Determining the difference between important and unimportant DNA changes in childhood diseases can be tedious and difficult. The Grimes Lab works to understand how normal hematopoiesis is programmed, and how diseases like marrow failure and leukemia change the transcriptional programming.

I have a broad background in hematopoiesis, molecular biology and molecular oncology, including mouse modeling of hematopoiesis, myelopoiesis, marrow failure syndromes including myelodysplastic syndromes (MDS) and severe congenital neutropenia (SCN) and acute myeloid leukemia (AML).

I received a PhD in molecular pathology and immunology studying gene regulation with Maureen Goodenow (then at University of Florida). I then joined Philip Tsichlis (then at Fox Chase Cancer Center) when that lab was cloning novel genes activated by Moloney murine leukemia virus insertion mutagenesis (e.g., Akt, Tpl2).

I participated in the identification of the Growth factor independent-1 (Gfi1) transcription factor, its DNA binding specificity, named the “SNAG” transcription repressor domain, and genetically linked this domain to Gfi1-directed biology.

The Grimes Lab continues to focus on transcriptional integration of normal and malignant hematopoiesis.

With University of Washington colleague Marshall Horwitz, I identified humans with mutations in Gfi1 who display severe congenital neutropenia (SCN) and non-immune chronic idiopathic neutropenia of adults (NI-CINA).

The Grimes Lab has established multiple mouse models of human disease, including acute myeloid leukemia (AML), and more recently SCN. Their work has spanned both small molecule and RNA therapeutics.

In a 2016 study published in Cancer Discovery, the team proved that DNMT3A haploinsufficiency could facilitate AML genesis.

The Grimes Lab was one of the first labs to utilize deep scRNA-seq profiling to dissect homeostatic myeloid development and provide deep molecular insight into the process of differentiation. This work was published in Nature in 2016.

We went on to generate the first mouse models of human SCN using patient-derived mutations in the Gfi1 transcription factor. This work was published in Nature in 2020.

To determine the effects of SCN mutations, the team generated single-cell references for granulopoietic genomic states with linked epitopes, aligned mutant cells to their wild-type equivalents and identified differentially expressed genes and epigenetic loci. These insights facilitated the genetic rescue of granulocytic specification but not post-commitment defects in innate-immune effector function, and underscore the importance of evaluating the effects of mutations and therapy within each relevant cell state.

The Grimes Lab is actively harnessing both established and cutting-edge single-cell technologies to dissect the transcriptional and epigenetic programming of normal and malignant hematopoiesis. In collaboration with Nathan Salomonis here at Cincinnati Children’s, we develop biologically-centric informatics algorithms to process single-cell data, web portals to disseminate the work flows, and web browsers to make the data easily accessible to biologists.