News Release

Using genes to understand the brain's building blocks

New large-scale computational analysis of gene expression in single cells in the brain identifies distinct cell types

Peer-Reviewed Publication

Allen Institute

A Cellular Taxonomy of the Visual Cortex

video: The mammalian brain is composed of various cell populations that differ based on their molecular, morphological, electrophysiological and functional characteristics. Classifying these cells into types is one of the essential approaches to defining the diversity of brain's building blocks.

We created a cellular taxonomy of the mouse primary visual cortex by analyzing gene expression patterns, at the single cell level, of more than 1,600 cells. Using transgenic mice, we isolated fluorescently labeled cells from their brains and then sequenced the transcriptomes of individual cells. To identify the different cell types, we employed an iterative unbiased classification method (cluster analysis) that examined all expressed genes and was blind to the origin of cells. view more 

Credit: Allen Institute

Understanding the cellular building blocks of the brain, including the number and diversity of cell types, is a fundamental step toward understanding brain function. Researchers at the Allen Institute for Brain Science have created a detailed taxonomy of cells in the mouse visual cortex based on single-cell gene expression, identifying 49 distinct cell types in the largest collection of individual adult cortical neurons characterized by gene expression published to date. The work appears this month online in Nature Neuroscience.

"Studying any system requires knowing what the system is made of," says Bosiljka Tasic, Ph.D., Assistant Investigator at the Allen Institute for Brain Science. "There are many ways to define the brain's cellular building blocks. Our approach was to look at all the genes that are expressed in individual cells in the mouse visual cortex and use that information to classify the cells."

The team developed a technique to isolate single cells from the adult mouse brain, and then obtained genome-wide gene expression data from these individual cells. Each cell expresses thousands of genes, making the cell classification problem an enormous computational task.

"Initially, the problem of classifying cells is like sorting Skittles in the dark," says Vilas Menon, Scientist II at the Allen Institute for Brain Science. "With single-cell gene expression data, we get the equivalent of color, or type, information, but we still have to extract it from the large-scale data set. Ultimately, we wanted to figure out how many types there were in an unbiased, data-driven way."

Tasic, Menon and their team used computational dimension reduction techniques, which collapse genes with similar expression patterns into gene sets. When single cells were analyzed by clustering in this lower-dimensional space, 49 distinct groups appeared based on unique combinations of genes they express, including 42 neuronal cell types and 7 non-neuronal types.

"Our human cortex is what gives rise to our unique thoughts and perceptions," says Christof Koch, Ph.D., President and Chief Scientific Officer at the Allen Institute for Brain Science. "Having this kind of objective analysis of cell types in this region of the brain is a basic piece of understanding we need, and provides a baseline for looking at other regions of the mouse brain and also at the human brain."

The data from this single cell analysis approach agree with and complement the Allen Brain Atlas: a brain-wide gene expression atlas of the mouse brain.

"Our unit of analysis was a single cell and all genes within each cell, but in our process, we lost fine spatial information," says Tasic. "But then, we were able to use our Allen Brain Atlas, which has brain-wide analysis of each gene, one gene at a time at cellular resolution, to more precisely locate each cell type. Our work is one more step toward assigning genes to specific cell types and then helping investigate what these genes do, how they work together, and how they ultimately make our nervous systems and us who we are."

"Categorizing the cells in visual cortex into these distinct types that are marked by specific genes will enable us to begin to understand what these cells and types do in the brain," says Hongkui Zeng, Ph.D., Investigator of Cell and Circuit Genetics at the Allen Institute for Brain Science. "Next, we can investigate how gene expression correlates with the anatomical, physiological and functional properties of the cells, how these cell types are connected with each other, and how they work together to process and make sense of the visual information the brain receives from the outside world. This will ultimately shed light on the inner workings of the brain."

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About the Allen Institute for Brain Science

The Allen Institute for Brain Science, a division of the Allen Institute, is an independent, 501(c)(3) nonprofit medical research organization dedicated to accelerating the understanding of how the human brain works in health and disease. Using a big science approach, the Allen Institute generates useful public resources used by researchers and organizations around the globe, drives technological and analytical advances, and discovers fundamental brain properties through integration of experiments, modeling and theory. Launched in 2003 with a seed contribution from founder and philanthropist Paul G. Allen, the Allen Institute is supported by a diversity of government, foundation and private funds to enable its projects. Given the Institute's achievements, Mr. Allen committed an additional $300 million in 2012 for the first four years of a ten-year plan to further propel and expand the Institute's scientific programs, bringing his total commitment to date to $500 million. The Allen Institute's data and tools are publicly available online at http://www.brain-map.org.


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