Quantitative expression profiling of identified neurons reveals cell-specific constraints on highly variable levels of gene expression
Open accessAbstract
The postdevelopmental basis of cellular identity and the unique cellular output of a particular neuron type are of particular interest in the nervous system because a detailed understanding of circuits responsible for complex processes in the brain is impeded by the often ambiguous classification of neurons in these circuits. Neurons have been classified by morphological, electrophysiological, and neurochemical techniques. More recently, molecular approaches, particularly microarray, have been applied to the question of neuronal identity. With the realization that proteins expressed exclusively in only one type of neuron are rare, expression profiles obtained from neuronal subtypes are analyzed to search for diagnostic patterns of gene expression. However, this expression profiling hinges on one critical and implicit assumption: that neurons of the same type in different animals achieve their conserved functional output via conserved levels and quantitative relationships of gene expression. Here we exploit the unambiguously identifiable neurons in the crab stomatogastric ganglion to investigate the precise quantitative expression profiling of neurons at the level of single-cell ion channel expression. By measuring absolute mRNA levels of six different channels in the same individually identified neurons, we demonstrate that not only do individual cell types possess highly variable levels of channel expression but that this variability is constrained by unique patterns of correlated channel expression.
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In wild-type populations of animals with similar performance profiles, 2-7 fold variations in the mRNA expression of most cellular components are seen in identified neurons across individuals.
“In wild-type populations of animals with similar performance profiles, 2-7 fold variations in the mRNA expression of most cellular components are seen in identified neurons across individuals [25-30]”
From A feature and not a bug: Replication failures can lead to new biology (2026) · cites this paper as [26]
The Results report 3- to 5-fold variation in ion-channel mRNA among identified neurons of the same type, and the Discussion describes these neurons as maintaining constant network function. The paper measured six ion-channel genes in crab neurons; it does not establish a 2- to 7-fold range or extend the finding to most cellular components. No page number is available in our copy. (LLM, conf=0.88)
Experimental — accuracy not yet measuredIt is common for investigators to look for correlations between the expression of individual components or features to obtain insight into how individual system components contribute to system behavior.
“It is common for investigators to look for correlations between the expression of individual components or features to obtain insight into how individual system components contribute to system behavior [26,[60][61][62].”
From A feature and not a bug: Replication failures can lead to new biology (2026) · cites this paper as [26]
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- Authors
- Schulz, D. J., Goaillard, J.-M., & Marder, E. E.
- Affiliations
- University of Missouri (US)
- Brandeis University (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2007-08-07
- Volume
- 104
- Issue
- 32
- Pages
- 13187-13191
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC1933263
- OpenAlex
- W2065914874
- Cited by
- 288
- References
- 4
- Citations by year
- 2026: 8 · 2025: 6 · 2024: 16 · 2023: 12 · 2022: 13 · 2021: 19 · 2020: 9 · 2019: 19 · 2018: 20 · 2017: 11 · 2016: 13 · 2015: 21 · 2014: 26 · 2013: 15 · 2012: 20
- FWCI
- 5.55
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Science Foundation (0615160)
- James S. McDonnell Foundation
- University of Missouri
- National Institutes of Health
- National Institute of Mental Health (MH 46742, R37MH046742, R01MH046742)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Ion channel regulation and function
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Keywords
- neuronal identity, gene expression variation, stomatogastric ganglion, ion channels, single-cell expression profiling, mRNA levels, correlated gene expression, neuronal cell types, crabs
- MeSH terms
- Animals, Base Sequence, Brachyura, Ion Channels, Molecular Sequence Data, Neurons, Gene Expression Profiling
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