# Comparison of Nucleosome Landscapes Between Porcine Embryonic Fibroblasts and GV Oocytes

**Authors:** Minjun Zhao, Shunran Zhao, Zhaoqi Pang, Chunhui Jia, Chenyu Tao

PMC · DOI: 10.3390/ani14233392 · Animals : an Open Access Journal from MDPI · 2024-11-25

## TL;DR

This study compares chromatin structure and gene expression in pig oocytes and fibroblasts, revealing differences in nucleosome positioning that could aid in nuclear transplantation.

## Contribution

The study identifies unique nucleosome patterns and gene expression profiles in porcine oocytes versus fibroblasts, offering insights for cell reprogramming.

## Key findings

- Nucleosome occupancy in BF promoters was significantly higher (4.85%) than in PEF (3.3%).
- 51 genes were uniquely expressed in BF, and 80 in PEF, based on transcriptome reanalysis.
- Nucleosome distribution around TSSs correlated with expression in PEF but not in BF.

## Abstract

Nucleosomes serve as the basic structural components of chromatin and act as key regulators of gene expression and cellular function. In this study, we compared the nucleosome occupancy, distribution, and transcription of genes between two types of cells: fully grown germinal vesicle (GV) oocytes from big follicles (BF) and somatic cells (porcine embryonic fibroblast, PEF). The nucleosome occupancy in the BF promoter was significantly higher than in PEF. A reanalysis of published transcriptomes of fully grown GV oocytes and PEF identified 51 uniquely expressed genes in BF and 80 in PEF. The nucleosome distribution around gene transcription start sites (TSSs) correlated with expression levels in somatic cells, but results differed between BF and PEF. This research reveals the dynamic changes and crucial roles of nucleosome positioning and chromatin organization in different cell types, providing a theoretical basis for nuclear transplantation.

(1) Background: Nucleosomes represent the essential structural units of chromatin and serve as key regulators of cell function and gene expression. Oocytes in the germinal vesicle (GV) stage will later undergo meiosis and become haploid cells ready for fertilization, while somatic cells undergo mitosis after DNA replication. (2) Purpose: To furnish theoretical insights and data that support the process of cell reprogramming after nuclear transplantation. (3) Methods: We compared the nucleosome occupancy, distribution, and transcription of genes between two types of cells: fully grown GV oocytes from big follicles (BF) and somatic cells (porcine embryonic fibroblast, PEF). (4) Results: The nucleosome occupancy in the promoter of BF was 4.85%, which was significantly higher than that of 3.3% in PEF (p < 0.05), and the nucleosome distribution showed a noticeable increase surrounding transcriptional start sites (TSSs) in BF. Next, we reanalyzed the currently published transcriptome of fully grown GV oocytes and PEF, and a total of 51 genes in BF and 80 genes in PEF were identified as being uniquely expressed. The nucleosome distribution around gene TSSs correlated with expression levels in somatic cells, yet the results in BF differed from those in PEF. (5) Conclusion: This study uncovers the dynamic nature and significance of nucleosome positioning and chromatin organization across various cell types, providing a basis for nuclear transplantation.

## Full-text entities

- **Genes:** COL1A1 [NCBI Gene 397571], FN1 (fibronectin 1) [NCBI Gene 397620], NANOG (Nanog homeobox) [NCBI Gene 79923], GATA4 (GATA binding protein 4) [NCBI Gene 2626] {aka ASD2, TACHD, TOF, VSD1}, MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609] {aka MRTL, MYCC, bHLHe39, c-Myc}, SOX2 (SRY-box transcription factor 2) [NCBI Gene 6657] {aka ANOP3, MCOPS3}, POU5F1 (POU class 5 homeobox 1) [NCBI Gene 5460] {aka OCT3, OCT4, OCT4Borf1, OTF-3, OTF3, OTF4}, KLF4 (KLF transcription factor 4) [NCBI Gene 9314] {aka EZF, GKLF}, Obox6 (oocyte specific homeobox 6) [NCBI Gene 252830] {aka D17Ertd599e}, FOXA2 (forkhead box A2) [NCBI Gene 3170] {aka HNF-3-beta, HNF3B, TCF3B}, THBS1 (thrombospondin 1) [NCBI Gene 492313], ACTA2 (actin alpha 2, smooth muscle) [NCBI Gene 733615] {aka ACT-4, actin}, ZP2 (zona pellucida glycoprotein 2) [NCBI Gene 396846] {aka ZPA, Zp-2, pZP1}, SYCN (syncollin) [NCBI Gene 100628195], SPARC [NCBI Gene 100514136], OOEP (oocyte expressed protein) [NCBI Gene 100152355], TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, GLIS1 (GLIS family zinc finger 1) [NCBI Gene 148979], ZP3 (zona pellucida glycoprotein 3) [NCBI Gene 396927] {aka ZPC, Zp-3}, ZP4 (zona pellucida glycoprotein 4) [NCBI Gene 397111] {aka ZP3-ALPHA, ZPB, Zp-4}
- **Diseases:** PEF (MESH:D004682), injury to people or property (MESH:C000719191), BF (MESH:D000072717)
- **Chemicals:** lipids (MESH:D008055), BF (-)
- **Species:** Sus scrofa (pig, species) [taxon 9823], Homo sapiens (human, species) [taxon 9606], Bos taurus (bovine, species) [taxon 9913], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11840278/full.md

## References

27 references — full list in the complete paper: https://tomesphere.com/paper/PMC11840278/full.md

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Source: https://tomesphere.com/paper/PMC11840278