Ezer Shlomit, Ronin Nathan, Yanovsky-Dagan Shira, Rotem-Bamberger Shahar, Halstuk Orli, Wexler Yair, Ben-Moshe Zohar, Plaschkes Inbar, Benyamini Hadar, Saada Ann, Inbal Adi, Harel Tamar
Department of Genetics, Hadassah Medical Organization, Jerusalem, Israel.
Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.
Orphanet J Rare Dis. 2025 Apr 15;20(1):181. doi: 10.1186/s13023-025-03709-0.
ATAD3A, a nuclear gene encoding the ATAD3A protein, has diverse roles in mitochondrial processes, encompassing mitochondrial dynamics, mitochondrial DNA maintenance, metabolic pathways and inter-organellar interactions. Pathogenic variants in this gene cause neurological diseases in humans with recognizable genotype-phenotype correlations. Yet, gaps in knowledge remain regarding the underlying pathogenesis.
To further investigate the gene function and its implication in health and disease, we utilized CRISPR/Cas9 genome editing to generate a knockout model of the zebrafish ortholog gene, atad3. We characterized the phenotype of the null model, performed mitochondrial and functional tests, and compared the transcriptome of null embryos to their healthy siblings.
Analysis of atad3-null zebrafish embryos revealed microcephaly, small eyes, pericardial edema and musculature thinning, closely mirroring the human rare disease phenotype. Larvae exhibited delayed hatching and embryonic lethality by 13 days post-fertilization (dpf). Locomotor activity, ATP content, mitochondrial content, and mitochondrial activity were all reduced in the mutant embryos. Transcriptome analysis at 3 dpf via RNA-sequencing indicated decline in most mitochondrial pathways, accompanied by a global upregulation of cytosolic tRNA synthetases, presumably secondary to mitochondrial stress and possibly endoplasmic reticulum (ER)-stress. Differential expression of select genes was corroborated in fibroblasts from an affected individual.
The atad3-null zebrafish model emerges as a reliable representation of human ATAD3A-associated disorders, with similarities in differentially expressed pathways and processes. Furthermore, our study underscores mitochondrial dysfunction as the primary underlying pathogenic mechanism in ATAD3A-associated disorders and identifies potential readouts for therapeutic studies.
ATAD3A是一个编码ATAD3A蛋白的核基因,在线粒体过程中具有多种作用,包括线粒体动力学、线粒体DNA维持、代谢途径和细胞器间相互作用。该基因的致病变体在人类中会导致具有可识别基因型-表型相关性的神经疾病。然而,关于潜在发病机制的知识仍存在空白。
为了进一步研究该基因的功能及其在健康和疾病中的意义,我们利用CRISPR/Cas9基因组编辑技术构建了斑马鱼直系同源基因atad3的敲除模型。我们对该缺失模型的表型进行了特征描述,进行了线粒体和功能测试,并将缺失胚胎的转录组与其健康的同胞进行了比较。
对atad3基因缺失的斑马鱼胚胎的分析显示出小头畸形、小眼睛、心包水肿和肌肉组织变薄,与人类罕见疾病表型极为相似。幼虫在受精后13天(dpf)表现出孵化延迟和胚胎致死率。突变胚胎的运动活性、ATP含量、线粒体含量和线粒体活性均降低。在3 dpf通过RNA测序进行的转录组分析表明,大多数线粒体途径下降,同时胞质tRNA合成酶整体上调,推测这是线粒体应激以及可能的内质网(ER)应激的继发结果。在一名受影响个体的成纤维细胞中证实了选定基因的差异表达。
atad3基因缺失的斑马鱼模型成为人类ATAD3A相关疾病的可靠模型,在差异表达的途径和过程方面具有相似性。此外,我们的研究强调线粒体功能障碍是ATAD3A相关疾病的主要潜在致病机制,并确定了治疗研究的潜在指标。