Developmental Expression Mapping of a Gene Implicated in Multiple Neurodevelopmental Disorders, A2bp1 (Fox1)
Open accessAbstract
The neuronal transcription splicing factor, A2BP1, has been implicated in a variety of neurodevelopmental disorders; however, the role of A2BP1 in brain development and gene regulatory function remains to be explicated. Here, we map A2bp1 gene expression, focusing on the developing forebrain of the C57BL6J mouse. Early in forebrain development, A2bp1 expression is highly reminiscent of the expression of genes marking postmitotic GABAergic cells emanating from the ventral telencephalon during migration to the dorsal pallium. Ventral pallial expression remains low after the migratory period. Broader dorsal pallial expression becomes more evident late prenatally and early postnatally. This is paralleled by dense, restricted expression in the ventrobasal dorsal thalamic complex and mid-hypothalamic region. Outside of the forebrain, there is significant expression in motor pathways. These data indicate that A2BP1 mutations may clinically affect very selective forebrain neuron types from early periods of development.
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All three Rbfox genes are broadly expressed in the brain, with individual neuronal cell types expressing different combinations at different developmental times.
“All three Rbfox genes are broadly expressed in the brain, with individual neuronal cell types expressing different combinations at different developmental times51–55.”
From The neurogenetics of alternative splicing (2016) · cites this paper as [54]
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- Authors
- Hammock, E. A. D., & Levitt, P.
- Affiliations
- Vanderbilt University (US)
- University of Southern California (US)
- Venue
- Developmental Neuroscience
- Publisher
- S. Karger AG
- Published
- 2011
- Volume
- 33
- Issue
- 1
- Pages
- 64-74
- ISSN
- 0378-5866 (ISSN-L)
- 1421-9859
- PMC
- PMC3080782
- OpenAlex
- W2147389564
- Cited by
- 21
- References
- 21
- Citations by year
- 2024: 1 · 2023: 1 · 2020: 2 · 2019: 1 · 2018: 1 · 2017: 2 · 2016: 1 · 2015: 4 · 2014: 1 · 2013: 3 · 2012: 4
- FWCI
- 1.60
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Developmental Neuroscience (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Vanderbilt University
- National Institutes of Health (NIH T32, HD015052)
- Vanderbilt Kennedy Center, Vanderbilt University Medical Center
- National Institute of Mental Health (T32MH075883, T32MH065215)
- Eunice Kennedy Shriver National Institute of Child Health and Human Development (P30HD015052)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetics and Neurodevelopmental Disorders
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Developmental Biology and Gene Regulation
- Keywords
- A2BP1, neurodevelopmental disorders, forebrain development, gene expression mapping, GABAergic neurons, neuronal migration, pallium, thalamus, hypothalamus, motor pathways, C57BL/6J mice
- MeSH terms
- RNA Splicing Factors, Animals, Brain, Developmental Disabilities, Mice, Inbred C57BL, Nervous System Diseases, Neurons, RNA-Binding Proteins, Gene Expression Regulation, Developmental, Mice
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