Kemppainen Esko, Fernández-Ayala Daniel Jose Moreno, Galbraith Laura C A, O'Dell Kevin M C, Jacobs Howard T
Institute of Medical Technology and Tampere University Hospital, FI-33014 University of Tampere, Finland.
Mitochondrion. 2009 Sep;9(5):353-63. doi: 10.1016/j.mito.2009.07.002. Epub 2009 Jul 17.
A mutation in the Drosophila gene technical knockout (tko(25t)), encoding mitoribosomal protein S12, phenocopies human mitochondrial disease. We isolated three spontaneous X-dominant suppressors of tko(25t) (designated Weeble), exhibiting almost wild-type phenotype and containing overlapping segmental duplications including the mutant allele, plus a second mitoribosomal protein gene, mRpL14. Ectopic, expressed copies of tko(25t) and mRpL14 conferred no phenotypic suppression. When placed over a null allele of tko, Weeble retained the mutant phenotype, even in the presence of additional transgenic copies of tko(25t). Increased mutant gene dosage can thus compensate the mutant phenotype, but only when located in its normal chromosomal context.
果蝇基因技术敲除(tko(25t))发生突变,该基因编码线粒体核糖体蛋白S12,其表型模拟人类线粒体疾病。我们分离出了tko(25t)的三个自发的X显性抑制子(命名为Weeble),它们表现出几乎野生型的表型,并且包含重叠的节段性重复,其中包括突变等位基因,以及第二个线粒体核糖体蛋白基因mRpL14。tko(25t)和mRpL14的异位表达拷贝没有产生表型抑制作用。当置于tko的无效等位基因上时,即使存在额外的tko(25t)转基因拷贝,Weeble仍保留突变表型。因此,增加突变基因剂量可以补偿突变表型,但前提是该基因位于其正常的染色体背景中。