Researchers at Michigan State University have discovered a protein that does its best work with one foot in the grave. The study, which appears in the current issue of the Journal of Biological Chemistry, focuses on the nontraditional lifestyle of Retinoblastoma tumor¹ suppressor proteins, which could lead to new ways to treat cancer.

 

"Retinoblastoma proteins are unique in that they use controlled destruction to do their jobs in a timely but restrained（克制的） fashion," said Liang Zhang, a lead author and MSU cell and molecular² biology graduate student. "This is an unusual way for proteins to act."

 

As an organism grows, proteins essential for fueling its prosperity typically toe a tight line, performing their jobs at the right place and time. If these proteins go rogue³, disasters such as cancer can result.

 

Retinoblastoma proteins, which could be labeled as rebellious⁴ as opposed to rogue, perform acts of valor⁵ rather than destruction. And just like fireworks, they save their best work for the finale.

 

Proteins' lifecycles end with degradation⁶, and like most living things they become weaker and less efficient at their jobs near the end of their lives. For Retinoblastoma proteins, however, their destruction is linked to their ability to efficiently⁷ control excessive cell growth.

 

Using the fruit fly Drosophila, MSU researchers isolated⁸ the specific region that controls the protein's ability to degrade. Strikingly, this is the same region the protein uses to hit its stride and exert its full power to suppress genes¹⁰ related to unrestrained cell growth. Other categories of genes, such as those linked to cell death, may not be influenced by this specific region that controls degradation. This sheds light on a single mechanism¹¹ that controls both living and dying at the genetic¹² level.

 

Identifying this mechanism in fruit flies could be beneficial to humans. David Arnosti, MSU biochemist and director of MSU's Gene⁹ Expression in Disease Development initiative, noted¹³ the genetic similarities between humans and Drosophila, describing fruit flies as "resembling little people with wings."

 

"By revealing the molecular details about the regulation of the fly Retinoblastoma protein, we can start to understand the possible roles of the human counterparts in cancer," he said.

 

The research was a product of NIH-funded research between the laboratories of Arnosti and R. William Henry, MSU biochemist.

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