Cancer Research Takes A Closer Look At Zombie Cells
A new yeast model lets scientists investigate a gene mutation that interferes with DNA duplication, causing massive damage to a cell’s chromosomes, but somehow allowing the cell to keep dividing. The result of the mutation is zombie cells that by all accounts shouldn’t be able to survive, let alone divide, with their chromosomes shattered and strung out between tiny micronuclei.
Sometimes they’re connected to each other by ultrafine DNA bridges. Imagine tearing apart a hot pizza. These DNA bridges are like strings of cheese still draping between the separated pieces.
Often, the micronuclei, which are thought to retain the most damaged portions of the DNA, rejoin the parent nuclei and incorporate mutations into the survivors.
The mutation has been associated with cancer in mice, and micronuclei are often found in human cancer cells. With their new yeast model, researchers hope to learn more about each.
Senior author Susan Forsburg says:
“Using a simple yeast system, we have developed a powerful genetic model to investigate a recently identified characteristic of human cancer cells. This will enable us to rapidly identify genes responsible for this abnormal division.”
Because the genes that regulate division in human and yeast cells are the same, this simple organism provides a tool for human cell discovery, Forsburg says.
DNA is vulnerable to damage when it’s unzipped into two single strands for replication by a cell’s MCM helicase, a cellular component essential to DNA replication.
Typically, the single-stranded DNA triggers repair of damage by special enzymes or, in extreme cases, drives the damaged cell to suicide. Either way, cell division halts while the issue is dealt with.
But in cancer cells, despite the damaged DNA, the cells continue to divide—creating tumors full of genetic mutations. In this study, a mutation in the yeast’s MCM helicase triggered responses similar to those in mammals where mutations in this gene are associated with cancer and the formation of micronuclei.
Mutations on Video
To study the phenomenon, Forsburg and lead author Sarah Sabatinos collected videos of the damaged cells dividing so that they could maintain continuous monitoring of individual cells and record cell division from beginning to end.
They watched what happened in the mutant in real time and then used a super-resolution microscope that generates 3D images of objects at the nanometer scale to examine the damaged structures in crisp detail.
Says Sabatinos, who conducted the study as a postdoctoral researcher at USC. She is now an assistant professor at Ryerson University in Toronto:
“The devil’s in the division. In real time, we’re able to see that these mutant cells ignore the damage caused during DNA replication, which results in the creation of unusual structures like micronuclei.”
The work will inform future studies into how a cancer cell evades biological checkpoints that should halt its division and spread.