Gorman M, Kuroda M I, Baker B S
Department of Biological Sciences, Stanford University, California 94305.
Cell. 1993 Jan 15;72(1):39-49. doi: 10.1016/0092-8674(93)90048-u.
In Drosophila, the single male X chromosome is transcribed at twice the rate of a single female X chromosome. This hypertranscription requires the functions of at least four autosomal male-specific lethal genes (msls) and is under the control of the Sex-lethal (Sxl) gene. One of the msls, the maleless (mle) gene, encodes a protein that is associated with the male X chromosome. To investigate how dosage compensation is regulated, we have determined whether Sxl and the other msls are required for mle X chromosome binding. We have found that in females, Sxl functions to prevent mle from binding to the two X chromosomes. Additionally, we have found that mle X chromosome binding requires wild-type msl1, msl2, and msl3 functions. These data support a model whereby the activity of the mle protein is regulated through its association with one or more of the other msl proteins.
在果蝇中,单个雄性X染色体的转录速率是单个雌性X染色体的两倍。这种超转录需要至少四个常染色体雄性特异性致死基因(msls)的功能,并且受性别致死(Sxl)基因的控制。其中一个msls,即无雄性(mle)基因,编码一种与雄性X染色体相关的蛋白质。为了研究剂量补偿是如何被调控的,我们已经确定Sxl和其他msls对于mle与X染色体的结合是否是必需的。我们发现,在雌性中,Sxl发挥作用以阻止mle与两条X染色体结合。此外,我们还发现mle与X染色体的结合需要野生型msl1、msl2和msl3的功能。这些数据支持了一个模型,即mle蛋白的活性是通过其与一种或多种其他msl蛋白的结合来调控的。