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小鼠胚胎发育过程中HMG盒因子TCF-1和LEF-1的差异表达。

Differential expression of the HMG box factors TCF-1 and LEF-1 during murine embryogenesis.

作者信息

Oosterwegel M, van de Wetering M, Timmerman J, Kruisbeek A, Destree O, Meijlink F, Clevers H

机构信息

Department of Immunology, University Hospital, Utrecht, The Netherlands.

出版信息

Development. 1993 Jun;118(2):439-48. doi: 10.1242/dev.118.2.439.

Abstract

The recent identification of a number of T lymphocyte-specific enhancers has allowed the cloning of several novel transcription factors. Two of these, TCF-1 and LEF-1, contain a virtually identical DNA-binding domain of the High Mobility Group (HMG-1) box type. TCF-1 and LEF-1 originate from a recent gene duplication event as evidenced by comparison with the chicken homologue, chTCF. We have now analyzed the differential expression of these two transcription factors. In a panel of lymphoid cell lines, TCF-1 was exclusively expressed in the T cell lineage. In contrast, LEF-1 mRNA was detected at equivalent levels in pro- and pre-B cells and in all T lineage cells. In situ hybridization on murine embryos revealed that TCF-1 and LEF-1 were widely expressed at day 7.5 of gestation. At later stages, the expression patterns were complex and only partially overlapping. The expression of TCF-1 and LEF-1 coincided until day 10.5, when mRNAs were detected in limb buds, neural crest, pharyngeal arches and nasal process. At later time points (day 13.5 to 14.5), sites of overlapping expression included lung, the urogenital system, tooth buds, thymus and choroid plexus. Unique expression sites for TCF-1 included Reichert's membrane and trophectoderm-derived cells, the ribs and thoracic prevertebrae, craniofacial structures, the adrenal gland and meninges. Unique LEF-1 expression was observed in the tail prevertebrae, brain and inner ear. Postnatally, expression of both genes could only be detected in lymphoid tissues. These observations suggest that TCF-1 and LEF-1 exert differential functions during murine embryogenesis.

摘要

最近对一些T淋巴细胞特异性增强子的鉴定使得几个新的转录因子得以克隆。其中两个,即TCF-1和LEF-1,含有一个几乎相同的高迁移率族(HMG-1)盒型DNA结合结构域。与鸡同源物chTCF比较表明,TCF-1和LEF-1起源于最近的基因复制事件。我们现在分析了这两种转录因子的差异表达。在一组淋巴样细胞系中,TCF-1仅在T细胞谱系中表达。相反,在B前体细胞和前B细胞以及所有T谱系细胞中,LEF-1 mRNA的检测水平相当。对小鼠胚胎进行原位杂交显示,在妊娠第7.5天时,TCF-1和LEF-1广泛表达。在后期阶段,表达模式复杂且仅部分重叠。TCF-1和LEF-1的表达在第10.5天之前是一致的,此时在肢芽、神经嵴、咽弓和鼻突中检测到mRNA。在随后的时间点(第13.5天至14.5天),重叠表达的部位包括肺、泌尿生殖系统、牙胚、胸腺和脉络丛。TCF-1的独特表达部位包括赖歇特膜和滋养外胚层衍生细胞、肋骨和胸段椎体、颅面结构、肾上腺和脑膜。在尾段椎体、脑和内耳中观察到LEF-1的独特表达。出生后,仅在淋巴组织中能检测到这两个基因的表达。这些观察结果表明,TCF-1和LEF-1在小鼠胚胎发育过程中发挥不同的功能。

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