Wu Z G, Murphy C, Gall J G
Chromosoma. 1986;93(4):291-7. doi: 10.1007/BF00327586.
We have cloned and sequenced a 360 bp repeated sequence from genomic DNA of the bullfrog Rana catesbeiana. This sequence, which we call satellite 1, makes up 0.7% of the genome (1.6 X 10(5) repeats) and is scattered throughout the length of all the chromosomes. In situ hybridization with strand-specific probes demonstrated that transcripts from both strands of satellite 1 occur on lamp-brush chromosome loops. We suggest that these transcripts arise by readthrough from upstream structural gene promoters. Sequences that cross-react with satellite 1 were found in genomic DNA of four out of five other Rana species that we tested, but were absent from the DNA of Xenopus, Bombina, and Acris.
我们从牛蛙(Rana catesbeiana)的基因组DNA中克隆并测序了一段360 bp的重复序列。这个序列,我们称之为卫星1,占基因组的0.7%(1.6×10⁵个重复序列),并散布在所有染色体的全长上。用链特异性探针进行的原位杂交表明,卫星1两条链的转录本都出现在灯刷染色体环上。我们认为这些转录本是由上游结构基因启动子的通读产生的。在我们测试的其他五种蛙类中的四种的基因组DNA中发现了与卫星1交叉反应的序列,但在非洲爪蟾、铃蟾和蝗蛙的DNA中没有。