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结构多态性水平高,由 Chaetognath Spadella cephaloptera 的 Hox 基因组区域中的移动元件驱动。

High level of structural polymorphism driven by mobile elements in the Hox genomic region of the Chaetognath Spadella cephaloptera.

机构信息

Centre d'Océanologie de Marseille, Université de la Méditerranée, Station Marine d'Endoume, Marseille, France.

出版信息

Genome Biol Evol. 2010;2:665-77. doi: 10.1093/gbe/evq047. Epub 2010 Aug 1.

Abstract

Little is known about the relationships between genome polymorphism, mobile element dynamics, and population size among animal populations. The chaetognath species Spadella cephaloptera offers a unique perspective to examine this issue because they display a high level of genetic polymorphism at the population level. Here, we have investigated in detail the extent of nucleotide and structural polymorphism in a region harboring Hox1 and several coding genes and presumptive functional elements. Sequencing of several bacterial artificial chromosome inserts representative of this nuclear region uncovered a high level of structural heterogeneity, which is mainly caused by the polymorphic insertion of a diversity of genetic mobile elements. By anchoring this variation through individual genotyping, we demonstrated that sequence diversity could be attributed to the allelic pool of a single population, which was confirmed by detection of extensive recombination within the genomic region studied. The high average level of nucleotide heterozygosity provides clues of selection in both coding and noncoding domains. This pattern stresses how selective processes remarkably cope with intense sequence turnover due to substitutions, mobile element insertions, and recombination to preserve the integrity of functional landscape. These findings suggest that genome polymorphism could provide pivotal information for future functional annotation of genomes.

摘要

关于动物种群中基因组多态性、移动元件动态和种群大小之间的关系,人们知之甚少。齿吻沙蚕(Spadella cephaloptera)物种提供了一个独特的视角来研究这个问题,因为它们在种群水平上表现出高度的遗传多态性。在这里,我们详细研究了包含 Hox1 和几个编码基因和假定功能元件的区域中的核苷酸和结构多态性的程度。对代表该核区域的几个细菌人工染色体插入物进行测序,揭示了高水平的结构异质性,这主要是由多种遗传移动元件的多态性插入引起的。通过对个体基因型进行锚定,我们证明了序列多样性可以归因于单一种群的等位基因库,这通过在所研究的基因组区域内检测到广泛的重组得到了证实。高平均核苷酸杂合度水平为编码和非编码区域的选择提供了线索。这种模式强调了选择过程如何通过替换、移动元件插入和重组来应对强烈的序列转换,以保持功能景观的完整性。这些发现表明,基因组多态性可以为未来的基因组功能注释提供关键信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3cf6/2997562/4d7ff56f6dcc/gbeevq047f01_3c.jpg

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