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FTDP‐17 mutants S320F and S352L have subtle differential effects on 4R tau isoform aggregation in vitro
Author(s) -
Yenjerla Mythili,
Gamblin Chris T
Publication year - 2017
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.31.1_supplement.lb101
Subject(s) - gene isoform , mutant , tau protein , chemistry , microbiology and biotechnology , microtubule , gene , biochemistry , biology , genetics , alzheimer's disease , medicine , disease , pathology
Frontotemporal Dementia with Parkinsonism linked to chromosome‐17 (FTDP‐17) is a class of inherited neurodegenerative diseases caused by mutations in the tau gene. Tau protein is a microtubule associated protein that stabilizes microtubules in neurons. During neurodegeneration, tau protein aggregates to form toxic filaments. Tau isoforms have either three or four 18‐amino acid microtubule binding repeats, known as 3‐repeat tau (3R tau) or 4‐repeat tau (4R tau). The 4R and 3R tau isoforms are further classified into 0N, 1N and 2N isoforms based on the number of N‐terminal exons. Forty four different mutations in various positions of the tau gene have been reported. FTDP‐17 tau mutants 2N4R S320F and S352L cause neuropathology through different mechanisms of tau aggregation. The mutant S320F forms short tau oligomers while S352L forms long tau filaments in vitro . Here, we determined whether the 4R tau isoforms (0N, 1N, 2N) of S320F and S352L affect tau aggregation differently in vitro . We used right angle laser light scattering, thioflavin S florescence assay and transmission electron microscopy (TEM) to study arachidonic acid induced tau aggregation. All wild type 4R tau isoforms (0N, 1N, 2N) showed the same effect on polymerization of tau into filaments upon addition of arachidonic acid. All S320F isoforms (0N, 1N, 2N) showed a significant decrease (p < 0.01) and S352L isoforms (0N, 1N, 2N) showed no significant change in laser light scattering when compared to the corresponding wild type 4R isoforms. However, S320F isoform 1N showed a significant decrease (p < 0.01) in percentage change from the respective wild type isoform when compared to 0N, 2N S320F by one way ANOVA analysis of laser light scattering. S320F isoforms 0N, 2N showed an increase (p < 0.05, 0.01) and 2N S352L also showed an increase (p < 0.001) in thioflavin S fluorescence when compared to the corresponding wild type 4R isoform. TEM images of all 4R S320F filaments showed very short tau fibrils which could be tau oligomers while all S352L filaments showed an increase in length of tau polymer. The 2N S352L filaments were longer than filaments from 0N and 1N isoforms. Though the mutant isoforms have the same effect on tau polymerization, the extent of polymerization varies. These results show that the presence of N‐terminal exons have small, but significant, alterations in the pro‐aggregation properties of FTDP‐17 4R tau. Support or Funding Information NIH grant R01NS083391