Murphy S P, Garbern J, Odenwald W F, Lazzarini R A, Linney E
Department of Microbiology and Immunology, Duke University Medical Center, Durham, NC 27710.
Proc Natl Acad Sci U S A. 1988 Aug;85(15):5587-91. doi: 10.1073/pnas.85.15.5587.
The Hox-1.3 gene is located on mouse chromosome 6 and has been previously shown to be expressed in mouse embryos and adults. In this study, we have examined the steady-state levels of the Hox-1.3 transcripts in undifferentiated and differentiated F9 embryonal carcinoma cells. We find that there is a rapid increase of Hox-1.3 transcripts after differentiation induction of F9 cells. The level of the major 1.85-kilobase (kb) transcript peaks at 16-24 hr after differentiation induction of F9 cells. By using primer extension techniques the 5' ends of the major 1.85-kb transcript have been mapped to two sites in induced F9 cells. Cellular fractionation of RNA and transfer blot gel analysis has localized one minor transcript to the nucleus, whereas the major transcript and two additional minor transcripts appear in the nucleus and the cytoplasm of induced F9 cells. The results of nuclear run-off experiments with uninduced and induced F9 cell nuclei indicate that there is a substantial increase in the rate of Hox-1.3 transcription upon induction of F9 cells with retinoic acid.
Hox - 1.3基因位于小鼠的6号染色体上,先前已证明它在小鼠胚胎和成年个体中表达。在本研究中,我们检测了未分化和分化的F9胚胎癌细胞中Hox - 1.3转录本的稳态水平。我们发现,F9细胞分化诱导后,Hox - 1.3转录本迅速增加。主要的1.85千碱基(kb)转录本水平在F9细胞分化诱导后16 - 24小时达到峰值。通过引物延伸技术,已将主要的1.85 - kb转录本的5'端定位到诱导的F9细胞中的两个位点。RNA的细胞分级分离和转印凝胶分析已将一种次要转录本定位到细胞核,而主要转录本和另外两种次要转录本出现在诱导的F9细胞的细胞核和细胞质中。用未诱导和诱导的F9细胞核进行的核转录实验结果表明,用视黄酸诱导F9细胞后,Hox - 1.3转录速率大幅增加。