Jongens T A, Fowler T, Shermoen A W, Beckendorf S K
Department of Molecular Biology, University of California, Berkeley 94720.
EMBO J. 1988 Aug;7(8):2559-67. doi: 10.1002/j.1460-2075.1988.tb03105.x.
During the last day of larval development, the Sgs-4 glue gene of Drosophila melanogaster is expressed at high levels in a single tissue, the larval salivary glands. As shown by transformation experiments and by DNA sequence analysis of Sgs-4 underproducing strains, an essential regulatory region for Sgs-4 expression lies between 149 and 568 bp upstream from the transcribed part of the gene. This region shows the positional independence of a transcriptional enhancer and directs at least three regulatory activities: tissue specificity, developmental timing and high-level expression. Here we use a transient transformation assay to identify three elements within this enhancer that are involved in tissue specificity. For at least this regulatory activity the enhancer is internally redundant. Any pairwise combination of the three elements is sufficient to direct salivary gland expression, although none of the three can act alone.
在幼虫发育的最后一天,黑腹果蝇的Sgs-4胶水基因在单一组织即幼虫唾液腺中高水平表达。转化实验以及Sgs-4产量不足菌株的DNA序列分析表明,Sgs-4表达的一个关键调控区域位于该基因转录部分上游149至568 bp之间。该区域显示出转录增强子的位置独立性,并至少指导三种调控活性:组织特异性、发育时间和高水平表达。在这里,我们使用瞬时转化分析来鉴定该增强子中参与组织特异性的三个元件。对于至少这种调控活性而言,增强子在内部是冗余的。这三个元件的任何两两组合都足以指导唾液腺表达,尽管这三个元件都不能单独起作用。