CEP78 functions downstream of CEP350 to control biogenesis of primary cilia by negatively regulating CP110 levels
CEP78 is a centrosomal protein implicated in ciliogenesis and ciliary length control, and mutations in the CEP78 gene cause retinal cone-rod dystrophy associated with hearing loss. However, the mechanism by which CEP78 affects cilia formation is unknown. Based on a recently discovered disease-causin...
Main Authors: | , , , , , , , , , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
eLife Sciences Publications Ltd
2021-07-01
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Series: | eLife |
Subjects: | |
Online Access: | https://elifesciences.org/articles/63731 |