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WDR4 缺失导致的纤毛缺陷与蛋白酶体过度活跃和泛素短缺有关。

Cilia defects upon loss of WDR4 are linked to proteasomal hyperactivity and ubiquitin shortage.

机构信息

Department of Experimental and Clinical Pharmacology and Pharmacogenomics, Section of Pharmacogenomics, Eberhard-Karls-University Tübingen, 72074, Tübingen, Germany.

Genome Damage and Stability Centre, University of Sussex, Brighton, BN1 9RQ, UK.

出版信息

Cell Death Dis. 2024 Sep 9;15(9):660. doi: 10.1038/s41419-024-07042-5.

Abstract

The WD repeat-containing protein 4 (WDR4) has repeatedly been associated with primary microcephaly, a condition of impaired brain and skull growth. Often, faulty centrosomes cause microcephaly, yet aberrant cilia may also be involved. Here, we show using a combination of approaches in human fibroblasts, zebrafish embryos and patient-derived cells that WDR4 facilitates cilium formation. Molecularly, we associated WDR4 loss-of-function with increased protein synthesis and concomitant upregulation of proteasomal activity, while ubiquitin precursor pools are reduced. Inhibition of proteasomal activity as well as supplementation with free ubiquitin restored normal ciliogenesis. Proteasome inhibition ameliorated microcephaly phenotypes. Thus, we propose that WDR4 loss-of-function impairs head growth and neurogenesis via aberrant cilia formation, initially caused by disturbed protein and ubiquitin homeostasis.

摘要

WD 重复蛋白 4(WDR4)与原发性小头畸形(一种大脑和颅骨生长受损的疾病)反复相关。通常,有缺陷的中心体导致小头畸形,但异常的纤毛也可能涉及其中。在这里,我们使用人类成纤维细胞、斑马鱼胚胎和患者来源的细胞的组合方法表明,WDR4 有助于纤毛形成。从分子角度来看,我们将 WDR4 功能丧失与蛋白质合成增加以及蛋白酶体活性的伴随上调相关联,而泛素前体池减少。蛋白酶体抑制以及补充游离泛素可恢复正常的纤毛发生。蛋白酶体抑制可改善小头畸形表型。因此,我们提出 WDR4 功能丧失通过异常的纤毛形成损害头部生长和神经发生,最初是由蛋白质和泛素稳态失调引起的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5f10/11384789/44ffe5f98b62/41419_2024_7042_Fig1_HTML.jpg

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