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Multiple redundant sequence elements within the fission yeast ura4 replication origin enhancer

机译:裂变酵母ura4复制起点增强子内的多个冗余序列元件

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Background Some origins in eukaryotic chromosomes fire more frequently than others. In the fission yeast, Schizosaccharomyces pombe, the relative firing frequencies of the three origins clustered 4-8 kbp upstream of the ura4 gene are controlled by a replication enhancer - an element that stimulates nearby origins in a relatively position-and orientation-independent fashion. The important sequence motifs within this enhancer were not previously localized. Results Systematic deletion of consecutive segments of ~50, ~100 or ~150 bp within the enhancer and its adjacent core origin (ars3002) revealed that several of the ~50-bp stretches within the enhancer contribute to its function in partially redundant fashion. Other stretches within the enhancer are inhibitory. Some of the stretches within the enhancer proved to be redundant with sequences within core ars3002. Consequently the collection of sequences important for core origin function was found to depend on whether the core origin is assayed in the presence or absence of the enhancer. Some of the important sequences in the core origin and enhancer co-localize with short runs of adenines or thymines, which may serve as binding sites for the fission yeast Origin Recognition Complex (ORC). Others co-localize with matches to consensus sequences commonly found in fission yeast replication origins. Conclusions The enhancer within the ura4 origin cluster in fission yeast contains multiple sequence motifs. Many of these stimulate origin function in partially redundant fashion. Some of them resemble motifs also found in core origins. The next step is to identify the proteins that bind to these stimulatory sequences.
机译:背景真核染色体的某些起源比其他起源更频繁地发射。在裂殖酵母裂殖酵母中,簇集在ura4基因上游4-8 kbp的三个起源的相对激发频率受复制增强子的控制,复制增强子以相对于位置和方向独立的方式刺激附近的起源。该增强子内的重要序列基序先前未定位。结果系统性删除了增强子及其邻近核心起点(ars3002)中〜50,〜100或〜150 bp的连续段,这表明增强子中的〜50 bp延伸片段中有几个以部分冗余的方式对其功能起作用。增强剂内的其他延伸是抑制性的。增强子内的某些延伸被证明与核心ars3002中的序列是多余的。因此,发现对于核心起源功能重要的序列的收集取决于是否在增强子存在或不存在下测定核心起源。核心起源和增强子中的一些重要序列与腺嘌呤或胸腺嘧啶的短期共定位,这些腺嘌呤或胸腺嘧啶可作为裂变酵母起源识别复合物(ORC)的结合位点。其他的则与裂变酵母复制起源中常见的共有序列的匹配共定位。结论裂变酵母中ura4起源簇内的增强子具有多个序列基序。其中许多以部分冗余的方式刺激起源功能。其中一些类似于在核心起源中也发现的图案。下一步是鉴定与这些刺激序列结合的蛋白质。

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