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A KDM5-Prospero transcriptional axis functions during early neurodevelopment to regulate mushroom body formation.KDM5-Prospero 转录轴在早期神经发育过程中发挥作用,调节蘑菇体的形成。
Elife. 2021 Mar 17;10:e63886. doi: 10.7554/eLife.63886.
2
The histone demethylase KDM5 is required for synaptic structure and function at the Drosophila neuromuscular junction.组蛋白去甲基化酶 KDM5 对于果蝇神经肌肉接头的突触结构和功能是必需的。
Cell Rep. 2021 Feb 16;34(7):108753. doi: 10.1016/j.celrep.2021.108753.
3
Mutually suppressive roles of KMT2A and KDM5C in behaviour, neuronal structure, and histone H3K4 methylation.KMT2A 和 KDM5C 在行为、神经元结构和组蛋白 H3K4 甲基化中的相互抑制作用。
Commun Biol. 2020 Jun 1;3(1):278. doi: 10.1038/s42003-020-1001-6.
4
Further delineation of the female phenotype with KDM5C disease causing variants: 19 new individuals and review of the literature.进一步描述 KDM5C 致病变异导致的女性表型:19 例新病例及文献复习。
Clin Genet. 2020 Jul;98(1):43-55. doi: 10.1111/cge.13755. Epub 2020 May 29.
5
Down syndrome.唐氏综合征。
Nat Rev Dis Primers. 2020 Feb 6;6(1):9. doi: 10.1038/s41572-019-0143-7.
6
The histone demethylase KDM5 controls developmental timing in by promoting prothoracic gland endocycles.组蛋白去甲基化酶 KDM5 通过促进前胸腺内周期促进的发育定时。
Development. 2019 Dec 20;146(24):dev182568. doi: 10.1242/dev.182568.
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The Histone Demethylase KDM5 Is Essential for Larval Growth in .组蛋白去甲基化酶 KDM5 对 的幼虫生长至关重要。
Genetics. 2018 Jul;209(3):773-787. doi: 10.1534/genetics.118.301004. Epub 2018 May 15.
8
Altered Gene-Regulatory Function of KDM5C by a Novel Mutation Associated With Autism and Intellectual Disability.与自闭症和智力残疾相关的新型突变导致KDM5C基因调控功能改变。
Front Mol Neurosci. 2018 Apr 4;11:104. doi: 10.3389/fnmol.2018.00104. eCollection 2018.
9
A Drosophila Model of Intellectual Disability Caused by Mutations in the Histone Demethylase KDM5.果蝇模型研究组蛋白去甲基化酶 KDM5 突变导致的智力残疾
Cell Rep. 2018 Feb 27;22(9):2359-2369. doi: 10.1016/j.celrep.2018.02.018.
10
Peripheral blood epi-signature of Claes-Jensen syndrome enables sensitive and specific identification of patients and healthy carriers with pathogenic mutations in .Claes-Jensen 综合征外周血 epi 特征可敏感且特异地识别. 致病性突变的患者和健康携带者
Clin Epigenetics. 2018 Feb 14;10:21. doi: 10.1186/s13148-018-0453-8. eCollection 2018.

照顾者报告的 KDM5C 致病性变异患儿特征。

Caregiver-reported characteristics of children diagnosed with pathogenic variants in KDM5C.

机构信息

Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, USA.

Rose F. Kennedy Children's Evaluation and Rehabilitation Center, The Children's Hospital at Montefiore, Bronx, New York, USA.

出版信息

Am J Med Genet A. 2021 Oct;185(10):2951-2958. doi: 10.1002/ajmg.a.62381. Epub 2021 Jun 4.

DOI:10.1002/ajmg.a.62381
PMID:34089235
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8446302/
Abstract

Loss of function variants in the lysine demethylase 5C (KDM5C) gene account for approximately 0.7-2.8% of X-linked intellectual disability (ID) cases and pose significant burdens for patients and their caregivers. To date, 45 unique variants in KDM5C have been reported in individuals with ID. As a rare disorder, its etiology and natural history remain an area of active investigation, with treatment limited to symptom management. Previous studies have found that males present with moderate to severe ID with significant syndromic comorbidities such as epilepsy, short stature, and craniofacial abnormalities. Although not as well characterized, females have been reported to predominantly display mild to moderate ID with approximately half being asymptomatic. Here, we present caregiver-reported data for 37 unrelated individuals with pathogenic variants in KDM5C; the largest cohort reported to-date. We find that up to 70% of affected females were reported to display syndromic features including gastrointestinal dysfunction and hearing impairment. Additionally, more than half of individuals reported a diagnosis of autism spectrum disorder or described features consistent with this spectrum. Our data thus provide further evidence of sexually dimorphic heterogeneity in disease presentation and suggest that pathogenic variants in KDM5C may be more common than previously assumed.

摘要

赖氨酸去甲基酶 5C(KDM5C)基因的功能丧失变异约占 X 连锁智力障碍(ID)病例的 0.7-2.8%,给患者及其照顾者带来了巨大的负担。迄今为止,已有 45 种独特的 KDM5C 变异在 ID 患者中被报道。由于这种疾病比较罕见,其病因和自然史仍然是一个活跃的研究领域,治疗方法仅限于症状管理。先前的研究发现,男性表现为中重度 ID,并伴有明显的综合征性合并症,如癫痫、身材矮小和颅面异常。虽然女性的特征不如男性明显,但据报道,她们主要表现为轻度至中度 ID,约有一半无症状。在这里,我们提供了 37 名无关的 KDM5C 致病性变异患者的照顾者报告数据;这是迄今为止报告的最大队列。我们发现,多达 70%的受影响女性被报告有综合征特征,包括胃肠道功能障碍和听力损伤。此外,超过一半的患者被诊断为自闭症谱系障碍或具有与该谱系一致的特征。我们的数据因此提供了疾病表现存在性别二态性异质性的进一步证据,并表明 KDM5C 的致病性变异可能比之前假设的更为常见。