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微管(B3)和大脑发育。

MicroTUB(B3)ules and brain development.

机构信息

Howard Hughes Medical Institute, Cambridge, MA 02139, USA.

出版信息

Cell. 2010 Jan 8;140(1):30-2. doi: 10.1016/j.cell.2009.12.038.

DOI:10.1016/j.cell.2009.12.038
PMID:20085703
Abstract

The microtubule network is crucial for the developing nervous system, and mutations in tubulin-encoding genes disrupt neuronal migration. Tischfield et al. (2010) now report that mutations in the tubulin-encoding gene TUBB3 have a striking impact on microtubule dynamics in neurons, resulting in a diverse set of disease symptoms.

摘要

微管网络对于发育中的神经系统至关重要,微管蛋白编码基因的突变会破坏神经元迁移。Tischfield 等人(2010 年)现在报告称,微管蛋白编码基因 TUBB3 的突变对神经元中的微管动力学有显著影响,导致一系列不同的疾病症状。

相似文献

1
MicroTUB(B3)ules and brain development.微管(B3)和大脑发育。
Cell. 2010 Jan 8;140(1):30-2. doi: 10.1016/j.cell.2009.12.038.
2
Tubulin-related cortical dysgeneses: microtubule dysfunction underlying neuronal migration defects.微管蛋白相关的皮质发育异常:神经元迁移缺陷背后的微管功能障碍
Trends Genet. 2009 Dec;25(12):555-66. doi: 10.1016/j.tig.2009.10.003. Epub 2009 Oct 26.
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Elongator bridges tubulin acetylation and neuronal migration.延伸体连接微管蛋白乙酰化与神经元迁移。
Cell. 2009 Feb 6;136(3):393-4. doi: 10.1016/j.cell.2009.01.024.
4
[Microtubules: functional polymorphisms of tubulin and associated proteins (structural and motor MAP's)].[微管:微管蛋白及相关蛋白(结构和运动微管相关蛋白)的功能多态性]
C R Seances Soc Biol Fil. 1996;190(2-3):255-68.
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Zebrafish beta tubulin 1 expression is limited to the nervous system throughout development, and in the adult brain is restricted to a subset of proliferative regions.
Gene Expr Patterns. 2004 Mar;4(2):191-8. doi: 10.1016/j.modgep.2003.09.001.
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Microtubule-associated protein 1B interaction with tubulin tyrosine ligase contributes to the control of microtubule tyrosination.微管相关蛋白1B与微管蛋白酪氨酸连接酶的相互作用有助于控制微管酪氨酸化。
Dev Neurosci. 2008;30(1-3):200-10. doi: 10.1159/000109863.
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Tumor cells resistant to a microtubule-depolymerizing hemiasterlin analogue, HTI-286, have mutations in alpha- or beta-tubulin and increased microtubule stability.对微管解聚的海胆环肽类似物HTI-286耐药的肿瘤细胞,其α-微管蛋白或β-微管蛋白发生了突变,且微管稳定性增加。
Biochemistry. 2004 Nov 9;43(44):13944-54. doi: 10.1021/bi049300+.
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Echinoderm microtubule-associated protein like protein 4, a member of the echinoderm microtubule-associated protein family, stabilizes microtubules.棘皮动物微管相关蛋白样蛋白4是棘皮动物微管相关蛋白家族的成员之一,可使微管稳定。
Neuroscience. 2007 Feb 23;144(4):1373-82. doi: 10.1016/j.neuroscience.2006.11.015. Epub 2006 Dec 27.
9
TUBA1A mutations identified in lissencephaly patients dominantly disrupt neuronal migration and impair dynein activity.在无脑回畸形患者中鉴定到 TUBA1A 突变,其主要破坏神经元迁移并损害动力蛋白活性。
Hum Mol Genet. 2019 Apr 15;28(8):1227-1243. doi: 10.1093/hmg/ddy416.
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Mutations in the neuronal ß-tubulin subunit TUBB3 result in malformation of cortical development and neuronal migration defects.神经元β-微管蛋白亚基 TUBB3 的突变导致皮质发育畸形和神经元迁移缺陷。
Hum Mol Genet. 2010 Nov 15;19(22):4462-73. doi: 10.1093/hmg/ddq377. Epub 2010 Sep 9.

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Multiplicity of acquired cross-resistance in paclitaxel-resistant cancer cells is associated with feedback control of TUBB3 via FOXO3a-mediated ABCB1 regulation.
耐紫杉醇癌细胞中获得性交叉耐药的多样性与通过FOXO3a介导的ABCB1调控对TUBB3的反馈控制有关。
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Reversal of axonal growth defects in an extraocular fibrosis model by engineering the kinesin-microtubule interface.通过改造驱动蛋白-微管界面逆转眼外肌纤维化模型中的轴突生长缺陷
Nat Commun. 2016 Jan 18;7:10058. doi: 10.1038/ncomms10058.
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Pathogenic variants in TUBB4A are not found in primary dystonia.TUBB4A 中的致病变异在原发性肌张力障碍中未发现。
Neurology. 2014 Apr 8;82(14):1227-30. doi: 10.1212/WNL.0000000000000294. Epub 2014 Mar 5.
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Major epigenetic development distinguishing neuronal and non-neuronal cells occurs postnatally in the murine hypothalamus.区分神经元细胞和非神经元细胞的主要表观遗传发育在小鼠下丘脑出生后发生。
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Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene.发声低语困难(DYT4 型肌张力障碍)是由 TUBB4 基因突变引起的。
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Cerebellum-specific and age-dependent expression of an endogenous retrovirus with intact coding potential.小脑特异性和年龄依赖性表达具有完整编码潜力的内源性逆转录病毒。
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Microtubule-based localization of a synaptic calcium-signaling complex is required for left-right neuronal asymmetry in C. elegans.微管基定位的突触钙信号复合物是秀丽隐杆线虫左右神经元不对称所必需的。
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