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Ana1的N端和C端部分的相互作用允许中心粒复制但不允许其延长。

Interactions of N- and C-terminal parts of Ana1 permitting centriole duplication but not elongation.

作者信息

Nagy Agota, Kovacs Levente, Rangone Helene, Fu Jingyan, Ladinsky Mark, Glover David M

机构信息

Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, California 91125, USA.

Babeş-Bolyai University, Cluj-Napoca, Romania.

出版信息

bioRxiv. 2024 Oct 31:2024.10.28.620588. doi: 10.1101/2024.10.28.620588.

Abstract

The conserved process of centriole duplication requires establishment of a Sas6-centred cartwheel initiated by Plk4's phosphorylation of Ana1/STIL. Subsequently the centriole undergoes conversion to a centrosome requiring its radial expansion and elongation, mediated by a network requiring interactions between Cep135, Ana1/Cep295, and Asterless/Cep152. Here we show that mutant alleles encoding overlapping N- and C-terminal parts of Ana1 are capable of intragenic complementation to rescue radial expansion. This permits recruitment of Asl and thereby centriole duplication and mechanosensory cilia formation to restore the coordination defects of these mutants. This genetic combination also rescues centriole duplication in the male germ line but does not rescue the elongation of the triplet microtubule-containing centrioles of primary spermatocytes and consequently these males are coordinated but sterile. Such centriole elongation is rescued by the continuous, full-length Ana1 sequence. We define a region that when deleted within otherwise intact Ana1 does not permit primary spermatocyte centrioles to elongate but still allows recruitment of Asl. Our findings point to differing demands upon the physical organization of Ana1 for the distinct processes of radial expansion and elongation of centrioles.

摘要

中心粒复制的保守过程需要由Plk4对Ana1/STIL的磷酸化启动,建立以Sas6为中心的轮辐结构。随后,中心粒经历向中心体的转变,这需要其径向扩展和伸长,由一个需要Cep135、Ana1/Cep295和Asterless/Cep152之间相互作用的网络介导。在这里,我们表明,编码Ana1重叠的N端和C端部分的突变等位基因能够进行基因内互补以挽救径向扩展。这允许招募Asl,从而实现中心粒复制和机械感觉纤毛形成,以恢复这些突变体的协调缺陷。这种遗传组合也挽救了雄性生殖系中的中心粒复制,但不能挽救初级精母细胞中含三联体微管的中心粒的伸长,因此这些雄性是协调的但不育。这种中心粒伸长可通过连续的全长Ana1序列挽救。我们定义了一个区域,当在其他方面完整的Ana1内缺失该区域时,不允许初级精母细胞中心粒伸长,但仍允许招募Asl。我们的研究结果表明,对于中心粒径向扩展和伸长的不同过程,对Ana1的物理组织有不同的要求。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/41ad/11565839/0502c71b9597/nihpp-2024.10.28.620588v1-f0001.jpg

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