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Isolation of Murine Spermatogenic Cells using a Violet-Excited Cell-Permeable DNA Binding Dye
Published on: January 14, 2021
INO80 requires a polycomb subunit to regulate the establishment of poised chromatin in murine spermatocytes
Prabuddha Chakraborty1, Terry Magnuson1,2
1Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599-7264, USA.
Abstract:
INO80 is the catalytic subunit of the INO80-chromatin remodeling complex that is involved in DNA replication, repair and transcription regulation. Ino80 deficiency in murine spermatocytes (Ino80cKO) results in pachytene arrest of spermatocytes due to incomplete synapsis and aberrant DNA double-strand break repair, which leads to apoptosis. RNA-seq on Ino80cKO spermatocytes revealed major changes in transcription, indicating that an aberrant transcription program arises upon INO80 depletion. In Ino80WT spermatocytes, genome-wide analysis showed that INO80-binding sites were mostly promoter proximal and necessary for the regulation of spermatogenic gene expression, primarily of premeiotic and meiotic genes. Furthermore, most of the genes poised for activity, as well as those genes that are active, shared INO80 binding. In Ino80cKO spermatocytes, most poised genes demonstrated de-repression due to reduced H3K27me3 enrichment and, in turn, showed increased expression levels. INO80 interacts with the core PRC2 complex member SUZ12 and promotes its recruitment. Furthermore, INO80 mediates H2A.Z incorporation at the poised promoters, which was reduced in Ino80cKO spermatocytes. Taken together, INO80 is emerging as a major regulator of the meiotic transcription program by mediating poised chromatin establishment through SUZ12 binding.
Insights
The INO80 chromatin remodeler regulates gene expression during meiosis. Its depletion disrupts spermatocyte development by altering gene transcription and chromatin states.
Area of Science:
- Reproductive Biology
- Epigenetics
- Chromatin Biology
Background:
- The INO80 complex is crucial for DNA replication, repair, and transcription regulation.
- INO80 deficiency in mouse spermatocytes causes meiotic arrest and apoptosis due to faulty DNA repair and transcription.
Purpose of the Study:
- To investigate the role of INO80 in regulating the meiotic transcription program.
- To understand how INO80 depletion affects chromatin states and gene expression in spermatocytes.
Main Methods:
- RNA sequencing (RNA-seq) to analyze transcription changes in Ino80-deficient spermatocytes.
- Genome-wide analysis of INO80 binding sites in wild-type spermatocytes.
- Chromatin immunoprecipitation to assess H3K27me3 enrichment and H2A.Z incorporation.
Main Results:
- INO80 binds near promoters and regulates spermatogenic gene expression, particularly meiotic genes.
- Loss of INO80 leads to de-repression of poised genes, increased H3K27me3, and altered expression.
- INO80 interacts with SUZ12 and mediates H2A.Z incorporation at poised promoters.
Conclusions:
- INO80 is essential for establishing poised chromatin states during meiosis.
- INO80 regulates the meiotic transcription program through SUZ12 recruitment and H2A.Z incorporation.
- Disruption of INO80 function impairs spermatogenesis by altering epigenetic regulation.
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