Biomedical Research Foundation Academy Of AthensAcademy Of Athens
Scientific Personnel

Eleni Eleni Katsantoni, PhD
Researcher C'

Telephone : +30 210 6597 444, -220 (office), 439 (lab)
Fax : +30 210 6597 545
e-mail : ekatsantoni@bioacademy.gr


Center :

Basic Research

Lab Site :

Katsantoni Lab


Brief Bio

Eleni Katsantoni received her degree in Biology from the University of Athens, Greece (1995), Master of Science in Medical Genetics from the University of Newcastle, UK (1996) and PhD in Molecular Biology and Biomedicine from the University of Crete, Greece (2002). During her undergraduate and MSc studies she was involved in research on human follicular fluid proteins (Human Genetics Laboratory, Department of Biology, University of Athens) and on mapping 12q23-24.1 human chromosome region for the cloning of Darier’s disease gene (Human Molecular Genetics Laboratory, University of Newcastle, UK). Her PhD research (Molecular Biology Laboratory, Medical School, University of Crete and IMBB) focused on investigation of the molecular mechanisms of globin genes transcriptional regulation and hemoglobin switching. She analysed the role of cis acting elements of the beta globin gene cluster and her work identified an enhancer element, capable of altering the developmental pattern of expression of A-gamma globin gene, which was later successfully used in gene therapy vectors. She also defined two silencer elements capable of altering the developmental pattern of expression of A-gamma globin gene. During her PhD she was awarded 2 short term EMBO fellowships to visit the Department of Cell biology, Erasmus Medical Center, Netherlands. For the period 1999-2005, Katsantoni worked in the Department of Cell biology, Erasmus Medical Center, Rotterdam, Netherlands, initially as a visiting PhD student and then as a postdoctoral fellow, funded by a Marie Curie post-doctoral fellowship (EU) and by Erasmus MC. Her post-doctoral work focused on understanding the role of transcription factors in erythroid differentiation by characterization of transcription factor complexes and target genes. She developed inducible systems in transgenic mice and bioinformatics tools for analysis of target genes networks. In May 2005 Katsantoni returned in Greece, supported by a Marie Curie European Reintegration Grant (EU) and since then she is working in BRFAA, as Investigator. Her research focuses on mechanisms of transcriptional activation and repression mediated by transcription factors (erythropoietic and Signal Transducers and Activators of Transcription, STATs) in normal and pathologic hematopoiesis. Her Laboratory uses genomics, transcriptomics and proteomics approaches to understand the transcriptional role of STAT factors in hematopoietic cells (pro-B, erythropoietic and leukemic cells). Her Laboratory identified two novel STAT5 interacting partners and defined a dual role of both factors in STAT5-dependent transcription, a novel STAT5 target gene which provided insights in B-chronic lymphocytic leukemia, and gender specific differences in transcriptomic profiles of thalassemia (a model of ineffective erythropoiesis used in the Laboratory). Her projects are funded from EU (FP6, FP7, H2020), Research Promotion Foundation (Cyprus) and General Secretariat for Research & Development and Ministry of Education (Greece).

Selected Publications

Nanou A, Toumpeki C, Lavigne MD, Lazou V, Demmers J, Paparountas T, Thanos D, Katsantoni E. The dual role of LSD1 and HDAC3 in STAT5-dependent transcription is determined by protein interactions, binding affinities, motifs and genomic positions. Nucleic Acids Res. 2016 Sep 19. pii: gkw832. [Epub ahead of print]

Theodorou M, Speletas M, Mamara A, Papachristopoulou G, Lazou V, Scorilas A, Katsantoni E. Identification of a STAT5 target gene, Dpf3, provides novel insights in chronic lymphocytic leukemia. PLoS One. 2013 Oct 14;8(10):e76155.

E. Katsantoni, Protein complexes and target genes identification by in vivo biotinylation: The STAT5 paradigm. Sci. Signal. 5, pt13 (2012).

Gazouli M, Katsantoni E et al. Persistent fetal gamma-globin expression in adult transgenic mice following deletion of two silencer elements located 3' to the human Agamma-globin gene. Mol Med. 2009 Nov-Dec;15 (11-12):415-24.

Katsantoni EZ et al. Ubiquitous expression of the rtTA2S-M2 inducible system in transgenic mice driven by the human hnRNPA2B1/CBX3 CpG island. BMC Dev Biol. 2007 Sep 27;7:108.

Horsman S, Moorhouse MJ, de Jager VC, van der Spek P, Grosveld F, Strouboulis J, Katsantoni EZ. TF Target Mapper: a BLAST search tool for the identification of Transcription Factor target genes. BMC Bioinformatics. 2006 Mar 8;7:120

Katsantoni EZ et al. An embryonic-specific repressor element located 3' to the Agamma-globin gene influences transcription of the human beta-globin locus in transgenic mice. Exp Hematol. 2004 Feb;32(2):224-33.

Katsantoni EZ, et al. Persistent gamma-globin expression in adult transgenic mice is mediated by HPFH-2, HPFH-3, and HPFH-6 breakpoint sequences. Blood. 2003 Nov 1;102(9):3412-9.

de Boer E, Rodriguez P, Bonte E, Krijgsveld J, Katsantoni E et al. Efficient biotinylation and single-step purification of tagged transcription factors in mammalian cells and transgenic mice. Proc Natl Acad Sci U S A. 2003 Jun 24;100(13):7480-5.

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