Save
Email
Print
ShareMay 4, 2011 — Scientists have discovered a new component of mitochondria that plays a key part in their function. The discovery, which is presented in the journal Cell Metabolism, is of potential significance to our understanding of both inherited and age-related diseases.
Mitochondria are normally called the cell's power plants since they convert the energy in our food into a form that the body can use. To work properly, the mitochondria have to form new proteins, which they do in their ribosomes.
A group of researchers at Karolinska Institutet in Sweden and the Max Planck Institute for Biology of Ageing, Germany, has discovered that a protein called MTERF4 combines with another protein called NSUN4 to form a complex that controls the formation and function of the mitochondrial ribosomes. In mice lacking MTERF4 no functional ribosomes are formed, leading to a reduction in energy production.
"Reduced mitochondrial function is involved in several inherited diseases, normal aging and age-related diseases," says Professor Nils Göran Larsson, who co-led the study with Professor Claes Gustafsson. "Fundamental knowledge of how mitochondrial function is regulated can therefore be of great clinical significance in the future."
The research group previously discovered similar regulation mechanisms in the mitochondria that were found to be related to the development of diabetes.
Other social bookmarking and sharing tools:
Story Source:
The above story is reprinted from materials provided by Karolinska Institutet.
Note: Materials may be edited for content and length. For further information, please contact the source cited above.
Journal Reference:
- Yolanda Cámara, Jorge Asin-Cayuela, Chan Bae Park, Metodi D. Metodiev, Yonghong Shi, Benedetta Ruzzenente, Christian Kukat, Bianca Habermann, Rolf Wibom, Kjell Hultenby, Thomas Franz, Hediye Erdjument-Bromage, Paul Tempst, B. Martin Hallberg, Claes M. Gustafsson, Nils-Göran Larsson. MTERF4 Regulates Translation by Targeting the Methyltransferase NSUN4 to the Mammalian Mitochondrial Ribosome. Cell Metabolism, 2011; 13 (5): 527-539 DOI: 10.1016/j.cmet.2011.04.002
Note: If no author is given, the source is cited instead.
more 
