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组织特异性富含AT的DNA序列结合蛋白在淋巴细胞分化中的作用。

Role of tissue-specific AT-rich DNA sequence-binding proteins in lymphocyte differentiation.

作者信息

Yokota Takafumi, Kanakura Yuzuru

机构信息

Department of Hematology and Oncology, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka, 565-0871, Japan,

出版信息

Int J Hematol. 2014 Sep;100(3):238-45. doi: 10.1007/s12185-014-1602-2. Epub 2014 Jun 18.

DOI:10.1007/s12185-014-1602-2
PMID:24938377
Abstract

A great many transcription factors, cytokines, and cytokine receptors have been identified as indispensable elements in lymphocyte differentiation, but the molecular mechanism that orchestrates the expression and function of these molecular factors is unknown. The process of lymphocyte differentiation involves both the simultaneous activation of lymphoid-related genes and the inactivation of non-lymphoid lineage-related genes, suggesting that there should be critical molecules that regulate such gene expression in both temporal and spatial dimensions. Recent studies of chromatin-remodeling proteins shed light on this complex process. In particular, special AT-rich sequence-binding protein 1 has been studied extensively. In this article, we review the wealth of information characterizing this protein.

摘要

许多转录因子、细胞因子和细胞因子受体已被确定为淋巴细胞分化中不可或缺的元素,但协调这些分子因子表达和功能的分子机制尚不清楚。淋巴细胞分化过程涉及淋巴相关基因的同时激活和非淋巴谱系相关基因的失活,这表明应该存在在时间和空间维度上调节此类基因表达的关键分子。最近对染色质重塑蛋白的研究为这一复杂过程提供了线索。特别是,富含AT序列的特殊结合蛋白1已得到广泛研究。在本文中,我们综述了有关该蛋白的丰富信息。

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Role of tissue-specific AT-rich DNA sequence-binding proteins in lymphocyte differentiation.组织特异性富含AT的DNA序列结合蛋白在淋巴细胞分化中的作用。
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2
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Guest editorial: molecular mechanisms of lymphocyte development: recent findings.特邀社论:淋巴细胞发育的分子机制:最新发现
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Small RNA as a regulator of hematopoietic development, immune response in infection and tumorigenesis.小RNA作为造血发育、感染中的免疫反应和肿瘤发生的调节因子。
Int J Hematol. 2014;99(5):553-60. doi: 10.1007/s12185-014-1564-4. Epub 2014 Apr 1.
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Bright/Arid3A acts as a barrier to somatic cell reprogramming through direct regulation of Oct4, Sox2, and Nanog.Bright/Arid3A 通过直接调控 Oct4、Sox2 和 Nanog 来充当体细胞核重编程的屏障。
Stem Cell Reports. 2014 Jan 14;2(1):26-35. doi: 10.1016/j.stemcr.2013.12.002.
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Complementary regulation of early B-lymphoid differentiation by genetic and epigenetic mechanisms.
通过整合基因组网络分析鉴定急性淋巴细胞白血病的潜在治疗方法。
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SATB1-mediated chromatin landscape in T cells.SATB1 介导的 T 细胞染色质景观。
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The Role of ARID5B in Acute Lymphoblastic Leukemia and Beyond.ARID5B在急性淋巴细胞白血病及其他方面的作用。
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The expression of special AT-rich binding protein 1 in cervical cancer and its clinical significance.特异性富含AT序列结合蛋白1在宫颈癌中的表达及其临床意义。
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Molecular studies reveal and gene fusions displaced in a case of infantile acute lymphoblastic leukemia with complex karyotype.分子研究揭示了一例具有复杂核型的婴儿急性淋巴细胞白血病中存在的[未提及具体基因]基因融合和[未提及具体基因]基因融合。
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Satb1 Regulates Contactin 5 to Pattern Dendrites of a Mammalian Retinal Ganglion Cell.Satb1通过调控Contactin 5来塑造哺乳动物视网膜神经节细胞的树突形态。
Neuron. 2017 Aug 16;95(4):869-883.e6. doi: 10.1016/j.neuron.2017.07.019. Epub 2017 Aug 3.
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Coordination of matrix attachment and ATP-dependent chromatin remodeling regulate auxin biosynthesis and Arabidopsis hypocotyl elongation.基质附着与ATP依赖的染色质重塑的协调调控生长素生物合成及拟南芥下胚轴伸长。
PLoS One. 2017 Jul 26;12(7):e0181804. doi: 10.1371/journal.pone.0181804. eCollection 2017.
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Genome-Wide AnkA-DNA Interactions Are Enriched in Intergenic Regions and Gene Promoters and Correlate with Infection-Induced Differential Gene Expression.全基因组AnkA-DNA相互作用在基因间区域和基因启动子中富集,并与感染诱导的差异基因表达相关。
Front Cell Infect Microbiol. 2016 Sep 20;6:97. doi: 10.3389/fcimb.2016.00097. eCollection 2016.
遗传和表观遗传机制对早期 B 淋巴细胞分化的互补调控。
Int J Hematol. 2013 Oct;98(4):382-9. doi: 10.1007/s12185-013-1424-7. Epub 2013 Sep 3.
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The Satb1 protein directs hematopoietic stem cell differentiation toward lymphoid lineages.Satb1 蛋白将造血干细胞向淋巴系分化。
Immunity. 2013 Jun 27;38(6):1105-15. doi: 10.1016/j.immuni.2013.05.014. Epub 2013 Jun 20.
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Satb1 regulates the self-renewal of hematopoietic stem cells by promoting quiescence and repressing differentiation commitment.Satb1 通过促进静止和抑制分化承诺来调节造血干细胞的自我更新。
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Nuclear location and the control of developmental progression.核定位与发育进程的控制。
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Satb1 and Satb2 are dispensable for X chromosome inactivation in mice.Satb1 和 Satb2 对于小鼠 X 染色体失活是可有可无的。
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Genome organizing function of SATB1 in tumor progression.SATB1 在肿瘤进展中的基因组组织功能。
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