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迪多基因突变引发围产期死亡,并在存活的成年小鼠中产生脑部异常和行为改变。

Dido mutations trigger perinatal death and generate brain abnormalities and behavioral alterations in surviving adult mice.

作者信息

Villares Ricardo, Gutiérrez Julio, Fütterer Agnes, Trachana Varvara, Gutiérrez del Burgo Fernando, Martínez-A Carlos

机构信息

Department of Immunology and Oncology, Centro Nacional de Biotecnología, Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid, 28049 Madrid, Spain.

Department of Immunology and Oncology, Centro Nacional de Biotecnología, Consejo Superior de Investigaciones Científicas, Universidad Autónoma de Madrid, 28049 Madrid, Spain

出版信息

Proc Natl Acad Sci U S A. 2015 Apr 14;112(15):4803-8. doi: 10.1073/pnas.1419300112. Epub 2015 Mar 30.

Abstract

Nearly all vertebrate cells have a single cilium protruding from their surface. This threadlike organelle, once considered vestigial, is now seen as a pivotal element for detection of extracellular signals that trigger crucial morphogenetic pathways. We recently proposed a role for Dido3, the main product of the death inducer-obliterator (dido) gene, in histone deacetylase 6 delivery to the primary cilium [Sánchez de Diego A, et al. (2014) Nat Commun 5:3500]. Here we used mice that express truncated forms of Dido proteins to determine the link with cilium-associated disorders. We describe dido mutant mice with high incidence of perinatal lethality and distinct neurodevelopmental, morphogenetic, and metabolic alterations. The anatomical abnormalities were related to brain and orofacial development, consistent with the known roles of primary cilia in brain patterning, hydrocephalus incidence, and cleft palate. Mutant mice that reached adulthood showed reduced life expectancy, brain malformations including hippocampus hypoplasia and agenesis of corpus callosum, as well as neuromuscular and behavioral alterations. These mice can be considered a model for the study of ciliopathies and provide information for assessing diagnosis and therapy of genetic disorders linked to the deregulation of primary cilia.

摘要

几乎所有脊椎动物细胞都有一根从其表面伸出的单根纤毛。这种丝状细胞器曾被认为是退化器官,现在则被视为检测触发关键形态发生途径的细胞外信号的关键元件。我们最近提出死亡诱导物消除因子(dido)基因的主要产物Dido3在组蛋白去乙酰化酶6转运至初级纤毛过程中发挥作用[Sánchez de Diego A等人(2014年),《自然通讯》5:3500]。在此,我们使用表达截短形式Dido蛋白的小鼠来确定与纤毛相关疾病的联系。我们描述了围产期致死率高且伴有明显神经发育、形态发生和代谢改变的dido突变小鼠。解剖学异常与脑和口面部发育有关,这与初级纤毛在脑模式形成、脑积水发生率和腭裂方面的已知作用一致。存活至成年的突变小鼠预期寿命缩短,出现脑畸形,包括海马体发育不全和胼胝体发育不全,以及神经肌肉和行为改变。这些小鼠可被视为研究纤毛病的模型,并为评估与初级纤毛失调相关的遗传疾病的诊断和治疗提供信息。

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