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本文引用的文献

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EPO-mediated expansion of late-stage erythroid progenitors in the bone marrow initiates recovery from sublethal radiation stress.EPO 介导的骨髓晚期红系祖细胞的扩增启动了对亚致死性辐射应激的恢复。
Blood. 2012 Sep 20;120(12):2501-11. doi: 10.1182/blood-2011-11-394304. Epub 2012 Aug 13.
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Gene induction and repression during terminal erythropoiesis are mediated by distinct epigenetic changes.终末红细胞生成过程中的基因诱导和抑制是由不同的表观遗传变化介导的。
Blood. 2011 Oct 20;118(16):e128-38. doi: 10.1182/blood-2011-03-341404. Epub 2011 Aug 22.
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The Strategies WDK: a graphical search interface and web development kit for functional genomics databases.WDK 策略:功能基因组学数据库的图形搜索界面和网络开发工具包。
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The multifunctional role of EKLF/KLF1 during erythropoiesis.EKLF/KLF1 在红细胞生成过程中的多功能作用。
Blood. 2011 Aug 25;118(8):2044-54. doi: 10.1182/blood-2011-03-331371. Epub 2011 May 25.
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Formation of mammalian erythrocytes: chromatin condensation and enucleation.哺乳动物红细胞的形成:染色质浓缩和去核。
Trends Cell Biol. 2011 Jul;21(7):409-15. doi: 10.1016/j.tcb.2011.04.003. Epub 2011 May 17.
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Global gene expression analysis of human erythroid progenitors.人类红系祖细胞的全基因表达分析。
Blood. 2011 Mar 31;117(13):e96-108. doi: 10.1182/blood-2010-07-290825. Epub 2011 Jan 26.
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Single-lineage transcriptome analysis reveals key regulatory pathways in primitive erythroid progenitors in the mouse embryo.单细胞转录组分析揭示了小鼠胚胎原始红细胞祖细胞中的关键调控途径。
Blood. 2011 May 5;117(18):4924-34. doi: 10.1182/blood-2010-10-313676. Epub 2011 Jan 24.
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Aquaporin-3 mediates hydrogen peroxide uptake to regulate downstream intracellular signaling.水通道蛋白 3 介导过氧化氢摄取以调节下游细胞内信号转导。
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Identification of ROS using oxidized DCFDA and flow-cytometry.使用氧化型DCFDA和流式细胞术鉴定活性氧。
Methods Mol Biol. 2010;594:57-72. doi: 10.1007/978-1-60761-411-1_4.
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Resolving the distinct stages in erythroid differentiation based on dynamic changes in membrane protein expression during erythropoiesis.基于红细胞生成过程中膜蛋白表达的动态变化解析红细胞分化的不同阶段。
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红细胞基因表达的个体发生。

Ontogeny of erythroid gene expression.

机构信息

Department of Pediatrics, University of Rochester Medical Center, Center for Pediatric Biomedical Research, Rochester, NY 14642, USA.

出版信息

Blood. 2013 Feb 7;121(6):e5-e13. doi: 10.1182/blood-2012-04-422394. Epub 2012 Dec 12.

DOI:10.1182/blood-2012-04-422394
PMID:23243273
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3567347/
Abstract

Erythroid ontogeny is characterized by overlapping waves of primitive and definitive erythroid lineages that share many morphologic features during terminal maturation but have marked differences in cell size and globin expression. In the present study, we compared global gene expression in primitive, fetal definitive, and adult definitive erythroid cells at morphologically equivalent stages of maturation purified from embryonic, fetal, and adult mice. Surprisingly, most transcriptional complexity in erythroid precursors is already present by the proerythroblast stage. Transcript levels are markedly modulated during terminal erythroid maturation, but housekeeping genes are not preferentially lost. Although primitive and definitive erythroid lineages share a large set of nonhousekeeping genes, annotation of lineage-restricted genes shows that alternate gene usage occurs within shared functional categories, as exemplified by the selective expression of aquaporins 3 and 8 in primitive erythroblasts and aquaporins 1 and 9 in adult definitive erythroblasts. Consistent with the known functions of Aqp3 and Aqp8 as H2O2 transporters, primitive, but not definitive, erythroblasts preferentially accumulate reactive oxygen species after exogenous H2O2 exposure. We have created a user-friendly Web site (http://www.cbil.upenn.edu/ErythronDB) to make these global expression data readily accessible and amenable to complex search strategies by the scientific community.

摘要

红细胞发生的特点是原始和定型红细胞谱系的重叠波,它们在终末成熟过程中具有许多形态特征,但在细胞大小和珠蛋白表达上有明显的差异。在本研究中,我们比较了从胚胎、胎儿和成年小鼠中分离出的形态学上相同成熟阶段的原始、胎儿定型和成人定型红细胞中的全局基因表达。令人惊讶的是,红细胞前体细胞中的大多数转录复杂性在原红细胞阶段就已经存在。在终末红细胞成熟过程中,转录水平有明显的调节,但管家基因并没有优先丢失。虽然原始和定型红细胞谱系共享一大组非管家基因,但谱系特异性基因的注释表明,在共享的功能类别中会发生替代基因的使用,例如水通道蛋白 3 和 8 在原始红细胞中的选择性表达,以及水通道蛋白 1 和 9 在成人定型红细胞中的选择性表达。与 Aqp3 和 Aqp8 作为 H2O2 转运体的已知功能一致,原始红细胞,而不是定型红细胞,在体外 H2O2 暴露后优先积累活性氧。我们创建了一个用户友好的网站(http://www.cbil.upenn.edu/ErythronDB),以便科学界能够方便地访问这些全局表达数据,并采用复杂的搜索策略。