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首页> 外文期刊>Human Molecular Genetics >Temporal and parental-specific expression of imprinted genes in a newly derived Chinese human embryonic stem cell line and embryoid bodies.
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Temporal and parental-specific expression of imprinted genes in a newly derived Chinese human embryonic stem cell line and embryoid bodies.

机译:印记基因在新衍生的中国人胚胎干细胞系和拟胚体中的时间和亲本特异性表达。

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Although the study of imprinted genes in human development is very important, little is known about their expression and regulation in the early differentiation of human tissues due to lack of an appropriate model. In this study, a Chinese human embryonic stem (hES) cell line, SHhES1, was derived and fully characterized. Expression profiles of human imprinted genes were determined by Affymetrix Oligo micro-array in undifferentiated SHhES1 cells and SHhES1-derived embryoid bodies (EBs) at day 3, 8, 13 and 18. Thirty-two known human imprinted genes were detected in undifferentiated ES cells. Significantly, differential expression was found in nine genes at different stages of EB formation. Expression profile changes were confirmed by quantitative real-time reverse transcriptase-polymerase chain reaction in SHhES1 cells as well as in another independently derived hES cell line, HUES-7. In addition, the monoallelic expressions of four imprinted genes were examined in three different passages of undifferentiated ES cells and EBs of both hES cell lines. The monoallelic expressions of imprinted genes, H19, PEG10, NDNL1 and KCNQ1 were maintained in both undifferentiated hES cells and derived EBs. More importantly, with the availability of maternal peripheral blood lymphocyte sample, we demonstrated that the maternal expression of KCNQ1 and the paternal expression of NDNL1 and PEG10 were maintained in SHhES1 cells. These data provide the first demonstration that the parental-specific expression of imprinted genes is stable in EBs after extensive differentiation, also indicating that in vitro fertilization protocol does not disrupt the parental monoallelic expression of the imprinted genes examined.
机译:尽管在人类发育中研究印迹基因非常重要,但由于缺乏合适的模型,人们对它们在人类组织早期分化中的表达和调控知之甚少。在这项研究中,中国人类胚胎干(hES)细胞系SHhES1被衍生并得到充分表征。在第3、8、13和18天,通过Affymetrix Oligo微阵列在未分化的SHhES1细胞和SHhES1来源的胚状体(EBs)中确定了人类印迹基因的表达谱。 。显着地,在EB形成的不同阶段的9个基因中发现差异表达。在SHhES1细胞以及另一种独立衍生的hES细胞系HUES-7中,通过定量实时逆转录酶-聚合酶链反应确认了表达谱的变化。另外,在两个未分化的ES细胞和两种hES细胞系的EB的三个不同的传代中检查了四个印迹基因的单等位基因表达。印迹基因H19,PEG10,NDNL1和KCNQ1的单等位基因表达在未分化的hES细胞和衍生的EB中均得以维持。更重要的是,随着母体外周血淋巴细胞样品的获得,我们证明了SHhES1细胞中母体KCNQ1的表达以及NDNL1和PEG10的母体表达得以维持。这些数据提供了第一个证明,即在广泛分化后,印迹基因的亲本特异性表达在EB中是稳定的,也表明体外受精方案不会破坏所检测印迹基因的亲本单等位基因表达。

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