Thermos aquaticus
Well-Known Member
In this thread I will be presenting evidence that supports the origin of humans. That origin is descent through modification (i.e. evolution) from ape-like ancestors. The specific evidence I will be presenting is focused on endogenous retroviruses, or ERVs.
Retroviruses are usually RNA based viruses that reverse transcribe their genomes into DNA and then insert that DNA into the host genome. The long terminal repeats at the ends of the inserted viral genome act as strong gene promoters causing the host genetic systems to transcribe and translate the genes found in the viral genome. This results in the construction of new virus that buds off from the host cell and moves to new cells where the process is repeated. Retroviruses that invade and insert into the genome of a sperm or egg have the chance of being passed on to the next generation. When this happens it is called an endogenous retrovirus, or ERV.
We can watch this process in action in both the wild and in the lab. We have also constructed viral genomes from the consensus sequence of several human ERVs, and the result is a viable retrovirus. Again, we can observe new retroviral insertions occurring in real time, and ERVs already in the human genome can be reconstructed into retroviruses. There is absolutely no reason to doubt that ERVs are from retroviral insertions.
We also know that retroviral insertion can occur almost anywhere in the genome. When scientists infect cells with retroviruses and determine where in the genome the insertion occurred these are the results they get:
click here:
http://journals.plos.org/plosbiology/article/figure?id=10.1371/journal.pbio.0020234.g001
Those are the 22 human chromosomes, and each colored circle marks a retroviral insertion that occurred in the lab. As you can see, insertions happened all over the place in each of the chromosomes.
What this means is that two insertions that happen independently of one another should occur at different spots in the genome in the vast majority of cases. Therefore, when we find the same insertion at the same spot in the genomes of two individuals this means that the insertion happened only once in a common ancestor. Again, if two individuals do not share common ancestry then their ERVs should be found at different places in their genome. If they share a relatively recent ancestor then they should share nearly all of their ERVs at the same location in their genomes which are called orthologous ERVs. This is the scientific test for common ancestry.
So how does this apply to human ancestry? The human genome has over 200,000 ERVs. There are about the same number in the chimp genome. Of the ERVs in the human genome, nearly all of them are found at the same position in the chimp genome. Less than 100 human ERVs do not have an ortholog (i.e. same ERV at the same position) in the chimp genome. This is smoking gun evidence for common ancestry between chimps and humans.
References:
https://www.nature.com/articles/35057062
https://www.nature.com/articles/nature04072
Retroviruses are usually RNA based viruses that reverse transcribe their genomes into DNA and then insert that DNA into the host genome. The long terminal repeats at the ends of the inserted viral genome act as strong gene promoters causing the host genetic systems to transcribe and translate the genes found in the viral genome. This results in the construction of new virus that buds off from the host cell and moves to new cells where the process is repeated. Retroviruses that invade and insert into the genome of a sperm or egg have the chance of being passed on to the next generation. When this happens it is called an endogenous retrovirus, or ERV.
We can watch this process in action in both the wild and in the lab. We have also constructed viral genomes from the consensus sequence of several human ERVs, and the result is a viable retrovirus. Again, we can observe new retroviral insertions occurring in real time, and ERVs already in the human genome can be reconstructed into retroviruses. There is absolutely no reason to doubt that ERVs are from retroviral insertions.
We also know that retroviral insertion can occur almost anywhere in the genome. When scientists infect cells with retroviruses and determine where in the genome the insertion occurred these are the results they get:
click here:
http://journals.plos.org/plosbiology/article/figure?id=10.1371/journal.pbio.0020234.g001
Those are the 22 human chromosomes, and each colored circle marks a retroviral insertion that occurred in the lab. As you can see, insertions happened all over the place in each of the chromosomes.
What this means is that two insertions that happen independently of one another should occur at different spots in the genome in the vast majority of cases. Therefore, when we find the same insertion at the same spot in the genomes of two individuals this means that the insertion happened only once in a common ancestor. Again, if two individuals do not share common ancestry then their ERVs should be found at different places in their genome. If they share a relatively recent ancestor then they should share nearly all of their ERVs at the same location in their genomes which are called orthologous ERVs. This is the scientific test for common ancestry.
So how does this apply to human ancestry? The human genome has over 200,000 ERVs. There are about the same number in the chimp genome. Of the ERVs in the human genome, nearly all of them are found at the same position in the chimp genome. Less than 100 human ERVs do not have an ortholog (i.e. same ERV at the same position) in the chimp genome. This is smoking gun evidence for common ancestry between chimps and humans.
References:
https://www.nature.com/articles/35057062
https://www.nature.com/articles/nature04072