Hi,
I have two questions:
1) If most of HERV-Ks integrated before the separation of hominids and Old World monkeys +-30-45 million years ago, why was no RhERV-K found to be (yet) orthologous to closely related HERV-K's and CERV-K's? (Article: Demographic Histories of ERV-K in Humans, Chimpanzees and Rhesus Monkeys)
Your age of integration is way off. Here is the entire abstract with added emphasis on the important bits.
PLoS ONE. 2007 Oct 10;2(10):e1026.
Demographic Histories of ERV-K in Humans, Chimpanzees and Rhesus Monkeys.
Romano CM, de Melo FL, Corsini MA, Holmes EC, de A Zanotto PM.
Laboratory of Molecular Evolution and Bioinformatics, Department of Microbiology, Biomedical Sciences Institute-ICBII, University of São Paulo, Brazil.
We detected 19 complete endogenous retroviruses of the K family in the genome of rhesus monkey (Macaca mulatta; RhERV-K) and 12 full length elements in the genome of the common chimpanzee (Pan troglodytes; CERV-K). These sequences were compared with 55 human HERV-K and 20 CERV-K reported previously, producing a total data set of 106 full-length ERV-K genomes. Overall, 61% of the human elements compared to 21% of the chimpanzee and 47% of rhesus elements had estimated integration times less than 4.5 million years before present (MYBP), with an average integration times of 7.8 MYBP, 13.4 MYBP and 10.3 MYBP for HERV-K, CERV-K and RhERV-K, respectively. By excluding those ERV-K sequences generated by chromosomal duplication, we used 63 of the 106 elements to compare the population dynamics of ERV-K among species. This analysis indicated that both HERV-K and RhERV-K had similar demographic histories, including markedly smaller effective population sizes, compared to CERV-K. We propose that these differing ERV-K dynamics reflect underlying differences in the evolutionary ecology of the host species, such that host ecology and demography represent important determinants of ERV-K dynamics.
The average insertion time for RhERV-K was ~10 million years before present, well after the Old World monkeys lineage split off.
2) Is there an example of any mammal that is capable of reproduction without ERV envelope genes playing a role in placental physiology?
Thank you!
It hasn't been confirmed that every mammal requires ERV genes, but there are several where this has been confirmed. Your point? (see Red Herring in my previous post).
Edit: Wait, make that 3 (sorry):
3) Why was one of the CERV1 subfamilies dated to 7.8my and two CERV2 families dated at 21.9my and 14.1my? They have no orthologues in humans... (Article: Identification, characterization and comparative genomics of chimpanzee endogenous retroviruses)
From the paper:
The estimated ages of the two subfamilies are 5 MY and 7.8 MY, respectively, suggesting that at least one subfamily was present in the lineage prior to the time chimpanzees and humans diverged from a common ancestor (about 6 MYA). This conclusion, however, is inconsistent with the fact that no CERV 1/PTERV1 orthologues were detected in the sequenced human genome. Moreover, we were able to detect pre-integration sites at those regions in the human genome orthologous to the CERV 1/PTERV1 insertion sites in chimpanzees, effectively eliminating the possibility that the elements were once present in humans but subsequently excised. Consistent with our findings, the results of a previously published Southern hybridization survey indicated that sequences orthologous to CERV 1/PTERV1 elements are present in the African great apes and old world monkeys but not in Asian apes or humans [30]. These results suggest that some members of the CERV 1/PTERV1 subfamily entered the chimpanzee genome after the split from humans through exogenous infections from closely related species and subsequently increased in copy number by retrotransposition.
In other words, the estimated time of integration based on sequence is thrown off by the ERV jumping around on the chromosome and from older ERV's from closely related species jumping into the chimp lineage (some researchers even suggest that this was caused by eating meat that contained CERV1).
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