Beyond telomerase: another enzyme discovered critical to maintaining telomere length
Researchers have uncovered the role of an another enzyme crucial to telomere length in addition to the telomerase. The researchers say the new test they used to find the enzyme should speed discovery of other proteins and processes that determine telomere length.
Shortened telomeres have been implicated in aging and in diseases as diverse as lung and bone marrow disorders, while overly long telomeres are linked to cancer.
“We’ve known for a long time that telomerase doesn’t tell the whole story of why chromosomes’ telomeres are a given length, but with the tools we had, it was difficult to figure out which proteins were responsible for getting telomerase to do its work,” says Carol Greider, Ph.D., the Daniel Nathans Professor and Director of Molecular Biology and Genetics in the Johns Hopkins Institute for Basic Biomedical Sciences. Greider won the 2009 Nobel Prize in Physiology or Medicine for the discovery of telomerase.
Figuring out exactly what’s needed to lengthen telomeres has broad health implications, Greider notes. Telomeres naturally shorten each time DNA is copied in preparation for cell division, so cells need a well-tuned process to keep adding the right number of building blocks back onto telomeres over an organism’s lifetime.
But until now, researchers have been saddled with a limiting and time-consuming test for whether a given protein is involved in maintaining telomere length, a test that first requires blocking a suspected protein’s action in lab-grown cells, then getting the cells to grow and divide for about three months so that detectable differences in telomere length can emerge. In addition to being time consuming, the test could not be used at all for proteins whose loss would kill the cells before the three-month mark.
For their trial run of the new test, dubbed “addition of de novo initiated telomeres (ADDIT),” Greider’s group examined an enzyme called ATM kinase. “ATM kinase was known to be involved in DNA repair, but there were conflicting reports about whether it had a role in telomere lengthening,” says Greider.
Her team blocked the enzyme in lab-grown mouse cells, and used ADDIT to find that it was indeed needed to lengthen telomeres. They verified the result using the old, three-month-long telomere test, and got the same result.
The team also found that in normal mouse cells, a drug that blocks an enzyme called PARP1 would activate ATM kinase and spur telomere lengthening. This finding offers a proof of principle for drug-based telomere elongation to treat short-telomere diseases, such as bone marrow failure, Greider says, but she cautions that PARP1 inhibitor drug itself doesn’t have the same telomere-elongating effect in human cells as it does in mouse cells.
Greider’s group plans to use ADDIT to find out more about the telomere-lengthening biochemical pathway that ATM kinase is a part of, as well as other pathways that help determine telomere length.
“The potential applications are very exciting,” says graduate student Stella Suyong Lee, who conducted the research, which took nearly five years. “Ultimately ADDIT can help us understand how cells strike a balance between aging and the uncontrolled cell growth of cancer, which is very intriguing.”