Jelena Perovanović

ORCID: 0000-0003-2348-2332
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About
Contact & Profiles
Research Areas
  • Immune Cell Function and Interaction
  • T-cell and B-cell Immunology
  • Diabetes and associated disorders
  • RNA Research and Splicing
  • Genomics and Chromatin Dynamics
  • CRISPR and Genetic Engineering
  • Pluripotent Stem Cells Research
  • Immunotherapy and Immune Responses
  • Nuclear Structure and Function
  • Epigenetics and DNA Methylation
  • Single-cell and spatial transcriptomics
  • Muscle Physiology and Disorders
  • RNA modifications and cancer
  • 3D Printing in Biomedical Research
  • Immune responses and vaccinations
  • Congenital limb and hand anomalies
  • Neuroinflammation and Neurodegeneration Mechanisms
  • Cancer-related molecular mechanisms research
  • Plant and animal studies
  • Adipose Tissue and Metabolism
  • Atherosclerosis and Cardiovascular Diseases
  • Antibiotic Resistance in Bacteria
  • RNA regulation and disease
  • Prosthetics and Rehabilitation Robotics
  • Bone fractures and treatments

University of Utah
2019-2024

Huntsman Cancer Institute
2019-2024

National Institute of Arthritis and Musculoskeletal and Skin Diseases
2018-2022

National Institutes of Health
2018

Children's National
2016

George Washington University
2013-2016

Military Medical Academy
2013

University of Belgrade
2011

ABSTRACT Dedicated stem cells ensure postnatal growth, repair and homeostasis of skeletal muscle. Following injury, muscle (MuSCs) exit from quiescence divide to reconstitute the cell pool give rise progenitors. The transcriptomes pooled MuSCs have provided a rich source information for describing genetic programs distinct static states; however, bulk microarray RNA sequencing provide only averaged gene expression profiles, blurring heterogeneity developmental dynamics asynchronous MuSC...

10.1242/dev.174177 article EN Development 2019-03-19

Mutations in lamin A/C and emerin change myogenic cell fate by disrupting heterochromatin tethering to the nuclear envelope.

10.1126/scitranslmed.aad4991 article EN Science Translational Medicine 2016-04-20

The genetic context of the blaNDM-1 gene in genome Pseudomonas aeruginosa MMA83 was investigated. Sequencing cosmid selected for revealed presence two copies P. a unique environment. Additionally, mating assays, DNA-DNA hybridization, and an S1 nuclease assay strongly suggest that is chromosome borne.

10.1128/aac.02312-12 article EN Antimicrobial Agents and Chemotherapy 2013-04-23

The transition between pluripotent and tissue-specific states is a key aspect of development. Understanding the pathways driving these transitions will facilitate engineering properly differentiated cells for experimental therapeutic uses. Here, we showed that during mesoderm differentiation, transcription factor Oct1 activated developmental lineage–appropriate genes were silent in cells. Using mouse embryonic stem (ESCs) with an inducible knockout Oct1, deficiency resulted poor induction...

10.1126/scisignal.add5750 article EN Science Signaling 2023-04-18

The molecular mechanisms leading to the establishment of immunological memory are inadequately understood, limiting development effective vaccines and durable antitumor immune therapies. Here, we show that ectopic OCA-B expression is sufficient improve antiviral recall responses, while having minimal effects on primary effector responses. At peak viral response, short-lived T cell populations expanded but increased Gadd45b Socs2 expression, precursor cells Bcl2 , Il7r, Tcf7 a per-cell basis....

10.1073/pnas.2309153121 article EN cc-by-nc-nd Proceedings of the National Academy of Sciences 2024-02-22

The transcriptional coregulator OCA-B promotes expression of T cell target genes in cases repeated antigen exposure, a necessary feature autoimmunity. We hypothesized that cell–specific deletion and pharmacologic inhibition would protect mice from autoimmune diabetes. developed an Ocab conditional allele backcrossed it onto diabetes-prone NOD/ShiLtJ strain background. loss protected spontaneous disease. Protection was associated with large reductions islet CD8+ receptor specificities...

10.1084/jem.20200533 article EN cc-by-nc-sa The Journal of Experimental Medicine 2020-12-09

Embryonic stem cells (ESCs) can adopt lineage-specific gene-expression programs by stepwise exposure to defined factors, resulting in the generation of functional cell types. Bulk and single-cell-based assays were employed catalog gene expression, histone modifications, chromatin conformation, accessibility transitions ESC populations individual acquiring a presomitic mesoderm fate undergoing further specification toward myogenic neurogenic lineages. These identified cis-regulatory regions...

10.1016/j.celrep.2022.111219 article EN cc-by Cell Reports 2022-08-01

We evaluated the degree of reproductive isolation between laboratory populations seed beetle (Acanthoscelides obtectus) selected to reproduce early (E) or late (L) in life, where different levels sexual activity and discrimination have been detected. found a significant level behavioral among within E selection regime which beetles showed enhanced early-life fitness traits low activity. In contrast, substantially higher an indiscriminate mating system inhibited rather than promoted...

10.1111/j.1439-0310.2011.01936.x article EN Ethology 2011-08-12

Thymic presentation of self-antigens is critical for establishing a functional yet self-tolerant T-cell population. Hybrid peptides formed through transpeptidation within pancreatic β-cell lysosomes have been proposed as new class autoantigens in type 1 diabetes (T1D). While the production hybrid thymus has not explored, due to nature their generation, it thought be highly unlikely. Therefore, peptide-reactive thymocytes may preferentially escape thymic selection and contribute significantly...

10.2337/db21-1069 article EN Diabetes 2022-05-27

Background During terminal differentiation of cells, there is typically a transition the nuclear envelope from Lamin B protein to A/C proteins. This commensurate with exit cell cycle, and maintenance transcriptional programs associated terminally differentiated cells. Dominant missense mutations in cause broad spectrum human genetic disorders, where specific point are defects organs or tissues. We have previously presented model disrupt developmentally appropriate interactions between...

10.1186/1756-8935-6-s1-p65 article EN cc-by Epigenetics & Chromatin 2013-03-01

ABSTRACT The transition between pluripotent and tissue-specific states is a key aspect of development. Understanding the pathways driving these transitions will facilitate engineering properly differentiated cells for experimental therapeutic uses. Here, we showed that during mesoderm differentiation, transcription factor Oct1 activated developmental lineage-appropriate genes were silent in cells. Using mouse embryonic stem (ESCs) with an inducible knockout Oct1, deficiency resulted poor...

10.1101/2020.12.01.406488 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2020-12-01

Abstract The molecular mechanisms leading to the establishment of immunological memory are inadequately understood, limiting development effective vaccines and durable anti-tumor immune therapies. Here we show that ectopic OCA-B expression is sufficient improve antiviral recall responses, while having minimal effects on primary effector responses. At peak viral response short lived T cell populations expanded but increased Gadd45b Socs2 expression, precursor cells Bcl2 , Il7r Tcf7 a per-cell...

10.1101/2022.09.21.508912 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2022-09-21

Abstract The establishment of durable immunological memory remains a poorly understood aspect lymphocyte biology and limiting factor in vaccine development. Using T cell-conditional OCA-B (Pou2af1) knockout model mouse viral pathogen, we show that expression the transcription cofactor within cells is necessary for proper CD4+ cell formation. We also ectopic sufficient to drive towards fate while having no effect on primary antiviral effector response. Bulk single-cell gene profiling...

10.4049/jimmunol.208.supp.56.11 article EN The Journal of Immunology 2022-05-01

Abstract The transcriptional coregulator OCA-B promotes expression of T cell target genes in cases repeated antigen exposure, a necessary feature autoimmunity. We hypothesized that cell-specific deletion and pharmacologic inhibition would protect mice from autoimmune diabetes. developed an Ocab conditional allele backcrossed it onto diabetes-prone NOD/ShiLtJ strain background. loss protected spontaneous disease. Protection was associated with large reductions islet CD8 + receptor...

10.1101/2020.02.06.937839 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2020-02-07

Abstract Treatments for autoimmunity aim to inhibit autoreactivity while preserving normal immune function. The transcriptional coregulator OCA-B (gene symbol Pou2af1) is induced in stimulated naïve CD4+ T cells, where docks with transcription factor Oct1 regulate genes such as Il2 and Ifng. only their targets cases of persistent antigen exposure, a common feature autoimmunity. We hypothesized that cell-specific deletion would protect mice from autoimmune diabetes, pharmacologic inhibition...

10.4049/jimmunol.204.supp.142.11 article EN The Journal of Immunology 2020-05-01

SUMMARY ESCs can adopt lineage-specific gene expression programs by stepwise exposure to defined factors, resulting in the generation of functional cell types. Bulk and single cell-based assays were employed catalogue expression, histone modifications, chromatin conformation, accessibility transitions ESC populations individual cells acquiring a presomitic mesoderm fate undergoing further lineage specification. These identified cis -regulatory regions transcription factors presiding...

10.1101/2022.03.29.486247 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2022-03-30

<p> </p> <p>Thymic presentation of self-antigens is critical for establishing a functional yet self-tolerant T cell population. Hybrid peptides formed through transpeptidation within pancreatic beta lysosomes have been proposed as new class autoantigens in Type 1 Diabetes (T1D). While the production hybrid thymus has not explored, due to nature their generation, it thought be highly unlikely. Therefore, peptide-reactive thymocytes may preferentially escape thymic selection...

10.2337/figshare.19799728.v1 preprint EN cc-by-nc-sa 2022-05-27

<p> </p> <p>Thymic presentation of self-antigens is critical for establishing a functional yet self-tolerant T cell population. Hybrid peptides formed through transpeptidation within pancreatic beta lysosomes have been proposed as new class autoantigens in Type 1 Diabetes (T1D). While the production hybrid thymus has not explored, due to nature their generation, it thought be highly unlikely. Therefore, peptide-reactive thymocytes may preferentially escape thymic selection...

10.2337/figshare.19799728 preprint EN cc-by-nc-sa 2022-05-27

Abstract The differentiation of CD4+ T cell subsets in response to infection has been studied extensively, however the epigenetic programs that regulate these processes remain poorly understood. Active demethylation by tet methylcytosine dioxygenases CpG dinucleotides within DNA is a key component programing promotes lineage specific gene expression and contributes cellular function. Here we report Tet2 acts restrict follicular helper (Tfh) cells responding viral infection. Using an adoptive...

10.4049/jimmunol.208.supp.112.24 article EN The Journal of Immunology 2022-05-01
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