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果蝇剂量补偿X染色体上,roX RNA有序组装成MSL复合体。

Ordered assembly of roX RNAs into MSL complexes on the dosage-compensated X chromosome in Drosophila.

作者信息

Meller V H, Gordadze P R, Park Y, Chu X, Stuckenholz C, Kelley R L, Kuroda M I

机构信息

Department of Molecular and Cellular Biology, Department of Biology, Baylor College of Medicine, Tufts University, Houston, Medford 77030, 02155, USA.

出版信息

Curr Biol. 2000 Feb 10;10(3):136-43. doi: 10.1016/s0960-9822(00)00311-0.

Abstract

BACKGROUND

In the male Drosophila, the X chromosome is transcriptionally upregulated to achieve dosage compensation, in a process that depends on association of the MSL proteins with the X chromosome. A role for non-coding RNAs has been suggested in recent studies. The roX1 and roX2 RNAs are male-specific, non-coding RNAs that are produced by, and also found associated with, the dosage-compensated male X chromosome. Whether roX RNAs are physically part of the MSL complex has not been resolved.

RESULTS

We found that roX RNAs colocalize with the MSL proteins and are highly unstable unless the MSL complex is coexpressed, suggesting a physical interaction. We were able to immunoprecipitate roX2 RNA from male tissue-culture cells with antibodies to the proteins Msl1 and Mle, consistent with an integral association with MSL complexes. Localization of roX1 and roX2 RNAs in mutants indicated an order of MSL-complex assembly in which roX2 RNA is incorporated early in a process requiring the Mle helicase. We also found that the roX2 gene, like roX1, is a nucleation site for MSL complex spreading into flanking chromatin in cis.

CONCLUSIONS

Our results support a model in which MSL proteins assemble at specific chromatin entry sites (including the roX1 and roX2 genes); the roX RNAs join the complex at their sites of synthesis; and complete complexes spread in cis to dosage compensate most genes on the X chromosome.

摘要

背景

在雄性果蝇中,X染色体转录上调以实现剂量补偿,这一过程依赖于MSL蛋白与X染色体的结合。最近的研究表明非编码RNA在其中发挥作用。roX1和roX2 RNA是雄性特异性非编码RNA,由剂量补偿后的雄性X染色体产生,并且也与其相关联。roX RNA是否是MSL复合体的物理组成部分尚未明确。

结果

我们发现roX RNA与MSL蛋白共定位,并且除非共表达MSL复合体,否则其极不稳定,这表明存在物理相互作用。我们能够用针对Msl1和Mle蛋白的抗体从雄性组织培养细胞中免疫沉淀roX2 RNA,这与它与MSL复合体的整体关联一致。roX1和roX2 RNA在突变体中的定位表明了MSL复合体的组装顺序,其中roX2 RNA在一个需要Mle解旋酶的过程中早期就被整合进去。我们还发现,与roX1一样,roX2基因是MSL复合体顺式扩散到侧翼染色质的成核位点。

结论

我们的结果支持这样一个模型,即MSL蛋白在特定的染色质进入位点(包括roX1和roX2基因)组装;roX RNA在其合成位点加入复合体;完整的复合体顺式扩散以对X染色体上的大多数基因进行剂量补偿。

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