Genomic and proteomic analysis of the myeloid differentiation program

被引:89
作者
Lian, Z
Wang, L
Yamaga, S
Bonds, W
Beazer-Barclay, Y
Kluger, Y
Gerstein, M
Newburger, PE
Berliner, N
Weissman, SM
机构
[1] Yale Univ, Sch Med, Boyer Ctr Mol Med, Dept Genet, New Haven, CT 06536 USA
[2] Yale Univ, Sch Med, Dept Internal Med, Sect Hematol, New Haven, CT 06536 USA
[3] Yale Univ, Sch Med, Dept Mol Biophys & Biochem, New Haven, CT 06536 USA
[4] Univ Massachusetts, Sch Med, Dept Pediat, Worcester, MA USA
[5] Gene Log, Gaithersburg, MD USA
关键词
D O I
10.1182/blood.V98.3.513
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Although the mature neutrophil Is one of the better characterized mammalian cell types, the mechanisms of myeloid differentiation are Incompletely understood at the molecular level. A mouse promyelocytic cell line (MPRO), derived from murine bone marrow cells and arrested developmentally by a dominant-negative retinoic acid receptor, morphologically differentiates to mature neutrophils In the presence of 10 muM retinoic acid. An extensive catalog was prepared of the gene expression changes that occur during morphologic maturation. To do this, 3 ' -end differential display, oligonucleotide, chip array hybridization, and 2-dimensional protein electrophoresis were used. A large number of genes whose mRNA levels are modulated during differentiation of MPRO cells were identified. The results suggest the involvement of several transcription regulatory factors not previously implicated in this process, but they also emphasize the importance of events other than the production of new transcription factors. Furthermore, gene expression patterns were compared at the level of mRNA and protein, and the correlation between 2 parameters was studied.
引用
收藏
页码:513 / 524
页数:12
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