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鉴定参与嗜热四膜虫程序性基因组重排的新型染色质相关蛋白。

Identification of novel chromatin-associated proteins involved in programmed genome rearrangements in Tetrahymena.

作者信息

Yao Meng-Chao, Yao Ching-Ho, Halasz Lia M, Fuller Patrick, Rexer Charles H, Wang Sidney H, Jain Rajat, Coyne Robert S, Chalker Douglas L

机构信息

Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA 98109, and Department of Biology, Washington University, St. Louis, MO 63130, USA.

出版信息

J Cell Sci. 2007 Jun 15;120(Pt 12):1978-89. doi: 10.1242/jcs.006502. Epub 2007 May 22.

Abstract

Extensive DNA rearrangements occur during the differentiation of the developing somatic macronuclear genome from the germ line micronuclear genome of Tetrahymena thermophila. To identify genes encoding proteins likely to be involved in this process, we devised a cytological screen to find proteins that specifically localize in macronuclear anlagen (Lia proteins) at the stage when rearrangements occur. We compared the localization of these with that of the chromodomain protein, Pdd1p, which is the most abundant known participant in this genome reorganization. We show that in live cells, Pdd1p exhibits dynamic localization, apparently shuttling from the parental to the developing nuclei through cytoplasmic bodies called conjusomes. Visualization of GFP-tagged Pdd1p also highlights the substantial three-dimensional nuclear reorganization in the formation of nuclear foci that occur coincident with DNA rearrangements. We found that late in macronuclear differentiation, four of the newly identified proteins are organized into nuclear foci that also contain Pdd1p. These Lia proteins are encoded by primarily novel genes expressed at the beginning of macronuclear differentiation and have properties or recognizable domains that implicate them in chromatin or nucleic acid binding. Three of the Lia proteins also localize to conjusomes, a result that further implicates this structure in the regulation of DNA rearrangement.

摘要

嗜热四膜虫发育中的体大核基因组由种系小核基因组分化而来的过程中会发生广泛的DNA重排。为了鉴定可能参与这一过程的蛋白质编码基因,我们设计了一种细胞学筛选方法,以寻找在重排发生阶段特异性定位于大核原基(Lia蛋白)的蛋白质。我们将这些蛋白质的定位与色域蛋白Pdd1p的定位进行了比较,Pdd1p是已知参与这种基因组重组的最丰富的蛋白质。我们发现,在活细胞中,Pdd1p表现出动态定位,显然是通过称为接合小体的细胞质体从亲代细胞核穿梭到发育中的细胞核。绿色荧光蛋白标记的Pdd1p的可视化也突出了与DNA重排同时发生的核灶形成过程中大量的三维核重组。我们发现,在大核分化后期,新鉴定的四种蛋白质被组织成也含有Pdd1p的核灶。这些Lia蛋白主要由在大核分化开始时表达的新基因编码,并且具有使其参与染色质或核酸结合的特性或可识别的结构域。其中三种Lia蛋白也定位于接合小体,这一结果进一步表明这种结构参与了DNA重排的调控。

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