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Mapping the mind with BARseq

image of BARseq brain mapping shapes
鈥淚 think of BARseq鈥檚 maps as sort of like a painting aid,鈥 says former CSHL postdoc Xiaoyin Chen. 鈥淎ll these little dots make up shapes. And you can actually zoom in and look at different parts and distinguish different cell types.鈥 Image: Chen lab/Allen Institute for Brain Science

Understanding the connections between different brain areas could pave the way to better treatment strategies for conditions like Alzheimer鈥檚, schizophrenia, and depression.

In 2019, as a postdoc in 黑料吃瓜资源鈥檚 (CSHL鈥檚) Zador lab, Xiaoyin Chen helped develop a technique to map these connections. BARseq identifies cells in the brain by the genes they use and traces the connecting neural circuitry. Early versions of BARseq mapped gene expression across thousands of neural pathways, using 鈥渂arcodes鈥 or short snippets of RNA.

Chen is now an assistant investigator at the Allen Brain Institute. He recently reunited with CSHL Professor Anthony Zador to upgrade BARseq鈥檚 capabilities. What does that look like? Instead of thousands of neurons, BARseq can now map millions. Chen says:

鈥淲e are focused on pushing BARseq forward. We want to make this easy for everybody to use, faster, more sensitive. Can we read out more information with it? With much higher scale, you can start to answer different questions.鈥

The team began their search for answers in the brain鈥檚 visual cortex. Sight is one of the most common ways humans perceive the world. Information travels from the eyes to the visual cortex for processing. But what happens in the brain when the visual cortex鈥檚 neural inroads are cut or don鈥檛 form at all?

鈥淧eople have known for a while that visual inputs are very important in shaping the brain,鈥 Chen explains. 鈥淏ut we don鈥檛 know, at the exact cell-type resolution BARseq provides, what actually happens.鈥

image of BARseq gene clusters side by side
Left: Each colored dot in this image of the brain鈥檚 outer layer, or cortex, is an individual gene. Right: Using BARseq, scientists can see how genes are clustered and identify the corresponding neurons, the larger colored dots seen here. Images: Chen lab/Allen Institute for Brain Science

The team used BARseq to map the brains of nine mice and traced gene expression in each mouse鈥檚 visual cortex. It鈥檚 the first time the technique has been used to map this many entire brains. Amazingly, the team found that if the mice went blind, the genes in the visual cortex started to look like those in neighboring cortical areas of the brain.

鈥淭he effects of losing vision were very broad,鈥 Chen explains. 鈥淭he visual cortex itself changes. It becomes more similar to the areas around it. There are still a lot of questions about how development controls this patterning.鈥

Chen is now working to expand BARseq鈥檚 capabilities even further. He and his team are using the technique to investigate how connections are wired in developing brains and how these connections evolve.

鈥淯nderstanding how cortical areas are set up is the first step in understanding these connections,鈥 he says. 鈥淏ut it鈥檚 not enough. We still need to discover how they progress during development. BARseq can bring us closer to that goal.鈥

Written by: Nick Wurm, Communications Specialist | [email protected] | 516-367-5940


Funding

U.S. Department of Health & Human Services, National Institutes of Health, Brain Research Foundation, Intelligence Advanced Research Projects Activity, Paul G. Allen Frontiers Group

Citation

Chen, X., et al., 鈥淲hole-cortex in situ sequencing reveals input-dependent area identity鈥, Nature, April 24, 2024. DOI:

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Principal Investigator

Anthony Zador

Anthony Zador

Professor
The Alle Davis and Maxine Harrison Professor of Neurosciences
M.D., Ph.D., Yale University, 1994

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