PUBLICATION

miR-129-3p controls cilia assembly by regulating CP110 and actin dynamics

Authors
Cao, J., Shen, Y., Zhu, L., Xu, Y., Zhou, Y., Wu, Z., Li, Y., Yan, X., and Zhu, X.
ID
ZDB-PUB-120612-8
Date
2012
Source
Nature cell biology   14(7): 697-706 (Journal)
Registered Authors
Cao, Jingli
Keywords
none
MeSH Terms
  • Humans
  • RNA Processing, Post-Transcriptional
  • Signal Transduction
  • Transfection
  • Gene Expression Regulation, Developmental
  • Gene Knockdown Techniques
  • Phosphoproteins/genetics
  • Phosphoproteins/metabolism*
  • Base Sequence
  • MicroRNAs/metabolism*
  • Genes, Reporter
  • Cell Proliferation
  • Time Factors
  • Carrier Proteins/genetics
  • Carrier Proteins/metabolism
  • HEK293 Cells
  • Microfilament Proteins/genetics
  • Microfilament Proteins/metabolism
  • Animals
  • Mice
  • LIM Domain Proteins/genetics
  • LIM Domain Proteins/metabolism
  • Actins/metabolism*
  • Cilia/metabolism
  • Binding Sites
  • 3' Untranslated Regions
  • Actin-Related Protein 2/genetics
  • Actin-Related Protein 2/metabolism
  • Centrioles/metabolism*
  • Conserved Sequence
  • Morphogenesis
  • Retinal Pigment Epithelium/metabolism*
  • Actin Cytoskeleton/metabolism*
  • Cell Cycle Proteins/genetics
  • Cell Cycle Proteins/metabolism*
  • Zebrafish/embryology
  • Zebrafish/genetics
  • Pronephros/metabolism
  • Microtubule-Associated Proteins/genetics
  • Microtubule-Associated Proteins/metabolism*
  • Molecular Sequence Data
PubMed
22684256 Full text @ Nat. Cell Biol.
Abstract

Ciliogenesis requires the removal of CP110 from the mother centriole; actin dynamics also influence ciliation, at least partly by affecting the centrosomal accumulation of ciliogenic membrane vesicles. How these distinct processes are properly regulated remains unknown. Here we show that miR-129-3p, a microRNA conserved in vertebrates, controlled cilia biogenesis in cultured cells by concomitantly downregulating CP110 and repressing branched F-actin formation. Blocking miR-129-3p inhibited serum-starvation-induced ciliogenesis, whereas its overexpression potently induced ciliation in proliferating cells and also promoted cilia elongation. Gene expression analysis further identified ARP2, TOCA1, ABLIM1 and ABLIM3 as its targets in ciliation-related actin dynamics. Moreover, miR-129-3p inhibition in zebrafish embryos suppressed ciliation in Kupffer?s vesicle and the pronephros, and induced developmental abnormalities including a curved body, pericardial oedema and defective left?right asymmetry. Therefore, our results reveal a mechanism that orchestrates both the centriole-to-basal body transition and subsequent cilia assembly through microRNA-mediated post-transcriptional regulation.

Genes / Markers
Figures
Show all Figures
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Antibodies
Orthology
Engineered Foreign Genes
Mapping