Hans M. Dalton
- Assistant Professor
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Biography —
My research interests involve exploring essential gene biology (i.e. genes we need in order to survive). This includes their impact on rare diseases, their biological mechanisms, and their other impacts on humans (e.g. aging biology, genomics). We use therapeutic screens with Drosophila and human cell models to create evidence for potential therapeutics as well as better understand the underlying biology. I believe science can and should be accessible and inclusive to all who want to pursue it - no matter your background. I grew up in a small town in northern Michigan in a small graduating class, and I feel grateful to be where I am now and have the opportunity to do scientific research. I wanted to be a scientist because I wanted to help find the answers to yet-unanswered scientific questions (and it turns out there are still millions of them). Our lab goals are to help people, help science, and hopefully have some fun along the way.
I earned my B.S. in Biochemistry with Honors at the University of Michigan, where I studied a G-protein coupled receptor disorder in mice in the laboratory of Dr. Rick Neubig (now at Michigan State University). I went on to earn my Ph.D. in Molecular Biology at the University of Southern California, where I studied aging biology in C. elegans in the laboratory of Dr. Sean Curran. I then worked for 5 years as a postdoc at the University of Utah, where I studied rare diseases called Congenital Disorders of Glycosylation (CDGs) in Drosophila and cells in the laboratory of Dr. Clement Chow.
Education —
Research —
Lab research vision:
Around 2,000 genes (~10%) are essential - necessary to live or for fitness. These represent a diverse set of biological functions, including metabolism, protein synthesis, transcription, the cytoskeleton, and more. Relative to their importance, there is still much unknown about these genes - including ~50 that have no known function!
Given their biological importance, mutations in essential genes often underlie rare diseases in humans. Some of these, such as Congenital Disorders of Glycosylation (CDGs), are so rare that any individual disorder can have less than 50 documented patients. Despite this, 7000+ rare diseases collectively affect over 30 million people in the U.S. alone, and there is a great need for new therapies for these diseases. Right now, our lab is focused on studying CDGs, but we are expanding into additional diseases soon. This work is currently funded by a K99/R00 transition grant from the National Institute of Child Health and Human Development (NICHD).
Medium-throughput in vivo drug screens:
Our lab develops Drosophila models of a given disease that have strong, reproducible phenotypes - typically impacting development such as eye size or ability to grow into an adult. Using these models, we use a drug repurposing library of FDA-approved drugs to find drugs that can improve our disease models. The use of these libraries is critical, as they have the potential to identify more readily-available therapeutics.
Validating top drugs and confirming their mechanism:
Top suppressor (because they “suppress” the phenotype) drugs can have strong effects on our disease models – sometimes almost completely rescuing their phenotypes. These top suppressors are validated by using an independent drug source and by dose-response in case certain concentrations are better or worse. We focus on the strongest drugs as well as those that have highly enriched mechanisms among the identified suppressors.
One of the best properties of drug repurposing is that most of the drugs tested already have known mechanisms of action. This means we can also utilize the power of fruit fly and cell genetics to test the targets of these drugs directly through genetic manipulation. This is a powerful method to confirm our hit mechanisms. Because many of these genes are conserved (especially true of essential genes), these data are very relevant for humans even regardless of whether a new therapy is found.
Beyond drug screening:
Essential genes are also fascinating from a basic science perspective. For example, in the context of aging biology, some essential genes can actually be beneficial to inhibit as an adult animal - increasing both healthspan and lifespan! The genomics of essential genes are also interesting - for example, why are there so many essential genes when other, similar genes have been duplicated as a form of genetic redundancy? We are very interested in studying these questions and more.
Some technologies used in the lab:Drosophila models (genetic crosses, RNAi, Auxin-Gal80), Drosophila behavior analysis (movement, seizure), drug repurposing screens, cell culture (proliferation, siRNA, metabolomics), molecular biology techniques (PCR, qPCR, Western blots, cloning).
Selected Publications —
See all papers by Hans Dalton on PubMed