A team of scientists at the Friedrich Miescher Institute for Biomedical Research and the University of Geneva has functionally dissected the molecular processes that ensure the stability of chromosomes. They show in the renowned scientific journal Cell, how three proteins interact on the repetitive sequences at the chromosomal ends, the telomeres, to form a powerful protein scaffold required for telomere homeostasis.
The genome is full of sequence repetitions. Sequence motive is added after sequence motive, sometimes more than a hundred times. Erratically it seems. And these sequence motives bind proteins that control transcription factors in regions of the genome where no transcription should occur. A conundrum.
Nicolas Thomä, group leader at the Friedrich Miescher Institute for Biomedical Research, and his team together with the team of David Shore at the University of Geneva, have now been able to give an answer and assign a function to this seeming inconsistency. In a study published today in Cell, they elucidated how sequence repeats in telomeres help stabilize these regions and prevent cell death.
Telomeres are at the ends of chromosomes and are composed of DNA repeats. With each cell division, because of the nature of DNA replication, one strand of the DNA becomes shorter and would hence trigger processes leading to cell cycle arrest and eventually cell death. There are a variety of processes in place to ensure that both DNA strands are maintained and that the loss of telomeric sequences through unwanted degradation is minimal. One strategy that has been known for a while is the protective capping of the telomeric ends using a set of dedicated proteins.
Read more at: Phys.org