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人胚胎干细胞与其分化的成纤维细胞的蛋白质组学比较:鉴定出 206 个受 hES 细胞特异性 microRNAs 靶向的基因。

Proteomic comparison of human embryonic stem cells with their differentiated fibroblasts: Identification of 206 genes targeted by hES cell-specific microRNAs.

机构信息

Institute of Clinical Medicine, Kaohsiung Medical University, Taiwan.

出版信息

Kaohsiung J Med Sci. 2011 Aug;27(8):299-306. doi: 10.1016/j.kjms.2011.03.010. Epub 2011 May 12.

DOI:10.1016/j.kjms.2011.03.010
PMID:21802640
Abstract

Human embryonic stem (hES)-T3 (T3ES) cells were spontaneously differentiated into autogeneic fibroblast-like T3DF cells, as feeder cells with the capacity to support the growth of undifferentiated hES cells. The proteomes of undifferentiated T3ES cells and their differentiated T3DF fibroblasts were quantitatively compared. Several heterogeneous nuclear ribonucleoproteins and glycolytic enzymes, including l-lactate dehydrogenase A (M), were found to be abundantly and differentially expressed in T3ES cells and T3DF fibroblasts, respectively. Both miRNA and mRNA profiles from the undifferentiated T3ES cells and their differentiated T3DF fibroblasts had been previously determined. In this investigation, 206 genes were found to be targets of the four hES cell-specific miRNAs of miR-302d, miR-372, miR-200c, and/or miR-367 by using two-fold differential expression and inverse expression levels (highly negative correlations) of miRNAs to their target mRNAs. That YWHAZ (14-3-3 zeta) is a target of miR-302d and miR-372 was further confirmed by proteomic comparison between T3ES cells and their differentiated T3DF fibroblasts. According to GeneOntology analyses, almost 50% of these 206 target proteins are nuclear and are involved in gene transcription. Identifying the target mRNAs of hES cell-specific miRNAs will provide a better understanding of the complex regulatory networks in hES cells. Furthermore, these miRNA-targeted proteins play important roles in differentiation of hES cells and during embryo development.

摘要

人胚胎干细胞(hES)-T3(T3ES)细胞自发分化为自体成纤维样 T3DF 细胞,作为具有支持未分化 hES 细胞生长能力的饲养细胞。定量比较了未分化的 T3ES 细胞和其分化的 T3DF 成纤维细胞的蛋白质组。发现几种异质核核糖核蛋白和糖酵解酶,包括 l-乳酸脱氢酶 A(M),在 T3ES 细胞和 T3DF 成纤维细胞中分别大量且差异表达。之前已经确定了未分化的 T3ES 细胞及其分化的 T3DF 成纤维细胞的 miRNA 和 mRNA 图谱。在这项研究中,通过使用 miRNA 与其靶 mRNA 的两倍差异表达和反向表达水平(高度负相关),发现 206 个基因是四个 hES 细胞特异性 miRNA(miR-302d、miR-372、miR-200c 和/或 miR-367)的靶基因。进一步通过 T3ES 细胞与其分化的 T3DF 成纤维细胞之间的蛋白质组比较证实,YWHAZ(14-3-3 zeta)是 miR-302d 和 miR-372 的靶标。根据 GeneOntology 分析,这些 206 个靶蛋白中的近 50%位于核内,参与基因转录。鉴定 hES 细胞特异性 miRNA 的靶 mRNA 将有助于更好地理解 hES 细胞中的复杂调控网络。此外,这些 miRNA 靶向的蛋白质在 hES 细胞的分化和胚胎发育过程中发挥重要作用。

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