Research interests
SEx specific differences in aging
Metabolism
Sex specific differences in aging in C. elegans
A focus of the Rottiers lab is to understand sex specific differences in aging. We use the worm, C. elegans, to study how the removal of germline stem cells increases the lifespan in a sex-specific manner. Like many stem cell systems, the C. elegans germ line contains a self-renewing germ cell population that is maintained by a niche. Interestingly, specific removal of the proliferating germline stem cells (GSCs) in the gonad ofC. elegans hermaphrodites robustly increases their lifespan while male lifespan is not changed. We are using metabolomic and genetic tools to investigate the changes that occur (or fail to occur) upon germ cell stem cell loss in hermaphrodites and males and determine the nature of the sex-specific differences in response to GSC loss. Such research will help us understand how changes in GSCs pools or different responses to signals from the germ cell stem affect the lifespan of organisms in a sex specific way.
Regulation of lipid homeostasis in C. elegans
More than one-third of U.S. adults are currently obese, causing an alarming rise in obesity associated diseases as well health care costs. Numerous human Genome-Wide Association Studies have found significant associations between many specific genetic loci and obesity. However, the importance or mechanism of action these genetic loci is lacking and hard to obtain. Functional studies of conserved genes in model organisms have the potential to determine the role of associated genes and identify those that could be targeted for treatment. Through cross referencing the results of genome wide screens for fat regulators in C. elegans with human obesity GWAS lists, we identified potential conserved pathways of lipid homeostasis. We are using a variety of genetic and molecular techniques in C. elegans and mammalian cell culture to assign functions to these genes and assess their therapeutic potential.
Funding
LAB MEMBERS
Veerle Rottiers
Principal Investigator
Dr. Rottiers received her PhD from Ghent University working on C. elegans hormonal regulation in the lab of Adam Antebi. She did her postdoctoral work at MGH Cancer Center/Harvard Medical School in Boston studying conserved regulation of lipid homeostasis.
In 2013, Dr. Rottiers moved to the Molecular Biology and Genetics Department at Cornell as an independent researcher where she secured funding from the American Heart Association as well as the National Institute on aging (NIA/NIH) for her work on metabolism and aging in C. elegans .
She joined the department of Nutritional Sciences and Toxicology at UC Berkeley in February 2019 as a PI where she is working with together with Dr. Anders Naar as well as lead independent research.
Melissa BOLDRIDGE
Graduate student
Melissa Boldridge is from Little Egg Harbor, NJ. She did her Bachelors is Cambridge, MA and has since lived in Biloxi, MS, Honolulu, HI, and Washington, DC. She joined the lab in 2020 and has worked on understanding the role of of the mitochondrial carrier homolog MTCH2 in mammalian lipid homeostasis.
Amandine Rapp
Graduate student
Amandine hails from Switzerland. She came to UC Berkeley for the world-class research, the metabolic biology focus of the program and the beautiful Bay area. She joined the lab in 2022. Her research focus is on Transketolase, an enzyme of the Pentose Phosphate Pathway and its role in the regulation of lipid homeostasis in C. elegans.
VIVIAN da CRUZ RODRIGUES
Graduate student
Vivian is joining us as a Visiting Research Student from the lab of Leandro Pereira de Moura at the University of Campinas in Brazil. She will study the role of MTCH2 in lipid homeostasis in mice.
Rottiers Lab
Department of Nutritional Sciences & Toxicology
244 Morgan Hall
Berkeley, CA 94720
USA