Literature DB >> 1944892

In situ localization of tau mRNA in developing rat brain.

R Takemura1, Y Kanai, N Hirokawa.   

Abstract

A microtubule-associated protein, tau, promotes microtubule assembly, forms characteristic short cross-bridges (less than 20 nm) between microtubules, and switches isoforms from juvenile to adult at the end of the first postnatal week in the rat brain. The developmental expression of tau was studied in rat central nervous system, mainly the cerebrum and cerebellum, by in situ hybridization. Tau mRNAs were localized in a wide variety of neural cells. The expression of tau mRNAs in the spinal cord appeared to precede that in the brain, and the expression in the brainstem appeared to precede that in the cerebral cortex and cerebellum. On neural cells throughout the cortical plate of the cerebral cortex, tau mRNAs were expressed in large amounts during the first postnatal week, but by the third postnatal week the expression had become reduced. In the cerebellum, tau mRNAs were enriched in granule cells. The expression in the internal granular layer peaked during the second and third postnatal weeks, and the relatively high level of expression persisted to young adulthood. Thin section transmission electron microscopic study revealed that the proportion of neighboring microtubules in parallel fiber axons of cerebellar granule cells with the distance less than 20 nm was as low as 10% at the end of the first postnatal week, but this proportion increased to as high as 35% at the end of the second postnatal week. Northern blot analysis showed that tau mRNAs were congruent to 6 kb as was reported previously, and those detected in the first postnatal week were three- to five-fold more abundant and approximately 0.2 kb smaller than those detected in the second or third postnatal weeks. The data suggest that (a) tau mRNAs are abundantly expressed in a wide variety of neurons in the central nervous system at the stage of neurite formation, and (b) tau mRNAs are expressed in more basal levels at later stages, but may be important in the formation and maintenance of characteristic microtubule bundles typically found in parallel fiber axons and in other axons.

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Year:  1991        PMID: 1944892     DOI: 10.1016/0306-4522(91)90064-u

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  9 in total

1.  The rate of Tau synthesis is differentially regulated during postnatal development in mouse cerebellum.

Authors:  G J Vilá-Ortiz; T A Santa-Coloma; H Carminatti; M Radrizzani
Journal:  Cell Mol Neurobiol       Date:  2001-10       Impact factor: 5.046

Review 2.  Regulated phosphorylation and dephosphorylation of tau protein: effects on microtubule interaction, intracellular trafficking and neurodegeneration.

Authors:  M L Billingsley; R L Kincaid
Journal:  Biochem J       Date:  1997-05-01       Impact factor: 3.857

3.  Widespread cytoskeletal pathology characterizes corticobasal degeneration.

Authors:  M B Feany; D W Dickson
Journal:  Am J Pathol       Date:  1995-06       Impact factor: 4.307

4.  In situ localization with digoxigenin-labelled probes of tau-related mRNAs in the rat pancreas.

Authors:  P Neuville; M T Vanier; L Michalik; J F Launay
Journal:  Histochem J       Date:  1995-08

5.  Respective roles of neurofilaments, microtubules, MAP1B, and tau in neurite outgrowth and stabilization.

Authors:  T B Shea; M L Beermann
Journal:  Mol Biol Cell       Date:  1994-08       Impact factor: 4.138

6.  Microtubule bundling by tau proteins in vivo: analysis of functional domains.

Authors:  Y Kanai; J Chen; N Hirokawa
Journal:  EMBO J       Date:  1992-11       Impact factor: 11.598

7.  Kinesin family in murine central nervous system.

Authors:  H Aizawa; Y Sekine; R Takemura; Z Zhang; M Nangaku; N Hirokawa
Journal:  J Cell Biol       Date:  1992-12       Impact factor: 10.539

8.  Human TTBK1, TTBK2 and MARK1 kinase toxicity in Drosophila melanogaster is exacerbated by co-expression of human Tau.

Authors:  Josefin Fernius; Annika Starkenberg; Malgorzata Pokrzywa; Stefan Thor
Journal:  Biol Open       Date:  2017-07-15       Impact factor: 2.422

9.  A novel microtubule-based motor protein (KIF4) for organelle transports, whose expression is regulated developmentally.

Authors:  Y Sekine; Y Okada; Y Noda; S Kondo; H Aizawa; R Takemura; N Hirokawa
Journal:  J Cell Biol       Date:  1994-10       Impact factor: 10.539

  9 in total

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