Abstract / Description of output
Microtubule actin crosslinking factor 1 (MACF1) plays a role in the coordination of microtubules and actin in multiple cellular processes. Here, we show that MACF1 is also critical for ciliogenesis in multiple cell types. Ablation of Macf1 in the developing retina abolishes ciliogenesis, and basal bodies fail to dock to ciliary vesicles or migrate apically. Photoreceptor polarity is randomized, while inner retinal cells laminate correctly, suggesting that photoreceptor maturation is guided by polarity cues provided by cilia. Deletion of MACF1 in adult photoreceptors causes reversal of basal body docking and loss of outer segments, reflecting a continuous requirement for MACF1 function. MACF1 also interacts with the ciliary proteins MKKS and TALPID3. We propose that a disruption of trafficking across microtubles to actin filaments underlies the ciliogenesis defect in cells lacking MACF1 and that MKKS and TALPID3 are involved in the coordination of microtubule and actin interactions.
Original language | English |
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Pages (from-to) | 1399-1413 |
Number of pages | 15 |
Journal | Cell Reports |
Volume | 17 |
Issue number | 5 |
DOIs | |
Publication status | Published - 25 Oct 2016 |
Keywords / Materials (for Non-textual outputs)
- retina
- cilia
- ciliogenesis
- ciliopathy
- polarity
- retinal degeneration
- basal body
- centrosome
- microtubule
- actin
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Megan Davey
- Royal (Dick) School of Veterinary Studies - Senior Research Fellow
Person: Academic: Research Active