Shpiz Sergey, Kalmykova Alla
Institute of Molecular Genetics of Russian Academy of Sciences, Kurchatov, Moscow, Russia.
Methods Mol Biol. 2014;1093:149-59. doi: 10.1007/978-1-62703-694-8_12.
In the Drosophila germline, retrotransposons are silenced by the PIWI-interacting RNA (piRNA) pathway. piRNA pathway mutations lead to overexpression and mobilization of retrotransposons in the germline. In different organisms, small RNAs were shown to be implicated in the posttranscriptional degradation of mRNA and/or transcriptional repression of the homologous locus. In Drosophila, the mechanism of piRNA-mediated silencing is still far from being understood. Transcriptional silencing implies a piRNA-mediated formation of repressive chromatin which diminishes the transcriptional capacity of the target locus. Nuclear Run-On (NRO) assay allows a direct estimation of the density of transcribing polymerases at specific genomic regions. Here we describe the NRO protocol on Drosophila ovarian tissues which can be useful for investigation of the transcriptional silencing in the female germline.
在果蝇生殖系中,逆转录转座子通过PIWI相互作用RNA(piRNA)途径被沉默。piRNA途径突变会导致生殖系中逆转录转座子的过表达和移动。在不同生物体中,小RNA被证明参与mRNA的转录后降解和/或同源基因座的转录抑制。在果蝇中,piRNA介导的沉默机制仍远未被理解。转录沉默意味着piRNA介导的抑制性染色质形成,这会降低靶基因座的转录能力。核运行分析(NRO)可以直接估计特定基因组区域中转录聚合酶的密度。在这里,我们描述了果蝇卵巢组织的NRO实验方案,该方案可用于研究雌性生殖系中的转录沉默。