Kelley R L, Solovyeva I, Lyman L M, Richman R, Solovyev V, Kuroda M I
Howard Hughes Medical Institute, Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030, USA.
Cell. 1995 Jun 16;81(6):867-77. doi: 10.1016/0092-8674(95)90007-1.
Male-specific lethal-2 (msl-2) is a RING finger protein that is required for X chromosome dosage compensation in Drosophila males. Consistent with the formation of a dosage compensation protein complex, msl-2 colocalizes with the other MSL proteins on the male X chromosome and coimmunoprecipitates with msl-1 from male larval extracts. Ectopic expression of msl-2 in females results in the appearance of the other MSL dosage compensation regulators on the female X chromosomes and decreased female viability. We suggest that msl-2 RNA is the primary target of SxI regulation in the dosage compensation pathway and present a speculative model for the regulation of two distinct modes of dosage compensation by SxI.
雄性特异性致死因子2(msl-2)是一种环状结构域蛋白,在果蝇雄性个体中,它是X染色体剂量补偿所必需的。与剂量补偿蛋白复合物的形成一致,msl-2与其他MSL蛋白在雄性X染色体上共定位,并与雄性幼虫提取物中的msl-1进行共免疫沉淀。在雌性个体中异位表达msl-2会导致其他MSL剂量补偿调节因子出现在雌性X染色体上,并降低雌性的生存能力。我们认为msl-2 RNA是剂量补偿途径中SxI调控的主要靶点,并提出了一个关于SxI调控两种不同剂量补偿模式的推测模型。