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A subset of Drosophila Myc sites remain associated with mitotic chromosomes co-localized with insulator proteins

机译:果蝇Myc位点的子集仍然与与绝缘子蛋白共定位的有丝分裂染色体相关

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摘要

Myc has been characterized as a transcription factor that activates expression of genes involved in pluripotency and cancer, and as a component of the replication complex. Here we find that Myc is present at promoters and enhancers of D. melanogaster genes during interphase. Myc co-localizes with Orc2, which is part of the pre-replication complex, during G1. As is the case in mammals, Myc associates preferentially with paused genes, suggesting that it may also be involved in the release of RNAPII from promoter proximal pausing in Drosophila. Interestingly, about 40% of Myc sites present in interphase persists during mitosis. None of the Myc mitotic sites correspond to enhancers and only some correspond to promoters. The rest of mitotic Myc sites overlap with binding sites for multiple insulator proteins that are also maintained in mitosis. These results suggest alternative mechanisms to explain the role of Myc in pluripotency and cancer.
机译:Myc被表征为激活多能性和癌症相关基因表达的转录因子,并且是复制复合物的组成部分。在这里,我们发现Myc在间期期间存在于D. melanogaster基因的启动子和增强子上。在G1期间,Myc与Orc2共定位,Orc2是复制前复合体的一部分。与哺乳动物的情况一样,Myc优先与暂停的基因缔合,这表明它也可能与果蝇中启动子近端暂停释放RNAPII有关。有趣的是,相间存在的Myc位点约40%在有丝分裂期间持续存在。 Myc有丝分裂位点均不对应于增强子,仅某些对应于启动子。其余的有丝分裂Myc位点与多个绝缘子蛋白的结合位点重叠,这些蛋白也保持在有丝分裂中。这些结果提示了其他机制来解释Myc在多能性和癌症中的作用。

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