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DmRP140基因的转录,该基因编码RNA聚合酶II的第二大亚基。

Transcription of DmRP140, the gene coding for the second-largest subunit of RNA polymerase II.

作者信息

Wiedemann M, Oldenburg I, Sitzler S, Petersen G

机构信息

Institute of Molecular Genetics, University Heidelberg, Germany.

出版信息

Biochim Biophys Acta. 1997 Feb 28;1350(3):282-6. doi: 10.1016/s0167-4781(96)00230-8.

Abstract

To analyze transcriptional control regions of Drosophila melanogaster housekeeping genes, we have characterized the promoter of the gene coding for the second-largest subunit of RNA polymerase II (DmRP140). Upstream of DmRP140 the genomic region harbors a gene which is transcribed in the opposite direction (DmRP140up). By determination of the transcription start sites of both genes we found a short non-transcribed intergenic region of 220 bp. Functional analysis of various promoter reportergene constructs by transient transfection of cultured cells revealed that sequences important for transcription of DmRP140 are located in the untranslated leader of the upstream gene. The onset of DmRP140 transcription during embryonic development was studied in transgenic flies using beta-galactosidase as reportergene. To distinguish between the maternally provided DmRP140 transcripts and the embryonically transcribed RNA the offspring of nontransformed females and male transformants was examined. The development of a sensitive detection assay based on a chemiluminescent substrate for beta-galactosidase allowed us to determine the onset of DmRP140 transcription to between 8-10 h after oviposition. Thus, DmRP140 transcription does not start following the transcriptional transition period between 2-3 h of development but occurs much later in embryogenesis coinciding with decreasing DNA synthesis and cell division rates.

摘要

为了分析黑腹果蝇管家基因的转录控制区域,我们对编码RNA聚合酶II第二大亚基(DmRP140)的基因启动子进行了表征。在DmRP140上游的基因组区域含有一个以相反方向转录的基因(DmRP140up)。通过确定这两个基因的转录起始位点,我们发现了一个220 bp的短非转录基因间区域。通过培养细胞的瞬时转染对各种启动子报告基因构建体进行功能分析,结果表明,对DmRP140转录重要的序列位于上游基因的非翻译前导区。在转基因果蝇中,以β-半乳糖苷酶作为报告基因,研究了胚胎发育过程中DmRP140转录的起始情况。为了区分母本提供的DmRP140转录本和胚胎转录的RNA,我们检查了未转化雌性和雄性转化体的后代。基于β-半乳糖苷酶化学发光底物的灵敏检测方法的开发,使我们能够确定DmRP140转录起始于产卵后8至10小时之间。因此,DmRP140转录并非在发育2至3小时的转录过渡期之后开始,而是在胚胎发生过程中晚得多的时候发生,这与DNA合成和细胞分裂速率的降低相吻合。

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