In silico analysis on frequency and distribution of microsatellites in genes associated with spinal cord astrocytoma

IF 0.5 Q4 GENETICS & HEREDITY
Tahir Shehzad Ahmed , Kashif Mahmood , Muhammad Sabtain Nazish Ali Khattak , Azizullah Noor , Huiying Liang , Siddiq Ur Rahman
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Abstract

Microsatellites, also called short tandem repeats (STRs) or simple sequence repeats (SSRs) are short DNA sequence segments consisting of tandemly repeated motifs. SSRs are regarded as one of the most effective tools for genetic research. In this study, we conducted an in silico analysis to investigate the presence, distribution, and characteristics of SSRs within the genes associated with spinal cord astrocytoma. The aim of this study was to identify SSRs in coding and non-coding regions, analyze their correlation with gene parameters, and determine the GC content in the gene sequences. The results revealed that the widespread presence of SSRs within the genes is associated with spinal cord astrocytoma (SCA). The distribution of SSR motifs varied among the analyzed genes, and certain motifs were common across multiple genes. Additionally, we observed a strong positive correlation between the total number of SSRs and gene size, indicating that larger genes tend to have a higher number of microsatellites. Furthermore, we identified SSRs in both coding and non-coding regions of the genes. The incidence of SSRs and cSSRs differed among genes, suggesting potential functional implications for gene expression and regulation. Our study provides valuable insights into the genetic diversity within the astrocytoma genes and highlights the potential significance of SSRs in gene regulation. In conclusion, this study contributes to a better understanding of the role of microsatellites within the genes associated with spinal cord astrocytoma. The observed patterns of SSR distribution and characteristics suggest their potential functional relevance in the development and progression of astrocytoma.

脊髓星形细胞瘤相关基因中微卫星频率和分布的硅学分析
微卫星又称短串联重复序列(STR)或简单序列重复序列(SSR),是由串联重复图案组成的短 DNA 序列片段。SSR 被认为是遗传研究最有效的工具之一。在本研究中,我们对脊髓星形细胞瘤相关基因中 SSR 的存在、分布和特征进行了硅分析。本研究旨在识别编码区和非编码区的 SSR,分析其与基因参数的相关性,并确定基因序列中的 GC 含量。结果发现,基因中广泛存在的 SSR 与脊髓星形细胞瘤(SCA)有关。在分析的基因中,SSR基团的分布各不相同,某些基团在多个基因中具有共性。此外,我们还观察到 SSR 总数与基因大小之间存在很强的正相关性,这表明较大的基因往往具有较多的微卫星。此外,我们在基因的编码区和非编码区都发现了 SSR。不同基因的 SSR 和 cSSR 发生率不同,这表明它们对基因表达和调控有潜在的功能影响。我们的研究为了解星形细胞瘤基因的遗传多样性提供了有价值的见解,并强调了 SSR 在基因调控中的潜在意义。总之,这项研究有助于更好地理解微卫星在脊髓星形细胞瘤相关基因中的作用。所观察到的 SSR 分布模式和特征表明,它们在星形细胞瘤的发生和发展过程中具有潜在的功能相关性。
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来源期刊
Human Gene
Human Gene Biochemistry, Genetics and Molecular Biology (General), Genetics
CiteScore
1.60
自引率
0.00%
发文量
0
审稿时长
54 days
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