Larschan E, Alekseyenko A A, Lai W R, Park P J, Kuroda M I
Harvard-Partners Center for Genetics and Genomics, Brigham & Women's Hospital, Boston, Massachusetts 02115, USA.
Cold Spring Harb Symp Quant Biol. 2006;71:385-94. doi: 10.1101/sqb.2006.71.026.
Dosage compensation in Drosophila serves as a model system for understanding the targeting of chromatin-modifying complexes to their sites of action. The MSL (male-specific lethal) complex up-regulates transcription of the single male X chromosome, thereby equalizing levels of transcription of X-linked genes between the sexes. Recruitment of the MSL complex to its binding sites on the male X chromosome requires each of the MSL proteins and at least one of the two large noncoding roX RNAs. To better understand how the MSL complex specifically targets the X chromosome, we have defined the binding using high-resolution genomic tiling arrays. Our results indicate that the MSL complex largely associates with transcribed genes that are present in clusters along the X chromosome. We hypothesize that after initial recruitment of the MSL complex to the X chromosome by unknown mechanisms, nascent transcripts or chromatin marks associated with active transcription attract the MSL complex to its final targets. Defining MSL-complex-binding sites will provide a tool for understanding functions of large noncoding RNAs that have remained elusive.
果蝇中的剂量补偿作为一个模型系统,用于理解染色质修饰复合物靶向其作用位点的机制。雄性特异性致死(MSL)复合物上调单个雄性X染色体的转录,从而使两性之间X连锁基因的转录水平相等。MSL复合物募集到雄性X染色体上的结合位点需要每个MSL蛋白以及两个大型非编码roX RNA中的至少一个。为了更好地理解MSL复合物如何特异性靶向X染色体,我们使用高分辨率基因组平铺阵列定义了其结合情况。我们的结果表明,MSL复合物主要与沿X染色体成簇存在的转录基因相关联。我们推测,在MSL复合物通过未知机制最初募集到X染色体后,与活跃转录相关的新生转录本或染色质标记将MSL复合物吸引到其最终靶标。定义MSL复合物结合位点将为理解一直难以捉摸的大型非编码RNA的功能提供一个工具。