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Genesis of gene structures and computational analysis of U12-type introns.

机译:U12型内含子的基因结构成因和计算分析。

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摘要

Accurate and prompt gene structure annotation is a necessity for the utilization of genomic sequence data and large scale biological research. As the number of genomes being sequenced rapidly increases, there is a need for immediate gene structure annotation, which is distinct from the whole genome annotation that is conducted at the completion of sequencing. In completely sequenced genomes, inaccuracies in gene structure annotations can make subsequent analysis problematic. For instance, the incorrect assignment of exons to a gene can change the protein coded by the gene, which would have effects on the functional and evolutionary descriptions of the gene.; To address both of these needs, the Tracembler and yrGATE tools were developed. Tracembler provides the unique utility of sequence search, assembly and gene structure annotation upon the latest available fragmented sequence data. Discovery of microsynteny in soybean using adjacent Medicago truncatula genes as seeds was demonstrated using Tracembler. yrGATE ("your Gene Structure Annotation Tool for Eukaryotes") allows users to create their own gene structure annotations using high quality evidence, which can then be submitted to a community for review. yrGATE has been successfully used in re-annotating inaccurate published gene annotations and in annotating emerging genomes. Using both of these tools, on-demand gene annotation is a reality.; A thorough genome-wide identification of U12-type introns across seven organisms revealed that some U12-type introns did not have accurate corresponding gene structure annotations. In these cases, novel gene structure annotations were created. A subsequent investigation of orthologous genes with these introns yielded new discoveries. The first instances of U12-type intron conversion to U2-type and loss were recorded in orthologous genes among vertebrates and among plants. Since the divergence of plants and animals, U12-type introns were shown to have been primarily lost. Orthologs with conserved U12-type introns were found to experience reduced evolution in terms of gene structure, global protein sequence, and local protein sequence. A correlation between phase frequencies and exonic sequence conservation of these introns was described. The results of this investigation are presented through the CIWOG ("Common Introns Within Orthologous Genes") database to aid future research.
机译:准确而迅速的基因结构注释是利用基因组序列数据和大规模生物学研究的必要条件。随着被测序的基因组数量的迅速增加,需要立即进行基因结构注释,这与在测序完成时进行的全基因组注释不同。在完全测序的基因组中,基因结构注释的不准确性可能会使后续分析成为问题。例如,错误地将外显子分配给基因会改变该基因编码的蛋白质,从而影响该基因的功能和进化描述。为了满足这两个需求,开发了Tracembler和yrGATE工具。 Tracembler根据最新的可用片段化序列数据提供独特的序列搜索,组装和基因结构注释实用程序。使用Trammbler证明了使用邻近的苜蓿苜蓿基因作为种子在大豆中发现微同调。 yrGATE(“您的真核生物基因结构注释工具”)允许用户使用高质量的证据创建自己的基因结构注释,然后将其提交给社区以供审查。 yrGATE已成功用于重新注释不准确的已发表基因注释和新出现的基因组。使用这两种工具,按需基因注释已成为现实。横跨七个生物的U12型内含子的全基因组范围内的全面鉴定表明,某些U12型内含子没有准确的相应基因结构注释。在这些情况下,创建了新颖的基因结构注释。随后用这些内含子研究直系同源基因产生了新发现。在脊椎动物和植物之间的直系同源基因中记录了U12型内含子向U2型转化和丢失的最初情况。由于动植物的差异,U12型内含子已被证明主要丢失。发现具有保守的U12型内含子的直向同源物在基因结构,整体蛋白序列和局部蛋白序列方面经历减少的进化。描述了这些内含子的相频率与外显子序列保守性之间的相关性。该调查的结果通过CIWOG(“直系同源基因内的普通内含子”)数据库提供,以帮助将来的研究。

著录项

  • 作者

    Wilkerson, Matthew Devin.;

  • 作者单位

    Iowa State University.$bGenetics, Development and Cell Biology.;

  • 授予单位 Iowa State University.$bGenetics, Development and Cell Biology.;
  • 学科 Biology Molecular.; Biology Genetics.; Biology Bioinformatics.
  • 学位 Ph.D.
  • 年度 2007
  • 页码 117 p.
  • 总页数 117
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分子遗传学;遗传学;
  • 关键词

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