The Heterotaxy Gene CCDC11 Is Important for Cytokinesis via RhoA Regulation.

Saurabh S Kulkarni, Rachel E Stephenson, Sarah Amalraj, Angelo Arrigo, Ewelina Betleja, James J Moresco, John R Yates, Moe R Mahjoub, Ann L Miller, Mustafa K Khokha
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Abstract

Mutations in CCDC11 (cfap53) have been identified in multiple patients with heterotaxy (Htx), a disorder of left-right (LR) patterning of the internal organs. In Xenopus, depletion of Ccdc11 causes defects in LR patterning, recapitulating the patient phenotype. Upon Ccdc11 depletion, monociliated cells of the Left-Right Organizer (LRO) exhibit multiple cilia per cell. Unexpectedly, we found that Ccdc11 is necessary for successful cytokinesis, explaining the multiciliation phenotype observed in Ccdc11-depleted cells. The small GTPase RhoA is critical for cytokinesis, and our Ccdc11 depletion phenotypes are reminiscent of RhoA loss of function. Here, we demonstrate that during cytokinesis CCDC11 is localized to the cytokinetic contractile ring overlapping with RhoA, and CCDC11 regulates total RhoA protein levels. Our results connect CCDC11 to cytokinesis and LR patterning via RhoA regulation, providing a potential mechanism for heterotaxy disease pathogenesis.

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异位基因 CCDC11 通过 RhoA 调节对细胞分裂很重要
CCDC11 (cfap53)突变已在多名异位症(Htx)患者中发现,异位症是一种内脏器官左右(LR)模式化障碍。在爪蟾中,Ccdc11的缺失会导致LR模式化缺陷,重现患者的表型。Ccdc11 缺失后,左-右器官(LRO)的单纤毛细胞表现出每个细胞多个纤毛。意想不到的是,我们发现 Ccdc11 是细胞分裂成功的必要条件,这也解释了在 Ccdc11 缺失的细胞中观察到的多纤毛表型。小 GTPase RhoA 对细胞运动至关重要,我们的 Ccdc11 缺失表型与 RhoA 功能缺失相似。在这里,我们证明了在细胞运动过程中,CCDC11 定位于与 RhoA 重叠的细胞运动收缩环上,并且 CCDC11 可调节 RhoA 蛋白的总水平。我们的研究结果通过 RhoA 的调控将 CCDC11 与细胞分裂和 LR 模式化联系起来,为异位发育疾病的发病机制提供了一种潜在的机制。
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