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首页> 外文期刊>Scientific reports. >Genome-wide In Silico Analysis, Characterization and Identification of Microsatellites in Spodoptera littoralis Multiple nucleopolyhedrovirus (SpliMNPV)
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Genome-wide In Silico Analysis, Characterization and Identification of Microsatellites in Spodoptera littoralis Multiple nucleopolyhedrovirus (SpliMNPV)

机译:基因组 - 在Spodoptera littoralis多核多核血症(SplimnPV)中微卫星的硅分析,表征和鉴定

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In this study, we undertook a survey to analyze the distribution and frequency of microsatellites or Simple Sequence Repeats (SSRs) in Spodoptera littoralis multiple nucleopolyhedrovirus (SpliMNPV) genome (isolate AN-1956). Out of the 55 microsatellite motifs, identified in the SpliMNPV-AN1956 genome using in silico analysis (inclusive of mono-, di-, tri- and hexa-nucleotide repeats), 39 were found to be distributed within coding regions (cSSRs), whereas 16 were observed to lie within intergenic or noncoding regions. Among the 39 motifs located in coding regions, 21 were located in annotated functional genes whilst 18 were identified in unknown functional genes (hypothetical proteins). Among the identified motifs, trinucleotide (80%) repeats were found to be the most abundant followed by dinucleotide (13%), mononucleotide (5%) and hexanucleotide (2%) repeats. The 39 motifs located within coding regions were further validated in vitro by using PCR analysis, while the 21 motifs located within known functional genes (15 genes) were characterized using nucleotide sequencing. A comparison of the sequence analysis data of the 21 sequenced cSSRs with the published sequences is presented. Finally, the developed SSR markers of the 39 motifs were further mapped/localized onto the SpliMNPV-AN1956 genome. In conclusion, the SSR markers specific to SpliMNPV, developed in this study, could be a useful tool for the identification of isolates and analysis of genetic diversity and viral evolutionary status.
机译:在这项研究中,我们对Spodoptera Littoralis(SplimNPV)基因组(分离An-1956)中的微卫星或简单序列重复(SSRS)的分布和频率进行了调查。在55个微卫星基质中,在SPLIMNPV-AN1956基因组中鉴定在SILICO分析中(包括单,二 - ,三核苷酸核苷酸重复),发现39个分布在编码区(CSSR)内分布。 16被观察到位于亚因子或非编码区域内。在位于编码区的39个图案中,在未知的功能基因(假设蛋白质)中鉴定出18℃的注释功能基因中。在鉴定的基序中,发现三核苷酸(80%)重复是最丰富的后跟二核苷酸(13%),单核苷酸(5%)和己核苷酸(2%)重复。通过使用PCR分析进一步验证位于编码区域内的39个图案,而使用核苷酸测序表征位于已知功能基因(15基因)内的21个基序。呈现了21个测序CSSR​​的序列分析数据的比较,具有发布的序列。最后,将39个图案的显影SSR标记进一步映射到SplimNPV-An1956基因组上。总之,在本研究中开发的SPLIMNPV特异性的SSR标记可能是识别分离物和遗传多样性和病毒进化状态的有用工具。

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