Chen Y, Hu H, Atkinson B G
Department of Zoology, University of Western Ontario, London, Canada.
Dev Genet. 1994;15(4):366-77. doi: 10.1002/dvg.1020150408.
Tissue-specific changes in gene expression occur in the liver of Rana catesbeiana tadpoles undergoing metamorphosis. Many of these changes can be induced precociously by administration of thyroid hormone (TH) to a tadpole or to cultured tadpole liver. While the precise molecular means by which TH exerts a tissue-specific response is unknown, recent studies suggest that the expression of genes which are liver-specific and characteristic of the adult liver phenotype may rely on TH-induction of tissue-specific transcription factors, as well as the thyroid hormone receptor proteins. Guided by this notion, we screened our Rana catesbeiana liver cDNA library and isolated clones, RcC/EBP-1 and -2, encoding Rana homologues of a mammalian transcription factor, C/EBP (CCAAT/enhancer core binding protein), implicated in the expression of liver-specific genes and terminal differentiation of hepatocytes. Gel mobility shift assays demonstrate that the proteins synthesized from these cDNAs bind specifically to the consensus binding site for C/EBP-related proteins. Characterization of the amino acid sequence in the bZIP DNA-binding domains of these proteins suggests that RcC/EBP-1 and -2 encode Rana homologues of C/EBP alpha and delta, respectively. Hybridization analyses demonstrate that the amount of RcC/EBP-2 mRNAs in tadpole liver remains constant throughout metamorphosis, whereas RcC/EBP-1 mRNAs are up-regulated during both spontaneous and TH-induced metamorphosis. The TH-induced up-regulation of RcC/EBP-1 mRNAs precedes the up-regulation of liver-specific urea cycle enzyme mRNAs by 6 to 12 hours. These results, coupled with in situ hybridization studies, suggest that RcC/EBP-1 mRNAs encode a transcription factor which may play an early role(s) in the terminal differentiation and/or reprogramming of gene expression in this tadpole's liver cells during both spontaneous and TH-induced metamorphosis.
在经历变态发育的牛蛙蝌蚪肝脏中会发生基因表达的组织特异性变化。通过向蝌蚪或培养的蝌蚪肝脏施用甲状腺激素(TH),可以过早诱导其中许多变化。虽然TH发挥组织特异性反应的确切分子机制尚不清楚,但最近的研究表明,肝脏特异性且具有成年肝脏表型特征的基因表达可能依赖于TH对组织特异性转录因子以及甲状腺激素受体蛋白的诱导。基于这一观点,我们筛选了牛蛙肝脏cDNA文库并分离出克隆RcC/EBP-1和-2,它们编码一种哺乳动物转录因子C/EBP(CCAAT/增强子核心结合蛋白)的牛蛙同源物,该转录因子与肝脏特异性基因的表达以及肝细胞的终末分化有关。凝胶迁移率变动分析表明,由这些cDNA合成的蛋白质特异性结合C/EBP相关蛋白的共有结合位点。对这些蛋白质bZIP DNA结合结构域中氨基酸序列的表征表明,RcC/EBP-1和-2分别编码C/EBPα和δ的牛蛙同源物。杂交分析表明,蝌蚪肝脏中RcC/EBP-2 mRNA的量在整个变态发育过程中保持恒定,而RcC/EBP-1 mRNA在自发变态发育和TH诱导的变态发育过程中均上调。TH诱导的RcC/EBP-1 mRNA上调比肝脏特异性尿素循环酶mRNA上调提前6至12小时。这些结果,再结合原位杂交研究,表明RcC/EBP-1 mRNA编码一种转录因子,在自发变态发育和TH诱导的变态发育过程中,该转录因子可能在这种蝌蚪肝细胞的终末分化和/或基因表达重编程中发挥早期作用。