Institute for Molecular Biology, OE5250, Hannover Medical School, Carl-Neuberg-Str. 1, 30625, Hannover, Germany.
Institute of Biology, University of Hohenheim, Garbenstraße 30, 70593, Stuttgart, Germany.
Sci Rep. 2021 Jun 25;11(1):13333. doi: 10.1038/s41598-021-92495-3.
Cilia are protrusions of the cell surface and composed of hundreds of proteins many of which are evolutionary and functionally well conserved. In cells assembling motile cilia the expression of numerous ciliary components is under the control of the transcription factor FOXJ1. Here, we analyse the evolutionary conserved FOXJ1 target CFAP161 in Xenopus and mouse. In both species Cfap161 expression correlates with the presence of motile cilia and depends on FOXJ1. Tagged CFAP161 localises to the basal bodies of multiciliated cells of the Xenopus larval epidermis, and in mice CFAP161 protein localises to the axoneme. Surprisingly, disruption of the Cfap161 gene in both species did not lead to motile cilia-related phenotypes, which contrasts with the conserved expression in cells carrying motile cilia and high sequence conservation. In mice mutation of Cfap161 stabilised the mutant mRNA making genetic compensation triggered by mRNA decay unlikely. However, genes related to microtubules and cilia, microtubule motor activity and inner dyneins were dysregulated, which might buffer the Cfap161 mutation.
纤毛是细胞表面的突起,由数百种蛋白质组成,其中许多在进化和功能上都很好地保守。在组装运动纤毛的细胞中,许多纤毛成分的表达受到转录因子 FOXJ1 的控制。在这里,我们分析了爪蟾和小鼠中进化保守的 FOXJ1 靶标 CFAP161。在这两种物种中,Cfap161 的表达与运动纤毛的存在相关,并依赖于 FOXJ1。标记的 CFAP161 定位于爪蟾幼虫表皮多纤毛细胞的基体上,而在小鼠中,CFAP161 蛋白定位于轴丝。令人惊讶的是,在这两种物种中破坏 Cfap161 基因并没有导致与运动纤毛相关的表型,这与在携带运动纤毛的细胞中保守表达和高度序列保守形成对比。在小鼠中,Cfap161 基因的突变稳定了突变的 mRNA,使得由 mRNA 降解引发的遗传补偿不太可能发生。然而,与微管和纤毛、微管马达活性和内动力蛋白相关的基因被失调,这可能缓冲 Cfap161 突变的影响。