Proteins are the executive agents that carry out all processes in a cell. Their activity is controlled and modified with the help of small chemical tags that can be dynamically added to and removed from the protein. 25 years after its first discovery, researchers at the European Molecular Biology Laboratory (EMBL) in Heidelberg have now gained insight into the role of one of these tags, a small sugar residue, that is found on many different proteins across species. In the current online issue of Science they report that the addition of this sugar tag to proteins in the nucleus of a cell is vital for normal development in fruit flies.
Over 25 years ago scientists discovered that many proteins in the nucleus and cytoplasm have a small sugar molecule, called GlcNAc, attached to them. The enzyme that adds this sugar is called Ogt but since its discovery it has remained elusive why attaching GlcNAc to proteins is important. Researchers in the group of Jrg Mller at EMBL have now discovered that flies lacking Ogt show dramatic developmental defects. In the absence of Ogt cells do not develop into the appropriate cell types and body segments do not differentiate according to plan.
"Expressing the right genes at the right time is critical for a developing organism," says Jrg Mller. "It is the appropriate combination of genes that tells a cell to turn into muscle, nerve or skin. This is why a tight control system regulates gene expression throughout development."
One important component of this control system is a group of regulatory proteins, called Polycomb proteins. They switch off developmental genes when and where their activity is not needed and thereby prevent the formation of specialised tissues and organs in the wrong places.
The scientists found that in the absence of Ogt, Polycomb proteins are no longer able to inactivate developmental genes. They showed that one specific Polycomb protein, called Polyhomeotic, is modi
|Contact: Anna-Lynn Wegener|
European Molecular Biology Laboratory