BACKGROUND: Mutations in centrosomal protein genes have been identified in a number of genetic diseases in brain development, including microcephaly. Centrosomal P4.1-associated protein (CPAP) is one of the causal genes implicated in primary microcephaly. We previously proposed that CPAP is essential for mother centriole maturation during mitosis. METHODS: We immunostained CPAP-depleted cells using the ninein antibody, which selectively detects subdistal appendages in mature mother centrioles. RESULTS: Ninein signals were significantly impaired in CPAP-depleted cells. CONCLUSION: The results suggest that CPAP is required for mother centriole maturation in mammalian cells. The selective absence of centriolar appendages in young mother centrioles may be responsible for asymmetric spindle pole formation in CPAP-depleted cells.
Determination of Mother Centriole Maturation in CPAP-Depleted Cells Using the Ninein Antibody.
利用 Ninein 抗体测定 CPAP 耗竭细胞中母中心粒的成熟度
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作者:Lee Miseon, Rhee Kunsoo
| 期刊: | Endocrinology and Metabolism | 影响因子: | 4.200 |
| 时间: | 2015 | 起止号: | 2015 Mar 27; 30(1):53-7 |
| doi: | 10.3803/EnM.2015.30.1.53 | 研究方向: | 细胞生物学 |
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