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E3 泛素连接酶 RLIM/RNF12 中的致病性变异导致综合征性 X 连锁智力残疾和行为障碍。

Pathogenic variants in E3 ubiquitin ligase RLIM/RNF12 lead to a syndromic X-linked intellectual disability and behavior disorder.

机构信息

Department of Clinical Genetics, Maastricht University Medical Center+, azM, Maastricht, 6202 AZ, The Netherlands.

Department of Genetics and Cell Biology, School for Oncology and Developmental Biology, GROW, FHML, Maastricht University, Maastricht, 6200 MD, The Netherlands.

出版信息

Mol Psychiatry. 2019 Nov;24(11):1748-1768. doi: 10.1038/s41380-018-0065-x. Epub 2018 May 4.

DOI:10.1038/s41380-018-0065-x
PMID:29728705
Abstract

RLIM, also known as RNF12, is an X-linked E3 ubiquitin ligase acting as a negative regulator of LIM-domain containing transcription factors and participates in X-chromosome inactivation (XCI) in mice. We report the genetic and clinical findings of 84 individuals from nine unrelated families, eight of whom who have pathogenic variants in RLIM (RING finger LIM domain-interacting protein). A total of 40 affected males have X-linked intellectual disability (XLID) and variable behavioral anomalies with or without congenital malformations. In contrast, 44 heterozygous female carriers have normal cognition and behavior, but eight showed mild physical features. All RLIM variants identified are missense changes co-segregating with the phenotype and predicted to affect protein function. Eight of the nine altered amino acids are conserved and lie either within a domain essential for binding interacting proteins or in the C-terminal RING finger catalytic domain. In vitro experiments revealed that these amino acid changes in the RLIM RING finger impaired RLIM ubiquitin ligase activity. In vivo experiments in rlim mutant zebrafish showed that wild type RLIM rescued the zebrafish rlim phenotype, whereas the patient-specific missense RLIM variants failed to rescue the phenotype and thus represent likely severe loss-of-function mutations. In summary, we identified a spectrum of RLIM missense variants causing syndromic XLID and affecting the ubiquitin ligase activity of RLIM, suggesting that enzymatic activity of RLIM is required for normal development, cognition and behavior.

摘要

RLIM,也称为 RNF12,是一种 X 连锁的 E3 泛素连接酶,作为 LIM 结构域转录因子的负调节剂,参与小鼠的 X 染色体失活(XCI)。我们报告了来自九个无关家庭的 84 名个体的遗传和临床发现,其中 8 名个体在 RLIM(环指 LIM 结构域相互作用蛋白)中存在致病性变异。共有 40 名受影响的男性患有 X 连锁智力障碍(XLID)和可变的行为异常,伴有或不伴有先天性畸形。相比之下,44 名杂合子女性携带者认知和行为正常,但有 8 名表现出轻微的身体特征。鉴定的所有 RLIM 变体都是错义变化,与表型共分离,并预测会影响蛋白功能。九个改变的氨基酸中有八个是保守的,位于与相互作用蛋白结合相关的结构域内或 C 末端 RING 指催化结构域内。体外实验表明,RLIM RING 指中的这些氨基酸变化会损害 RLIM 泛素连接酶的活性。在 rlim 突变斑马鱼的体内实验中,野生型 RLIM 挽救了斑马鱼 rlim 表型,而患者特异性错义 RLIM 变体未能挽救表型,因此可能是严重的功能丧失突变。总之,我们鉴定了一系列导致综合征性 XLID 的 RLIM 错义变体,并影响 RLIM 的泛素连接酶活性,表明 RLIM 的酶活性对于正常发育、认知和行为是必需的。

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1
Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic features.《E3泛素蛋白连接酶基因TRIP12单倍剂量不足导致伴有或不伴有自闭症谱系障碍、语言发育迟缓及畸形特征的智力障碍》勘误
Hum Genet. 2017 Aug;136(8):1009-1011. doi: 10.1007/s00439-017-1828-1.
2
E3 Ubiquitin Ligases Neurobiological Mechanisms: Development to Degeneration.E3泛素连接酶的神经生物学机制:从发育到退化
Front Mol Neurosci. 2017 May 19;10:151. doi: 10.3389/fnmol.2017.00151. eCollection 2017.
3
YY1 Haploinsufficiency Causes an Intellectual Disability Syndrome Featuring Transcriptional and Chromatin Dysfunction.
扩展 X 连锁 Tonne-Kalscheuer 综合征(TOKAS)的临床谱:来自胎儿视角的新见解。
J Med Genet. 2024 Aug 29;61(9):824-832. doi: 10.1136/jmg-2024-109854.
4
The role of s-palmitoylation in neurological diseases: implication for zDHHC family.S-棕榈酰化在神经疾病中的作用:对zDHHC家族的影响
Front Pharmacol. 2024 Jan 16;14:1342830. doi: 10.3389/fphar.2023.1342830. eCollection 2023.
5
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6
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FEBS Lett. 2023 Oct;597(19):2375-2415. doi: 10.1002/1873-3468.14723. Epub 2023 Sep 4.
7
Application of exome sequencing for prenatal diagnosis of fetal structural anomalies: clinical experience and lessons learned from a cohort of 1618 fetuses.外显子组测序在胎儿结构畸形产前诊断中的应用:1618 例胎儿队列的临床经验和教训。
Genome Med. 2022 Oct 28;14(1):123. doi: 10.1186/s13073-022-01130-x.
8
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9
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Life Sci Alliance. 2022 Jun 28;5(11). doi: 10.26508/lsa.202101248. Print 2022 Nov.
10
Therapeutic validation and targeting of signalling networks that are dysregulated in intellectual disability.治疗验证和针对智力障碍中失调的信号网络的靶向治疗。
FEBS J. 2023 Mar;290(6):1454-1460. doi: 10.1111/febs.16411. Epub 2022 Feb 28.
YY1单倍剂量不足导致一种以转录和染色质功能障碍为特征的智力障碍综合征。
Am J Hum Genet. 2017 Jun 1;100(6):907-925. doi: 10.1016/j.ajhg.2017.05.006.
4
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Prenat Diagn. 2017 Jun;37(6):602-610. doi: 10.1002/pd.5058. Epub 2017 May 23.
5
An interaction network of mental disorder proteins in neural stem cells.神经干细胞中精神障碍蛋白质的相互作用网络。
Transl Psychiatry. 2017 Apr 4;7(4):e1082. doi: 10.1038/tp.2017.52.
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8
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Hum Genet. 2017 Apr;136(4):377-386. doi: 10.1007/s00439-017-1763-1. Epub 2017 Mar 1.
9
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Mol Neuropsychiatry. 2016 Oct;2(3):133-144. doi: 10.1159/000447358. Epub 2016 Jul 27.
10
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