Hls5 regulated erythroid differentiation by modulating GATA-1 activity

被引:5
|
作者
Endersby, Raelene [1 ,2 ]
Majewski, Ian J. [1 ,3 ]
Winteringham, Louise [1 ]
Beaumont, Jennifer G. [1 ]
Samuels, Amy [1 ]
Scaife, Robin [1 ]
Lim, Esther [1 ]
Crossley, Merlin [4 ]
Klinken, S. Peter [1 ]
Lalonde, Jean-Philippe [1 ]
机构
[1] Univ Western Australia, Med Res Ctr, Western Australian Inst Med Res, Lab Canc Med, Crawley, Australia
[2] St Jude Childrens Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
[3] Walter & Eliza Hall Inst Med Res, Div Mol Med, Parkville, Vic, Australia
[4] Univ Sydney, Sch Mol & Microbial Biosci, Sydney, NSW 2006, Australia
关键词
D O I
10.1182/blood-2007-04-085746
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Hemopoietic lineage switch (His) 5 and 7 were originally isolated as genes upregulated during an erythroid-to-myeloid lineage switch. We have shown previously that HIs7/Mlf1 imposes a monoblastoid phenotype on erythroleukemic cells. Here we show that Hls5 impedes erythroid maturation by restricting proliferation and inhibiting hemoglobin synthesis; however, HIs5 does not influence the morphology of erythroid cells. Under the influence of GATA-1, HIs5 relocates from cytoplasmic granules to the nucleus where it associates with both FOG-1 and GATA-1. In the nucleus, HIs5 is able to suppress GATA-1-mediated transactivation and reduce GATA-1 binding to DNA. We conclude that HIs5 and Hls7/Mlf1 act cooperatively to induce biochemical and phenotypic changes associated with erythroid/myeloid lineage switching.
引用
收藏
页码:1946 / 1950
页数:5
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