Leukemogenesis in heterozygous PU.1 knockout mice

Paula C. Genik, Irina Vyazunova, Leta S. Steffen, Jeffery W. Bacher, Helle Bielefeldt-Ohmann, Scott McKercher, Robert L. Ullrich, Christina M. Fallgren, Michael M. Weil, F. Andrew Ray

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

Most murine radiation-induced acute myeloid leukemias involve biallelic inactivation of the PU.1 gene, with one allele being lost through a radiation-induced chromosomal deletion and the other allele affected by a recurrent point mutation in codon 235 that is likely to be spontaneous. The short latencies of acute myeloid leukemias occurring in nonirradiated mice engineered with PU.1 conditional knockout or knockdown alleles suggest that once both copies of PU.1 have been lost any other steps involved in leukemogenesis occur rapidly. Yet, spontaneous acute myeloid leukemias have not been reported in mice heterozygous for a PU.1 knockout allele, an observation that conflicts with the understanding that the PU.1 codon 235 mutation is spontaneous. Here we describe experiments that show that the lack of spontaneous leukemia in PU.1 heterozygous knockout mice is not due to insufficient monitoring times or mouse numbers or the genetic background of the knockout mice. The results reveal that spontaneous leukemias that develop in mice of the mixed 129S2/SvPas and C57BL/6 background of knockout mice arise by a pathway that does not involve biallelic PU.1 mutation. In addition, the latency of radiation-induced leukemia in PU.1 heterozygous mice on a genetic background susceptible to radiation-induced leukemia indicates that the codon 235 mutation is not a rate-limiting step in radiation leukemogenesis driven by PU.1 loss.

Original languageEnglish (US)
Pages (from-to)310-315
Number of pages6
JournalRadiation Research
Volume182
Issue number3
DOIs
StatePublished - 2014

Fingerprint

knockout mice
leukemias
Knockout Mice
Radiation-Induced Leukemia
mice
Alleles
mutations
Acute Myeloid Leukemia
Codon
Radiation
radiation
Mutation
Leukemia
Point Mutation
deletion
Observation
genes
deactivation
Genes

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging
  • Biophysics
  • Radiation

Cite this

Genik, P. C., Vyazunova, I., Steffen, L. S., Bacher, J. W., Bielefeldt-Ohmann, H., McKercher, S., ... Ray, F. A. (2014). Leukemogenesis in heterozygous PU.1 knockout mice. Radiation Research, 182(3), 310-315. https://doi.org/10.1667/RR13738.1

Leukemogenesis in heterozygous PU.1 knockout mice. / Genik, Paula C.; Vyazunova, Irina; Steffen, Leta S.; Bacher, Jeffery W.; Bielefeldt-Ohmann, Helle; McKercher, Scott; Ullrich, Robert L.; Fallgren, Christina M.; Weil, Michael M.; Ray, F. Andrew.

In: Radiation Research, Vol. 182, No. 3, 2014, p. 310-315.

Research output: Contribution to journalArticle

Genik, PC, Vyazunova, I, Steffen, LS, Bacher, JW, Bielefeldt-Ohmann, H, McKercher, S, Ullrich, RL, Fallgren, CM, Weil, MM & Ray, FA 2014, 'Leukemogenesis in heterozygous PU.1 knockout mice', Radiation Research, vol. 182, no. 3, pp. 310-315. https://doi.org/10.1667/RR13738.1
Genik PC, Vyazunova I, Steffen LS, Bacher JW, Bielefeldt-Ohmann H, McKercher S et al. Leukemogenesis in heterozygous PU.1 knockout mice. Radiation Research. 2014;182(3):310-315. https://doi.org/10.1667/RR13738.1
Genik, Paula C. ; Vyazunova, Irina ; Steffen, Leta S. ; Bacher, Jeffery W. ; Bielefeldt-Ohmann, Helle ; McKercher, Scott ; Ullrich, Robert L. ; Fallgren, Christina M. ; Weil, Michael M. ; Ray, F. Andrew. / Leukemogenesis in heterozygous PU.1 knockout mice. In: Radiation Research. 2014 ; Vol. 182, No. 3. pp. 310-315.
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