Cooperation between somatic Ikaros and Notch1 mutations at the inception of T-ALL.

Citation data:

Leukemia research, ISSN: 1873-5835, Vol: 35, Issue: 11, Page: 1512-9

Publication Year:
2011
Usage 339
Abstract Views 249
Downloads 90
Citations 1
Citation Indexes 1
Repository URL:
https://works.bepress.com/gerard-hoyne/1; https://researchonline.nd.edu.au/med_article/537; https://researchonline.nd.edu.au/health_article/54
PMID:
21840596
DOI:
10.1016/j.leukres.2011.07.024
Author(s):
Sontani, Yovina; Chapman, Gavin; Papathanasiou, Peter; Dunwoodie, Sally; Goodnow, Christopher C; Hoyne, Gerard F
Publisher(s):
Elsevier BV
Tags:
Biochemistry, Genetics and Molecular Biology; Medicine; Peer-reviewed; T cells; leukaemia; Notch; peer-reviewed; Medicine and Health Sciences; Life Sciences
article description
To understand the interactions between Notch1 and Ikaros in the evolution of T cell acute lymphoblastic leukemia (T-ALL), we traced the evolution of T-ALL in mice with an inherited Ikaros mutation, Ikzf1(Plstc) which inactivates DNA binding. DNA-binding Ikaros repressed Notch1 response in transfected cell lines and in CD4(+)8(+) (DP) thymocytes from young pre-leukemic Ikzf1(Plstc) heterozygous mice. In DP thymocytes, a 50-1000 fold escalation in mRNA for Notch1 target genes Hes1 and Dtx1 preceded thymic lymphoma or leukemia and was closely correlated with the first detectable differentiation abnormalities, loss of heterozygosity (LOH) eliminating wild-type Ikzf1, and multiple missense and truncating Notch1 mutations. These findings illuminate the early stages of leukemogenesis by demonstrating progressive exaggeration of Notch1 responsiveness at the DP thymocyte stage brought about by multiple mutations acting in concert upon the Notch1 pathway.