Yadav Mukesh P, Padmanabhan Sreedevi, Tripathi Vishnu P, Mishra Rahul K, Dubey Dharani D
Department of Biotechnology, Veer Bahadur Singh Purvanchal University, Jaunpur, Uttar Pradesh 222001, India.
BMC Res Notes. 2012 Nov 19;5:643. doi: 10.1186/1756-0500-5-643.
Replication and transcription, the two key functions of DNA, require unwinding of the DNA double helix. It has been shown that replication origins in the budding yeast, Saccharomyces cerevisiae contain an easily unwound stretch of DNA. We have used a recently developed method for determining the locations and degrees of stress-induced duplex destabilization (SIDD) for all the reported replication origins in the genome of the fission yeast, Schizosaccharomyces pombe.
We have found that the origins are more susceptible to SIDD as compared to the non-origin intergenic regions (NOIRs) and genes. SIDD analysis of many known origins in other eukaryotes suggests that SIDD is a common property of replication origins. Interestingly, the previously shown deletion-dependent changes in the activities of the origins of the ura4 origin region on chromosome 3 are paralleled by changes in SIDD properties, suggesting SIDD's role in origin activity. SIDD profiling following in silico deletions of some origins suggests that many of the closely spaced S. pombe origins could be clusters of two or three weak origins, similar to the ura4 origin region.
SIDD appears to be a highly conserved, functionally important property of replication origins in S. pombe and other organisms. The distinctly low SIDD scores of origins and the long range effects of genetic alterations on SIDD properties provide a unique predictive potential to the SIDD analysis. This could be used in exploring different aspects of structural and functional organization of origins including interactions between closely spaced origins.
复制和转录是DNA的两个关键功能,都需要解开DNA双螺旋。研究表明,芽殖酵母酿酒酵母中的复制起点包含一段易于解开的DNA。我们使用了一种最近开发的方法来确定裂殖酵母粟酒裂殖酵母基因组中所有已报道的复制起点的应激诱导双链去稳定化(SIDD)的位置和程度。
我们发现,与非起点基因间区域(NOIRs)和基因相比,起点更容易受到SIDD的影响。对其他真核生物中许多已知起点的SIDD分析表明,SIDD是复制起点的一个共同特性。有趣的是,先前显示的3号染色体上ura4起点区域起点活性的缺失依赖性变化与SIDD特性的变化平行,这表明SIDD在起点活性中起作用。对一些起点进行计算机删除后的SIDD分析表明,许多紧密间隔的粟酒裂殖酵母起点可能是两到三个弱起点的簇,类似于ura4起点区域。
SIDD似乎是粟酒裂殖酵母和其他生物中复制起点的一种高度保守、功能重要的特性。起点明显较低的SIDD分数以及基因改变对SIDD特性的长程影响为SIDD分析提供了独特的预测潜力。这可用于探索起点结构和功能组织的不同方面,包括紧密间隔起点之间的相互作用。