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在两细胞胚胎中特异性表达的 Eif1a 样基因和胚胎干细胞的短暂 Zscan4 阳性状态抑制了全球蛋白质合成。

Repression of global protein synthesis by Eif1a-like genes that are expressed specifically in the two-cell embryos and the transient Zscan4-positive state of embryonic stem cells.

机构信息

Developmental Genomics and Aging Section, Laboratory of Genetics, National Institute on Aging, NIH, 251 Bayview Boulevard, Suite 100, Baltimore, MD 21224, USA.

出版信息

DNA Res. 2013 Aug;20(4):391-402. doi: 10.1093/dnares/dst018. Epub 2013 May 5.

DOI:10.1093/dnares/dst018
PMID:23649898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3738165/
Abstract

Mouse embryonic stem (ES) cells are prototypical stem cells that remain undifferentiated in culture for long periods, yet maintain the ability to differentiate into essentially all cell types. Previously, we have reported that ES cells oscillate between two distinct states, which can be distinguished by the transient expression of Zscan4 genes originally identified for its specific expression in mouse two-cell stage embryos. Here, we report that the nascent protein synthesis is globally repressed in the Zscan4-positive state of ES cells, which is mediated by the transient expression of newly identified eukaryotic translation initiation factor 1A (Eif1a)-like genes. Eif1a-like genes, clustered on Chromosome 12, show the high sequence similarity to the Eifa1 and consist of 10 genes (Eif1al1-Eif1al10) and 9 pseudogenes (Eif1al-ps1-Eif1al-ps9). The analysis of the expressed sequence tag database showed that Eif1a-like genes are expressed mostly in the two-cell stage mouse embryos. Microarray analyses and quantitative real-time polymerase chain reaction analyses show that Eif1a-like genes are expressed specifically in the Zscan4-positive state of ES cells. These results indicate a novel mechanism to repress protein synthesis by Eif1a-like genes and a unique mode of protein synthesis regulation in ES cells, which undergo a transient and reversible repression of global protein synthesis in the Zscan4-positive state.

摘要

小鼠胚胎干细胞(ES 细胞)是典型的干细胞,在培养中能长时间保持未分化状态,同时保持分化为几乎所有细胞类型的能力。此前,我们报道 ES 细胞在两种截然不同的状态之间振荡,这两种状态可以通过瞬时表达最初在小鼠二细胞期胚胎中特异性表达的 Zscan4 基因来区分。在这里,我们报告说,新生蛋白质合成在 ES 细胞的 Zscan4 阳性状态下被全局抑制,这是由新鉴定的真核翻译起始因子 1A(Eif1a)样基因的瞬时表达介导的。Eif1a 样基因簇位于染色体 12 上,与 Eifa1 具有高度的序列相似性,由 10 个基因(Eif1al1-Eif1al10)和 9 个假基因(Eif1al-ps1-Eif1al-ps9)组成。对表达序列标签数据库的分析表明,Eif1a 样基因主要在小鼠二细胞期胚胎中表达。微阵列分析和定量实时聚合酶链反应分析表明,Eif1a 样基因特异性表达在 ES 细胞的 Zscan4 阳性状态。这些结果表明,Eif1a 样基因通过抑制蛋白质合成的一种新机制,以及 ES 细胞中蛋白质合成调控的一种独特模式,即在 Zscan4 阳性状态下,新生蛋白质合成被短暂和可逆地抑制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/3738165/0f65c73a5665/dst01805.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/3738165/5e3f2c4d5a78/dst01801.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/3738165/6911f006933c/dst01802.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/3738165/d94f787f8faa/dst01803.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/3738165/25f00ce81502/dst01804.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/3738165/0f65c73a5665/dst01805.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/3738165/5e3f2c4d5a78/dst01801.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/3738165/6911f006933c/dst01802.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/3738165/d94f787f8faa/dst01803.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/3738165/25f00ce81502/dst01804.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/27df/3738165/0f65c73a5665/dst01805.jpg

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