Welcome to the Genomic Stability Lab website!

 We study how cells signal and repair lesions to our genetic material, the DNA. We are particularly interested in how a post-translational modification called ADP-ribosylation accelerates DNA repair processes, and how mutations in genes involved in DNA damage signalling and repair cause rare genetic disorders characterized by neurodegeneration, cancer predisposition and premature aging.

Fluorescence microscopy of human cells in culture. Blue: DNA in the cell nucleus, green: actin filaments, red: mitochondria.
Fluorescence microscopy of a sister chromatid exchange assay. Chromosomes from a human cell are labelled such that one sister chromatid is seen in green and the other in blue. In response to DNA damage, homologous recombination may lead to the exchange of genetic information between sister chromatids, causing a reciprocal exchange in the colouring pattern of the chromosomes.

ADP-ribosylation is a post-translational modification of proteins with important roles in signaling the presence of DNA damage, in chromatin remodeling and recruitment of DNA repair factors to the damage site, as well as in a programmed cell death pathway called parthanatos. Recently we have also been interested in studying the role of ADP-ribosylation in other pathways, especially in the cellular response to viral infections.  

CONTACT US

Departamento de Bioquímica

Instituto de Química

Av. Prof. Lineu Prestes, 748
Cidade Universitária – USP
CEP: 05508-000
Brasil