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Protein Interactions on Telomeric Retrotransposons in Drosophila

机译:果蝇在眼球反转转移的蛋白质相互作用

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摘要

Telomere length in Drosophila is maintained by targeted transposition of three non-LTR retrotransposons: HeT-A, TART and TAHRE (HTT), but understanding the regulation of this process is hindered by our poor knowledge of HTT associated proteins. We have identified new protein components of the HTT array: Chromator (Chro), the TRF2/DREF complex and the sumoylation machinery. Chro was localized on telomeric HTT arrays by immunostaining, where it may interact with Prod directly, as indicated by yeast two-hybrid interaction, co-IP, and colocalization on polytene chromosomes. The TRF2/DREF complex may promote the open structure of HTT chromatin. The protein interactions controlling HTT chromatin structure and telomere length may be modulated by sumoylation.
机译:通过针对三个非LTR回收扫描疣的目标转换来维持果蝇的端粒长度:HET-A,TART和TAHRE(HTT),但了解该过程的调节因我们对HTT相关蛋白质的知识差而受阻。 我们已经确定了HTT阵列的新蛋白质组分:镀铬(CHRO),TRF2 / DREF复合物和雄性织物机械。 通过免疫染色,CHRO本地化在端粒HTT阵列上,可以直接与产品相互作用,如酵母双杂交相互作用,共同IP和聚对染色体上的分致化所示。 TRF2 / DREF复合物可以促进HTT染色质的开放结构。 控制HTT染色质结构和端粒长度的蛋白质相互作用可以通过SuMoylation调节。

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