Two distinct phenotypes in Snijders Blok-Campeau syndrome and characterization of the behavioral phenotype in a zebrafish model.

IF 3.7 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Yumi Enomoto, Takashi Shiromizu, Sakyo Yasojima, Junko Koiwa, Yukiko Kuroda, Hiroaki Ito, Mizuki Yuge, Momoka Ohkawa, Ryohei Shibata, Hiroaki Murakami, Takuya Naruto, Shizuka Shiiya, Naoko Omotani, Yuhei Nishimura, Kenji Kurosawa
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引用次数: 0

Abstract

Chromatin remodeling is an important system controlling gene expression. CHD3, which is a causative gene of Snijders Blok-Campeau syndrome (SNIBCPS), is a member of the chromodomain helicase DNA-binding (CHD) family related to chromatin remodeling. SNIBCPS is characterized by developmental delay (DD), intellectual disability (ID), macrocephaly, and facial features including a prominent forehead and hypertelorism. Hypersociability/overfriendliness is a notable behavioral feature in patients. Here, we describe five SNIBCPS patients with CHD3 variants from four families, including a sibling pair caused by parental gonosomal mosaicism. We observed two distinct phenotypes in our patients in accordance with previous observations. Phenotype 1: macrocephaly, hypertelorism, overgrowth, DD, and ID; and Phenotype 2: microcephaly, growth retardation, DD, and ID. Phenotype 1 was consistent with the typical SNIBCPS phenotype, while Phenotype 2 was distinct. To understand further the features of the patients with SNIBCPS, we generated chd3-knockout (KO) zebrafish using CRISPR-Cas9 genome editing. No morphological changes were observed in chd3-KO zebrafish. However, behavioral tests showed that chd3-KO zebrafish had strong and sustained interest in others, and were less aggressive toward others, suggesting a recapitulation of the hypersociability/overfriendliness phenotype in patients with SNIBCPS. Metabolomic analysis using whole brains showed changes in metabolites processed by specific mitochondrial enzymes in chd3-KO zebrafish. The administration of metformin, which reportedly ameliorates mitochondrial dysfunction and behavioral abnormalities, attenuated the abnormal behavior of chd3-KO zebrafish. Our study helps delineate the phenotypes of patients with SNIBCPS, provides insights into a characteristic behavior of the disease, and suggests a potential treatment to improve the behavioral symptoms of patients.

Snijders block - campeau综合征的两种不同表型和斑马鱼模型中行为表型的表征。
染色质重塑是调控基因表达的重要系统。CHD3是与染色质重塑相关的染色体结构解旋酶dna结合(CHD)家族成员,是Snijders block - campeau综合征(SNIBCPS)的致病基因。SNIBCPS的特征是发育迟缓(DD)、智力残疾(ID)、大头畸形和面部特征,包括前额突出和远端畸形。过度社交/过度友好是患者显著的行为特征。在这里,我们描述了来自四个家族的5例SNIBCPS CHD3变异患者,包括一对由亲代淋体嵌合引起的兄弟姐妹。根据先前的观察,我们在患者中观察到两种不同的表型。表型1:大头畸形、远端畸形、过度生长、DD、ID;表型2:小头畸形、生长迟缓、DD和ID。表型1与典型的SNIBCPS表型一致,而表型2则不同。为了进一步了解SNIBCPS患者的特征,我们使用CRISPR-Cas9基因组编辑技术生成了chd3敲除(KO)斑马鱼。chd3-KO斑马鱼未见形态学改变。然而,行为测试显示,chd3-KO斑马鱼对他人有强烈和持续的兴趣,并且对他人的攻击性较低,这表明SNIBCPS患者的过度社交/过度友好表型重现。全脑代谢组学分析显示chd3-KO斑马鱼特定线粒体酶处理的代谢物发生了变化。据报道,二甲双胍可以改善线粒体功能障碍和行为异常,减轻chd3-KO斑马鱼的异常行为。我们的研究有助于描述SNIBCPS患者的表型,提供了对疾病特征行为的见解,并提出了改善患者行为症状的潜在治疗方法。
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来源期刊
European Journal of Human Genetics
European Journal of Human Genetics 生物-生化与分子生物学
CiteScore
9.90
自引率
5.80%
发文量
216
审稿时长
2 months
期刊介绍: The European Journal of Human Genetics is the official journal of the European Society of Human Genetics, publishing high-quality, original research papers, short reports and reviews in the rapidly expanding field of human genetics and genomics. It covers molecular, clinical and cytogenetics, interfacing between advanced biomedical research and the clinician, and bridging the great diversity of facilities, resources and viewpoints in the genetics community. Key areas include: -Monogenic and multifactorial disorders -Development and malformation -Hereditary cancer -Medical Genomics -Gene mapping and functional studies -Genotype-phenotype correlations -Genetic variation and genome diversity -Statistical and computational genetics -Bioinformatics -Advances in diagnostics -Therapy and prevention -Animal models -Genetic services -Community genetics
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