Student or educator? Sign up with your school email and get 6 months of Pro free.
CoChat
Sign Up
Cited by 124

The DOI matches its Crossref record.

Zebrafish atlastin controls motility and spinal motor axon architecture via inhibition of the BMP pathway

Fassier, Coralie, Hutt, James A, Scholpp, Steffen, Lumsden, Andrew, Giros, Bruno, Nothias, Fatiha, Schneider-Maunoury, Sylvie, Houart, Corinne, Hazan, Jamilé·2010·Nature Neuroscience
DOI 10.1038/nn.2662
Open this paper in CoChat — free account

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1038/nn.2662

Cites

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

No references could be resolved yet.

Research works printed but not linked: 49

  1. Tessier-Lavigne, M. & Goodman, C.S. The molecular biology of axon guidance. Science 274, 1123–1133 (1996). · DOI · Paper page
  2. Dickson, B.J. Molecular mechanisms of axon guidance. Science 298, 1959–1964 (2002). · DOI · Paper page
  3. Charron, F. & Tessier-Lavigne, M. Novel brain wiring functions for classical morphogens: a role as graded positional cues in axon guidance. Development 132, 2251–2262 (2005). · DOI · Paper page
  4. Zou, Y. & Lyuksyutova, A.I. Morphogens as conserved axon guidance cues. Curr. Opin. Neurobiol. 17, 22–28 (2007). · DOI
  5. Colavita, A., Krishna, S., Zheng, H., Padgett, R.W. & Culotti, J.G. Pioneer axon guidance by UNC-129, a C. elegans TGF-beta. Science 281, 706–709 (1998). · DOI
  6. Aberle, H. et al. Wishful thinking encodes a BMP type II receptor that regulates synaptic growth in Drosophila. Neuron 33, 545–558 (2002). · DOI
  7. Marqués, G. et al. The Drosophila BMP type II receptor Wishful Thinking regulates neuromuscular synapse morphology and function. Neuron 33, 529–543 (2002). · DOI · Paper page
  8. McCabe, B.D. et al. The BMP homolog Gbb provides a retrograde signal that regulates synaptic growth at the Drosophila neuromuscular junction. Neuron 39, 241–254 (2003). · DOI · Paper page
  9. McCabe, B.D. et al. Highwire regulates presynaptic BMP signaling essential for synaptic growth. Neuron 41, 891–905 (2004). · DOI
  10. Wang, X., Shaw, W.R., Tsang, H.T., Reid, E. & O'Kane, C.J. Drosophila spichthyin inhibits BMP signaling and regulates synaptic growth and axonal microtubules. Nat. Neurosci. 10, 177–185 (2007). · DOI · Paper page
  11. Ratnaparkhi, A., Lawless, G.M., Schweizer, F.E., Golshani, P. & Jackson, G.R. A Drosophila model of ALS: human ALS-associated mutation in VAP33A suggests a dominant negative mechanism. PLoS ONE 3, e2334 (2008). · DOI
  12. Chang, H.C. et al. Modeling spinal muscular atrophy in Drosophila. PLoS ONE 3, e3209 (2008). · DOI
  13. Reid, E. Science in motion: common molecular pathological themes emerge in the hereditary spastic paraplegias. J. Med. Genet. 40, 81–86 (2003). · DOI
  14. Salinas, S., Proukakis, C., Crosby, A. & Warner, T.T. Hereditary spastic paraplegia: clinical features and pathogenetic mechanisms. Lancet Neurol. 7, 1127–1138 (2008). · DOI · Paper page
  15. Dürr, A. et al. Atlastin1 mutations are frequent in young-onset autosomal dominant spastic paraplegia. Arch. Neurol. 61, 1867–1872 (2004). · DOI
  16. Zhao, X. et al. Mutation in a newly identified GTPase gene cause autosomal dominant hereditary spastic paraplegia. Nat. Genet. 29, 326–331 (2001). · DOI · Paper page
  17. Zhu, P.P. et al. Cellular localization, oligomerization and membrane association of the hereditary spastic paraplegia 3A (SPG3A) protein atlastin. J. Biol. Chem. 278, 49063–49071 (2003). · DOI
  18. Scarano, V. et al. The R495W mutation in SPG3A causes spastic paraplegia associated with axonal neuropathy. J. Neurol. 252, 901–903 (2005). · DOI
  19. Smith, B.N. et al. Four novel SPG3A/atlastin mutations identified in autosomal dominant hereditary spastic paraplegia kindreds with intra-familial variability in age of onset and complex phenotype. Clin. Genet. 75, 485–489 (2009). · DOI
  20. Fusco, C. et al. Hereditary spastic paraplegia and axonal motor neuropathy caused by a novel SPG3A de novo mutation. Brain Dev. 32, 592–594 (2010). · DOI
  21. Rainier, S., Sher, C., Reish, O., Thomas, D. & Fink, J.K. De novo occurrence of novel SPG3A/atlastin mutation presenting as cerebral palsy. Arch. Neurol. 63, 445–447 (2006). · DOI
  22. Namekawa, M. et al. Mutations in the SPG3A gene encoding the GTPase atlastin interfere with vesicle trafficking in the ER/Golgi interface and Golgi morphogenesis. Mol. Cell. Neurosci. 35, 1–13 (2007). · DOI
  23. Sanderson, C.M. et al. Spastin and atlastin, two proteins mutated in autosomal-dominant hereditary spastic paraplegia, are binding partners. Hum. Mol. Genet. 15, 307–318 (2006). · DOI
  24. Rismanchi, N., Soderblom, C., Stadler, J., Zhu, P.P. & Blackstone, C. Atlastin GTPases are required for Golgi apparatus and ER morphogenesis. Hum. Mol. Genet. 17, 1591–1604 (2008). · DOI
  25. Orso, G. et al. Homotypic fusion of ER membranes requires the dynamin-like GTPase Atlastin. Nature 460, 978–983 (2009). · DOI · Paper page
  26. Hu, J. et al. A class of dynamin-like GTPases involved in the generation of the tubular ER network. Cell 138, 549–561 (2009). · DOI · Paper page
  27. Zhu, P.P., Soderblom, C., Tao-Cheng, J.H., Stadler, J. & Blackstone, C. SPG3A protein atlastin-1 is enriched in growth cones and promotes axon elongation during neuronal development. Hum. Mol. Genet. 15, 1343–1353 (2006). · DOI
  28. Park, H.C., Mehta, A., Richardson, J.S. & Appel, B. Olig2 is required for zebrafish primary motor neuron and oligodendrocyte development. Dev. Biol. 248, 356–368 (2002). · DOI · Paper page
  29. Flanagan-Steet, H., Fox, M.A., Meyer, D. & Sanes, J.R. Neuromuscular synapses can form in vivo by incorporation of initially aneural postsynaptic specializations. Development 132, 4471–4481 (2005). · DOI · Paper page
  30. Mintzer, K.A. et al. lost-a-fin encodes a type I BMP receptor, Alk8, acting maternally and zygotically in dorsoventral pattern formation. Development 128, 859–869 (2001). · DOI
  31. Schulte-Merker, S., Lee, K.J., McMahon, A.P. & Hammerschmidt, M. The zebrafish organizer requires chordino. Nature 387, 862–863 (1997). · DOI · Paper page
  32. Kobielak, K., Pasolli, H.A., Alonso, L., Polak, L. & Fuchs, E. Defining BMP functions in the hair follicle by conditional ablation of BMP receptor IA. J. Cell Biol. 163, 609–623 (2003). · DOI · Paper page
  33. Tsang, H.T. et al. The hereditary spastic paraplegia proteins NIPA1, spastin and spartin are inhibitors of mammalian BMP signaling. Hum. Mol. Genet. 18, 3805–3821 (2009). · DOI · Paper page
  34. Pyati, U.J., Webb, A.E. & Kimelman, D. Transgenic zebrafish reveal stage-specific roles for Bmp signaling in ventral and posterior mesoderm development. Development 132, 2333–2343 (2005). · DOI
  35. Yu, P.B. et al. Dorsomorphin inhibits BMP signals required for embryogenesis and iron metabolism. Nat. Chem. Biol. 4, 33–41 (2007). · DOI · Paper page
  36. Wen, Z. et al. BMP gradients steer nerve growth cones by a balancing act of LIM kinase and Slingshot phosphatase on ADF/cofilin. J. Cell Biol. 178, 107–119 (2007). · DOI
  37. Ball, R.W. et al. Retrograde BMP signaling controls synaptic growth at the NMJ by regulating Trio expression in motor neurons. Neuron 66, 536–549 (2010). · DOI
  38. Eaton, B.A. & Davies, G.W. LIM kinase1 controls synaptic stability downstream of the type II BMP receptor. Neuron 47, 695–708 (2005). · DOI
  39. Yang, Y.S. & Strittmatter, S.M. The reticulons: a family of proteins with diverse functions. Genome Biol. 8, 234 (2007). · DOI
  40. Liu, Y. et al. Reticulon RTN2B regulates trafficking and function of neuronal glutamate transporter EAAC1. J. Biol. Chem. 283, 6561–6571 (2008). · DOI
  41. Piddini, E. & Vincent, J.P. Modulation of developmental signals by endocytosis: different means and many ends. Curr. Opin. Cell Biol. 15, 474–481 (2003). · DOI
  42. O'Connor-Giles, K.M., Ho, L.L. & Ganetzky, B. Nervous wreck interacts with Thickveins and the endocytic machinery to attenuate retrograde BMP signaling during synaptic growth. Neuron 58, 507–518 (2008). · DOI
  43. Matsuura, I., Taniguchi, J., Hata, K., Saeki, N. & Yamashita, T. BMP inhibition enhances axonal growth and functional recovery after spinal cord injury. J. Neurochem. 105, 1471–1479 (2008). · DOI
  44. Higashijima, S., Hotta, Y. & Okamoto, H. Visualization of cranial motor neurons in live transgenic zebrafish expressing green fluorescent protein under the control of the islet-1 promoter/enhancer. J. Neurosci. 20, 206–218 (2000). · DOI · Paper page
  45. Kimmel, C.B., Ballard, W.W., Kimmel, S.R., Ullmann, B. & Schilling, T.F. Stages of embryonic development of the zebrafish. Dev. Dyn. 203, 253–310 (1995). · DOI · Paper page
  46. Macdonald, R. et al. Regulatory gene expression boundaries demarcate sites of neuronal differentiation in the embryonic zebrafish forebrain. Neuron 13, 1039–1053 (1994). · DOI
  47. Shanmugalingam, S. et al. Ace/Fgf8 is required for forebrain commissure formation and patterning of the telencephalon. Development 127, 2549–2561 (2000). · DOI
  48. Andersen, S.S.L. Preparation of dissociated zebrafish spinal neuron cultures. Methods Cell Sci. 23, 205–209 (2001). · DOI
  49. Tarrade, A. et al. A mutation of spastin is responsible for swellings and impairment of transport in a region of axon characterized by changes in microtubule composition. Hum. Mol. Genet. 15, 3544–3558 (2006). · DOI

Cited by

Metadata

Authors
Fassier, C., Hutt, J. A., Scholpp, S., Lumsden, A., Giros, B., Nothias, F., Schneider-Maunoury, S., Houart, C., & Hazan, J.
Venue
Nature Neuroscience
Publisher
Springer Science and Business Media LLC
Published
2010-10-10
Volume
13
Issue
11
Pages
1380-1387
ISSN
  • 1097-6256
  • 1546-1726
DOI
10.1038/nn.2662
Cited by
124
References
0
Language
en
Licence
www.springer.com/tdm (tdm)

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.