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本文引用的文献

1
CDKL5 ensures excitatory synapse stability by reinforcing NGL-1-PSD95 interaction in the postsynaptic compartment and is impaired in patient iPSC-derived neurons.CDKL5 通过增强突触后隔室中的 NGL-1-PSD95 相互作用来确保兴奋性突触稳定性,并且在患者诱导多能干细胞衍生的神经元中受到损害。
Nat Cell Biol. 2012 Sep;14(9):911-23. doi: 10.1038/ncb2566. Epub 2012 Aug 26.
2
Transient expression of Xpn, an XLMR protein related to neurite extension, during brain development and participation in neurite outgrowth.在大脑发育过程中,与轴突延伸相关的 XLMR 蛋白 Xpn 短暂表达,并参与轴突生长。
Neuroscience. 2012 Jul 12;214:181-91. doi: 10.1016/j.neuroscience.2012.04.030. Epub 2012 Apr 21.
3
Synaptic pathology of Down syndrome.唐氏综合征的突触病变。
Adv Exp Med Biol. 2012;970:451-68. doi: 10.1007/978-3-7091-0932-8_20.
4
Bioenergy sensing in the brain: the role of AMP-activated protein kinase in neuronal metabolism, development and neurological diseases.脑内生物能量感应:AMP 激活的蛋白激酶在神经元代谢、发育和神经疾病中的作用。
Cell Cycle. 2011 Oct 15;10(20):3452-60. doi: 10.4161/cc.10.20.17953.
5
Mutation screening in 86 known X-linked mental retardation genes by droplet-based multiplex PCR and massive parallel sequencing.通过基于微滴的多重PCR和大规模平行测序对86个已知的X连锁智力障碍基因进行突变筛查。
Hugo J. 2009 Dec;3(1-4):41-9. doi: 10.1007/s11568-010-9137-y. Epub 2010 Mar 25.
6
Synaptic microcircuit dysfunction in genetic models of neurodevelopmental disorders: focus on Mecp2 and Met.神经发育障碍遗传模型中的突触微电路功能障碍:以 Mecp2 和 Met 为例。
Curr Opin Neurobiol. 2011 Dec;21(6):827-33. doi: 10.1016/j.conb.2011.06.006. Epub 2011 Jul 4.
7
AMP-activated protein kinase regulates neuronal polarization by interfering with PI 3-kinase localization.AMP 激活的蛋白激酶通过干扰 PI 3-激酶的定位来调节神经元极化。
Science. 2011 Apr 8;332(6026):247-51. doi: 10.1126/science.1201678. Epub 2011 Mar 24.
8
Resequencing of 200 human exomes identifies an excess of low-frequency non-synonymous coding variants.200 个人类外显子组重测序发现低频非同义编码变异过度。
Nat Genet. 2010 Nov;42(11):969-72. doi: 10.1038/ng.680. Epub 2010 Oct 3.
9
Modulation of dendritic spine development and plasticity by BDNF and vesicular trafficking: fundamental roles in neurodevelopmental disorders associated with mental retardation and autism.脑源性神经营养因子(BDNF)和囊泡运输对树突棘发育和可塑性的调节:与智力迟钝和自闭症相关的神经发育障碍中的基本作用。
J Neurodev Disord. 2009 Sep;1(3):185-96. doi: 10.1007/s11689-009-9027-6.
10
Spatiotemporal expression in mouse brain of Kiaa2022, a gene disrupted in two patients with severe mental retardation.Kiaa2022基因在小鼠大脑中的时空表达,该基因在两名重度智力障碍患者中发生突变。
Gene Expr Patterns. 2009 Sep;9(6):423-9. doi: 10.1016/j.gep.2009.06.001. Epub 2009 Jun 11.

KIAA2022 功能丧失导致轻度至重度智力残疾伴自闭症谱系障碍,并损害轴突生长。

Loss of function of KIAA2022 causes mild to severe intellectual disability with an autism spectrum disorder and impairs neurite outgrowth.

机构信息

Centre de Génétique Humaine, Université de Franche-Comté, 25000 Besançon, France.

出版信息

Hum Mol Genet. 2013 Aug 15;22(16):3306-14. doi: 10.1093/hmg/ddt187. Epub 2013 Apr 24.

DOI:10.1093/hmg/ddt187
PMID:23615299
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3723314/
Abstract

Existence of a discrete new X-linked intellectual disability (XLID) syndrome due to KIAA2022 deficiency was questioned by disruption of KIAA2022 by an X-chromosome pericentric inversion in a XLID family we reported in 2004. Three additional families with likely pathogenic KIAA2022 mutations were discovered within the frame of systematic parallel sequencing of familial cases of XLID or in the context of routine array-CGH evaluation of sporadic intellectual deficiency (ID) cases. The c.186delC and c.3597dupA KIAA2022 truncating mutations were identified by X-chromosome exome sequencing, while array CGH discovered a 70 kb microduplication encompassing KIAA2022 exon 1 in the third family. This duplication decreased KIAA2022 mRNA level in patients' lymphocytes by 60%. Detailed clinical examination of all patients, including the two initially reported, indicated moderate-to-severe ID with autistic features, strabismus in all patients, with no specific dysmorphic features other than a round face in infancy and no structural brain abnormalities on magnetic resonance imaging (MRI). Interestingly, the patient with decreased KIAA2022 expression had only mild ID with severe language delay and repetitive behaviors falling in the range of an autism spectrum disorder (ASD). Since little is known about KIAA2022 function, we conducted morphometric studies in cultured rat hippocampal neurons. We found that siRNA-mediated KIAA2022 knockdown resulted in marked impairment in neurite outgrowth including both the dendrites and the axons, suggesting a major role for KIAA2022 in neuron development and brain function.

摘要

由于我们在 2004 年报道的一个 X 连锁智力障碍(XLID)家族中存在 X 染色体着丝粒倒位破坏 KIAA2022,因此存在一个离散的新的 X 连锁智力障碍(XLID)综合征的存在受到质疑。在 XLID 家族的系统平行测序或散发性智力障碍(ID)病例的常规阵列-CGH 评估范围内,发现了另外三个可能具有致病性 KIAA2022 突变的家族。通过 X 染色体外显子组测序鉴定了 c.186delC 和 c.3597dupA KIAA2022 截断突变,而阵列 CGH 发现了第三个家族中的 70 kb 微重复,包含 KIAA2022 外显子 1。该重复使患者淋巴细胞中的 KIAA2022 mRNA 水平降低了 60%。对所有患者进行了详细的临床检查,包括最初报告的两名患者,表明具有自闭症特征的中度至重度智力障碍,所有患者均有斜视,除了婴儿期的圆脸外,没有其他特定的畸形特征,磁共振成像(MRI)上也没有结构脑异常。有趣的是,表达 KIAA2022 减少的患者仅有轻度智力障碍,严重的语言延迟和重复行为属于自闭症谱系障碍(ASD)的范围。由于对 KIAA2022 的功能知之甚少,我们在培养的大鼠海马神经元中进行了形态计量学研究。我们发现,siRNA 介导的 KIAA2022 敲低导致神经突生长明显受损,包括树突和轴突,这表明 KIAA2022 在神经元发育和大脑功能中起主要作用。