Mastick G S, McKay R, Oligino T, Donovan K, López A J
Department of Biological Sciences, Carnegie Mellon University, Pittsburgh, Pennsylvania 15213.
Genetics. 1995 Jan;139(1):349-63. doi: 10.1093/genetics/139.1.349.
A method based on the transcriptional activation of a selectable reporter in yeast cells was used to identify genes regulated by the Ultrabithorax homeoproteins in Drosophila melanogaster. Fifty-three DNA fragments that can mediate activation by UBX isoform Ia in this test were recovered after screening 15% of the Drosophila genome. Half of these fragments represent single-copy sequences in the genome. Six single-copy fragments were investigated in detail, and each was found to reside near a transcription unit whose expression in the embryo is segmentally modulated as expected for targets of homoeotic genes. Four of these putative target genes are expressed in patterns that suggest roles in the development of regional specializations within mesoderm derivatives; in three cases these expression patterns depend on Ultrabithorax function. Extrapolation from this pilot study indicates that 85-170 candidate target genes can be identified by screening the entire Drosophila genome with UBX isoform Ia. With appropriate modifications, this approach should be applicable to other transcriptional regulators in diverse organisms.
一种基于酵母细胞中可选择报告基因转录激活的方法被用于鉴定黑腹果蝇中由超双胸同源蛋白调控的基因。在筛选了15%的果蝇基因组后,回收了53个在此测试中可介导由UBX同工型Ia激活的DNA片段。这些片段中有一半代表基因组中的单拷贝序列。对六个单拷贝片段进行了详细研究,发现每个片段都位于一个转录单元附近,其在胚胎中的表达如预期的同源异型基因靶标那样受到分段调节。这些假定的靶基因中有四个以暗示在中胚层衍生物区域特化发育中起作用的模式表达;在三种情况下,这些表达模式依赖于超双胸功能。从这项初步研究推断,通过用UBX同工型Ia筛选整个果蝇基因组,可以鉴定出85 - 170个候选靶基因。经过适当修改,这种方法应该适用于不同生物体中的其他转录调节因子。