Vermaak Danielle, Hayden Hillary S, Henikoff Steven
Howard Hughes Medical Institute, Basic Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Mol Cell Biol. 2002 Nov;22(21):7553-61. doi: 10.1128/MCB.22.21.7553-7561.2002.
Centromeres require specialized nucleosomes; however, the mechanism of localization is unknown. Drosophila sp. centromeric nucleosomes contain the Cid H3-like protein. We have devised a strategy for identifying elements within Cid responsible for its localization to centromeres. By expressing Cid from divergent Drosophila species fused to green fluorescent protein in Drosophila melanogaster cells, we found that D. bipectinata Cid fails to localize to centromeres. Cid chimeras consisting of the D. bipectinata histone fold domain (HFD) replaced with segments from D. melanogaster identified loop I of the HFD as being critical for targeting to centromeres. Conversely, substitution of D. bipectinata loop I into D. melanogaster abolished centromeric targeting. In either case, loop I was the only segment capable of conferring targeting. Within loop I, we identified residues that are critical for targeting. Most mutations of conserved residues abolished targeting, and length reductions were deleterious. Taken together with the fact that H3 loop I makes numerous contacts with DNA and with the adaptive evolution of Cid, our results point to the importance of DNA specificity for targeting. We suggest that the process of deposition of (Cid.H4)2 tetramers allows for discriminating contacts to be made between loop I and DNA, providing the specificity needed for targeting.
着丝粒需要特殊的核小体;然而,其定位机制尚不清楚。果蝇属物种的着丝粒核小体包含类Cid H3蛋白。我们设计了一种策略来鉴定Cid中负责其着丝粒定位的元件。通过在黑腹果蝇细胞中表达与绿色荧光蛋白融合的不同果蝇物种的Cid,我们发现双带果蝇的Cid不能定位于着丝粒。由双带果蝇组蛋白折叠结构域(HFD)被黑腹果蝇的片段取代组成的Cid嵌合体将HFD的环I鉴定为着丝粒靶向的关键区域。相反,将双带果蝇的环I替换到黑腹果蝇中则消除了着丝粒靶向。在任何一种情况下,环I都是唯一能够赋予靶向作用的片段。在环I内,我们鉴定出了对靶向至关重要的残基。保守残基的大多数突变消除了靶向作用,长度缩短是有害的。结合H3环I与DNA有大量接触以及Cid的适应性进化这一事实,我们的结果表明DNA特异性对着丝粒靶向的重要性。我们认为,(Cid.H4)2四聚体的沉积过程允许环I与DNA之间形成有区别的接触,从而提供靶向所需的特异性。