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Determination of Mother Centriole Maturation in CPAP-Depleted Cells Using the Ninein Antibody
Endocrinology and Metabolism ; : 53-57, 2015.
Article in English | WPRIM | ID: wpr-150119
ABSTRACT

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.
Subject(s)

Full text: Available Index: WPRIM (Western Pacific) Main subject: Brain / Cell Cycle / Centrioles / Centrosome / Spindle Poles / Microcephaly / Mitosis / Mothers Limits: Humans Language: English Journal: Endocrinology and Metabolism Year: 2015 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Brain / Cell Cycle / Centrioles / Centrosome / Spindle Poles / Microcephaly / Mitosis / Mothers Limits: Humans Language: English Journal: Endocrinology and Metabolism Year: 2015 Type: Article