Correlation Engine 2.0
Clear Search sequence regions


  • C21ORF59 (1)
  • cilia (1)
  • cytoplasm (1)
  • DNAI1 (4)
  • DNAI2 (2)
  • dynein (4)
  • dyskinesia (2)
  • DYX1C1 (1)
  • humans (1)
  • hydrocephalus (1)
  • LRRC6 (3)
  • mice (3)
  • mice knockout (1)
  • phenotypes (1)
  • rna (2)
  • ZMYND10 (10)
  • Sizes of these terms reflect their relevance to your search.

    Zinc finger MYND-type-containing 10 (ZMYND10), a cytoplasmic protein expressed in ciliated cells, causes primary ciliary dyskinesia (PCD) when mutated; however, its function is poorly understood. Therefore, in this study, we examined the roles of ZMYND10 using Zmynd10-/-mice exhibiting typical PCD phenotypes, including hydrocephalus and laterality defects. In these mutants, morphology, the number of motile cilia, and the 9+2 axoneme structure were normal; however, inner and outer dynein arms (IDA and ODA, respectively) were absent. ZMYND10 interacted with ODA components and proteins, including LRRC6, DYX1C1, and C21ORF59, implicated in the cytoplasmic pre-assembly of DAs, whose levels were significantly reduced in Zmynd10-/-mice. LRRC6 and DNAI1 were more stable when co-expressed with ZYMND10 than when expressed alone. DNAI2, which did not interact with ZMYND10, was not stabilized by co-expression with ZMYND10 alone, but was stabilized by co-expression with DNAI1 and ZMYND10, suggesting that ZMYND10 stabilized DNAI1, which subsequently stabilized DNAI2. Together, these results demonstrated that ZMYND10 regulated the early stage of DA cytoplasmic pre-assembly by stabilizing DNAI1.

    Citation

    Kyeong Jee Cho, Shin Hye Noh, Soo Min Han, Won-Il Choi, Hye-Youn Kim, Seyoung Yu, Joon Suk Lee, John Hoon Rim, Min Goo Lee, Friedhelm Hildebrandt, Heon Yung Gee. ZMYND10 stabilizes intermediate chain proteins in the cytoplasmic pre-assembly of dynein arms. PLoS genetics. 2018 Mar;14(3):e1007316

    Expand section icon Mesh Tags

    Expand section icon Substances


    PMID: 29601588

    View Full Text