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Runx1 Regulates c-Myc Expression And The Expansion Of Hematopoietic Precursors In A C-terminally Dependent Manner

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dc.contributor.advisorJanice C. Telfer
dc.contributor.advisorJuan Anguita
dc.contributor.advisorSurita R. Bhatia
dc.contributor.authorJacobs, Paejonette
dc.contributor.departmentUniversity of Massachusetts - Amherst
dc.date2023-09-23T09:22:33.000
dc.date.accessioned2024-04-26T14:17:56Z
dc.date.available2014-06-16T00:00:00Z
dc.date.issued2012-05-01
dc.description.abstractRunx1 regulates the expression of several important target genes and plays critical roles in the process of hematopoiesis. Runx1 by itself is a poor regulator of transcription and instead nucleates transcription complexes through its C-terminus to transactivate or repress the expression of target genes. We generated a C-terminally deleted Runx1 construct (Runx1.d190), which lacks important co-factor sites, to further investigate the function of Runx1 in development. A potential role for Runx1 in regulating the expression of another potent transcriptional regulator, c-Myc, has been suggested by published studies, which show that Runx1 and c-Myc collaborate in oncogenesis. In these studies, we show that endogenous Runx1 binds to three Runx consensus sites upstream of the c-Myc transcriptional start site in Jurkat T cells and murine primary splenocytes. Retroviral transduction of Jurkat T cells with Runx1.d190 results in the increased transcription of c-Myc as determined by microarray analysis. In order to monitor c-Myc expression in response to early-acting and transient Runx1.d190, we generated a cell membrane-permeable TAT-Runx1.d190 fusion protein. Treatment of murine primary splenocytes with TAT-Runx1.d190 protein results in a transient increase in the transcription of c-Myc and a corresponding increase in c-Myc protein levels. This effect is dependent on the ability of Runx1.d190 to bind to DNA. These data demonstrate that Runx1 directly regulates c-Myc expression in a C-terminally and DNA-binding dependent manner. In these studies, we also investigate the effects of the truncation of Runx1 C-terminus on hematopoietic stem cells (HSCs). We found that treatment of bone marrow cells enriched for HSCs with TAT-Runx1.d190 results in a 12.5 fold increase in hematopoietic precursors compared to untreated precursors in vitro as determined by Colony Forming Cell assays. We also show that hematopoietic precursors treated with TAT-Runx1.d190 are able to able to differentiate normally both in vitro and in vivo and thus represent functional hematopoietic precursors. Our findings show that we are able to transiently expand hematopoietic precursorsex vivo by treating the cells with a Runx1 construct that lacks the C-terminus. Collectively, this work demonstrates that Runx1 regulates the expression of c-Myc and the expansion of hematopoietic precursors in a C-terminally dependent manner.
dc.description.degreeDoctor of Philosophy (PhD)
dc.description.departmentMolecular and Cellular Biology
dc.identifier.doihttps://doi.org/10.7275/5691665
dc.identifier.urihttps://hdl.handle.net/20.500.14394/13855
dc.relation.urlhttps://scholarworks.umass.edu/cgi/viewcontent.cgi?article=1363&context=dissertations_1&unstamped=1
dc.source.statuspublished
dc.subjectBiological sciences
dc.subjectHealth and environmental sciences
dc.subjectC-myc
dc.subjectHematopoiesis
dc.subjectRunx1
dc.subjectTat peptides
dc.subjectImmunology and Infectious Disease
dc.subjectMolecular Biology
dc.titleRunx1 Regulates c-Myc Expression And The Expansion Of Hematopoietic Precursors In A C-terminally Dependent Manner
dc.typecampus
dc.typearticle
dc.typedissertation
digcom.contributor.authorJacobs, Paejonette
digcom.date.embargo2014-06-16T00:00:00-07:00
digcom.identifierdissertations_1/361
digcom.identifier.contextkey5691665
digcom.identifier.submissionpathdissertations_1/361
dspace.entity.typePublication
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