenes but expressed Oct4A at much lower levels compared with its pseudogenes.
机译:Oct4假基因和同工型严重混淆了体细胞中与多能性相关的Oct4A表达的检测,在许多情况下无法准确确定。最近已经讨论了这种混淆,但是不断得出错误的结论。大多数研究未能检测到体细胞中Oct4假基因和同工型的表达,但仅检测到Oct4A,其检测信号错误地来自其假基因和同工型。一些研究仅在体细胞中检测到Oct4假基因的表达,但未能检测到Oct4A。其他研究未能检测到任何Oct4基因的表达。 Oct4A与它的假基因相比,与它的同工型同源性更高,并且将Oct4A与它的假基因区分开来要困难得多,因此,本研究重点关注它们。在这项研究中,遵循严格的实验程序。通过对逆转录-聚合酶链反应(RT-PCR)克隆进行测序,精心设计并测试了三对Oct4A特异性聚合酶链反应(PCR)引物,这表明只有其中一个对Oct4A真正具有特异性。还使用扩增Oct4A及其假基因的引物进行RT-PCR,并对每种细胞类型的数百个PCR克隆进行了测序,以可靠地将低丰度的Oct4A与高丰度的假基因区分开。用三种Oct4抗体进行了蛋白质印迹,免疫细胞化学和流式细胞仪分析,以确认Oct4 mRNA表达的结果。毫无疑问,这项研究得出了有关人体细胞中Oct4表达的正确结论,并表明所有测试的人体细胞均表达Oct4A及其假基因,但与其假基因相比,其Oct4A的表达水平要低得多。

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