Magiorkinis Gkikas, Blanco-Melo Daniel, Belshaw Robert
Retrovirology. 2015 Feb 2;12:8. doi: 10.1186/s12977-015-0136-x.
Endogenous Retroviruses (ERVs) are retroviruses that over the course of evolution have integrated into germline cells and eventually become part of the host genome. They proliferate within the germline of their host, making up ~5% of the human and mouse genome sequences. Several lines of evidence have suggested a decline in the rate of ERV integration into the human genome in recent evolutionary history but this has not been investigated quantitatively or possible causes explored.
By dating the integration of ERV loci in 40 mammal species, we show that the human genome and that of other hominoids (great apes and gibbons) have experienced an approximately four-fold decline in the ERV integration rate over the last 10 million years. A major cause is the recent extinction of one very large ERV lineage (HERV-H), which is responsible for most of the integrations over the last 30 million years. The decline however affects most other ERV lineages. Only about 10% of the decline might be attributed to an accompanying increase in body mass (a trait we have shown recently to be negatively correlated with ERV integration rate). Humans are unusual compared to related species - Old World monkeys, great apes and gibbons - in (a) having not acquired any new ERV lineages during the last 30 million years and (b) the possession of an old ERV lineage that has continued to replicate up until at least the last few hundred thousand years - the potentially medically significant HERVK(HML2).
The human genome shares with the genome of other great apes and gibbons a recent decline in ERV integration that is not typical of other primates and mammals. The human genome differs from that of related species both in maintaining up until at least recently a replicating old ERV lineage and in not having acquired any new lineages. We speculate that the decline in ERV integration in the human genome has been exacerbated by a relatively low burden of horizontally-transmitted retroviruses and subsequent reduced risk of endogenization.
内源性逆转录病毒(ERVs)是在进化过程中整合到生殖细胞中并最终成为宿主基因组一部分的逆转录病毒。它们在宿主的生殖系中增殖,占人类和小鼠基因组序列的约5%。有几条证据表明,在最近的进化历史中,ERV整合到人类基因组中的速率有所下降,但尚未进行定量研究,也未探讨可能的原因。
通过对40种哺乳动物物种中ERV位点的整合时间进行测定,我们发现,在过去1000万年中,人类基因组以及其他类人猿(大猩猩和长臂猿)的基因组中ERV整合速率下降了约四倍。一个主要原因是一个非常大的ERV谱系(HERV-H)最近灭绝了,在过去3000万年中,大部分整合都是由它造成的。然而,这种下降影响了大多数其他ERV谱系。下降中只有约10%可能归因于体重的相应增加(我们最近已表明该性状与ERV整合速率呈负相关)。与相关物种——旧世界猴、大猩猩和长臂猿相比,人类的不同之处在于:(a)在过去3000万年中没有获得任何新的ERV谱系;(b)拥有一个古老的ERV谱系,该谱系至少一直复制到最近几十万年前——具有潜在医学意义的HERVK(HML2)。
人类基因组与其他大猩猩和长臂猿的基因组一样,ERV整合速率最近有所下降,这在其他灵长类动物和哺乳动物中并不典型。人类基因组与相关物种的不同之处在于,至少直到最近仍维持着一个复制的古老ERV谱系,且没有获得任何新谱系。我们推测,水平传播的逆转录病毒负担相对较低以及随后内源性化风险降低,加剧了人类基因组中ERV整合的下降。