- A study led by scientists of the Universitat Autònoma de Barcelona (UAB) and the National Centre for Genomic Analysis (CNAG-CRG) from the Centre for Genomic Regulation (CRG) reveals the three-dimensional genomic structure of male germ cells and how this structure determines their function.
- The study, published in the journal Cell Reports, represents a significant advance in our understanding of how the dynamics of insulator proteins and transcriptional activity are coupled during the 3D genome re-organisation that takes place during the formation of male germ cells.
The code of life (genome) is not just a linear sequence of letters, but is also folded (compartmentalised) into a specifically tailored chromatin structure within the cell nuclei. This three-dimensional genomic structure is fundamental, given that it determines which genes “turn on” and which are “turned off” in each cell types.
A new study led by scientists from the UAB and the CNAG-CRG and published in Cell Reports reveals the three-dimensional genomic structure of male germ cells. The study, carried out on mice, shows that this structure is extremely dynamic during the formation of germ cells (gamete precursor cells). Moreover, the study revealed a fine-tuned balance between chromatin remodelling, architectural proteins such as cohesins and gene expression during this process.
All sexually reproducing organisms form haploid gametes (oocytes and sperm) – each cell type carrying only one copy of each chromosome – through two consecutive cell divisions preceded by one round of genome replication. This process is known as meiosis and implies that the genome must be packaged and unpackaged in a precise and highly regulated manner.
“Our work shows the dynamics of chromatin remodelling during the formation of male gametes, by comparing changes in chromatin folding and gene transcription at different moments throughout male meiosis”, says coordinator of the study Aurora Ruiz-Herrera, researcher at the Department of Cell Biology, Physiology and Immunology of the Institute of Biotechnology and Biomedicine (IBB) at the UAB, where she leads the research group in Animal Genomics. “We have thus demonstrated the existence of different degrees of genome folding and how these different levels of genome organization are related to structural proteins such as cohesins and gene expression. The results will pave the way for new investigations into the molecular mechanisms regulating these changes.”
“This study has been possible only thanks to the combination of complementary techniques in biology such as molecular genetics, microscope imaging and computer simulations. It truly is a multidisciplinary project”, explains Marc A. Marti-Renom, ICREA researcher and head of the Structural Genomics Group at the CNAG-CRG and co-leader of the study.
The project represents a significant advance in the study of the mechanisms generating and regulating the 3D structure and function of the genome during the formation of gametes. Determining these mechanisms is fundamental, given that the deregulation of this process can lead to diseases such as infertility and chromosome alterations like trisomy 21.
According to scientists, the research also represents an example of the importance of synergy among specialists from different fields such as molecular and cell biology, genomics and bioinformatics in advancing in our knowledge of the regulation and structure of the genome. Participating in the study were seven research teams, including the UAB, the CNAG-CRG, the CSIC-University of Salamanca, the Sequentia Biotech and the University of New South Wales in Sydney.
The study has received funding from the Ministry for Economics, Industry and Competitiveness, the Government of Catalonia (AGAUR), the Institute of Health Carlos III, the Government of Castilla y León, the European Research Council (ERC) and the Horizon 2020 Programme.
Original article: C. Vara, A. Paytuví-Gallart, I. Cuartero et al. “Three-Dimensional Genomic Structure and Cohesin Occupancy Correlate with Transcriptional Activity during Spermatogenesis”. Cell Reports 28, 1-16 (2019). DOI: 10.1016/j.celrep.2019.06.037
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