Department of Molecular Biology, Umeå University, SE-90187 Umeå, Sweden.
G3 (Bethesda). 2013 Aug 7;3(8):1325-34. doi: 10.1534/g3.113.006866.
In Drosophila melanogaster, two chromosome-specific targeting and regulatory systems have been described. The male-specific lethal (MSL) complex supports dosage compensation by stimulating gene expression from the male X-chromosome, and the protein Painting of fourth (POF) specifically targets and stimulates expression from the heterochromatic 4(th) chromosome. The targeting sites of both systems are well characterized, but the principles underlying the targeting mechanisms have remained elusive. Here we present an original observation, namely that POF specifically targets two loci on the X-chromosome, PoX1 and PoX2 (POF-on-X). PoX1 and PoX2 are located close to the roX1 and roX2 genes, which encode noncoding RNAs important for the correct targeting and spreading of the MSL-complex. We also found that the targeting of POF to PoX1 and PoX2 is largely dependent on roX expression and identified a high-affinity target region that ectopically recruits POF. The results presented support a model linking the MSL-complex to POF and dosage compensation to regulation of heterochromatin.
在黑腹果蝇中,已经描述了两种染色体特异性靶向和调节系统。雄性特异性致死(MSL)复合物通过刺激雄性 X 染色体的基因表达来支持剂量补偿,而蛋白质第四(POF)特异性靶向并刺激异染色质 4(th)染色体的表达。这两个系统的靶向位点都得到了很好的描述,但靶向机制的原理仍然难以捉摸。在这里,我们提出了一个新的观察结果,即 POF 特异性靶向 X 染色体上的两个位点,PoX1 和 PoX2(POF-on-X)。PoX1 和 PoX2 靠近 roX1 和 roX2 基因,这些基因编码对 MSL 复合物的正确靶向和扩散很重要的非编码 RNA。我们还发现,POF 对 PoX1 和 PoX2 的靶向在很大程度上依赖于 roX 的表达,并鉴定了一个高亲和力的靶区,该靶区异位招募 POF。所提出的结果支持将 MSL 复合物与 POF 以及剂量补偿与异染色质调控联系起来的模型。