- Research article
- Open Access
Hypoxia alters expression of Zebrafish Microtubule-associated protein Tau (mapta, maptb) gene transcripts
BMC Research Notes volume 7, Article number: 767 (2014)
Microtubule-associated protein tau (MAPT) is abundant in neurons and functions in assembly and stabilization of microtubules to maintain cytoskeletal structure. Human MAPT transcripts undergo alternative splicing to produce 3R and 4R isoforms normally present at approximately equal levels in the adult brain. Imbalance of the 3R-4R isoform ratio can affect microtubule binding and assembly and may promote tau hyperphosphorylation and neurofibrillary tangle formation as seen in neurodegenerative diseases such as frontotemporal dementia (FTD) and Alzheimer’s disease (AD). Conditions involving hypoxia such as cerebral ischemia and stroke can promote similar tau pathology but whether hypoxic conditions cause changes in MAPT isoform formation has not been widely explored. We previously identified two paralogues (co-orthologues) of MAPT in zebrafish, mapta and maptb.
In this study we assess the splicing of transcripts of these genes in adult zebrafish brain under hypoxic conditions. We find hypoxia causes increases in particular mapta and maptb transcript isoforms, particularly the 6R and 4R isoforms of mapta and maptb respectively. Expression of the zebrafish orthologue of human TRA2B, tra2b, that encodes a protein binding to MAPT transcripts and regulating splicing, was reduced under hypoxic conditions, similar to observations in AD brain.
Overall, our findings indicate that hypoxia can alter splicing of zebrafish MAPT co-orthologues promoting formation of longer transcripts and possibly generating Mapt proteins more prone to hyperphosphorylation. This supports the use of zebrafish to provide insight into the mechanisms regulating MAPT transcript splicing under conditions that promote neuronal dysfunction and degeneration.
The MICROTUBULE-ASSOCIATED PROTEIN TAU (MAPT) gene encodes the soluble tau protein that is abundant in neurons and functions to assemble and stabilize microtubules to maintain cytoskeletal structure . As a result of alternative splicing of MAPT transcripts, six tau protein isoforms ranging from 352 to 441 amino acid residues in length are generated and expressed in the human brain. The isoforms differ by the regulated inclusion or exclusion of two regions of sequence near the N-terminus and the possession of either three (3R) or four (4R) repeat regions, (corresponding to the microtubule-binding domains), towards the C-terminus of tau . The 3R isoform is generated from mRNAs lacking exon 10, while mRNAs containing exon 10 encode 4R tau. These isoforms are normally present at approximately equal levels in the adult human brain . Changes in this isoform ratio and post-translational modifications of the 3R and 4R isoforms affect microtubule binding and assembly [4, 5].
Dysregulation of tau splicing is often observed in neurodegenerative diseases with aberrant tau deposition, including frontotemporal dementia (FTD), Pick disease (PiD), progressive supranuclear palsy (PSP)  and Alzheimer’s disease (AD) . Mutations reported in FTD cause aberrant exon 10 splicing, resulting in altered 4R/3R tau ratios [8, 9]. In PSP, aggregates of 4R tau predominate, whereas 3R isoforms are found in excess in Pick bodies in the majority of cases of PiD [10, 11]. In AD brains, increases in 4R tau isoforms have been reported resulting in altered 4R/3R tau ratios . Neurofibrillary tangles (NFTs), a major pathological hallmark of the AD brain, can result from the phosphorylation of 3R tau, 4R tau or both [13, 14]. Thus, any alternations in the levels of these isoforms could promote tangle formation and disease progression. It should be noted that changes in tau protein isoform ratios could result both from changes in the alternative splicing of transcripts and differential changes in the stability of their protein products.
Conditions such as cerebral ischemia and stroke that result in hypoxic conditions in affected brain areas can promote tau hyperphosphorylation and formation of NFTs. Acute hypoxic conditions have been shown to activate kinases that phosphorylate tau resulting in accumulation of phosphorylated tau in neurons . In a rodent stroke model, hyperphosphorylated tau accumulated in neurons of the cerebral cortex in areas where ischemic damage was prominent. This was associated with the up-regulation of the tau phosphorylating enzyme CdK5, and the consequent promotion of the formation of filaments similar to those present in human neurodegenerative tauopathies . It stands to reason that increases in tau isoforms may also contribute to this process by increasing the availability of the tau substrate to phosphorylating enzymes.
The zebrafish, Danio rerio, is an emerging model organism for the study of neurodegenerative disease . Zebrafish embryos represent normal collections of cells in which complex and subtle manipulations of gene activity can be performed to facilitate analyses of genes involved in human disease. The zebrafish genome is extensively annotated and regions of conservation of chromosomal synteny between humans and zebrafish have been defined . In many cases zebrafish genes are identifiable that are clear orthologues of human genes. For example, the AD-relevant PRESENILIN genes (PSEN1 and PSEN2) have zebrafish orthologues of psen1 and psen2 respectively. Tau phosphorylation and subsequent toxicity has been reported in zebrafish over-expressing the FTD associated human tau mutation, P301L [21, 22]. However this model does not reflect the pathology of other dementias such as AD where factors that regulate levels of wild-type tau isoforms promote hyper-phosphorylation and neurodegeneration.
We have previously identified two paralogues (co-orthologues) of MAPT in zebrafish, denoted mapta and maptb and have shown that both genes are expressed in the developing central nervous system . (Teleosts appear to have undergone an additional round of genome duplication since their separation from the tetrapod lineage followed by loss of many of the duplicated genes ). Similar to human MAPT, a complex pattern of alternative splicing of the mapta and maptb transcripts occurs. Zebrafish mapta gives rise to transcripts encoding 4R-6R isoforms, whereas maptb is predominantly expressed as a 3R isoform  (Figure 1) and is also alternatively spliced to form a “big tau” isoform. In mammals “big tau” is expressed in the peripheral nervous system and other tissues [24–26] while in zebrafish we observed “big tau” expression (at 24 hours post fertilization, hpf) in the trigeminal ganglion and dorsal spinal cord neurons (possibly dorsal sensory neurons) . However, whether hypoxic conditions lead to changes in tau isoform expression has not been widely explored in zebrafish. In the work described in this paper we extend our examination of expression of the zebrafish tau co-orthologues to study their response to actual hypoxia in adult fish brains and to chemical mimicry of hypoxia in explanted adult fish brains. We observe increases in the overall levels of both mapta and maptb transcripts due to specific increases in the levels of mapta 6R and maptb 4R transcript isoforms. This is consistent with dramatically decreased levels of transcripts of the zebrafish orthologue of the human TRA2B gene that codes for a splicing factor regulating alternative splicing of MAPT transcripts in human cells . We also observe an apparent increase under hypoxia in the levels of shorter transcripts of maptb relative to “big tau” transcripts of this gene. Overall, our findings indicate that hypoxia can alter splicing of zebrafish MAPT co-orthologues promoting formation of longer transcripts and possibly generating Mapt proteins more prone to hyperphosphorylation. This supports the use of zebrafish to provide insight into the mechanisms regulating MAPT transcript splicing under conditions that promote neuronal dysfunction and degeneration.
To determine whether hypoxic conditions regulate alternative splicing in MAPT co-orthologues in zebrafish, levels of mapta and maptb transcripts were assessed in adult zebrafish brains under conditions of actual hypoxia or in explanted adult brains subjected to chemical mimicry of hypoxia caused by NaN3.
In studies of hypoxia it is common to use chemical agents that can mimic (partially) hypoxic conditions (also known as “chemical hypoxia”). Agents commonly used are cobalt chloride (CoCl2), nickel chloride (NiCl2) and NaN3. Azides, including NaN3, have an action on the respiratory chain very similar to that of cyanide. We have previously shown that exposure to aqueous solutions of NaN3 can induce hypoxia-like responses in zebrafish . Exposure of adult fish to hypoxia or exposure of explanted adult brains to chemical mimicry of hypoxia increases the overall expression of tau transcripts in zebrafish brains. This was shown by qPCR measurement involving amplification of exonic sequence included in all transcripts of mapta or maptb (i.e. exon 6 of both genes – see Figure 2A and 2B). We also observed that the pattern of tau transcript splicing differs between hypoxia-exposed brains and controls. In terms of contributing isoforms, expression of the mapta 6R isoform was significantly increased, while expression of the mapta 4R isoform showed a significant decrease under hypoxia (Figure 2A). We also observed a significantly increased level of expression of maptb 4R transcripts, while expression of maptb 3R transcripts also showed a significant decrease under hypoxia (Figure 2B). An increase in expression of maptb 4R but not 3R corresponds to an overall increase in the 4R/3R ratio of tau transcripts (Figure 2B).
In rats (and humans) Mapt exon 4a contains a large open reading frame. Inclusion of this exonic sequence in MAPT mRNAs allows translation of “big tau” protein. Exon 3 of zebrafish maptb appears to be equivalent to rat exon 4a in size although no sequence homology is observed. Like rat MAPT exon 4a, zebrafish maptb exon 3 is subject to alternative splicing . Therefore, we performed qPCR to test whether this alternative splicing event is also influenced by hypoxic conditions. We observed that exclusion of exon 3 (here denoted as maptb − 3) from zebrafish maptb transcripts is significantly increased under hypoxia and chemical mimicry of hypoxia when compared with inclusion of exon 3 (here denoted as maptb +3) (Figure 2C).
In humans, differential splicing of MAPT transcripts in response to hypoxia can occur due to decreased binding of TRA2 protein to RNA . The TRA2 gene is duplicated in vertebrates, resulting in two TRA2 proteins with aprpoximately 63% amino acid residue identity in humans . These proteins are denoted TRA2A encoded by the TRA2A gene and TRA2B protein encoded by the gene TRA2B (also known as SFRS10). Nuclear magnetic resonance (NMR) analyses have recently shown that the optimal core RNA target sequence for binding TRA2B protein is AGAA. Conrad et al.  observed AD-specific changes in TRA2B expression, suggesting a potential mechanism for altered tau in AD. Suh et al. also observed a decrease in mouse Tra2b expression leading to a decrease in exon 10 exclusion and 3R-tau expression in cortical neurons after transient occlusion of the middle cerebral artery in mice. To examine whether this behavior is conserved for the zebrafish mapta and maptb genes we first observed whether hypoxia alters expression of the TRA2B orthologous gene, tra2b, in zebrafish brains. As shown in Figure 2D both actual hypoxia and chemical mimicry of hypoxia lead to decreased tra2b transcript levels presumably indicating reduction in the splice-regulating activity of Tra2b protein. We then examined whether the zebrafish mapta and maptb genes possess potential Tra2b binding sites within exons encoding tubulin-binding repeats and subject to alternative splicing. Using the online software, ESE finder (http://genes.mit.edu/burgelab/rescue-ese/) , zebrafish sequences for mapta exon 8 and maptb exon 9 were examined for putative tra2b binding sites. We found multiple exonic splicing enhancers (ESEs) but, for each gene, only one appeared significantly similar to the human TRA2B-binding site (Figure 3).
The human MAPT gene is located on chromosome 17 and contains 16 exons. Alternative splicing of the primary transcript leads to a family of mRNAs, encoding different protein isoforms. In adult human brain, six isoforms are expressed, produced by alternative splicing of exons 2, 3, and 10. Tau isoforms in the CNS contain either three or four copies of a tandem repeat containing tubulin-binding sequences (encoded by exon 10), referred to as 3R and 4R-tau . Optional inclusion of exon 2, or exons 2 and 3, gives rise to N-terminal inclusions of 29 or 58 amino acid residues respectively .
In this study we provide evidence that exposure to actual hypoxia and to chemical mimicry of hypoxia leads to overall increases in tau transcript levels and, simultaneously, marked relative changes in the alternative splicing of tau transcripts in adult zebrafish brains. Our results revealed that exposure to acute levels of actual hypoxia or chemical mimicry of hypoxia shifts the production of the predominantly expressed 3R transcript isoform of maptb towards formation of the 4R isoform, thus altering the 3R to 4R ratio. The precise regulation of the ratio of expression of 3R relative to 4R MAPT isoforms in human brain has been proposed to be critical for maintaining normal brain function . The disruption of this balance has been found to be correlated with tauopathies [8, 32]. We also observed a significant increase in expression of the 6R transcript isoform of zebrafish mapta relative to the mapta 4R transcript. As far as the behavior in alternative splicing of exons coding for tubulin-binding domain sequences is concerned, our data are in agreement with those of Conrad et al.  and Ichihara et al. showing that, in AD brains, the expression level of exon 10 is altered .
Imbalance of the 4R-3R tau isoform ratio has been observed in tauopathies such as FTDP-17 , PSP , and PiD . An altered 4R-3R tau isoform ratio has also been reported in the spinal cord after sciatic nerve axotomy . Suh et al. reported that cerebral ischemia changes the ratio of 4R-3R tau mRNAs and protein levels as well as causing tau hyperphosphorylation. Changes in tau isoform ratio and phosphorylation status can cause defects in the central nervous system by affecting microtubule dynamics and axonal transport resulting in neuronal loss . Therefore, it is conceivable that an alteration of tau isoform ratio and increased tau hyperphosphorylation after brain ischemic insult may contribute to the prevalence of AD in stroke patients [36, 37].
Exon 10 of the human MAPT gene, is flanked by a large intron 9 (13.6 kb) and intron 10 (3.8 kb), and has a stem-loop structure which spans the 5′ splice sites, which can sequester the 5′ splice site and leads to the use of alternative 5′ splice sites . Thus exon 10 can be included or skipped to produce tau proteins with or without exon 10, depending on the action of trans-acting or cis- elements located in exon 10. Hutton M, 1998  The pre-mRNA splicing factor Tra2b was shown to promote MAPT exon 10 splicing . Levels of Tra2b protein were found to be reduced in AD brains . Decreased levels of this splicing factor were also observed by Suh et al.  in cortical neurons and in mouse cerebral cortex following hypoxic-ischemic injury. Thus, decreased Tra2b expression under hypoxia may contribute to a shift in 4R-3R tau isoform ratio by increasing incorporation of exon 10 into mature MAPT mRNA. Consistent with this we detected putative Tra2b-binding sites in exon 8 of mapta and exon 9 of maptb. We also saw decreased expression of tra2b mRNA under hypoxic conditions.
High molecular weight (HMW) tau isoforms “big tau” have been detected in the neurons of the adult rat peripheral nervous system (PNS), optic nerve, spinal cord, several neuronal cell lines including PC12 and neuroblastoma N115  and non-neuronal tissues [25, 26]. “Big tau” appears to be the only tau isoform expressed in adult dorsal root ganglia (DRG) [24, 40]. “Big tau” is encoded by an 8 kb mRNA containing an additional exon 4a that is not present in any other tau isoforms. “Big tau” expression is developmentally regulated. It is expressed late in fetal life and its expression increases postnatally . Its presence has been correlated with increased neurite stability in adult DRG . Several studies have investigated “big tau” expression in non-neuronal tissues in AD patients but did not observe any significant changes [25, 26]. Chen et al. described an alternative splicing event involving maptb exon 3, which appears to be equivalent to human MAPT exon 4a. In our experiments we observed that hypoxia significantly increases the level of maptb transcripts from which exon 3 sequence is excluded but does not appear to change levels of the “big tau” form of maptb transcripts. However, we cannot exclude the possibility that this apparent increase in maptb expression with decreased exon 3 inclusion may be due to increased expression of the shorter transcript isoform in cells that do not express big tau, rather than a change in the ratio of splicing to form shorter transcript relative to “big tau” transcript within cells expressing both transcripts.
Overall, our findings show that exposure of zebrafish brains to actual hypoxia or chemical mimicry of hypoxia can produce changes in the expression ratio of different tau isoforms. These changes are similar to those observed in a number of neurodegenerative diseases and thus support the use of zebrafish as a model for providing further insight into the mechanisms underlying these disease processes.
This work was conducted under the auspices of The Animal Ethics Committee of The University of Adelaide and in accordance with EC Directive 86/609/EEC for animal experiments and the Uniform Requirements for Manuscripts Submitted to Biomedical Journals.
Zebrafish husbandry and experimental procedures
Danio rerio were bred and maintained at 28°C on a 14 h light/10 h dark cycle . Adult zebrafish (AB strain) at approximately 1 year of age were used for all experiments (n = 12). Fish for analysis were not selected on the basis of sex. For chemical mimicry of hypoxia adult explant brain tissue was exposed to 100 μM of sodium azide (NaN3, Sigma-Aldrich CHEMIE Gmbh, Steinheim, Germany) in DMEM medium for 3 hours. Untreated adult zebrafish brain explants that were dissected from zebrafish in the same way as for the treated adult zebrafish brains were used as in vitro controls. In the experiments conducted under low oxygen conditions, oxygen was depleted by bubbling nitrogen gas through the medium. Oxygen concentrations were then measured using a dissolved oxygen meter (DO 6+, EUTECH instruments, Singapore). The dissolved oxygen level in the actual hypoxia group was measured to be 1.15 ± 0.6 mg/l; whereas the normal ambient oxygen level was 6.6 ± 0.45 mg/l [27, 42]. Zebrafish were exposed to actual hypoxia for 3 hours. Briefly, after each hypoxia trial, the animals were euthanized by hypothermic shock and then decapitated to remove the brain. Total RNA was extracted from samples mentioned above using the QIAGEN RNeasy mini kit (QIAGEN, GmbH, Hilden, Germany) and stored at −80°C for further analysis. RNA concentration was determined with a NanoVue™ UV–vis spectrophotometer (GE Healthcare Life Sciences, Fairfield, USA). To insure quality of RNA, RNA samples were electrophoresed on 1% TBE agarose gels. 700 ng of total RNA were used to synthesize 25 μL of first-strand cDNA by reverse transcription (SuperScript® ΙΙΙ First-Strand DNA synthesis kit; Invitrogen, Camarillo, USA).
Quantitative real-time PCR for detection
The relative standard curve method for quantification was used to determine the expression of experimental samples compared to a basis sample. For experimental samples, target quantity was determined from the standard curve and then compared to the basis sample to determine fold changes in expression. Gene-specific primers were designed for amplification of target cDNA and the cDNA from the ubiquitously expressed control gene eef1a1a. The reaction mixture consisted of 50 ng/μ l of cDNA, 18 μ M of forward and reverse primers and Power SYBR green master mix PCR solution (Applied Biosystems, Warrington, UK).
To generate the standard curve cDNA was serially diluted (100 ng, 50 ng, 25 ng, 12.5 ng). Each sample and standard curve reaction was performed in triplicate for the control gene and experimental genes. Amplification conditions were 2 min at 50°C followed by 10 min at 95°C and then 40–45 cycles of 15 s at 95°C and 1 min at 60°C. Amplification was performed on an ABI 7000 Sequence Detection System (Applied Biosystems) using 96 well plates. Cycle thresholds obtained from each triplicate were averaged and normalized against the expression of eef1a1l1, which has previously been demonstrated to show unchanged levels of expression under hypoxia in embryos at 6, 12, 48 and 72 hpf and in adult gills . Each experimental sample was then compared to the basis sample to determine the fold change of expression. The primers used for quantitative real-time PCR analysis of relative zebrafish mapta/b mRNA levels are shown in Table 1. To reduce possible interference from unspliced RNA and/or contaminating genomic DNA primers were designed to bind in cDNA over exon-exon boundaries. All qPCRs were performed according to MIQE guidelines .
Statistical analysis of data
Means and standard deviations were calculated for all variables using conventional methods. Two-way ANOVA was used to evaluate significant differences between normoxia and samples from actual hypoxia or chemical mimicry of hypoxia. p- Values are shown in the figure legends, a criterion alpha level of P < 0.05 was used for all statistical comparisons. All qPCR assays were done in three biological replicates with three qPCRs per biological replicate). All the data were analysed using GraphPad Prism version 6.0 (GraphPad Prism, La Jolla, CA).
Bowen DM, Smith CB, White P, Davison AN: Neurotransmitter-related enzymes and indices of hypoxia in senile dementia and other abiotrophies. Brain. 1976, 99: 459-496. 10.1093/brain/99.3.459.
Johnson GV, Jenkins SM: Tau protein in normal and Alzheimer’s disease brain. J Alzheimers Dis. 1999, 1: 307-328.
Kosik KS, Crandall JE, Mufson EJ, Neve RL: Tau in situ hybridization in normal and Alzheimer brain: localization in the somatodendritic compartment. Ann Neurol. 1989, 26: 352-361. 10.1002/ana.410260308.
Bunker JM, Wilson L, Jordan MA, Feinstein SC: Modulation of microtubule dynamics by tau in living cells: implications for development and neurodegeneration. Mol Biol Cell. 2004, 15: 2720-2728. 10.1091/mbc.E04-01-0062.
Han D, Qureshi HY, Lu Y, Paudel HK: Familial FTDP-17 missense mutations inhibit microtubule assembly-promoting activity of tau by increasing phosphorylation at Ser202 in vitro. J Biol Chem. 2009, 284: 13422-13433. 10.1074/jbc.M901095200.
Brandt R, Hundelt M, Shahani N: Tau alteration and neuronal degeneration in tauopathies: mechanisms and models. Biochim Biophys Acta. 2005, 1739: 331-354. 10.1016/j.bbadis.2004.06.018.
Yasojima K, McGeer EG, McGeer PL: Tangled areas of Alzheimer brain have upregulated levels of exon 10 containing tau mRNA. Brain Res. 1999, 831: 301-305. 10.1016/S0006-8993(99)01486-9.
Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, Petersen RC, Stevens M, de Graaff E, Wauters E, van Baren J, Hillebrand M, Joosse M, Kwon JM, Nowotny P, Che LK, Norton J, Morris JC, Reed LA, Trojanowski J, Basun H, et al: Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17. Nature. 1998, 393: 702-705. 10.1038/31508.
Liu F, Gong CX: Tau exon 10 alternative splicing and tauopathies. Mol Neurodegener. 2008, 3: 8-10.1186/1750-1326-3-8.
Sergeant N, Wattez A, Delacourte A: Neurofibrillary degeneration in progressive supranuclear palsy and corticobasal degeneration: tau pathologies with exclusively “exon 10” isoforms. J Neurochem. 1999, 72: 1243-1249. 10.1046/j.1471-4159.1999.0721243.x.
de Silva R, Lashley T, Strand C, Shiarli AM, Shi J, Tian J, Bailey KL, Davies P, Bigio EH, Arima K, Iseki E, Murayama S, Kretzschmar H, Neumann M, Lippa C, Halliday G, MacKenzie J, Ravid R, Dickson D, Wszolek Z, Iwatsubo T, Pickering-Brown SM, Holton J, Lees A, Revesz T, Mann DM: An immunohistochemical study of cases of sporadic and inherited frontotemporal lobar degeneration using 3R- and 4R-specific tau monoclonal antibodies. Acta Neuropathol. 2006, 111: 329-340. 10.1007/s00401-006-0048-x.
Conrad C, Zhu J, Conrad C, Schoenfeld D, Fang Z, Ingelsson M, Stamm S, Church G, Hyman BT: Single molecule profiling of tau gene expression in Alzheimer’s disease. J Neurochem. 2007, 103: 1228-1236. 10.1111/j.1471-4159.2007.04857.x.
Espinoza M, de Silva R, Dickson DW, Davies P: Differential incorporation of tau isoforms in Alzheimer’s disease. J Alzheimers Dis. 2008, 14: 1-16.
Togo T, Akiyama H, Iseki E, Uchikado H, Kondo H, Ikeda K, Tsuchiya K, de Silva R, Lees A, Kosaka K: Immunohistochemical study of tau accumulation in early stages of Alzheimer-type neurofibrillary lesions. Acta Neuropathol. 2004, 107: 504-508. 10.1007/s00401-004-0842-2.
Chen GJ, Xu J, Lahousse SA, Caggiano NL, de la Monte SM: Transient hypoxia causes Alzheimer-type molecular and biochemical abnormalities in cortical neurons: potential strategies for neuroprotection. J Alzheimers Dis. 2003, 5: 209-228.
Wen Y, Yang SH, Liu R, Perez EJ, Brun-Zinkernagel AM, Koulen P, Simpkins JW: Cdk5 is involved in NFT-like tauopathy induced by transient cerebral ischemia in female rats. Biochim Biophys Acta. 2007, 1772: 473-483. 10.1016/j.bbadis.2006.10.011.
Newman M, Verdile G, Martins RN, Lardelli M: Zebrafish as a tool in Alzheimer’s disease research. Biochim Biophys Acta. 2011, 1812: 346-352. 10.1016/j.bbadis.2010.09.012.
Catchen JM, Braasch I, Postlethwait JH: Conserved synteny and the zebrafish genome. Methods Cell Biol. 2011, 104: 259-285.
Leimer U, Lun K, Romig H, Walter J, Grunberg J, Brand M, Haass C: Zebrafish (Danio rerio) presenilin promotes aberrant amyloid beta-peptide production and requires a critical aspartate residue for its function in amyloidogenesis. Biochemistry. 1999, 38: 13602-13609. 10.1021/bi991453n.
Groth C, Nornes S, McCarty R, Tamme R, Lardelli M: Identification of a second presenilin gene in zebrafish with similarity to the human Alzheimer’s disease gene presenilin2. Dev Genes Evol. 2002, 212: 486-490. 10.1007/s00427-002-0269-5.
Paquet D, Bhat R, Sydow A, Mandelkow EM, Berg S, Hellberg S, Falting J, Distel M, Koster RW, Schmid B, Haass C: A zebrafish model of tauopathy allows in vivo imaging of neuronal cell death and drug evaluation. J Clin Invest. 2009, 119: 1382-1395. 10.1172/JCI37537.
Giustiniani J, Chambraud B, Sardin E, Dounane O, Guillemeau K, Nakatani H, Paquet D, Kamah A, Landrieu I, Lippens G, Baulieu EE, Tawk M: Immunophilin FKBP52 induces Tau-P301L filamentous assembly in vitro and modulates its activity in a model of tauopathy. Proc Natl Acad Sci U S A. 2014, 111: 4584-4589. 10.1073/pnas.1402645111.
Chen M, Martins RN, Lardelli M: Complex splicing and neural expression of duplicated tau genes in zebrafish embryos. J Alzheimers Dis. 2009, 18: 305-317.
Goedert M, Wischik CM, Crowther RA, Walker JE, Klug A: Cloning and sequencing of the cDNA encoding a core protein of the paired helical filament of Alzheimer disease: identification as the microtubule-associated protein tau. Proc Natl Acad Sci U S A. 1988, 85: 4051-4055. 10.1073/pnas.85.11.4051.
Hattori H, Matsumoto M, Iwai K, Tsuchiya H, Miyauchi E, Takasaki M, Kamino K, Munehira J, Kimura Y, Kawanishi K, Hoshino T, Murai H, Ogata H, Maruyama H, Yoshida H: The tau protein of oral epithelium increases in Alzheimer’s disease. J Gerontol A Biol Sci Med Sci. 2002, 57: M64-M70. 10.1093/gerona/57.1.M64.
Ingelson M, Vanmechelen E, Lannfelt L: Microtubule-associated protein tau in human fibroblasts with the Swedish Alzheimer mutation. Neurosci Lett. 1996, 220: 9-12. 10.1016/S0304-3940(96)13218-3.
Moussavi Nik SH, Newman M, Lardelli M: The response of HMGA1 to changes in oxygen availability is evolutionarily conserved. Exp Cell Res. 2011, 317: 1503-1512. 10.1016/j.yexcr.2011.04.004.
Suh J, Im DS, Moon GJ, Ryu KS, de Silva R, Choi IS, Lees AJ, Guenette SY, Tanzi RE, Gwag BJ: Hypoxic ischemia and proteasome dysfunction alter tau isoform ratio by inhibiting exon 10 splicing. J Neurochem. 2010, 114: 160-170.
Tacke R, Tohyama M, Ogawa S, Manley JL: Human Tra2 proteins are sequence-specific activators of pre-mRNA splicing. Cell. 1998, 93: 139-148. 10.1016/S0092-8674(00)81153-8.
Fairbrother WG, Yeh RF, Sharp PA, Burge CB: Predictive identification of exonic splicing enhancers in human genes. Science. 2002, 297: 1007-1013. 10.1126/science.1073774.
Chen S, Townsend K, Goldberg TE, Davies P, Conejero-Goldberg C: MAPT isoforms: differential transcriptional profiles related to 3R and 4R splice variants. J Alzheimers Dis. 2010, 22: 1313-1329.
Spillantini MG, Murrell JR, Goedert M, Farlow MR, Klug A, Ghetti B: Mutation in the tau gene in familial multiple system tauopathy with presenile dementia. Proc Natl Acad Sci U S A. 1998, 95: 7737-7741. 10.1073/pnas.95.13.7737.
Ichihara K, Uchihara T, Nakamura A, Suzuki Y, Mizutani T: Selective deposition of 4-repeat tau in cerebral infarcts. J Neuropathol Exp Neurol. 2009, 68: 1029-1036. 10.1097/NEN.0b013e3181b56bf4.
de Silva R, Lashley T, Gibb G, Hanger D, Hope A, Reid A, Bandopadhyay R, Utton M, Strand C, Jowett T, Khan N, Anderton B, Wood N, Holton J, Revesz T, Lees A: Pathological inclusion bodies in tauopathies contain distinct complements of tau with three or four microtubule-binding repeat domains as demonstrated by new specific monoclonal antibodies. Neuropathol Appl Neurobiol. 2003, 29: 288-302. 10.1046/j.1365-2990.2003.00463.x.
Chambers CB, Muma NA: Neuronal gene expression in aluminum-induced neurofibrillary pathology: an in situ hybridization study. Neurotoxicology. 1997, 18: 77-88.
Tatemichi TK, Desmond DW, Mayeux R, Paik M, Stern Y, Sano M, Remien RH, Williams JB, Mohr JP, Hauser WA, Figueroa M: Dementia after stroke: baseline frequency, risks, and clinical features in a hospitalized cohort. Neurology. 1992, 42: 1185-1193. 10.1212/WNL.42.6.1185.
Guglielmotto M, Tamagno E, Danni O: Oxidative stress and hypoxia contribute to Alzheimer’s disease pathogenesis: two sides of the same coin. ScientificWorldJournal. 2009, 9: 781-791.
Eperon LP, Graham IR, Griffiths AD, Eperon IC: Effects of RNA secondary structure on alternative splicing of pre-mRNA: is folding limited to a region behind the transcribing RNA polymerase?. Cell. 1988, 54: 393-401. 10.1016/0092-8674(88)90202-4.
Kondo S, Yamamoto N, Murakami T, Okumura M, Mayeda A, Imaizumi K: Tra2 beta, SF2/ASF and SRp30c modulate the function of an exonic splicing enhancer in exon 10 of tau pre-mRNA. Genes Cells. 2004, 9: 121-130. 10.1111/j.1356-9597.2004.00709.x.
Boyne LJ, Tessler A, Murray M, Fischer I: Distribution of Big tau in the central nervous system of the adult and developing rat. J Comp Neurol. 1995, 358: 279-293. 10.1002/cne.903580209.
Westerfield M: The zebrafish book. A guide for the laboratory use of zebrafish (Danio rerio). 2007, University of Oregon Press, 5
Moussavi Nik SH, Croft K, Mori TA, Lardelli M: The comparison of methods for measuring oxidative stress in zebrafish brains. Zebrafish. 2014, 11: 248-254. 10.1089/zeb.2013.0958.
Tang R, Dodd A, Lai D, McNabb WC, Love DR: Validation of zebrafish (Danio rerio) reference genes for quantitative real-time RT-PCR normalization. Acta Biochim Biophys Sin (Shanghai). 2007, 39: 384-390. 10.1111/j.1745-7270.2007.00283.x.
Bustin SA, Benes V, Garson JA, Hellemans J, Huggett J, Kubista M, Mueller R, Nolan T, Pfaffl MW, Shipley GL, Vandesompele J, Wittwer CT: The MIQE guidelines: minimum information for publication of quantitative real-time PCR experiments. Clin Chem. 2009, 55: 611-622. 10.1373/clinchem.2008.112797.
This work was supported by funds from the School of Molecular and Biomedical Science at The University of Adelaide and by a Strategic Research Grant from Edith Cowan University. RM and GV are supported by grants from the McCusker Alzheimer’s Disease Research Foundation and NHMRC. MC is supported by a scholarship form the West Perth Rotary Club and the McCusker Alzheimer’s Disease Research Foundation. MV was generously supported by the family of Lindsay Carthew.
The authors declare that they have no competing interests.
SHMN completed experiments, participated in the design of the study and data analysis and drafted the manuscript. MN participated in the design of the study and revisions of the manuscript. SG completed experiments. MC participated in revision of the manuscript. RM participated in the revision of the manuscript. GV participated in the design of the study and the revision of the manuscript. ML predominantly designed the study and revised the manuscript. All authors read and approved the final manuscript.
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Moussavi Nik, S.H., Newman, M., Ganesan, S. et al. Hypoxia alters expression of Zebrafish Microtubule-associated protein Tau (mapta, maptb) gene transcripts. BMC Res Notes 7, 767 (2014). https://doi.org/10.1186/1756-0500-7-767
- Microtubule-associated protein tau (MAPT)
- Alternative splicing
- Alzheimer’s disease