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The Alzheimer's Transcriptome

Alzheimer's Disease and Alipoprotein E

    Alzheimer's Disease (AD) is a fatal neurodegenerative disease characterized by progressive memory loss. The disease is believed to be caused in part by the aggregation of insoluble fibrils of the protein amyloid-beta. Amyloid-beta is a domain of the membrane protein Amyloid Precursor Protein (APP), which is cleaved to release the extracellular amyloid-beta protein component. The aggregated clumps of amyloid-beta form amyloid plaques, a key histological hallmark of AD (Huang 2012) (Figure 1).

     

Figure 1: Amyloid Plaque. Image courtesy of neurodigitech.com.

    Alipoprotein (apo) E4 is an allele of the ApoE gene with a strong genetic link to the development of late-onset Alzheimer's Disease (LOAD). The exact functions of ApoE4 in AD development is a topic of intense debate and study. Some research shows that apoE may be involved in the removal of amyloid-beta deposits while other studies indicate amyloid-beta independent roles of ApoE in AD progression (Huang 2012). It is likely that ApoE4 plays a multifaceted role in human neurons, as it has been implicated in a variety of cellular processes (Huang 2012).

Gene Expression Changes in ApoE4 carriers

    A 2013 study published in Nature investigated whole-transcriptomes from healthy carriers of the ApoE4 allele and LOAD patients. In this study, gene expression in the cerebral cortices of ApoE4 allele carriers and LOAD patients were compared to each other and to a reference transcriptome (Rhinn 2013). The study found that ApoE4 carriers exhibited changes in gene expression that resembled the gene expression changes found in Alzhemier's patients. Additionally, the researchers identified novel genes with altered expression in ApoE4 carriers and LOAD patients, including APBA2, RNF219, and SV2A (Rhinn 2013).

Genomics as a Discovery Science

    This project began with a rather open-ended and perhaps almost obvious hypothesis: the transcriptomes of ApoE4 allele carriers and LOAD patients would differ from the transcriptomes of healthy patients. As the topic of study was so broad, this research study is a good example of discovery science. In discovery science, large volumes of experimental data are analyzed to identify patterns or correlations. In the present study, entire transcriptomes were evaluated in the effort to find differences transcriptional between genotypes and phenotypes.

    Despite the breadth of the research study, researchers were able to reach very specific conclusions: the discovery of precise genes with transcriptional differences in ApoE4 carriers and LOAD patients. This study is a wonderful example of how genomic methodologies can allow for successful management of what would be an otherwise overwhelming amount of raw experimental data.

Genomic Technology in This Study

    This study measured gene expression through quantitative reverse transcription polymerase chain reaction, or qRT-PCR (Rhinn 2013). This method is a combination of two common techniques in molecular biology, reverse transcription PCR (RT-PCR) and real-time PCR (qPCR). In RT-PCR, RNA is reverse transcribed to complementary DNA via reverse transcriptase and amplified through PCR. In qPCR, PCR products are labeled with fluorescent probes during thermal cycling. As the PCR product is amplified, fluorescent signal accumulates at a rate that is proportional to the amount of starting DNA. In qRT-PCR, the processes are combined, allowing for the quantitative analysis of RNA.

    In this study, qRT-PCR was used to quantify the entire transcriptome of patients in the various categories. This transcriptome-wide approach allowed for changes in total transcription in the ApoE4 genotype or LOAD phenotype to be evaluated.

Take Home Message

    This paper demonstrates how basic discovery science with genomics methodologies can be employed to make clinically relevant discoveries from immense data.

Evaluation of the Project

    This paper begins with a simple premise: the Alzheimer's transcriptome will bear considerable differences than a healthy transcriptome. Despite this basic and simple premise, the researchers are able to identify specific molecular differences in the respective transcriptomes and identify novel genes in ApoE4 signaling in Alzheimer's development. All in all, this was a very effective research strategy that yielded powerful results through the application of genomics methodologies. 

References

Huang, Y. and L. Mucke. 2012. Alzheimer mechanisms and therapeutic strategies. Cell 148 (6): 1204-1222.

Pittcon. 2015. Understanding Alzheimer's Disease through genomics and proteomics [Internet]. [Cited 2016 Jan 22]. Available from http://www.news-medical.net/whitepaper/20151111/Understanding-Alzheimere28099s-Disease-through-genomics-and-proteomics.aspx. 

Rhinn, H., Fujita, R., Qiang, L., Cheng, R., Lee, J. H., and A. Abeliovich. 2013. Integrative genomics identifies APOE e4 effectors in Alzheimer's Disease. Nature 500: 45-50.

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