[English] 日本語

- EMDB-35229: In situ structure of axonemal doublet microtubules in mouse sperm... -
+
Open data
-
Basic information
Entry | ![]() | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Title | In situ structure of axonemal doublet microtubules in mouse sperm with 16-nm repeat | |||||||||
![]() | Axonemal doublet microtubules in mouse sperm with 16-nm repeat | |||||||||
![]() |
| |||||||||
![]() | microtubules / axoneme / sperm / filament / STRUCTURAL PROTEIN | |||||||||
Function / homology | ![]() male germ-line stem cell population maintenance / axonemal microtubule doublet inner sheath / Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane / Cilium Assembly / Sealing of the nuclear envelope (NE) by ESCRT-III / outer acrosomal membrane / regulation of brood size / establishment of left/right asymmetry / 9+0 motile cilium / axonemal B tubule inner sheath ...male germ-line stem cell population maintenance / axonemal microtubule doublet inner sheath / Microtubule-dependent trafficking of connexons from Golgi to the plasma membrane / Cilium Assembly / Sealing of the nuclear envelope (NE) by ESCRT-III / outer acrosomal membrane / regulation of brood size / establishment of left/right asymmetry / 9+0 motile cilium / axonemal B tubule inner sheath / Intraflagellar transport / axonemal A tubule inner sheath / manchette / Carboxyterminal post-translational modifications of tubulin / protein polyglutamylation / inner dynein arm assembly / positive regulation of feeding behavior / COPI-independent Golgi-to-ER retrograde traffic / sperm principal piece / HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand / MAP kinase tyrosine/serine/threonine phosphatase activity / microtubule sliding / regulation of cilium beat frequency involved in ciliary motility / cilium movement involved in cell motility / COPI-mediated anterograde transport / Aggrephagy / protein localization to organelle / Kinesins / 9+2 motile cilium / Mitotic Prometaphase / EML4 and NUDC in mitotic spindle formation / acrosomal membrane / Resolution of Sister Chromatid Cohesion / PKR-mediated signaling / The role of GTSE1 in G2/M progression after G2 checkpoint / RHO GTPases activate IQGAPs / Recycling pathway of L1 / axoneme assembly / COPI-dependent Golgi-to-ER retrograde traffic / axonemal microtubule / RHO GTPases Activate Formins / cilium organization / Separation of Sister Chromatids / Hedgehog 'off' state / Loss of Nlp from mitotic centrosomes / Recruitment of mitotic centrosome proteins and complexes / Loss of proteins required for interphase microtubule organization from the centrosome / Recruitment of NuMA to mitotic centrosomes / Anchoring of the basal body to the plasma membrane / AURKA Activation by TPX2 / Regulation of PLK1 Activity at G2/M Transition / flagellated sperm motility / cell projection organization / MHC class II antigen presentation / protein targeting to membrane / protein targeting to mitochondrion / extrinsic component of membrane / positive regulation of cell motility / tubulin complex / histone H2AXS140 phosphatase activity / RNA polymerase II CTD heptapeptide repeat Y1 phosphatase activity / RNA polymerase II CTD heptapeptide repeat T4 phosphatase activity / RNA polymerase II CTD heptapeptide repeat S2 phosphatase activity / RNA polymerase II CTD heptapeptide repeat S5 phosphatase activity / RNA polymerase II CTD heptapeptide repeat S7 phosphatase activity / MAP kinase serine/threonine phosphatase activity / calmodulin-dependent protein phosphatase activity / myosin phosphatase activity / protein-serine/threonine phosphatase / ciliary base / intercellular bridge / beta-tubulin binding / spermatid development / phosphatase activity / microtubule organizing center / regulation of cell division / mitotic cytokinesis / phosphoprotein phosphatase activity / glial cell projection / sperm flagellum / axoneme / cilium assembly / single fertilization / alpha-tubulin binding / cellular response to unfolded protein / microtubule-based process / cytoplasmic microtubule / sperm midpiece / Neutrophil degranulation / centriole / Hsp70 protein binding / protein-tyrosine-phosphatase / protein tyrosine phosphatase activity, metal-dependent / histone H2AXY142 phosphatase activity / non-membrane spanning protein tyrosine phosphatase activity / cellular response to leukemia inhibitory factor / acrosomal vesicle / ciliary basal body / mitotic spindle organization / Hsp90 protein binding Similarity search - Function | |||||||||
Biological species | ![]() ![]() | |||||||||
Method | subtomogram averaging / cryo EM / Resolution: 4.5 Å | |||||||||
![]() | Zhu Y / Yin GL / Tai LH / Sun F | |||||||||
Funding support | ![]()
| |||||||||
![]() | ![]() Title: In-cell structural insight into the stability of sperm microtubule doublet. Authors: Linhua Tai / Guoliang Yin / Xiaojun Huang / Fei Sun / Yun Zhu / ![]() Abstract: The propulsion for mammalian sperm swimming is generated by flagella beating. Microtubule doublets (DMTs) along with microtubule inner proteins (MIPs) are essential structural blocks of flagella. ...The propulsion for mammalian sperm swimming is generated by flagella beating. Microtubule doublets (DMTs) along with microtubule inner proteins (MIPs) are essential structural blocks of flagella. However, the intricate molecular architecture of intact sperm DMT remains elusive. Here, by in situ cryo-electron tomography, we solved the in-cell structure of mouse sperm DMT at 4.5-7.5 Å resolutions, and built its model with 36 kinds of MIPs in 48 nm periodicity. We identified multiple copies of Tektin5 that reinforce Tektin bundle, and multiple MIPs with different periodicities that anchor the Tektin bundle to tubulin wall. This architecture contributes to a superior stability of A-tubule than B-tubule of DMT, which was revealed by structural comparison of DMTs from the intact and deformed axonemes. Our work provides an overall molecular picture of intact sperm DMT in 48 nm periodicity that is essential to understand the molecular mechanism of sperm motility as well as the related ciliopathies. | |||||||||
History |
|
-
Structure visualization
Supplemental images |
---|
-
Downloads & links
-EMDB archive
Map data | ![]() | 116.2 MB | ![]() | |
---|---|---|---|---|
Header (meta data) | ![]() ![]() | 38.9 KB 38.9 KB | Display Display | ![]() |
Images | ![]() | 190.2 KB | ||
Filedesc metadata | ![]() | 12.5 KB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Validation report
Summary document | ![]() | 785.2 KB | Display | ![]() |
---|---|---|---|---|
Full document | ![]() | 784.7 KB | Display | |
Data in XML | ![]() | 6.5 KB | Display | |
Data in CIF | ![]() | 7.5 KB | Display | |
Arichive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 8i7oMC ![]() 8i7rC C: citing same article ( M: atomic model generated by this map |
---|---|
Similar structure data | Similarity search - Function & homology ![]() |
-
Links
EMDB pages | ![]() ![]() |
---|---|
Related items in Molecule of the Month |
-
Map
File | ![]() | ||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Annotation | Axonemal doublet microtubules in mouse sperm with 16-nm repeat | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.76 Å | ||||||||||||||||||||||||||||||||||||
Density |
| ||||||||||||||||||||||||||||||||||||
Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
|
-Supplemental data
-
Sample components
+Entire : mouse sperm
+Supramolecule #1: mouse sperm
+Macromolecule #1: Tektin-1
+Macromolecule #2: Detyrosinated tubulin alpha-3 chain
+Macromolecule #3: Tubulin beta-4B chain
+Macromolecule #4: Tektin-2
+Macromolecule #5: Tektin-3
+Macromolecule #6: Tektin-4
+Macromolecule #7: Tektin bundle-interacting protein 1
+Macromolecule #8: Tektin-5
+Macromolecule #9: EF-hand domain-containing protein 1
+Macromolecule #10: EF-hand domain-containing family member C2
+Macromolecule #11: Protein FAM166A
+Macromolecule #12: Protein FAM166C
+Macromolecule #13: Dual specificity phosphatase 21
+Macromolecule #14: Coiled-coil domain-containing protein 105
+Macromolecule #15: Enkurin
+Macromolecule #16: Testis-expressed protein 43
+Macromolecule #17: Cilia- and flagella-associated protein 276
+Macromolecule #18: Protein Flattop
+Macromolecule #19: Cilia- and flagella-associated protein 52
+Macromolecule #20: EF-hand calcium-binding domain-containing protein 6
+Macromolecule #21: Cilia and flagella-associated protein 77
+Macromolecule #22: Cilia- and flagella-associated protein 20
+Macromolecule #23: Parkin coregulated gene protein homolog
+Macromolecule #24: Sperm acrosome-associated protein 9
+Macromolecule #25: GUANOSINE-5'-TRIPHOSPHATE
-Experimental details
-Structure determination
Method | cryo EM |
---|---|
![]() | subtomogram averaging |
Aggregation state | cell |
-
Sample preparation
Buffer | pH: 7 |
---|---|
Vitrification | Cryogen name: ETHANE |
-
Electron microscopy
Microscope | FEI TITAN KRIOS |
---|---|
Image recording | Film or detector model: GATAN K2 QUANTUM (4k x 4k) / Detector mode: SUPER-RESOLUTION / Average electron dose: 3.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Illumination mode: SPOT SCAN / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 5.0 µm / Nominal defocus min: 1.0 µm |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
-
Image processing
Final reconstruction | Applied symmetry - Point group: C1 (asymmetric) / Resolution.type: BY AUTHOR / Resolution: 4.5 Å / Resolution method: FSC 0.143 CUT-OFF / Number subtomograms used: 37018 |
---|---|
Extraction | Number tomograms: 689 / Number images used: 37018 |
Final angle assignment | Type: MAXIMUM LIKELIHOOD |