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本文引用的文献

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Functional consequences of AXL sequence variants in hypogonadotropic hypogonadism.AXL 序列变异在促性腺激素低下性性腺功能减退症中的功能后果。
J Clin Endocrinol Metab. 2014 Apr;99(4):1452-60. doi: 10.1210/jc.2013-3426. Epub 2014 Jan 29.
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Epigenetic control of gonadotropin releasing hormone neurons.促性腺激素释放激素神经元的表观遗传调控。
Front Endocrinol (Lausanne). 2013 May 27;4:61. doi: 10.3389/fendo.2013.00061. eCollection 2013.
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HDAC6 and SIRT2 regulate the acetylation state and oncogenic activity of mutant K-RAS.组蛋白去乙酰化酶 6 和 SIRT2 调节突变型 K-RAS 的乙酰化状态和致癌活性。
Mol Cancer Res. 2013 Sep;11(9):1072-7. doi: 10.1158/1541-7786.MCR-13-0040-T. Epub 2013 May 30.
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AXL and MET crosstalk to promote gonadotropin releasing hormone (GnRH) neuronal cell migration and survival.AXL 和 MET 相互作用促进促性腺激素释放激素(GnRH)神经元的迁移和存活。
Mol Cell Endocrinol. 2013 Jul 15;374(1-2):92-100. doi: 10.1016/j.mce.2013.04.018. Epub 2013 May 3.
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The tumor suppressor kinase LKB1 activates the downstream kinases SIK2 and SIK3 to stimulate nuclear export of class IIa histone deacetylases.肿瘤抑制激酶 LKB1 激活下游激酶 SIK2 和 SIK3,刺激 IIa 类组蛋白去乙酰化酶的核输出。
J Biol Chem. 2013 Mar 29;288(13):9345-62. doi: 10.1074/jbc.M113.456996. Epub 2013 Feb 7.
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Histone deacetylase 6 plays a role as a distinct regulator of diverse cellular processes.组蛋白去乙酰化酶 6 作为多种细胞过程的独特调节剂发挥作用。
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Histone deacetylase-1 (HDAC1) is a molecular switch between neuronal survival and death.组蛋白去乙酰化酶-1(HDAC1)是神经元存活和死亡之间的分子开关。
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Histone deacetylases regulate gonadotropin-releasing hormone I gene expression via modulating Otx2-driven transcriptional activity.组蛋白去乙酰化酶通过调节 Otx2 驱动的转录活性来调节促性腺激素释放激素 I 基因的表达。
PLoS One. 2012;7(6):e39770. doi: 10.1371/journal.pone.0039770. Epub 2012 Jun 25.
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Histone deacetylases 6 and 9 and sirtuin-1 control Foxp3+ regulatory T cell function through shared and isoform-specific mechanisms.组蛋白去乙酰化酶 6 和 9 以及 Sirtuin-1 通过共享和同工型特异性机制控制 Foxp3+调节性 T 细胞的功能。
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10
Histone deacetylase 9 as a negative regulator for choline acetyltransferase gene in NG108-15 neuronal cells.组蛋白去乙酰化酶 9 作为 NG108-15 神经元细胞中胆碱乙酰转移酶基因的负调控因子。
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IIb类组蛋白去乙酰化酶6(HDAC6)与IIa类HDAC9的新型相互作用控制促性腺激素释放激素(GnRH)神经元细胞的存活和移动。

Novel Interaction of Class IIb Histone Deacetylase 6 (HDAC6) with Class IIa HDAC9 Controls Gonadotropin Releasing Hormone (GnRH) Neuronal Cell Survival and Movement.

作者信息

Salian-Mehta Smita, Xu Mei, McKinsey Timothy A, Tobet Stuart, Wierman Margaret E

机构信息

From the Division of Endocrinology, Metabolism, and Diabetes and.

Division of Cardiology, University of Colorado School of Medicine, Aurora, Colorado 80045.

出版信息

J Biol Chem. 2015 May 29;290(22):14045-56. doi: 10.1074/jbc.M115.640482. Epub 2015 Apr 14.

DOI:10.1074/jbc.M115.640482
PMID:25873389
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4447976/
Abstract

The impact of histone deacetylases (HDACs) in the control of gonadotropin releasing hormone (GnRH) neuronal development is unknown. We identified an increase in many HDACs in GT1-7 (differentiated) compared with NLT (undifferentiated) GnRH neuronal cell lines. Increased HDAC9 mRNA and protein and specific deacetylase activity in GT1-7 cells suggested a functional role. Introduction of HDAC9 in NLT cells protected from serum withdrawal induced apoptosis and impaired basal neuronal cell movement. Conversely, silencing of endogenous HDAC9 in GT1-7 cells increased apoptosis and cell movement. Comparison of WT and mutant HDAC9 constructs demonstrated that the HDAC9 pro-survival effects required combined cytoplasmic and nuclear localization, whereas the effects on cell movement required a cytoplasmic site of action. Co-immunoprecipitation demonstrated a novel interaction of HDAC9 selectively with the Class IIb HDAC6. HDAC6 was also up-regulated at the mRNA and protein levels, and HDAC6 catalytic activity was significantly increased in GT1-7 compared with NLT cells. HDAC9 interacted with HDAC6 through its second catalytic domain. Silencing of HDAC6, HDAC9, or both, in GT1-7 cells augmented apoptosis compared with controls. HDAC6 and -9 had additive effects to promote cell survival via modulating the BAX/BCL2 pathway. Silencing of HDAC6 resulted in an activation of movement of GT1-7 cells with induction in acetylation of α-tubulin. Inhibition of HDAC6 and HDAC9 together resulted in an additive effect to increase cell movement but did not alter the acetylation of αtubulin. Together, these studies identify a novel interaction of Class IIa HDAC9 with Class IIb HDAC6 to modulate cell movement and survival in GnRH neurons.

摘要

组蛋白去乙酰化酶(HDACs)在促性腺激素释放激素(GnRH)神经元发育调控中的作用尚不清楚。我们发现,与未分化的NLT GnRH神经元细胞系相比,分化的GT1-7细胞中多种HDACs有所增加。GT1-7细胞中HDAC9 mRNA、蛋白及特异性去乙酰化酶活性的增加表明其具有功能性作用。在NLT细胞中引入HDAC9可保护细胞免受血清剥夺诱导的凋亡,并损害基础神经元细胞运动。相反,GT1-7细胞中内源性HDAC9的沉默增加了细胞凋亡和细胞运动。野生型和突变型HDAC9构建体的比较表明,HDAC9的促生存作用需要细胞质和细胞核的联合定位,而对细胞运动的影响则需要细胞质作用位点。免疫共沉淀证明HDAC9与IIb类HDAC6存在新型相互作用。与NLT细胞相比,GT1-7细胞中HDAC6在mRNA和蛋白水平也上调,且HDAC6催化活性显著增加。HDAC9通过其第二个催化结构域与HDAC6相互作用。与对照组相比,GT1-7细胞中HDAC6、HDAC9或二者的沉默均增加了细胞凋亡。HDAC6和-9通过调节BAX/BCL2途径对促进细胞存活具有累加效应。HDAC6的沉默导致GT1-7细胞运动激活,并诱导α-微管蛋白乙酰化。同时抑制HDAC6和HDAC9对增加细胞运动具有累加效应,但不改变α-微管蛋白的乙酰化。总之,这些研究确定了IIa类HDAC9与IIb类HDAC6之间的新型相互作用,以调节GnRH神经元中的细胞运动和存活。