Cited by 90Skin and Cellular Biology ResearchNuclear Structure and FunctionProtein Structure and Dynamics

The effects of dephosphorylation on the structure of the projections of neurofilament

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Hisanaga, S, Hirokawa, N·1989·The Journal of Neuroscience

Abstract

Carboxy-terminal tail domains of larger molecular mass subunits (NF-M and NF-H) of neurofilaments (NFs), which are the highly phosphorylated moieties, were observed as thin flexible filaments projecting from NF core filaments by rotary shadowing (Hisanaga and Hirokawa, 1988). Dephosphorylation of NFs has been suspected to affect the structures and the functions of the carboxy-terminal tail projections. We report here the effects of the dephosphorylation on the structure of NFs studied by electron microscopy. (1) The structures of carboxy-terminal tail projections after dephosphorylation were compared with those of the control NFs by low-angle rotary shadowing. This was examined with 2 samples; the isolated neurofilaments and the short filaments assembled from NF-H. Both the dephosphorylated NFs and the short filaments showed many projections laterally extending from core filaments similar to those observed in the control samples. (2) With respect to the structure of NF in physiological solution, the density of NFs in the precipitates was examined by thin-section electron microscopy. No difference in the density was noted between control and dephosphorylated NFs. (3) The ability to form cross-bridges in vitro was examined by quick-freeze, deep-etch electron microscopy. The structure and frequency of cross-bridges appeared to be similar in both control and dephosphorylated NFs. (4) Phosphate determination revealed that about 90% of the phosphate groups of NF-H subunit were removed by treatment with E. coli alkaline phosphatase. These results indicated that the dephosphorylation of NF did not affect the structure and the ability to form cross-bridges of the carboxy-terminal tail projections in vitro.

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Crossref · 10.1523/jneurosci.09-03-00959.1989

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  • The C-terminal tail domains of neurofilament M and H subunits extrude outward from core filaments, as does the projection domain of Tau, to make spaces between neurofilaments.

    “The C-terminal tail domains of neurofilament M and H subunits extrude outward from core filaments, as does the projection domain of Tau, to make spaces between neurofilaments (NFs) (Hisanaga and Hirokawa, 1989).”

    From Regulation of Mitochondrial Transport and Inter-Microtubule Spacing by Tau Phosphorylation at the Sites Hyperphosphorylated in Alzheimer's Disease (2012) · cites this paper as Hisanaga and Hirokawa, 1989

    The section “Structure of the projections of control and dephosphorylated NFs” (page unavailable) describes projections extending from NF core filaments, and the Discussion describes cross-bridges between NFs that seem to comprise NF-H and NF-M tail domains. The copy does not discuss Tau’s projection domain or establish that these projections create the spaces between neurofilaments. (LLM, conf=0.86)

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Research works printed but not linked: 1

  1. Zackroff, R. V., W. W. Idler, P. M. Steinert, and R. D. Goldman (1982) In vitro reconstitution of intermediate filaments from mammalian neurofilament triplet polypeptides. Proc. Natl. Acad. Sci. USA 79: 754-757.

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Authors
Hisanaga, S., & Hirokawa, N.
Affiliations
The University of Tokyo (JP)
Venue
The Journal of Neuroscience
Published
1989-03-01
Volume
9
Issue
3
Pages
959-966
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W1567061101
Cited by
90
References
1
Citations by year
2024: 1 · 2021: 1 · 2018: 2 · 2017: 1 · 2016: 2 · 2015: 2 · 2012: 5
FWCI
3.97
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
  • Europe PMC (PubMed Central) (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • Muscular Dystrophy Association
  • Japan Society for the Promotion of Science (62065007)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Cell Biology › Skin and Cellular Biology Research
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Nuclear Structure and Function
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
Keywords
neurofilaments, dephosphorylation, neurofilament heavy chain, NF-M, cross-bridges, alkaline phosphatase, filament structure, cytoskeleton
MeSH terms
Animals, Cattle, Cytoskeleton, Intermediate Filament Proteins, Intermediate Filaments, Microscopy, Electron, Neural Pathways, Synaptic Transmission, Phosphates, Phosphorylation, Neurofilament Proteins

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