Suppr超能文献

果蝇同源物 SUPT16H 是与神经发育障碍相关的基因,其以细胞自主的方式对于细胞存活是必需的。

The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survival.

机构信息

Department of Molecular and Human Genetics, Baylor College of Medicine, Houston, TX 77030, USA.

Jan and Dan Duncan Neurological Research Institute, Texas Children's Hospital, Houston, TX 77030, USA.

出版信息

Hum Mol Genet. 2023 Mar 6;32(6):984-997. doi: 10.1093/hmg/ddac259.

Abstract

SUPT16H encodes the large subunit of the FAcilitate Chromatin Transcription (FACT) complex, which functions as a nucleosome organizer during transcription. We identified two individuals from unrelated families carrying de novo missense variants in SUPT16H. The probands exhibit global developmental delay, intellectual disability, epilepsy, facial dysmorphism and brain structural abnormalities. We used Drosophila to characterize two variants: p.T171I and p.G808R. Loss of the fly ortholog, dre4, causes lethality at an early developmental stage. RNAi-mediated knockdown of dre4 in either glia or neurons causes severely reduced eclosion and longevity. Tissue-specific knockdown of dre4 in the eye or wing leads to the loss of these tissues, whereas overexpression of SUPT16H has no dominant effect. Moreover, expression of the reference SUPT16H significantly rescues the loss-of-function phenotypes in the nervous system as well as wing and eye. In contrast, expression of SUPT16H p.T171I or p.G808R rescues the phenotypes poorly, indicating that the variants are partial loss-of-function alleles. While previous studies argued that the developmental arrest caused by loss of dre4 is due to impaired ecdysone production in the prothoracic gland, our data show that dre4 is required for proper cell growth and survival in multiple tissues in a cell-autonomous manner. Altogether, our data indicate that the de novo loss-of-function variants in SUPT16H are indeed associated with developmental and neurological defects observed in the probands.

摘要

SUPT16H编码 FAcilitate Chromatin Transcription(FACT)复合物的大亚基,该复合物在转录过程中作为核小体组织者发挥作用。我们在两个无亲缘关系的家庭中发现了两个携带 SUPT16H 中新发错义变异的个体。先证者表现为全面发育迟缓、智力障碍、癫痫、面型异常和脑结构异常。我们使用果蝇来描述两种变体:p.T171I 和 p.G808R。果蝇同源物 dre4 的缺失导致早期发育阶段的致死性。RNAi 介导的 dre4 在神经胶质或神经元中的敲低导致孵化和寿命严重降低。dre4在眼睛或翅膀中的组织特异性敲低导致这些组织的丧失,而 SUPT16H 的过表达没有显性效应。此外,参考 SUPT16H 的表达显著挽救了神经系统以及翅膀和眼睛的功能丧失表型。相比之下,SUPT16H p.T171I 或 p.G808R 的表达仅能部分挽救表型,表明这些变体是部分功能丧失等位基因。虽然之前的研究认为 dre4 的缺失引起的发育停滞是由于前胸腺中蜕皮激素产生受损,但我们的数据表明,dre4以细胞自主的方式在多个组织中对于细胞的正常生长和存活是必需的。总之,我们的数据表明,SUPT16H中的新发功能丧失变异确实与先证者中观察到的发育和神经缺陷有关。

相似文献

2
De novo variants in cause neurodevelopmental disorders associated with corpus callosum abnormalities.
J Med Genet. 2020 Jul;57(7):461-465. doi: 10.1136/jmedgenet-2019-106193. Epub 2020 Jan 10.
3
Monoallelic and bi-allelic variants in NCDN cause neurodevelopmental delay, intellectual disability, and epilepsy.
Am J Hum Genet. 2021 Apr 1;108(4):739-748. doi: 10.1016/j.ajhg.2021.02.015. Epub 2021 Mar 11.
4
De Novo Variants in CDK19 Are Associated with a Syndrome Involving Intellectual Disability and Epileptic Encephalopathy.
Am J Hum Genet. 2020 May 7;106(5):717-725. doi: 10.1016/j.ajhg.2020.04.001. Epub 2020 Apr 23.
5
Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.
Am J Hum Genet. 2023 Jan 5;110(1):120-145. doi: 10.1016/j.ajhg.2022.11.011. Epub 2022 Dec 16.
6
De novo and bi-allelic variants in AP1G1 cause neurodevelopmental disorder with developmental delay, intellectual disability, and epilepsy.
Am J Hum Genet. 2021 Jul 1;108(7):1330-1341. doi: 10.1016/j.ajhg.2021.05.007. Epub 2021 Jun 7.
7
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.
Am J Hum Genet. 2021 Sep 2;108(9):1669-1691. doi: 10.1016/j.ajhg.2021.06.019. Epub 2021 Jul 26.
8
A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3.
Am J Hum Genet. 2024 Jan 4;111(1):96-118. doi: 10.1016/j.ajhg.2023.12.004.
10
De novo variants in FRYL are associated with developmental delay, intellectual disability, and dysmorphic features.
Am J Hum Genet. 2024 Apr 4;111(4):742-760. doi: 10.1016/j.ajhg.2024.02.007. Epub 2024 Mar 12.

引用本文的文献

本文引用的文献

2
Brain inflammation triggers macrophage invasion across the blood-brain barrier in during pupal stages.
Sci Adv. 2021 Oct 29;7(44):eabh0050. doi: 10.1126/sciadv.abh0050. Epub 2021 Oct 27.
4
TNPO2 variants associate with human developmental delays, neurologic deficits, and dysmorphic features and alter TNPO2 activity in Drosophila.
Am J Hum Genet. 2021 Sep 2;108(9):1669-1691. doi: 10.1016/j.ajhg.2021.06.019. Epub 2021 Jul 26.
5
Haematopoietic stem cell-dependent Notch transcription is mediated by p53 through the Histone chaperone Supt16h.
Nat Cell Biol. 2020 Dec;22(12):1411-1422. doi: 10.1038/s41556-020-00604-7. Epub 2020 Nov 23.
7
The mutational constraint spectrum quantified from variation in 141,456 humans.
Nature. 2020 May;581(7809):434-443. doi: 10.1038/s41586-020-2308-7. Epub 2020 May 27.
8
Large-Scale Transgenic Resource Collections for Loss- and Gain-of-Function Studies.
Genetics. 2020 Apr;214(4):755-767. doi: 10.1534/genetics.119.302964. Epub 2020 Feb 18.
9
A perinuclear microtubule-organizing centre controls nuclear positioning and basement membrane secretion.
Nat Cell Biol. 2020 Mar;22(3):297-309. doi: 10.1038/s41556-020-0470-7. Epub 2020 Feb 17.
10
De novo variants in cause neurodevelopmental disorders associated with corpus callosum abnormalities.
J Med Genet. 2020 Jul;57(7):461-465. doi: 10.1136/jmedgenet-2019-106193. Epub 2020 Jan 10.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验