Suter B, Kubli E
Zoological Institute, University of Zurich-Irchel, Switzerland.
Mol Cell Biol. 1988 Aug;8(8):3322-31. doi: 10.1128/mcb.8.8.3322-3331.1988.
Six Drosophila melanogaster tRNA(Tyr) genes have been isolated and sequenced. They contained introns of different sequences and two size classes: 20 or 21 base pairs (bp) (five genes) and 113 bp (one gene). However, the sequences coding for the mature tRNA(Tyr) were identical in all six genes. The 113-bp intron-containing gene was a single-copy gene. Hence, its primary transcript could be traced by S1 mapping. The gene was turned on during embryogenesis and continually expressed to various degrees during the following developmental stages. Thus, S1 mapping is a feasible method to follow the transcriptional activity of individual genes with identical mature products, provided that their primary transcripts are unique. The six genes were organized in two clusters of three and two genes, respectively (each containing a 20- or a 21-bp intron; cytological localization, 85A), and a single-copy gene (113-bp intron; cytological localization, 28C). We show that four of the six tRNA(Tyr) genes characterized were localized in putative 5' control regions of developmentally controlled genes transcribed by polymerase II.
已分离并测序了六个黑腹果蝇tRNA(Tyr)基因。它们含有不同序列和两个大小类别的内含子:20或21个碱基对(bp)(五个基因)和113 bp(一个基因)。然而,在所有六个基因中,编码成熟tRNA(Tyr)的序列是相同的。含有113 bp内含子的基因是单拷贝基因。因此,其初级转录本可通过S1作图追踪。该基因在胚胎发生期间开启,并在随后的发育阶段持续以不同程度表达。因此,S1作图是一种可行的方法,可用于追踪具有相同成熟产物的单个基因的转录活性,前提是它们的初级转录本是独特的。这六个基因分别组织成两个簇,一个簇包含三个基因,另一个簇包含两个基因(每个簇都含有一个20或21 bp的内含子;细胞学定位,85A),以及一个单拷贝基因(113 bp内含子;细胞学定位,28C)。我们表明,所鉴定的六个tRNA(Tyr)基因中的四个位于由聚合酶II转录的发育调控基因的假定5'控制区域中。