What New Insights Have Scientists Uncovered About Evolution and Major Diseases?

Synopsis
Key Takeaways
- Viruses utilize human cellular machinery to replicate.
- Transposable elements are remnants left by viruses in human DNA.
- LINE-1 can still migrate within the genome.
- Research may lead to new therapies targeting LINE-1 replication.
- Understanding these mechanisms is crucial for human health.
New York, May 4 (NationPress) A groundbreaking study has shed light on how a genetic component, comprising a significant portion of human DNA, can effectively invade the nucleus to replicate itself. Viruses are known to hijack the genetic machinery of human cells they penetrate to create copies of themselves.
During this process, viruses leave behind traces throughout the genetic material (genomes) of humans.
The virus-like insertions, referred to as “transposable elements,” are fragments of genetic material that are even more primitive than viruses and also utilize host cell machinery for replication, as detailed in the study published in the journal Science Advances.
While most of these inserted elements have been silenced by our cellular defense mechanisms over time, a select few, dubbed “jumping genes,” can still navigate the human genome just like viruses.
One such element, known as long interspersed nuclear element 1 (LINE-1), retains the ability to move independently.
According to Liam J Holt, associate professor in the Department of Biochemistry and Molecular Pharmacology and the Institute for Systems Genetics at NYU Grossman School of Medicine, these findings regarding the specific mechanisms behind LINE-1 insertion pave the way for developing future therapies aimed at preventing LINE-1 replication.
To replicate itself, LINE-1 must infiltrate each cell’s nucleus, the protective barrier that contains DNA.
Directed by researchers from NYU Langone Health and the Munich Gene Center at Ludwig-Maximilians-Universität (LMU) München in Germany, the study demonstrated that LINE-1 attaches to cellular DNA during the fleeting moments when nuclei temporarily open as cells undergo division, creating replacements to ensure tissue viability as we age.
The research team discovered that LINE-1 RNA capitalizes on these instances, forming clusters with one of the two proteins it encodes, ORF1p, to tightly bind to DNA until the nucleus reassembles post-cell division.
“In the future, we aim to explore whether other condensates experience functional alterations as the ratios among their components shift,” stated Dr. Holt.