# GATAD2B regulates spindle assembly by affecting protein deacetylation during oocyte meiotic maturation

## TL;DR

This study shows that GATAD2B helps oocytes mature properly by regulating protein deacetylation, which is important for forming the spindle needed for cell division.

## Contribution

The study identifies GATAD2B as a novel regulator of histone deacetylation during oocyte meiotic maturation.

## Key findings

- GATAD2B is stably expressed during oocyte meiosis and increases at the MII stage.
- Knocking down GATAD2B leads to abnormal spindle formation, chromosome misalignment, and increased aneuploidy.
- Deacetylation-related genes are downregulated and acetylated proteins accumulate in GATAD2B-deficient oocytes.

## Abstract

Oocyte quality is critical for the stable transmission of genetic information and affects early embryonic development. But the precise mechanisms governing oocyte meiotic progression remains largely unclear. Transcription regulation through chromatin compaction and decompaction is regulated through various chromatin-remodeling complexes such as nucleosome remodeling and histone deacetylation (NuRD) complex. GATAD2B is known to be a component of the NuRD complex but whether GATAD2B regulates chromatin modification in mouse oocyte meiosis remains unclear. We hope to explore the role of GATAD2B in mouse oocyte meiosis.

In this study, we initially utilized western blot and immunofluorescence to delineate the expression and subcellular localization of GATAD2B during oocyte meiotic maturation. To further elucidate the role of GATAD2B in regulating oocyte meiotic division, we employed the method of microinjection of Gatad2b-specific siRNA to knock down the protein expression of GATAD2B. Subsequently, dynamic changes in oocyte meiotic division were captured in real-time using live-cell imaging with Geri. Additionally, spindle staining, DNA staining, spread analysis, and reanalysis of RNA-seq data were performed to investigate the mechanisms through which GATAD2B regulates oocyte meiotic division.

GATAD2B was stably expressed during oocyte meiosis and was significantly increased during the metaphase II (MII) stage. To further explore the effect of GATAD2B on oocyte meiotic maturation, we observed increased abnormal spindle, severe chromosome misalignment and metaphase I (MI) block in GATAD2B knocked-down (GATAD2B-KD) oocytes. Interestingly, the distribution of microtubule organizing center was abnormal and aneuploidy was significantly increased in GATAD2B-KD oocytes. In addition, some deacetylation-related genes were significantly downregulated and acetylated proteins accumulated abnormally in GATAD2B-KD oocytes.

These findings implicate GATAD2B as a novel regulator of histone deacetylation during oocyte maturation and provide evidence that such deacetylation is required for proper spindle assembly.