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Generation of a Maize B Centromere Minimal Map Containing the Central Core Domain

机译:包含中央核心域的玉米B着丝粒最小图的生成

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摘要

The maize B centromere has been used as a model for centromere epigenetics and as the basis for building artificial chromosomes. However, there are no sequence resources for this important centromere. Here we used transposon display for the centromere-specific retroelement CRM2 to identify a collection of 40 sequence tags that flank CRM2 insertion points on the B chromosome. These were confirmed to lie within the centromere by assaying deletion breakpoints from centromere misdivision derivatives (intracentromere breakages caused by centromere fission). Markers were grouped together on the basis of their association with other markers in the misdivision series and assembled into a pseudocontig containing 10.1 kb of sequence. To identify sequences that interact directly with centromere proteins, we carried out chromatin immunoprecipitation using antibodies to centromeric histone H3 (CENH3), a defining feature of functional centromeric sequences. The CENH3 chromatin immunoprecipitation map was interpreted relative to the known transmission rates of centromere misdivision derivatives to identify a centromere core domain spanning 33 markers. A subset of seven markers was mapped in additional B centromere misdivision derivatives with the use of unique primer pairs. A derivative previously shown to have no canonical centromere sequences (Telo3-3) lacks these core markers. Our results provide a molecular map of the B chromosome centromere and identify key sequences within the map that interact directly with centromeric histone H3.
机译:玉米B着丝粒已被用作着丝粒表观遗传学的模型,并被用作构建人工染色体的基础。但是,此重要着丝粒没有序列资源。在这里,我们对着丝粒特异的逆转录因子CRM2使用了转座子展示,以鉴定B染色体上CRM2插入点侧翼的40个序列标签的集合。通过测定来自着丝粒错分衍生物的缺失断点(由着丝粒裂变引起的着丝粒内破损),证实它们位于着丝粒内。根据标记与错分系列中的其他标记的关联将标记分组在一起,并组装成包含10.1 kb序列的假重叠群。为了鉴定与着丝粒蛋白直接相互作用的序列,我们使用针对着丝粒的组蛋白H3(CENH3)(功能着丝粒的序列的定义特征)的抗体进行了染色质免疫沉淀。相对于着丝粒错分衍生物的已知传播速率解释了CENH3染色质免疫沉淀图,以鉴定跨越33个标记的着丝粒核心结构域。使用独特的引物对,将七个标记的子集映射到其他B着丝粒错分衍生物中。先前显示的不具有规范着丝粒序列的衍生物(Telo3-3)缺少这些核心标记。我们的结果提供了B染色体着丝粒的分子图,并确定了图中与着丝粒组蛋白H3直接相互作用的关键序列。

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