Gene Center Munich
print


Breadcrumb Navigation


Content

Ribosome Biogenesis

Finding form by folding

05.01.2018

Ribosomes are the organelles responsible for protein synthesis in cells. LMU researchers have now dissected early steps in their assembly and visualized how their RNA components fold correctly and find their places in the growing structure.

kater paper

 

 

Three-dimensional structure of a nucleolar ribosomal complex. Assembly factors are indicated in various colors, while ribosomal RNAs and proteins are indicated in light and dark gray, respectively. Image: L.Kater, LMU

In actively growing cells, a huge variety of proteins must be synthesized in widely varying amounts. To meet these demands, the cell’s protein factories – the ribosomes – which are made up of proteins and several RNAs must themselves be built in considerable numbers. A growing yeast cell produces on the order of 100,000 ribosomes per hour, each of which consists around 80 ribosomal proteins and four ribosomal RNAs (rRNAs), distributed between two distinct subunits that functionally interact with each other. In addition, ribosomal assembly requires the intervention of approximately 200 other proteins that serve as biogenesis factors, which are not part of the final structure. These factors orchestrate the construction of the ribosome and direct the sequential folding of the rRNAs, which provides the appropriate binding sites for the insertion of the ribosomal proteins. LMU researchers led by Professor Roland Beckmann, in cooperation with Professor Ed Hurt’s group at Heidelberg University, have now determined, for the first time in three-dimensional detail, how the early steps in the assembly of the large subunit take place in yeast cells. The findings appear in the leading journal Cell.

More information please visit LMU.de/news


Original Publication:

Visualizing the Assembly Pathway of Nucleolar Pre-60S Ribosomes.
Kater L, Thoms M, Barrio-Garcia C, Cheng J, Ismail S, Ahmed YL, Bange G, Kressler D, Berninghausen O, Sinning I, Hurt E, Beckmann R.
Cell. 2017 Dec 14;171(7):1599-1610.e14. doi: 10.1016/j.cell.2017.11.039