Studies at the Intersection of Ribosome Function and Cellular Homeostasis

The ribosome is a complex molecular machine that translates the genetic code into functional polypeptides. Our work focuses on understanding how the ribosome functions at a molecular level and how changes in its activity lead to mRNA quality control and the induction of cellular stress responses. Work in the Green lab ranges widely in scope, from detailed mechanistic questions in ribosome rescue to surveying global changes in gene expression and dissecting the complex interplay of mammalian signaling pathways. We use a wide range of genetic, genomic, and biochemical approaches to explore these questions in bacteria, yeast, and increasingly in mammalian systems. Much of our ongoing work focuses on the importance of ribosome collisions in activating signaling pathways such as the integrated stress response (ISR) and various MAP kinase cascades.

Watch Rachel Green’s iBiology.org video explaining Protein Synthesis at https://www.ibiology.org/biochemistry/protein-synthesis/

Click on each figure to read more!

collided-ribosome.jpg
 
 

The Legionella pneumophila effector SidL is an adenylyltransferase that modifies the glycolytic intermediate 3-phosphoglycerate

 
 

ZAK activation at the collided ribosome

 
 

RIOK3 mediates the degradation of 40S ribosomes

 

The RNA helicase HrpA rescues collided ribosomes in E. coli

 

EDF1 coordinates cellular responses to ribosome collisions

 

LARP1 binds ribosomes and TOP mRNAs in repressed complexes

 

Ribosome collisions trigger general stress responses to regulate cell fate

 

The ribotoxic stress response drives UV-mediated cell death



 

Ribosome collisions induce mRNA cleavage and ribosome rescue in bacteria