Novel binding partners of Ldb1 are required for haematopoietic development

被引:106
作者
Meier, Natalia
Krpic, Sanja
Rodriguez, Patrick
Strouboulis, John
Monti, Maria
Krijgsveld, Jeroen
Gering, Martin
Patient, Roger
Hostert, Arnd
Grosveld, Frank
机构
[1] Erasmus MC, Dept Cell Biol & Genet, NL-3000 CA Rotterdam, Netherlands
[2] Univ Utrecht, Dept Biomol Mass Spect, Bijvoet Ctr Biomol Res, NL-3584 CA Utrecht, Netherlands
[3] Univ Utrecht, Utrecht Inst Pharmaceut Sci, NL-3584 CA Utrecht, Netherlands
[4] Univ Oxford, Weatherall Inst Mol Med, MRC Mol Haematol Unit, Oxford OX3 9DS, England
来源
DEVELOPMENT | 2006年 / 133卷 / 24期
基金
英国医学研究理事会;
关键词
Ldb1; transcription factor complexes; haematopoietic stem cells; haematopoiesis;
D O I
10.1242/dev.02656
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Ldb1, a ubiquitously expressed LIM domain binding protein, is essential in a number of tissues during development. It interacts with Gata1, Tal1, E2A and Lmo2 to form a transcription factor complex regulating late erythroid genes. We identify a number of novel Ldb1 interacting proteins in erythroleukaemic cells, in particular the repressor protein Eto-2 (and its family member Mtgr1), the cyclin-dependent kinase Cdk9, and the bridging factor Lmo4. MO-mediated knockdowns in zebrafish show these factors to be essential for definitive haematopoiesis. In accordance with the zebrafish results these factors are coexpressed in prehaematopoietic cells of the early mouse embryo, although we originally identified the complex in late erythroid cells. Based on the change in subcellullar localisation of Eto-2 we postulate that it plays a central role in the transition from the migration and expansion phase of the prehaematopoietic cells to the establishment of definitive haematopoietic stem cells.
引用
收藏
页码:4913 / 4924
页数:12
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