Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

Developmentally regulated expression of specific tau sequences.

K S Kosik1, L D Orecchio, S Bakalis

  • 1Department of Neurology (Neuroscience), Harvard Medical School, Brigham and Women's Hospital, Boston, Massachusetts 02115.

Neuron
|April 1, 1989
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Transplacental metoprolol for fetal supraventricular tachycardia.

Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology·2019
Same author

Ubiquitin-proteasomal regulation of chromatin remodeler INO80 in the nucleus accumbens mediates persistent cocaine craving.

Science advances·2019
Same author

Exploring the Role of Cereal Dietary Fiber in Digestion.

Journal of agricultural and food chemistry·2019
Same author

Biological and Cognitive Markers of Presenilin1 E280A Autosomal Dominant Alzheimer's Disease: A Comprehensive Review of the Colombian Kindred.

The journal of prevention of Alzheimer's disease·2019
Same author

Evaluation of dry heat treatment of soft wheat flour for the production of high ratio cakes.

Food research international (Ottawa, Ont.)·2018
Same author

The dendritic spine morphogenic effects of repeated cocaine use occur through the regulation of serum response factor signaling.

Molecular psychiatry·2017
Same journal

Fast-conducting mechanonociceptors uniquely engage reflexive and affective pain circuitry to drive protective responses.

Neuron·2026
Same journal

Sparse component analysis: A method that uncovers separable computations within neural population activity.

Neuron·2026
Same journal

Spatiomolecular mapping reveals anatomical organization of heterogeneous cell types in the human nucleus accumbens.

Neuron·2026
Same journal

TGF-β1-induced endothelial transcytosis drives blood-brain barrier leakage during aging.

Neuron·2026
Same journal

Image space opens up for visual neuroscience.

Neuron·2026
Same journal

Septal GLP-1 receptors control alcohol taking and seeking.

Neuron·2026
See all related articles

Researchers identified a novel tau protein sequence variant during early brain development. This immature tau mRNA form declines after birth, but reappears in Alzheimer's disease.

Area of Science:

  • Neuroscience
  • Molecular Biology
  • Developmental Biology

Background:

  • Tau protein is crucial for microtubule stability.
  • Tau protein undergoes developmental changes in molecular mass and complexity.
  • Tau is implicated in neurodegenerative diseases like Alzheimer's.

Purpose of the Study:

  • To characterize the molecular changes in tau protein during early postnatal development.
  • To identify novel tau protein sequences and their developmental expression patterns.
  • To compare developmentally expressed tau sequences with those found in Alzheimer's disease.

Main Methods:

  • Sequencing of tau cDNA from adult rat brain expression library.
  • Oligonucleotide probe hybridization to detect tau mRNA expression.

Related Experiment Videos

  • Analysis of tau mRNA expression across different developmental time points (embryonic to postnatal).
  • Comparison of developmental tau sequences with those from Alzheimer's paired helical filaments.
  • Main Results:

    • Two inserted sequences were found in adult rat brain tau cDNA, one predicting a fourth microtubule-binding repeat.
    • An immature tau mRNA form, lacking the insert, is expressed from embryonic day 14 to postnatal day 8, then declines.
    • A mature tau mRNA form containing the insert is expressed postnatally.
    • Both mature and immature tau mRNA sequences were detected in Alzheimer's paired helical filaments.

    Conclusions:

    • A novel, immature tau mRNA sequence is developmentally regulated during early postnatal brain development.
    • This immature tau mRNA form reappears in the context of Alzheimer's disease pathology.
    • Understanding these developmental tau isoforms may provide insights into Alzheimer's disease mechanisms.