scholarly journals Mutation in microtubule-associated protein tau MAPT coding gene and its correlation with Alzheimer’s disease

2020 ◽  
Vol 11 (4) ◽  
pp. 5150-5157
Author(s):  
Sabah Subhi Ismael ◽  
Sarab D. Al-Shamaa

Alzheimer's disease (AD) is a progressive irreversible neuronal dysfunction characterized by progressive memory loss along with neuropsychiatric symptoms and a decline in daily activities. Disturbances in microtubule-associated protein tau (MAPT) gene expression result in disruption of the neuronal cytoskeleton and formation of neurofibrillary tangles. The study aims are to highlight the correlation between MAPT gene's exons mutations and AD. Beside the possibility of utilizing serum's tau protein concentration as an indicator for AD due to the accumulation of intracellular neurofibrillary filaments of highly phosphorylated Tau in AD patient's brain. DNA had been extracted from participant's blood that divided into three groups 30 participants in each ,AD patients ,Positive family history and healthy or control groups. The results of this research showed that serum's Tau protein concentration in AD patient group was significantly higher than healthy control and positive family history group and according to this result serum's tau concentration could be utilized as a good indicator for AD .Beside mutation in each 1,9 and 13 exons had been identified by PCR product analysis utilizing specific primers for each , Amplification PCR products in exon (1) showed 428bp band in AD patients group does not exist in 26.66% and in positive family history for AD group does not exist in 23.33%, In exon (9) PCR product of 604bp band in AD patients group does not exist in 53.33%, and in positive family history group does not exist in 43.33%. While amplification PCR product of exon 13 showed 299bps band in all healthy control and positive family history but not in AD patient group instead it band in 263bp had been appeared in 36.66%. These results confirmed the important role of tau protein and its coding gene in the pathology of AD.

2015 ◽  
Vol 28 (2) ◽  
pp. 211-219 ◽  
Author(s):  
Mei Zhao ◽  
Xiaozhen Lv ◽  
Maimaitirexiati Tuerxun ◽  
Jincai He ◽  
Benyan Luo ◽  
...  

ABSTRACTBackground:The prevalence and factors associated with delays in help seeking for people with dementia in China are unknown.Methods:Within 1,010 consecutively registered participants in the Clinical Pathway for Alzheimer's Disease in China (CPAD) study (NCT01779310), 576 persons with dementia (PWDs) and their informants reported the estimated time from symptom onset to first medical visit seeking diagnosis. Univariate analysis of general linear model was used to examine the potential factors associated with the delayed diagnosis seeking.Results:The median duration from the first noticeable symptom to the first visit seeking diagnosis or treatment was 1.77 years. Individuals with a positive family history of dementia had longer duration (p= 0.05). Compared with other types of dementia, people with vascular dementia (VaD) were referred for diagnosis earliest, and the sequence for such delays was: VaD < Alzheimer's disease (AD) < frontotemporal dementia (FTD) (p< 0.001). Subtypes of dementia (p< 0.001), family history (p= 0.01), and education level (p= 0.03) were associated with the increased delay in help seeking.Conclusions:In China, seeking diagnosis for PWDs is delayed for approximately 2 years, even in well-established memory clinics. Clinical features, family history, and less education may impede help seeking in dementia care.


Biochemistry ◽  
2013 ◽  
Vol 52 (37) ◽  
pp. 6445-6455 ◽  
Author(s):  
Hamid Y. Qureshi ◽  
Tong Li ◽  
Ryen MacDonald ◽  
Chul Min Cho ◽  
Nicole Leclerc ◽  
...  

2001 ◽  
Vol 356 (1406) ◽  
pp. 213-227 ◽  
Author(s):  
Michel Goedert ◽  
Maria Grazia Spillantini ◽  
Louise C. Serpell ◽  
John Berriman ◽  
Michael J. Smith ◽  
...  

The most common degenerative diseases of the human brain are characterized by the presence of abnormal filamentous inclusions in affected nerve cells and glial cells. These diseases can be grouped into two classes, based on the identity of the major proteinaceous components of the filamentous assemblies. The filaments are made of either the microtubule–associated protein tau or the protein α–synuclein. Importantly, the discovery of mutations in the tau gene in familial forms of frontotemporal dementia and of mutations in the α–synuclein gene in familial forms of Parkinson's disease has established that dysfunction of tau protein and α–synuclein can cause neurodegeneration.


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