Literature DB >> 1832678

Distinct ankyrin isoforms at neuron cell bodies and nodes of Ranvier resolved using erythrocyte ankyrin-deficient mice.

E Kordeli1, V Bennett.   

Abstract

Isoforms of ankyrin (ankyrinsR) immunologically related to erythrocyte ankyrin (ankyrinRo) are associated with distinct neuronal plasma membrane domains of functional importance, such as cell bodies and dendrites, axonal hillock and initial segments, and nodes of Ranvier. AnkyrinRo is expressed in brain, and accounts for at least one of the ankyrinR isoforms. Another ankyrin isoform of brain, ankyrinB, is encoded by a distinct gene and is immunologically distinct from ankyrinsR. Mutant mice with normoblastosis (nb/nb) constitute the first described genetic model of ankyrin deficiency: they display a severe hemolytic anemia due to a significantly reduced expression of the ankyrinRo gene in reticulocytes as well as brain (Peters L. L., C. S. Birkenmeier, R. T. Bronson, R. A. White, S. E. Lux, E. Otto, V. Bennett, A. Higgins, and J. E. Barker. 1991. J. Cell Biol. 114:1233-1241). In the present report, we distinguish between ankyrinRo and other ankyrinR isoforms using immunoblot analysis and immunofluorescence localization of ankyrinsR throughout the nervous system (forebrain, cerebellum, brain stem, spinal cord, and sciatic nerve) of nb/nb and normal mice. This is the first immunocytochemical characterization of the neurological component of the nb mutation and shows the following. (a) The isoform of ankyrin at the nodes of Ranvier and initial axonal segments is present in the nb/nb mice and does not cross-react with an ankyrinRo-specific antibody; this isoform, therefore, is distinct from both ankyrin isoforms identified in brain, ankyrinRo and ankyrinB, and is probably the product of a distinct gene and a unique component of the specialized membrane skeleton associated with nodes of Ranvier. (b) AnkyrinRo missing from nb/nb mice is selectively associated with neuronal cell bodies and dendrites, excluded from myelinated axons, and displays a selective pattern of expression in the nervous system whereby expression is almost ubiquitous in neurons of the cerebellum (Purkinje and granule cells) and spinal cord, and restricted to a very minor subset of neurons in hippocampus and neocortex of forebrain.

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Year:  1991        PMID: 1832678      PMCID: PMC2289136          DOI: 10.1083/jcb.114.6.1243

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  42 in total

Review 1.  Spectrin-based membrane skeleton: a multipotential adaptor between plasma membrane and cytoplasm.

Authors:  V Bennett
Journal:  Physiol Rev       Date:  1990-10       Impact factor: 37.312

2.  Linkage of dominant hereditary spherocytosis to the gene for the erythrocyte membrane-skeleton protein ankyrin.

Authors:  F F Costa; P Agre; P C Watkins; J C Winkelmann; T K Tang; K M John; S E Lux; B G Forget
Journal:  N Engl J Med       Date:  1990-10-11       Impact factor: 91.245

3.  Brain ankyrin. Purification of a 72,000 Mr spectrin-binding domain.

Authors:  J Q Davis; V Bennett
Journal:  J Biol Chem       Date:  1984-02-10       Impact factor: 5.157

4.  Proteins involved in membrane--cytoskeleton association in human erythrocytes: spectrin, ankyrin, and band 3.

Authors:  V Bennett
Journal:  Methods Enzymol       Date:  1983       Impact factor: 1.600

5.  Brain spectrin, a membrane-associated protein related in structure and function to erythrocyte spectrin.

Authors:  V Bennett; J Davis; W E Fowler
Journal:  Nature       Date:  1982-09-09       Impact factor: 49.962

6.  Human erythrocyte ankyrin. Purification and properties.

Authors:  V Bennett; P J Stenbuck
Journal:  J Biol Chem       Date:  1980-03-25       Impact factor: 5.157

7.  Development of axonal membrane specializations defines nodes of Ranvier and precedes Schwann cell myelin elaboration.

Authors:  C Wiley-Livingston; M H Ellisman
Journal:  Dev Biol       Date:  1980-10       Impact factor: 3.582

8.  Spectrin deficient inherited hemolytic anemias in the mouse: characterization by spectrin synthesis and mRNA activity in reticulocytes.

Authors:  D M Bodine; C S Birkenmeier; J E Barker
Journal:  Cell       Date:  1984-07       Impact factor: 41.582

9.  Isolation and characterization of cDNAs encoding human brain ankyrins reveal a family of alternatively spliced genes.

Authors:  E Otto; M Kunimoto; T McLaughlin; V Bennett
Journal:  J Cell Biol       Date:  1991-07       Impact factor: 10.539

10.  Purkinje cell degeneration associated with erythroid ankyrin deficiency in nb/nb mice.

Authors:  L L Peters; C S Birkenmeier; R T Bronson; R A White; S E Lux; E Otto; V Bennett; A Higgins; J E Barker
Journal:  J Cell Biol       Date:  1991-09       Impact factor: 10.539

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  32 in total

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Journal:  J Neurosci       Date:  2000-06-15       Impact factor: 6.167

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Authors:  G Pietrini; M Matteoli; G Banker; M J Caplan
Journal:  Proc Natl Acad Sci U S A       Date:  1992-09-15       Impact factor: 11.205

3.  A novel ENU-generated truncation mutation lacking the spectrin-binding and C-terminal regulatory domains of Ank1 models severe hemolytic hereditary spherocytosis.

Authors:  Michael R Hughes; Nicole Anderson; Steven Maltby; Justin Wong; Zorana Berberovic; Connie S Birkenmeier; D James Haddon; Kamal Garcha; Ann Flenniken; Lucy R Osborne; S Lee Adamson; Janet Rossant; Luanne L Peters; Mark D Minden; Robert F Paulson; Chen Wang; Dwayne L Barber; Kelly M McNagny; William L Stanford
Journal:  Exp Hematol       Date:  2010-12-28       Impact factor: 3.084

4.  440-kD ankyrinB: structure of the major developmentally regulated domain and selective localization in unmyelinated axons.

Authors:  W Chan; E Kordeli; V Bennett
Journal:  J Cell Biol       Date:  1993-12       Impact factor: 10.539

5.  Of mice and men: the mice were right.

Authors:  V Bennett
Journal:  J Clin Invest       Date:  1995-03       Impact factor: 14.808

6.  Ankyrin gene mutations in japanese patients with hereditary spherocytosis.

Authors:  H Nakanishi; A Kanzaki; A Yawata; O Yamada; Y Yawata
Journal:  Int J Hematol       Date:  2001-01       Impact factor: 2.490

7.  Giant ankyrin-G: a critical innovation in vertebrate evolution of fast and integrated neuronal signaling.

Authors:  Paul M Jenkins; Namsoo Kim; Steven L Jones; Wei Chou Tseng; Tatyana M Svitkina; Henry H Yin; Vann Bennett
Journal:  Proc Natl Acad Sci U S A       Date:  2014-12-31       Impact factor: 11.205

8.  Hyaluronan-CD44 interaction activates stem cell marker Nanog, Stat-3-mediated MDR1 gene expression, and ankyrin-regulated multidrug efflux in breast and ovarian tumor cells.

Authors:  Lilly Y W Bourguignon; Karine Peyrollier; Weiliang Xia; Eli Gilad
Journal:  J Biol Chem       Date:  2008-04-25       Impact factor: 5.157

9.  β-III-spectrin spinocerebellar ataxia type 5 mutation reveals a dominant cytoskeletal mechanism that underlies dendritic arborization.

Authors:  Adam W Avery; David D Thomas; Thomas S Hays
Journal:  Proc Natl Acad Sci U S A       Date:  2017-10-16       Impact factor: 11.205

10.  An isoform-specific mutation in the protein 4.1 gene results in hereditary elliptocytosis and complete deficiency of protein 4.1 in erythrocytes but not in nonerythroid cells.

Authors:  J G Conboy; J A Chasis; R Winardi; G Tchernia; Y W Kan; N Mohandas
Journal:  J Clin Invest       Date:  1993-01       Impact factor: 14.808

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