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FACT 组蛋白伴侣在酿酒酵母中将组蛋白 H4 引导到核小体构象中。

The FACT histone chaperone guides histone H4 into its nucleosomal conformation in Saccharomyces cerevisiae.

机构信息

Department of Biochemistry, University of Utah School of Medicine, Salt Lake City, Utah 84112.

出版信息

Genetics. 2013 Sep;195(1):101-13. doi: 10.1534/genetics.113.153080. Epub 2013 Jul 5.

Abstract

The pob3-Q308K mutation alters the small subunit of the Saccharomyces cerevisiae histone/nucleosome chaperone Facilitates Chromatin Transactions (FACT), causing defects in both transcription and DNA replication. We describe histone mutations that suppress some of these defects, providing new insight into the mechanism of FACT activity in vivo. FACT is primarily known for its ability to promote reorganization of nucleosomes into a more open form, but neither the pob3-Q308K mutation nor the compensating histone mutations affect this activity. Instead, purified mutant FACT complexes fail to release from nucleosomes efficiently, and the histone mutations correct this flaw. We confirm that pob3-T252E also suppresses pob3-Q308K and show that combining two suppressor mutations can be detrimental, further demonstrating the importance of balance between association and dissociation for efficient FACT:nucleosome interactions. To explain our results, we propose that histone H4 can adopt multiple conformations, most of which are incompatible with nucleosome assembly. FACT guides H4 to adopt appropriate conformations, and this activity can be enhanced or diminished by mutations in Pob3 or histones. FACT can therefore destabilize nucleosomes by favoring the reorganized state, but it can also promote assembly by tethering histones and DNA together and maintaining them in conformations that promote canonical nucleosome formation.

摘要

pob3-Q308K 突变改变了酿酒酵母组蛋白/核小体伴侣 Facilitates Chromatin Transactions(FACT)的小亚基,导致转录和 DNA 复制缺陷。我们描述了一些能够抑制这些缺陷的组蛋白突变,为 FACT 体内活性的机制提供了新的见解。FACT 主要以其促进核小体重组为更开放形式的能力而闻名,但 pob3-Q308K 突变和补偿性组蛋白突变都不会影响这种活性。相反,纯化的突变 FACT 复合物不能有效地从核小体中释放出来,而组蛋白突变则纠正了这一缺陷。我们证实了 pob3-T252E 也能抑制 pob3-Q308K,并表明结合两种抑制突变可能是有害的,进一步证明了 FACT:核小体相互作用中缔合和解离之间的平衡对于高效 FACT 的重要性。为了解释我们的结果,我们提出组蛋白 H4 可以采用多种构象,其中大多数与核小体组装不兼容。FACT 指导 H4 采用适当的构象,而 Pob3 或组蛋白的突变可以增强或减弱这种活性。因此,FACT 可以通过有利于重组状态来破坏核小体,但它也可以通过将组蛋白和 DNA 束缚在一起并保持它们有利于形成规范核小体的构象来促进组装。

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