- EMDB-0628: The axonemal doublet microtubule focusing on the inner junction r... -
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Basic information
Entry
Database: EMDB / ID: EMD-0628
Title
The axonemal doublet microtubule focusing on the inner junction region extracted from the cryo-electron tomography and subtomographic average of isolated Chlamydomonas wild type cilia
Map data
The doublet microtubule focusing on the inner junction region of Chlamydomonas wild type cilia
Sample
Organelle or cellular component: The inner junction region of axonemal doublet microtubule averaged from Chlamydomonas wild type cilia
Biological species
Chlamydomonas reinhardtii (plant)
Method
subtomogram averaging / cryo EM / Resolution: 23.0 Å
National Institutes of Health/National Institute of General Medical Sciences
R01GM112050
United States
National Institutes of Health/National Institute of General Medical Sciences
R01GM055667
United States
National Institutes of Health/National Institute of General Medical Sciences
R01GM083122
United States
Citation
Journal: Mol Biol Cell / Year: 2019 Title: PACRG and FAP20 form the inner junction of axonemal doublet microtubules and regulate ciliary motility. Authors: Erin E Dymek / Jianfeng Lin / Gang Fu / Mary E Porter / Daniela Nicastro / Elizabeth F Smith / Abstract: We previously demonstrated that PACRG plays a role in regulating dynein-driven microtubule sliding in motile cilia. To expand our understanding of the role of PACRG in ciliary assembly and motility, ...We previously demonstrated that PACRG plays a role in regulating dynein-driven microtubule sliding in motile cilia. To expand our understanding of the role of PACRG in ciliary assembly and motility, we used a combination of functional and structural studies, including newly identified mutants. Using cryo-electron tomography we show that PACRG and FAP20 form the inner junction between the A- and B-tubule along the length of all nine ciliary doublet microtubules. The lack of PACRG and FAP20 also results in reduced assembly of inner-arm dynein IDA and the beak-MIP structures. In addition, our functional studies reveal that loss of PACRG and/or FAP20 causes severe cell motility defects and reduced in vitro microtubule sliding velocities. Interestingly, the addition of exogenous PACRG and/or FAP20 protein to isolated mutant axonemes restores microtubule sliding velocities, but not ciliary beating. Taken together, these studies show that PACRG and FAP20 comprise the inner junction bridge that serves as a hub for both directly modulating dynein-driven microtubule sliding, as well as for the assembly of additional ciliary components that play essential roles in generating coordinated ciliary beating.
History
Deposition
Mar 4, 2019
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Header (metadata) release
Mar 27, 2019
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Map release
Jun 5, 2019
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Update
Aug 12, 2020
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Current status
Aug 12, 2020
Processing site: RCSB / Status: Released
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Structure visualization
Movie
Surface view with section colored by density value
A: 441.83997 Å / B: 386.61 Å / C: 524.685 Å α=β=γ: 90.0 °
CCP4 map header:
mode
Image stored as Reals
Å/pix. X/Y/Z
5.523
5.523
5.523
M x/y/z
80
70
95
origin x/y/z
0.000
0.000
0.000
length x/y/z
441.840
386.610
524.685
α/β/γ
90.000
90.000
90.000
MAP C/R/S
1
2
3
start NC/NR/NS
-14
-73
-21
NC/NR/NS
80
70
95
D min/max/mean
116.729
137.514
125.731
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Supplemental data
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Sample components
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Entire : The inner junction region of axonemal doublet microtubule average...
Entire
Name: The inner junction region of axonemal doublet microtubule averaged from Chlamydomonas wild type cilia
Components
Organelle or cellular component: The inner junction region of axonemal doublet microtubule averaged from Chlamydomonas wild type cilia
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Supramolecule #1: The inner junction region of axonemal doublet microtubule average...
Supramolecule
Name: The inner junction region of axonemal doublet microtubule averaged from Chlamydomonas wild type cilia type: organelle_or_cellular_component / ID: 1 / Parent: 0
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