Dr. De Jesus is an Assistant Professor of Medicine in the Department of Medicine, Section of Genetic Medicine, at the University of Chicago. With over a decade of experience in molecular biology and metabolism research, his work focuses on uncovering how molecular mechanisms govern health and metabolic disease, particularly in the context of RNA modifications, diabetes, and aging.
His scientific journey began during his Master’s studies as a Fulbright Research Scholar in the laboratory of Professor Rohit N. Kulkarni at the Joslin Diabetes Center. This work continued through his PhD in the Graduate Program of Basic and Applied Biology (GABBA) at the University of Porto, where he investigated the epigenetic reprogramming of hepatic metabolism.
Before joining the University of Chicago, he served as an Instructor in Medicine at Harvard Medical School and as a Research Associate at the Joslin Diabetes Center in Boston. His independent research has been supported by the European Association for the Study of Diabetes (EASD), the American Diabetes Association (ADA), and more recently by the National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) through a K99/R00 award. His current projects focus on understanding how RNA modifications, particularly m⁶A, shape metabolic regulation and aging — with the ultimate goal of paving the way for new therapeutic strategies against metabolic disease.
Beyond research, he is deeply passionate about academia, teaching, and mentoring. Having once worked as a high school biology teacher in Portugal, he remains committed to advancing the careers of trainees at all levels, creating an environment where young scientists can thrive and achieve their professional goals.
m6A mRNA methylation regulates pancreatic a-cell plasticity.
m6A mRNA methylation regulates pancreatic a-cell plasticity. Nat Metab. 2026 Sep; 8(9):1948-1970.
PMID: 42760315
Pancreatic ß-cell aging in physiology and diabetes: emerging roles of m6A mRNA methylation.
Pancreatic ß-cell aging in physiology and diabetes: emerging roles of m6A mRNA methylation. J Mol Endocrinol. 2026 Jul 01; 77(1).
PMID: 42274290
Author Correction: Redox regulation of m6A methyltransferase METTL3 in ß-cells controls the innate immune response in type 1 diabetes.
Author Correction: Redox regulation of m6A methyltransferase METTL3 in ß-cells controls the innate immune response in type 1 diabetes. Nat Cell Biol. 2026 Jan; 28(1):208.
PMID: 41249573
Regulatory Roles of IGF2R in Insulin Secretion and Adaptive ß-Cell Proliferation.
Regulatory Roles of IGF2R in Insulin Secretion and Adaptive ß-Cell Proliferation. Diabetes. 2025 Dec 01; 74(12):2351-2364.
PMID: 41042627
Corrigendum to "Insulin receptor-mediated signaling regulates pluripotency markers and lineage differentiation" [Mol Metab 18 (2018) 153-163].
Corrigendum to "Insulin receptor-mediated signaling regulates pluripotency markers and lineage differentiation" [Mol Metab 18 (2018) 153-163]. Mol Metab. 2026 Jan; 103:102285.
PMID: 41285400
Genome-wide CRISPR Screen Identifies Sec31A as a Key Regulator of Alpha Cell Survival.
Genome-wide CRISPR Screen Identifies Sec31A as a Key Regulator of Alpha Cell Survival. Nat Commun. 2025 Oct 15; 16(1):9159.
PMID: 41093834
m6A mRNA methylation decorates genes involved in fibrinogen synthesis to regulate liver regeneration in mice.
m6A mRNA methylation decorates genes involved in fibrinogen synthesis to regulate liver regeneration in mice. Am J Physiol Gastrointest Liver Physiol. 2025 11 01; 329(5):G614-G627.
PMID: 41056353
Divergent roles of m6A in orchestrating brown and white adipocyte transcriptomes and systemic metabolism.
Divergent roles of m6A in orchestrating brown and white adipocyte transcriptomes and systemic metabolism. Nat Commun. 2025 Jan 09; 16(1):533.
PMID: 39788955
m6A mRNA methylation by METTL14 regulates early pancreatic cell differentiation.
m6A mRNA methylation by METTL14 regulates early pancreatic cell differentiation. EMBO J. 2024 Nov; 43(22):5445-5468.
PMID: 39322760
m6A mRNA methylation in brown fat regulates systemic insulin sensitivity via an inter-organ prostaglandin signaling axis independent of UCP1.
m6A mRNA methylation in brown fat regulates systemic insulin sensitivity via an inter-organ prostaglandin signaling axis independent of UCP1. Cell Metab. 2024 Oct 01; 36(10):2207-2227.e9.
PMID: 39255799