Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease
- PMID: 2484340
- DOI: 10.1016/0896-6273(89)90210-9
Multiple isoforms of human microtubule-associated protein tau: sequences and localization in neurofibrillary tangles of Alzheimer's disease
Abstract
We have determined the sequences of isoforms of human tau protein, which differ from previously reported forms by insertions of 29 or 58 amino acids in the amino-terminal region. Complementary DNA cloning shows that the insertions occur in combination with both three and four tandem repeats. RNAase protection assays indicate that transcripts encoding isoforms with the insertions are expressed in an adult-specific manner. Transcripts encoding four tandem repeats are also expressed in an adult-specific manner, whereas mRNAs encoding three tandem repeats are expressed throughout life, including in fetal brain. The levels of transcripts encoding the 29 or 58 amino acid inserts were not significantly changed in cerebral cortex from patients with Alzheimer's disease. Antisera raised against synthetic peptides corresponding to these different human tau isoforms demonstrate that multiple tau protein isoforms are incorporated into the neurofibrillary tangles of Alzheimer's disease.
Similar articles
-
The repeat region of microtubule-associated protein tau forms part of the core of the paired helical filament of Alzheimer's disease.Ann Med. 1989;21(2):127-32. doi: 10.3109/07853898909149199. Ann Med. 1989. PMID: 2504257 Review.
-
Cloning and sequencing of the cDNA encoding an isoform of microtubule-associated protein tau containing four tandem repeats: differential expression of tau protein mRNAs in human brain.EMBO J. 1989 Feb;8(2):393-9. doi: 10.1002/j.1460-2075.1989.tb03390.x. EMBO J. 1989. PMID: 2498079 Free PMC article.
-
Tau protein immunoreactivity in dementia of the Alzheimer type: II. Electron microscopy and pathogenetic implications. Effects of fixation on the morphology of the Alzheimer's abnormal filaments.Lab Invest. 1989 Mar;60(3):375-89. Lab Invest. 1989. PMID: 2494388
-
Tau in Alzheimer neurofibrillary tangles. N- and C-terminal regions are differentially associated with paired helical filaments and the location of a putative abnormal phosphorylation site.Biochem J. 1991 Jan 1;273(Pt 1)(Pt 1):127-33. doi: 10.1042/bj2730127. Biochem J. 1991. PMID: 1899184 Free PMC article.
-
The molecular and cellular pathology of Alzheimer neurofibrillary lesions.J Gerontol. 1989 May;44(3):B55-8. doi: 10.1093/geronj/44.3.b55. J Gerontol. 1989. PMID: 2497170 Review. No abstract available.
Cited by
-
CELF2 promotes tau exon 10 inclusion via hinge domain-mediated nuclear condensation.bioRxiv [Preprint]. 2024 Nov 3:2024.11.02.621395. doi: 10.1101/2024.11.02.621395. bioRxiv. 2024. PMID: 39553957 Free PMC article. Preprint.
-
The structure of a Tau fragment bound to tubulin prompts new hypotheses on Tau mechanism and oligomerization.PNAS Nexus. 2024 Oct 30;3(11):pgae487. doi: 10.1093/pnasnexus/pgae487. eCollection 2024 Nov. PNAS Nexus. 2024. PMID: 39534653 Free PMC article.
-
Real-Time Tracking of Vesicles in Living Cells Reveals That Tau-Hyperphosphorylation Suppresses Unidirectional Transport by Motor Proteins.Chem Biomed Imaging. 2024 Apr 23;2(5):362-373. doi: 10.1021/cbmi.4c00016. eCollection 2024 May 27. Chem Biomed Imaging. 2024. PMID: 39474119 Free PMC article.
-
A Survey on Computational Methods in Drug Discovery for Neurodegenerative Diseases.Biomolecules. 2024 Oct 19;14(10):1330. doi: 10.3390/biom14101330. Biomolecules. 2024. PMID: 39456263 Free PMC article. Review.
-
Neuronal Vulnerability of the Entorhinal Cortex to Tau Pathology in Alzheimer's Disease.Br J Biomed Sci. 2024 Oct 7;81:13169. doi: 10.3389/bjbs.2024.13169. eCollection 2024. Br J Biomed Sci. 2024. PMID: 39435008 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Molecular Biology Databases
Miscellaneous
