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SUV39h-independent association of HP1β with fibrillarin-positive nucleolar regions

机译:HP1β与原纤维蛋白阳性核仁区域的SUV39h独立性

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Heterochromatin protein 1 (HP1), which binds to sites of histone H3 lysine 9 (H3K9) methylation, is primarily responsible for gene silencing and the formation of heterochromatin. We observed that HP1β is located in both the chromocenters and fibrillarin-positive nucleoli interiors. However, HP1α and HP1γ occupied fibrillarin-positive compartments to a lesser extent, corresponding to the distinct levels of HP1 subtypes at the promoter of rDNA genes. Deficiency of histone methyltransferases SUV39h and/or inhibition of histone deacetylases (HDACi) decreased HP1β and H3K9 trimethylation at chromocenters, but not in fibrillarin-positive regions that co-localized with RNA polymerase I. Similarly, SUV39h- and HDACi-dependent nucleolar rearrangement and inhibition of rDNA transcription did not affect the association between HP1β and fibrillarin. Moreover, the presence of HP1β in nucleoli is likely connected with transcription of ribosomal genes and with the role of fibrillarin in nucleolar processes.
机译:异染色质蛋白1(HP1)与组蛋白H3赖氨酸9(H3K9)甲基化位点结合,主要负责基因沉默和异染色质的形成。我们观察到HP1β位于色中心和原纤维蛋白阳性的核仁内部。但是,HP1α和HP1γ在较小的程度上占据了原纤维蛋白阳性腔室,这与rDNA基因启动子上HP1亚型的不同水平相对应。组蛋白甲基转移酶SUV39h的缺乏和/或组蛋白脱乙酰基酶(HDACi)的抑制降低了色中心的HP1β和H3K9三甲基化,但在与RNA聚合酶I共同定位的原纤维蛋白阳性区域中没有。类似地,SUV39h和HDACi依赖性核仁重排和rDNA转录的抑制不影响HP1β和原纤维蛋白之间的关联。此外,HP1β在核仁中的存在​​可能与核糖体基因的转录以及原核蛋白在核仁过程中的作用有关。

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