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| From left, Qixiang He, Ci Ji Lim, Xiuhua Lin. Resized Image using AI by SFLORG Credit: University of Wisconsin–Madison |
Researchers at the University of Wisconsin–Madison have described the way an enzyme and proteins interact to maintain the protective caps, called telomeres, at the end of chromosomes, a new insight into how a human cell preserves the integrity of its DNA through repeated cell division.
DNA replication is essential for perpetuating life as we know it, but many of the complexities of the process — how myriad biomolecules get where they need to go and interact over a series of intricately orchestrated steps — remain mysterious.
“The mechanisms behind how this enzyme, called Polα-primase, works have been elusive for decades,” says Ci Ji Lim, an assistant professor of biochemistry and principal investigator on new research into DNA replication published recently in Nature. “Our study provides a big breakthrough in understanding DNA synthesis at the ends of chromosomes, and it generates new hypotheses about how Polα-primase — a central cog in the DNA replication machine — operates.”
Every time a cell divides, the telomeres at the end of the long DNA molecule that makes up a single chromosome shorten slightly. Telomeres protect chromosomes like an aglet protects the end of a shoelace. Eventually, the telomeres are so short that vital genetic code on a chromosome is exposed and the cell, unable to function normally, enters a zombie state. Part of a cell’s routine maintenance includes preventing excessive shortening by replenishing this DNA using Polα-primase.














