麻豆淫院

Over half of our genomes consist of thousands of remnants of ancient viral DNA, known as transposable elements, which are widespread across the tree of life. Once dismissed as the "dark side" of the genome, researchers at Helmholtz Munich and Ludwig-Maximilians-Universit盲t (LMU) have now revealed their crucial role in early embryo development. The study is in the journal Cell.

Transposable elements, remnants of ancient viral DNA, are reactivated during the first hours and days following fertilization. This dynamic period of early development sees embryonic cells displaying remarkable plasticity, yet the molecular mechanisms and factors that regulate this plasticity remain unclear.

Research in models such as mice suggests that transposable elements play a crucial role in cellular plasticity, but it is still uncertain whether this is a universal feature across all mammalian species. The diverse evolutionary origins of these viral remnants raise further questions about their conservation across mammalian genomes. Understanding the regulatory mechanisms governing the activation of transposable elements is essential for advancing reproductive medicine and uncovering the fundamental principles of genome regulation.

A team of researchers led by Prof. Maria-Elena Torres-Padilla at Helmholtz Munich and LMU set out to explore these ancient DNA sequences by developing a novel method to study their transcription. They created a single-embryo atlas by comparing embryos from several mammalian species, including mouse, cow, pig, rabbit, and the non-human primate, rhesus macaque.

Their findings were surprising: The researchers discovered that very old viral elements, previously thought to be extinct, are re-expressed in mammalian embryos. They also found that each species studied expresses distinct types of these elements.

These observations show that the activation of transposable elements is conserved across species, and identifying specific elements provides exciting opportunities to manipulate thousands of genes in cells at the same time.

"This approach offers a novel way to influence cell fate, such as directing stem cell differentiation, which typically requires the simultaneous manipulation of hundreds of genes," says co-first author Dr. Marlies Oomen. "Our work highlights the importance of understanding the regulatory principles behind transposable elements."

Prof. Torres-Padilla further explains, "Our research uncovered that transposable element activation is a distinctive feature of early embryos in several mammalian species. This finding is significant because these early-stage cells can differentiate into all body cell types.

"By understanding how these cells regulate ancient viral elements, we gain crucial insights into the mechanisms of cellular plasticity. This study sets the stage for future research into specific regulatory elements, with broad implications for health, disease, and how manipulating these elements could impact cellular processes."

In addition to developing a novel methodology that opens new avenues for researchers working with single cells and embryos, this study has generated an unprecedented dataset. Early embryo development is a highly dynamic process that is of great interest to scientists, but most studies tend to focus on a single species, typically mouse or human.

This study, however, took an evolutionary approach by comparing multiple mammalian species, allowing the identification of key regulatory pathways shared across mammals. The biological insights gained from this research, combined with the rich dataset, will serve as a valuable resource for researchers in developmental and reproductive biology.