Tanaka Satomi S, Nagamatsu Go, Tokitake Yuko, Kasa Miyuki, Tam Patrick P L, Matsui Yasuhisa
Department of Molecular Embryology, Research Institute, Osaka Medical Center for Maternal and Child Health, Osaka, Japan.
Dev Dyn. 2004 Aug;230(4):651-9. doi: 10.1002/dvdy.20085.
Mouse interferon-induced transmembrane protein (IFITM) gene, Ifitm3 (previously known as mil-1 and fragilis), is expressed in primordial germ cells (PGCs), in their precursors, and in germ cells of the fetal gonads (Saitou et al. [2002] Nature 418:293-300; Tanaka and Matsui [2002] Mech Dev 119S:S261-S267). By examining the expression of green fluorescent protein transgene under the control of DNA sequences flanking exon 1, we have identified domains that direct Ifitm3 transcription in PGCs and their precursors in gastrula stage and 13.5 days post coitum embryos. Germ cell-specific expression is achieved by the activity of a consensus element unique to the Ifitm genes, which may act to suppress Ifitm3 expression in somatic tissues. The lack of any influence of the interferon-stimulable response elements on transgene expression in the germ-line suggests that interferon-mediated response is not critical for activating Ifitm3.
小鼠干扰素诱导跨膜蛋白(IFITM)基因Ifitm3(以前称为mil-1和fragilis)在原始生殖细胞(PGC)、其前体细胞以及胎儿性腺的生殖细胞中表达(斋藤等人[2002]《自然》418:293 - 300;田中与松井[2002]《机制与发育》119S:S261 - S267)。通过检测外显子1侧翼DNA序列控制下的绿色荧光蛋白转基因的表达,我们确定了在原肠胚阶段和交配后13.5天胚胎的PGC及其前体细胞中指导Ifitm3转录的结构域。生殖细胞特异性表达是通过Ifitm基因特有的共有元件的活性实现的,该元件可能在体细胞组织中抑制Ifitm3的表达。干扰素刺激反应元件对种系中转基因表达没有任何影响,这表明干扰素介导的反应对于激活Ifitm3并不关键。