Janice C. Telfer

Janice C. Telfer

Associate Professor

Undergraduate Program Director
Chair, Pre-Vet Advisory Committee

Photo of Janice Telfer

Office phone: 413-545-5564

Fax: 413-545-6326

Email: telfer [at] vasci [dot] umass [dot] edu

Office location: 427D ISB

Mailing address:

460 (lab) or 427D (office) ISB
661 North Pleasant St.
University of Massachusetts
Amherst, MA 01003

Ph.D.: Harvard University, 1995
Postdoctoral Training: California Institute of Technology

ANIML SCI 200 Animal Cellular and Molecular Biology
ANIML SCI H01 Honors Colloquium for AnSci 200

Role of RUNX Family Transcription Factors in Immune System Development

All of the cells of the blood descend from the progeny of hematopoietic stem cells resident in the bone marrow. Hematopoietic stem cells are very long-lived: they survive and divide for the life of the organism. Their daughter cells go through a period of development in which they become more and more specialized, turning on and off the expression of specific genes, until they are fully differentiated. The subversion of this process of normal development often results in cancer. My laboratory is interested in how the regulation of gene expression by the RUNX family of transcription factors influences the development and cancerous transformation of cells of the immune system.

RUNX family transcription factors (RUNX1, RUNX2, and RUNX3) bind to DNA and other proteins to activate or suppress transcription of specific genes. We have previously found that expression of RUNX1 has profound effects on the development of T cells and the myeloid cells known as neutrophils. We use a retroviral expression system that allows us to express normal and mutated RUNX proteins in both primary cells and cell lines, which can then be cultured. The projects currently pursued by my laboratory include:

  1. We have found that the expression of RUNX1 in the myeloid cell line 32Dcl3 promotes the cells’ continued proliferation, which is reminiscent of the high proportion of immature proliferating myeloid cells seen in patients with the cancer acute myelogenous leukemia. The fact that increased expression of RUNX1 in humans is associated with a predisposition to develop acute myelogenous leukemia supports our hypothesis that an increase of RUNX1 expression in immature myeloid cells leads to a pre-cancerous state of extended proliferative capacity. We will express mutated forms of RUNX1 in 32Dcl3 cells and primary myeloid cells to discover the mechanism by which RUNX1 works.
  2. We have found that expression of the transcription factor RUNX1 suppresses the development of gamma delta T cells (Fig. 1 gd TCR) and silences the expression of CD4 specifically at the immature alpha beta TCR double-positive thymocyte stage (Fig. 2 ab TCR DP). This leads to a bias first towards the production of ab T cells and later, to a bias towards the production of CD8 cytotoxic T cells (Fig. 1 CD8+ TCRbhi). RUNX1 is the first transcription factor known to influence production of either of these types of T cells. It is important to understand how production of different kinds of T cells is regulated: for instance, one can see from AIDS that neither gd T cells nor CD8+ ab T cells can make up for the lack of CD4+ ab T cells. We are characterizing the nature of RUNX family member regulation of CD4 expression, seeking to identify RUNX gene targets in early thymocytes, and investigating what signals normally control the level of RUNX family members in thymocytes.
  3. RUNX1 is associated with the development of pediatric acute lymphoblastic leukemia (ALL). We have discovered truncated splice isoforms of RUNX1 that, when expressed via retroviral transduction in immature thymocytes, cause a proliferative expansion or give a survival advantage to these cells. We have localized this effect to a short domain in the N-terminus of RUNX1 and are working on identifying specific amino acids and potential interacting proteins responsible for this effect.

Thymocyte Development

Thymocyte Development: Arrows indicate the direction and timing of branches in the thymocyte maturation pathway, which involves natural killer cells (NK, orange), gamma delta T cells (gd TCR, green), alpha beta T cells (ab TCR, blue and purple), immature “double-negative” thymocytes (DN1-DN4), “double-positive” thymocytes expressing both the CD4 and CD8 proteins (DP, light blue), and “single-positive” thymocytes expressing either CD4 or CD8 proteins (SP, blue or purple).

Tezgel ÖA, Gonzalez-Perez G, Telfer JC, Osborne BA, Minter LM, Tew GN.  2013.  Novel protein transduction domain mimics as nonviral delivery vectors for siRNA targeting NOTCH1 in primary human T cells.. Mol Ther. 21(1):201-9.
Chen C, Herzig CTA, Alexander LJ, Keele JW, McDaneld TG, Telfer JC, Baldwin CL.  2012.  Gene number determination and genetic polymorphism of the gamma delta T cell co-receptor WC1 genes.. BMC Genet. 13:86.
Tezgel ÖA, Telfer JC, Tew GN.  2011.  De novo designed protein transduction domain mimics from simple synthetic polymers.. Biomacromolecules. 12(8):3078-83.
Wang F, Herzig CTA, Chen C, Hsu H, Baldwin CL, Telfer JC.  2011.  Scavenger receptor WC1 contributes to the γδ T cell response to Leptospira.. Molecular immunology. 48(6-7):801-9.
Bockstal V, Guirnalda P, Caljon G, Goenka R, Telfer JC, Frenkel D, Radwanska M, Magez S, Black SJ.  2011.  T. brucei infection reduces B lymphopoiesis in bone marrow and truncates compensatory splenic lymphopoiesis through transitional B-cell apoptosis.. PLoS pathogens. 7(6):e1002089.
Herzig CTA, Waters RW, Baldwin CL, Telfer JC.  2010.  Evolution of the CD163 family and its relationship to the bovine gamma delta T cell co-receptor WC1.. BMC evolutionary biology. 10:181.
Joshi I, Minter LM, Telfer J, Demarest RM, Capobianco AJ, Aster JC, Sicinski P, Fauq A, Golde TE, Osborne BA.  2009.  Notch signaling mediates G1/S cell-cycle progression in T cells via cyclin D3 and its dependent kinases.. Blood. 113(8):1689-98.
Bruno L, Mazzarella L, Hoogenkamp M, Hertweck A, Cobb BS, Sauer S, Hadjur S, Leleu M, Naoe Y, Telfer JC et al..  2009.  Runx proteins regulate Foxp3 expression.. The Journal of experimental medicine. 206(11):2329-37.
Chen C, Herzig CTA, Telfer JC, Baldwin CL.  2009.  Antigenic basis of diversity in the gammadelta T cell co-receptor WC1 family.. Molecular immunology. 46(13):2565-75.
Samon JB, Champhekar A, Minter LM, Telfer JC, Miele L, Fauq A, Das P, Golde TE, Osborne BA.  2008.  Notch1 and TGFbeta1 cooperatively regulate Foxp3 expression and the maintenance of peripheral regulatory T cells.. Blood. 112(5):1813-21.
Rogers AN, Vanburen DG, Zou B, Lahmers KK, Herzig CTA, Brown WC, Telfer JC, Baldwin CL.  2006.  Characterization of WC1 co-receptors on functionally distinct subpopulations of ruminant gamma delta T cells.. Cellular immunology. 239(2):151-61.
Rogers AN, Vanburen DG, Hedblom EE, Tilahun ME, Telfer JC, Baldwin CL.  2005.  Gammadelta T cell function varies with the expressed WC1 coreceptor.. Journal of immunology (Baltimore, Md. : 1950). 174(6):3386-93.
Minter LM, Turley DM, Das P, Shin HM, Joshi I, Lawlor RG, Cho OH, Palaga T, Gottipati S, Telfer JC et al..  2005.  Inhibitors of gamma-secretase block in vivo and in vitro T helper type 1 polarization by preventing Notch upregulation of Tbx21.. Nature immunology. 6(7):680-8.
Rogers AN, Vanburen DG, Hedblom E, Tilahun ME, Telfer JC, Baldwin CL.  2005.  Function of ruminant gammadelta T cells is defined by WC1.1 or WC1.2 isoform expression.. Veterinary immunology and immunopathology. 108(1-2):211-7.
Telfer JC, Hedblom EE, Anderson MK, Laurent MN, Rothenberg EV.  2004.  Localization of the domains in Runx transcription factors required for the repression of CD4 in thymocytes.. Journal of immunology (Baltimore, Md. : 1950). 172(7):4359-70.
Name Phone Office
LePage , Lauren ISB 460
Former Lab Personnel