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Comparative Genomics Search for Losses of Long-Established Genes on the Human Lineage

机译:比较基因组学研究人类谱系中长期存在的基因的丢失

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摘要

Taking advantage of the complete genome sequences of several mammals, we developed a novel method to detect losses of well-established genes in the human genome through syntenic mapping of gene structures between the human, mouse, and dog genomes. Unlike most previous genomic methods for pseudogene identification, this analysis is able to differentiate losses of well-established genes from pseudogenes formed shortly after segmental duplication or generated via retrotransposition. Therefore, it enables us to find genes that were inactivated long after their birth, which were likely to have evolved nonredundant biological functions before being inactivated. The method was used to look for gene losses along the human lineage during the approximately 75 million years (My) since the common ancestor of primates and rodents (the euarchontoglire crown group). We identified 26 losses of well-established genes in the human genome that were all lost at least 50 My after their birth. Many of them were previously characterized pseudogenes in the human genome, such as GULO and UOX. Our methodology is highly effective at identifying losses of single-copy genes of ancient origin, allowing us to find a few well-known pseudogenes in the human genome missed by previous high-throughput genome-wide studies. In addition to confirming previously known gene losses, we identified 16 previously uncharacterized human pseudogenes that are definitive losses of long-established genes. Among them is ACYL3, an ancient enzyme present in archaea, bacteria, and eukaryotes, but lost approximately 6 to 8 Mya in the ancestor of humans and chimps. Although losses of well-established genes do not equate to adaptive gene losses, they are a useful proxy to use when searching for such genetic changes. This is especially true for adaptive losses that occurred more than 250,000 years ago, since any genetic evidence of the selective sweep indicative of such an event has been erased.
机译:利用几种哺乳动物的完整基因组序列,我们开发了一种新颖的方法,可以通过对人类,小鼠和狗基因组之间的基因结构进行同步映射来检测人类基因组中已建立好的基因的丢失。与大多数以前的用于假基因鉴定的基因组方法不同,该分析能够从片段复制后不久形成或通过逆转座产生的假基因中区分出已建立基因的损失。因此,它使我们能够找到在出生后很长时间就失活的基因,这些基因在失活之前可能已经进化出非冗余的生物学功能。自从灵长类和啮齿类动物的共同祖先以来,该方法一直被用于寻找人类谱系中大约7500万年间的基因损失(真人弓形目冠群)。我们确定了人类基因组中26个成熟基因的丢失,这些基因在出生后都丢失了至少50 My。他们中的许多先前已被人类基因组中的伪基因表征,例如GULO和UOX。我们的方法在识别古代起源的单拷贝基因的丢失方面非常有效,这使我们能够在人类基因组中找到一些先前的高通量全基因组研究遗漏的知名假基因。除了确认先前已知的基因缺失外,我们还鉴定了16种先前未表征的人假基因,它们是长期存在的基因的确定性缺失。其中有ACYL3,这是一种古老的酶,存在于古细菌,细菌和真核生物中,但在人类和黑猩猩的祖先中约损失6至8个Mya。尽管建立良好的基因的丧失并不等同于适应性基因的丧失,但是当寻找此类遗传变化时,它们是有用的代理。对于超过25万年前发生的适应性损失尤其如此,因为已删除了指示此类事件的选择性扫描的任何遗传证据。

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