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基于原位杂交技术对小鼠胚胎干细胞中异质表达基因的筛选。

An in situ hybridization-based screen for heterogeneously expressed genes in mouse ES cells.

作者信息

Carter Mark G, Stagg Carole A, Falco Geppino, Yoshikawa Toshiyuki, Bassey Uwem C, Aiba Kazuhiro, Sharova Lioudmila V, Shaik Nabeebi, Ko Minoru S H

机构信息

Developmental Genomics and Aging Section, Laboratory of Genetics, National Institute on Aging, NIH, Baltimore, MD 21224, USA.

出版信息

Gene Expr Patterns. 2008 Feb;8(3):181-98. doi: 10.1016/j.gep.2007.10.009. Epub 2007 Nov 4.

Abstract

We previously reported that Zscan4 showed heterogeneous expression patterns in mouse embryonic stem (ES) cells. To identify genes that show similar expression patterns, we carried out high-throughput in situ hybridization assays on ES cell cultures for 244 genes. Most of the genes are involved in transcriptional regulation, and were selected using microarray-based comparisons of gene expression profiles in ES and embryonal carcinoma (EC) cells versus differentiated cell types. Pou5f1 (Oct4, Oct3/4) and Krt8 (EndoA) were used as controls. Hybridization signals were detected on ES cell colonies for 147 genes (60%). The majority (136 genes) of them showed relatively homogeneous expression in ES cell colonies. However, we found that two genes unequivocally showed Zscan4-like spotted expression pattern (spot-in-colony pattern; Whsc2 and Rhox9). We also found that nine genes showed relatively heterogeneous expression pattern (mosaic-in-colony pattern: Zfp42/Rex1, Rest, Atf4, Pa2g4, E2f2, Nanog, Dppa3/Pgc7/Stella, Esrrb, and Fscn1). Among these genes, Zfp42/Rex1 showed unequivocally heterogeneous expression in individual ES cells prepared by the CytoSpin. These results show the presence of different types or states of cells within ES cell cultures otherwise thought to be undifferentiated and homogeneous, suggesting a previously unappreciated complexity in ES cell cultures.

摘要

我们之前报道过Zscan4在小鼠胚胎干细胞(ES细胞)中呈现出异质性表达模式。为了鉴定具有相似表达模式的基因,我们对ES细胞培养物中的244个基因进行了高通量原位杂交分析。这些基因大多参与转录调控,是通过基于微阵列的ES细胞和胚胎癌细胞(EC细胞)与分化细胞类型的基因表达谱比较来选择的。Pou5f1(Oct4,Oct3/4)和Krt8(EndoA)用作对照。在ES细胞集落中检测到147个基因(60%)的杂交信号。其中大多数(136个基因)在ES细胞集落中呈现相对均匀的表达。然而,我们发现有两个基因明确呈现出类似Zscan4的斑点状表达模式(集落内斑点模式;Whsc2和Rhox9)。我们还发现有九个基因呈现相对异质性的表达模式(集落内镶嵌模式:Zfp42/Rex1、Rest,、Atf4、Pa2g4、E2f2、Nanog、Dppa3/Pgc7/Stella、Esrrb和Fscn1)。在这些基因中,Zfp42/Rex1在通过细胞离心机制备的单个ES细胞中明确呈现异质性表达。这些结果表明,在原本被认为是未分化且均匀的ES细胞培养物中存在不同类型或状态的细胞,这表明ES细胞培养物中存在此前未被认识到的复杂性。

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