Oikawa T, Yamada T, Kihara-Negishi F, Yamamoto H, Kondoh N, Hitomi Y, Hashimoto Y
Department of Cell Genetics, Sasaki Institute, 2-2, Kanda-Surugadai, Chiyoda-ku, Tokyo 101-0062, Japan. toikawa@goldfish sasaki.or.jp
Cell Death Differ. 1999 Jul;6(7):599-608. doi: 10.1038/sj.cdd.4400534.
The PU.1 gene encodes an Ets family transcription factor which controls expression of many B cell- and macrophage-specific genes. Expression of the gene is critical for development of lymphoid and myeloid cell lineages, since PU.1-deficient mice exhibit defects in the development of these cell lineages. The PU.1 gene is identical to the Spi-1 gene isolated from common proviral integration sites in Friend virus-induced murine erythroleukemia (MEL), and deregulated expression of the gene is believed to be an essential step of the disease. We recently demonstrated that overexpression of PU.1 inhibits erythroid differentiation of MEL cells induced with the differentiating agent DMSO. We also noticed unexpectedly that overexpression of PU.1 together with DMSO induces marked growth arrest and apoptosis in MEL cells, supporting the notion that some oncogenes induce growth inhibition and apoptosis rather than cell proliferation and transformation under specific circumstances as shown with the c-myc gene. In this review, the role of PU.1 in hematopoietic cell differentiation, proliferation and apoptosis is described and the possible molecular mechanisms of PU.1-induced effects in MEL cells are discussed.
PU.1基因编码一种Ets家族转录因子,该因子控制许多B细胞和巨噬细胞特异性基因的表达。该基因的表达对于淋巴样和髓样细胞谱系的发育至关重要,因为PU.1缺陷型小鼠在这些细胞谱系的发育中表现出缺陷。PU.1基因与从Friend病毒诱导的小鼠红白血病(MEL)中常见的前病毒整合位点分离出的Spi-1基因相同,并且该基因的失调表达被认为是该疾病的一个关键步骤。我们最近证明,PU.1的过表达抑制了用分化剂二甲基亚砜(DMSO)诱导的MEL细胞的红系分化。我们还意外地注意到,PU.1与DMSO共同过表达会诱导MEL细胞显著的生长停滞和凋亡,这支持了一种观点,即某些癌基因在特定情况下会诱导生长抑制和凋亡,而不是细胞增殖和转化,就像c-myc基因所显示的那样。在这篇综述中,描述了PU.1在造血细胞分化、增殖和凋亡中的作用,并讨论了PU.1在MEL细胞中诱导效应的可能分子机制。