Yin Yang 1 controls cerebellar astrocyte maturation

Author:

Mockenhaupt Karli1,Tyc Katarzyna M.23,McQuiston Adam4,Gonsiewski Alexandra K.1,Zarei‐Kheirabadi Masoumeh1,Hariprashad Avani1,Biswas Debolina D.1,Gupta Angela S.1,Olex Amy L.5,Singh Sandeep K.1ORCID,Waters Michael R.1,Dupree Jeff L.6,Dozmorov Mikhail G.2,Kordula Tomasz17ORCID

Affiliation:

1. Department of Biochemistry and Molecular Biology The Massey Cancer Center, Virginia Commonwealth University Richmond Virginia USA

2. Department of Biostatistics The Massey Cancer Center Virginia Commonwealth University Richmond Virginia USA

3. Massey Cancer Center Bioinformatics Shared Resource Core The Massey Cancer Center, Virginia Commonwealth University Richmond Virginia USA

4. Department of Anatomy and Neurobiology The Massey Cancer Center Virginia Commonwealth University Richmond Virginia USA

5. C. Kenneth and Dianne Wright Center for Clinical and Translational Research The Massey Cancer Center, Virginia Commonwealth University Richmond Virginia USA

6. Research Service, Central Virginia VA Health Care System Richmond Virginia USA

7. The Massey Cancer Center, Virginia Commonwealth University Richmond Virginia USA

Abstract

AbstractDiverse subpopulations of astrocytes tile different brain regions to accommodate local requirements of neurons and associated neuronal circuits. Nevertheless, molecular mechanisms governing astrocyte diversity remain mostly unknown. We explored the role of a zinc finger transcription factor Yin Yang 1 (YY1) that is expressed in astrocytes. We found that specific deletion of YY1 from astrocytes causes severe motor deficits in mice, induces Bergmann gliosis, and results in simultaneous loss of GFAP expression in velate and fibrous cerebellar astrocytes. Single cell RNA‐seq analysis showed that YY1 exerts specific effects on gene expression in subpopulations of cerebellar astrocytes. We found that although YY1 is dispensable for the initial stages of astrocyte development, it regulates subtype‐specific gene expression during astrocyte maturation. Moreover, YY1 is continuously needed to maintain mature astrocytes in the adult cerebellum. Our findings suggest that YY1 plays critical roles regulating cerebellar astrocyte maturation during development and maintaining a mature phenotype of astrocytes in the adult cerebellum.

Funder

National Cancer Institute

National Center for Advancing Translational Sciences

National Institute of Neurological Disorders and Stroke

Publisher

Wiley

Subject

Cellular and Molecular Neuroscience,Neurology

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