Negative regulatory elements are present in the human LMO2 oncogene and may contribute to its expression in leukemia.

Abstract:

:Ectopic expression of LMO2 occurs in approximately 45% of T-lineage acute lymphoblastic leukemias (T-ALL), sometimes in association with chromosomal translocations. Recently, a lymphoproliferative disorder developed in two participants in a gene therapy trial due to LMO2 activation via integration of the retroviral vector. To investigate these regulatory disruptions, we analyzed the promoter region and identified a tissue-specific repressor. The fragment containing this element could also produce tissue-specific suppression of transcription from the SV40 promoter. This suppression involves histone acetylation which can be relieved with Trichostatin A (TSA). The negative element is in a region consistently removed from LMO2 in the known chromosomal translocations.

journal_name

Leuk Res

journal_title

Leukemia research

authors

Hammond SM,Crable SC,Anderson KP

doi

10.1016/j.leukres.2004.05.013

keywords:

subject

Has Abstract

pub_date

2005-01-01 00:00:00

pages

89-97

issue

1

eissn

0145-2126

issn

1873-5835

pii

S0145212604002152

journal_volume

29

pub_type

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