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驱动蛋白-5 KIF11功能丧失通过染色体不稳定和细胞周期停滞导致小头畸形、脉络膜视网膜病变和发育障碍。

Loss-of-function of kinesin-5 KIF11 causes microcephaly, chorioretinopathy, and developmental disorders through chromosome instability and cell cycle arrest.

作者信息

Zhou Yi, Xu Meng-Fei, Chen Jie, Zhang Jing-Lian, Wang Xin-Yao, Huang Min-Hui, Wei Ya-Lan, She Zhen-Yu

机构信息

Department of Cell Biology and Genetics, The School of Basic Medical Sciences, Fujian Medical University, Fuzhou, Fujian, 350122, China; Key Laboratory of Stem Cell Engineering and Regenerative Medicine, Fujian Province University, Fuzhou, Fujian, 350122, China.

Medical Research Center, Fujian Maternity and Child Health Hospital, Fuzhou, Fujian, 350001, China; College of Clinical Medicine for Obstetrics & Gynecology and Pediatrics, Fujian Medical University, Fuzhou, Fujian, 350122, China.

出版信息

Exp Cell Res. 2024 Mar 1;436(1):113975. doi: 10.1016/j.yexcr.2024.113975. Epub 2024 Feb 16.

DOI:10.1016/j.yexcr.2024.113975
PMID:38367657
Abstract

Kinesin motors play a fundamental role in development by controlling intracellular transport, spindle assembly, and microtubule organization. In humans, patients carrying mutations in KIF11 suffer from an autosomal dominant inheritable disease called microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR). While mitotic functions of KIF11 proteins have been well documented in centrosome separation and spindle assembly, cellular mechanisms underlying KIF11 dysfunction and MCLMR remain unclear. In this study, we generate KIF11-inhibition chick and zebrafish models and find that KIF11 inhibition results in microcephaly, chorioretinopathy, and severe developmental defects in vivo. Notably, loss-of-function of KIF11 causes the formation of monopolar spindle and chromosome misalignment, which finally contribute to cell cycle arrest, chromosome instability, and cell death. Our results demonstrate that KIF11 is crucial for spindle assembly, chromosome alignment, and cell cycle progression of progenitor stem cells, indicating a potential link between polyploidy and MCLMR. Our data have revealed that KIF11 inhibition cause microcephaly, chorioretinopathy, and development disorders through the formation of monopolar spindle, polyploid, and cell cycle arrest.

摘要

驱动蛋白在通过控制细胞内运输、纺锤体组装和微管组织来进行发育过程中发挥着重要作用。在人类中,携带KIF11突变的患者患有常染色体显性遗传疾病,称为小头畸形,伴有或不伴有脉络膜视网膜病变、淋巴水肿或智力迟钝(MCLMR)。虽然KIF11蛋白的有丝分裂功能在中心体分离和纺锤体组装方面已有充分记录,但KIF11功能障碍和MCLMR的细胞机制仍不清楚。在本研究中,我们构建了KIF11抑制的鸡和斑马鱼模型,发现KIF11抑制在体内导致小头畸形、脉络膜视网膜病变和严重的发育缺陷。值得注意的是,KIF11功能丧失会导致单极纺锤体的形成和染色体排列错误,最终导致细胞周期停滞、染色体不稳定和细胞死亡。我们的结果表明,KIF11对于祖干细胞的纺锤体组装、染色体排列和细胞周期进程至关重要,这表明多倍体与MCLMR之间存在潜在联系。我们的数据显示,KIF11抑制通过单极纺锤体、多倍体的形成和细胞周期停滞导致小头畸形、脉络膜视网膜病变和发育障碍。

相似文献

1
Loss-of-function of kinesin-5 KIF11 causes microcephaly, chorioretinopathy, and developmental disorders through chromosome instability and cell cycle arrest.驱动蛋白-5 KIF11功能丧失通过染色体不稳定和细胞周期停滞导致小头畸形、脉络膜视网膜病变和发育障碍。
Exp Cell Res. 2024 Mar 1;436(1):113975. doi: 10.1016/j.yexcr.2024.113975. Epub 2024 Feb 16.
2
Mutations in KIF11 cause autosomal-dominant microcephaly variably associated with congenital lymphedema and chorioretinopathy.KIF11 基因突变导致常染色体显性小头畸形,可伴有先天性淋巴水肿和脉络膜视网膜病变。
Am J Hum Genet. 2012 Feb 10;90(2):356-62. doi: 10.1016/j.ajhg.2011.12.018. Epub 2012 Jan 26.
3
Ocular manifestations of microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) syndrome associated with mutations in KIF11.与KIF11基因突变相关的小头畸形伴或不伴脉络膜视网膜病变、淋巴水肿或智力障碍(MCLID)综合征的眼部表现。
Acta Ophthalmol. 2016 Feb;94(1):92-8. doi: 10.1111/aos.12759. Epub 2015 May 21.
4
No evidence of locus heterogeneity in familial microcephaly with or without chorioretinopathy, lymphedema, or mental retardation syndrome.在伴有或不伴有脉络膜视网膜病变、淋巴水肿或智力迟钝综合征的家族性小头畸形中,没有基因座异质性的证据。
Orphanet J Rare Dis. 2015 May 2;10:52. doi: 10.1186/s13023-015-0271-4.
5
Microcephaly with or without chorioretinopathy, lymphoedema, or mental retardation (MCLMR): review of phenotype associated with KIF11 mutations.伴有或不伴有脉络膜视网膜病变、淋巴水肿或智力障碍的小头畸形(MCLMR):与KIF11突变相关的表型综述
Eur J Hum Genet. 2014 Jul;22(7):881-7. doi: 10.1038/ejhg.2013.263. Epub 2013 Nov 27.
6
Congenital microcephaly and chorioretinopathy due to de novo heterozygous KIF11 mutations: five novel mutations and review of the literature.新发杂合KIF11突变导致的先天性小头畸形和脉络膜视网膜病变:五个新突变及文献综述
Am J Med Genet A. 2014 Nov;164A(11):2879-86. doi: 10.1002/ajmg.a.36707. Epub 2014 Aug 12.
7
Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations.家族性渗出性玻璃体视网膜病变和微小头畸形、淋巴水肿及脉络膜视网膜发育不良与 KIF11 突变相关的表型重叠。
JAMA Ophthalmol. 2014 Dec;132(12):1393-9. doi: 10.1001/jamaophthalmol.2014.2814.
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Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation (MCLMR)- the new lacunae: a case report.无脑回畸形伴或不伴脉络膜视网膜病变、淋巴水肿或智力障碍(MCLMR)——新的腔隙:病例报告。
BMC Ophthalmol. 2024 Aug 26;24(1):372. doi: 10.1186/s12886-024-03627-y.
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A Novel Variant of the KIF11 Gene, c.2922G>T, Is Associated with Microcephaly by Affecting RNA Splicing.一种新型的 KIF11 基因突变,c.2922G>T,通过影响 RNA 剪接导致小头畸形。
Dev Neurosci. 2022;44(2):113-120. doi: 10.1159/000518923. Epub 2021 Aug 31.
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Novel variant of KIF11 associated with MCLMR syndrome.与MCLMR综合征相关的KIF11新变体。
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引用本文的文献

1
Novel Mutation Associated with Microcephaly, Chorioretinopathy and Impaired Intellectual Development: 20 Years of Follow-Up.与小头畸形、脉络膜视网膜病变及智力发育受损相关的新型突变:20年随访
Children (Basel). 2025 Apr 26;12(5):560. doi: 10.3390/children12050560.
2
The Kinesin Eg5 Inhibitor K858 Enhances Radiosensitivity in Esophageal Squamous Cell Carcinoma and Affects the Expression of Epithelial-mesenchymal Transition Related Markers: and Studies.驱动蛋白Eg5抑制剂K858增强食管鳞状细胞癌的放射敏感性并影响上皮-间质转化相关标志物的表达:体内和体外研究
Anticancer Agents Med Chem. 2025;25(15):1142-1159. doi: 10.2174/0118715206373782250211104402.
3
DNA tensiometer reveals catch-bond detachment kinetics of kinesin-1, -2 and -3.
DNA张力计揭示驱动蛋白-1、-2和-3的捕获键解离动力学。
bioRxiv. 2025 Mar 25:2024.12.03.626575. doi: 10.1101/2024.12.03.626575.