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Our work centers on the crosstalk between proteins and genes. We are studying how mechanisms that ensure protein quality regulate transcription, translation, and transcript stability. The goal of this research is to understand, and eventually control, molecular mechanisms that are critical for aging and cancer. 

We are currently pursuing the following research projects:

• How does the site-specific removal of nuclear proteins affect gene regulation in healthy cells and cancers?
• How does protein homeostasis impact mitochondrial activity?
• How do blood stem cells age and maintain a healthy proteome?
• Do chaperones provide a link between protein translation and mRNA decay?

Model systems include:

• Mammalian hematopoiesis
• Multiple myeloma
• Tissue culture and in vivo models

We employ the following approaches and techniques:

• Biochemistry
• Genome-wide genetic screens
• Metabolic activity
• Microscopy
• Molecular biology
• Next generation sequencing: RNA and ChIP

Our target organelles and pathways include:

• Mitochondria
• Nucleus
• Ribosomes
• Ubiquitin-proteasome system