The enhancer RNA, AANCR, regulates APOE expression in astrocytes and microglia

Enhancers, critical regulatory elements within the human genome, are often transcribed into enhancer RNAs. The dysregulation of enhancers leads to diseases collectively termed enhanceropathies. While it is known that enhancers play a role in diseases by regulating gene expression, the specific mechanisms by which individual enhancers cause diseases are not well understood. Studies of individual enhancers are needed to fill this gap. This study delves into the role of APOE-activating noncoding RNA, AANCR, in the central nervous system, elucidating its function as a genetic modifier in Alzheimer's Disease. We employed RNA interference, RNaseH-mediated degradation, and single-molecule RNA fluorescence in situ hybridization to demonstrate that mere transcription of AANCR is insufficient; rather, its transcripts are crucial for promoting APOE expression. Our findings revealed that AANCR is induced by ATM-mediated ERK phosphorylation and subsequent AP-1 transcription factor activation. Once activated, AANCR enhances APOE expression, which in turn imparts an inflammatory phenotype to astrocytes. These findings demonstrate that AANCR is a key enhancer RNA in some cell types within the nervous system, pivotal for regulating APOE expression and influencing inflammatory responses, underscoring its potential as a therapeutic target in neurodegenerative diseases.

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Publication Details

Journal
Nucleic Acids Research
Published
2024-08-20
DOI
https://doi.org/10.1093/nar/gkae696
Citations
7
Primary Topic
RNA Research and Splicing
Type
article
Field-Weighted Citation Impact
1.64

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article

The enhancer RNA, AANCR, regulates APOE expression in astrocytes and microglia

Ryan J. Snyder, Christopher R. Day, Robert W. Mahley, Yaojuan Liu et al.
7 citations
Nucleic Acids Research
RNA Research and Splicing
1.64
article

The enhancer RNA, AANCR, regulates APOE expression in astrocytes and microglia

Ryan J. Snyder, Christopher R. Day, Robert W. Mahley, Yaojuan Liu, Vivian G. Cheung, Jason A. Watts, Joseph Rodriguez, Dongjun Li, Ma Wan, Lillian B. Elkin, Christopher Grunseich
article en
7 citations

Abstract

Enhancers, critical regulatory elements within the human genome, are often transcribed into enhancer RNAs. The dysregulation of enhancers leads to diseases collectively termed enhanceropathies. While it is known that enhancers play a role in diseases by regulating gene expression, the specific mechanisms by which individual enhancers cause diseases are not well understood. Studies of individual enhancers are needed to fill this gap. This study delves into the role of APOE-activating noncoding RNA, AANCR, in the central nervous system, elucidating its function as a genetic modifier in Alzheimer's Disease. We employed RNA interference, RNaseH-mediated degradation, and single-molecule RNA fluorescence in situ hybridization to demonstrate that mere transcription of AANCR is insufficient; rather, its transcripts are crucial for promoting APOE expression. Our findings revealed that AANCR is induced by ATM-mediated ERK phosphorylation and subsequent AP-1 transcription factor activation. Once activated, AANCR enhances APOE expression, which in turn imparts an inflammatory phenotype to astrocytes. These findings demonstrate that AANCR is a key enhancer RNA in some cell types within the nervous system, pivotal for regulating APOE expression and influencing inflammatory responses, underscoring its potential as a therapeutic target in neurodegenerative diseases.

Nucleic Acids ResearchVol. 52(17)
National Institutes of Health (US), Gladstone Institutes (US), University of California, San Francisco (US), University of Michigan (US), National Institute of Environmental Health Sciences (US), National Institute of Neurological Disorders and Stroke (US)
Warren Alpert Foundation, National Institutes of Health, National Institute of Neurological Disorders and Stroke, National Institute of Environmental Health Sciences
Good health and well-being
Openalex Percentile: Top 16%
RNA Research and Splicing
1.64
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