Mahon Gwendolyn M, Wang Yan, Korus Malgorzata, Kostenko Elena, Cheng Li, Sun Tong, Arlinghaus Ralph B, Whitehead Ian P
Department of Microbiology and Molecular Genetics, UMDNJ-New Jersey Medical School, PO Box 1709, 225 Warren Street, Newark, NJ 07101-1709, USA.
Curr Biol. 2003 Mar 4;13(5):437-41. doi: 10.1016/s0960-9822(03)00090-3.
Bcr is a multifunctional protein that is the fusion partner for Abl (p210 Bcr-Abl) in Philadelphia chromosome positive leukemias. We have identified c-Myc as a binding partner for Bcr in both yeast and mammalian cells. We are also able to observe interactions between natively expressed c-Myc and Bcr in leukemic cell lines. Although Bcr and Max have overlapping binding sites on c-Myc, Bcr cannot interact with Max, or with the c-Myc.Max heterodimer. Bcr expression blocks activation of c-Myc-responsive genes, as well as the transformed phenotype induced by coexpression of c-Myc and H-Ras, and this finding suggests that one function of Bcr is to limit the activity of c-Myc. However, Bcr does not block c-Myc function by preventing its nuclear localization. Interestingly, increased Bcr dosage in COS-7 and K-562 cells correlates with a reduction in c-Myc protein levels, suggesting that Bcr may in fact be limiting c-Myc activity by regulating its stability. These data indicate that Bcr is a novel regulator of c-Myc function whose disrupted expression may contribute to the high level of c-Myc protein that is observed in Bcr-Abl transformed cells.
Bcr是一种多功能蛋白,在费城染色体阳性白血病中是Abl(p210 Bcr-Abl)的融合伴侣。我们已确定c-Myc在酵母和哺乳动物细胞中均为Bcr的结合伴侣。我们还能够观察到白血病细胞系中天然表达的c-Myc与Bcr之间的相互作用。尽管Bcr和Max在c-Myc上具有重叠的结合位点,但Bcr不能与Max或c-Myc.Max异二聚体相互作用。Bcr的表达会阻断c-Myc反应性基因的激活,以及由c-Myc和H-Ras共表达诱导的转化表型,这一发现表明Bcr的一个功能是限制c-Myc的活性。然而,Bcr不会通过阻止其核定位来阻断c-Myc的功能。有趣的是,COS-7和K-562细胞中Bcr剂量的增加与c-Myc蛋白水平的降低相关,这表明Bcr实际上可能通过调节其稳定性来限制c-Myc的活性。这些数据表明Bcr是c-Myc功能的一种新型调节因子,其表达的破坏可能导致在Bcr-Abl转化细胞中观察到的高水平c-Myc蛋白。