Like modern HIV, ancient human endogenous retroviruses (HERVs) had to insert their genetic material into their host’s genome to replicate.
Viruses insert their genomes into their hosts in the form of a provirus.
There are around 30 different kinds of HERVs in people today, amounting to over 60,000 proviruses in the human genome.
They demonstrate the long history of the many pandemics humanity has been subjected to over the course of evolution.
Scientists think these viruses once widely infected the population, since they have become fixed in not only the human genome but also in chimpanzee, gorilla and other primate genomes.
Research has demonstrated that HERV genes are active in diseased tissue, such as tumors, as well as during human embryonic development. But how active HERV genes are in healthy tissue was still largely unknown.
Role of HERVs in Human Health and Disease
The fact that thousands of pieces of ancient viruses still exist in the human genome and can even create protein has drawn a considerable amount of attention from researchers, particularly since related viruses still active today can cause breast cancer and AIDS-like disease in animals.
Whether the genetic remnants of human endogenous retroviruses can cause disease in people is still under study.
The new study adds a new angle to these data by showing that HERV genes are present even in healthy tissue.
This means that the presence of HERV RNA may not be enough to connect the virus to a disease.
Importantly, it also means that HERV genes or proteins may no longer be good targets for drugs.
HERVs have been explored as a target for a number of potential drugs, including antiretroviral medication, antibodies for breast cancer and T-cell therapies for melanoma.
Treatments using HERV genes as a cancer biomarker will also need to take into account their activity in healthy tissue.
On the other hand, the study also suggests that HERVs could even be beneficial to people.
The most famous HERV embedded in human and animal genomes, syncytin, is a gene derived from an ancient retrovirus that plays an important role in the formation of the placenta.
Pregnancy in all mammals is dependent on the virus-derived protein coded in this gene.
Unknowns Remain
The new study reveals a level of HERV activity in the human body that was previously unknown, raising as many questions as it answered.
There is still much to learn about the ancient viruses that linger in the human genome, including whether their presence is beneficial and what mechanism drives their activity.
Seeing if any of these genes are actually made into proteins will also be important.
Answering these questions could reveal previously unknown functions for these ancient viral genes and better help researchers understand how the human body reacts to evolution alongside these vestiges of ancient pandemics.
Full article at Sci News.
The presence of HERV’s in the human genome doesn’t necessarily demonstrate an evolutionary history of humans, just a history of humans. The relevant question to consider is where did the virus acquire the information to produce proteins in the first place?
When i first time heard about ERVs i was amazed …
As an engineer, i was amazed ….
At this moment, there are about 6000 known DNA mutations which cause serious genetic diseases.
But, when retroviruses repeatedly inserted pretty significant amounts of DNA into human genome, that is alright, nothing bad happened …
What amazes me even more, allegedly, these retroviruses take random places on human DNA to insert to …
In other words,… i will randomly insert into you 8% of new data, you are still here and intact … but few mutations known as genetic disorders kill you or will cause serious conditions …
Could some smart Darwinist explain to me, how is it possible that random ERV-insertions don’t do any harm ?
As to: “(Darwinists) think these (retro)viruses once widely infected the population, since they have become fixed in not only the human genome but also in chimpanzee, gorilla and other primate genomes.”
But alas, “retroviruses do not align with the expected evolutionary pattern”, and Darwinists have had to postulate that the “human lineage must, somehow, (mysteriously),, have been purged of these endemic viruses.”
Again, retroviruses do not fall into a common decent pattern
As to, “Research has demonstrated that HERV genes are active in diseased tissue, such as tumors, as well as during human embryonic development. But how active HERV genes are in healthy tissue was still largely unknown.,,, The new study adds a new angle to these data by showing that HERV genes are present even in healthy tissue.”
But alas, Darwinists also did not predict that ERVs would be functional in embryonic development, and in healthy tissues.
In fact, retroviruses were initially deemed, by Darwinists, to be non-functional ‘junk’ DNA. And thus finding important functions for ERVs ‘should’ count as, (yet another) empirical falsification of Darwinian ‘theory’,
As to: “The most famous HERV embedded in human and animal genomes, syncytin, is a gene derived from an ancient retrovirus that plays an important role in the formation of the placenta.”
And yet syncytins do not support common descent.
And again, retroviruses were initially deemed, by Darwinists, to be non-functional ‘junk’ DNA. So that retroviruses would now be found to be functional, even essential to embryonic development, and “that HERV genes are present even in healthy tissue”, (and yet not fall into a common descent pattern), should, if Darwinism were a normal science instead of being, basically, an unfalsifiable religion for atheists, count as yet another empirical falsification of their, ahem, ‘theory’.
and one more thing …
from an engineering point of view, i was also amazed to learn, that these retroviruses don’t insert into human DNA directly (as you may think)
They can’t. Because it is not physically possible …
Because there is AN INCOMPABILITY PROBLEM ….
and now comes some engineering in …
Human genome is made of DNA molecule and retroviruses use RNA molecules. SO THE VIRUS JUST CAN’T INSERT RNA INTO DNA… THIS IS THE INCOMPATIBILITY PROBLEM …
So, in order the insertion can be even done, retroviruses’ RNA molecule needs to be converted into a form of DNA … otherwise, the virus can’t insert its ‘data’ into ‘human storage’ … a clear incompatibility problem like we see everyday when using various computers /storage media or video codecs …
For the purpose of converting retroviruses’ RNA into DNA, a molecular machine called REVERSE TRANSCRIPTASE is being used – comes together with retroviruses 😉
here is a short but very informative 2 mins video on this conversion procedure:
https://youtu.be/eS1GODinO8w?t=95
PS: i, as an engineer, would love to understand, how a retrovirus knows, that in order to insert its ‘type of data’ into human ‘data storage’, its ‘data format’ has to be converted into a compatible one … and then some biologist comes in, claiming, that blind unguided process figured it out how to create a data format conversion tool … seriously, what is wrong with these people ???
A good explanation of why ERVs are strong evidence for evolution:
http://www.askabiologist.org.u.....hp?id=3914
Here is a good, easy to understand, explanation for why ERVs are NOT strong evidence for evolution.
https://answersingenesis.org/biology/microbiology/endogenous-retroviruses-common-ancestry/
of related note,
OT: recently uploaded Dr. Meyer video lecture on “Return of the God Hypothesis”
Pater @4
let me quote from the link you posted
… deposit a copy at a random location in the genome …
… it has ~3 billion places to choose from ….
Really ? What about this ?
From a mainstream paper:
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3185549/
or this one (another mainstream paper):
You guys are not reading far enough into the link I sent. ERVs express some preference for certain kinds of sites, but there are still billions of those for them to choose from. That means finding the same ERV at the same precise location in the genome can only be explained by common ancestry.
PK: “there are still billions of those for them to choose from.”
In trying to claim that it is all just random happenstance, It might help your case immensely if you did not assign agency, i.e. the ability to ‘choose’, to ERVs. 🙂
Ba77,
It look like a well oiled machine. Not, this car engine just assembled itself.
In. trying to claim that it is all just random happenstance, it might also help PK’s case immensely if viruses themselves did not give every indication of themselves being intelligently designed for essential purposes.
Of related note to viruses themselves giving every indication that they are Intelligently Designed for specific purposes, Bacteriophage viruses themselves “look like space ships from another world”,
Verse:
Virus function is not accidental. It has intention. For infectious viruses, they have intention and carry it out once in an appropriate environment.
Are you saying viruses are conscious and have a purpose in mind when they do what they do?
Martin_r @8,
Thanks for the great quotes and links. From the first one . . .
Emphasis added. Even mainstream papers make viruses seem sapient! LOL
Regarding the claim @9 that that common ERV insertion points support a common ancestor, it seems that the following from the same paper might explain this adequately:
-Q
Querius ….
Right!
Blind unguided process and non-living viruses have strategies :))))))))) These Darwinists … these guys are completely confused … as confused as it gets … today i don’t want to be rude, so i used the word “confused”.
PS: have you watched the REVERSE TRANSCRIPTASE videos i posted ? Have you noticed, that the Reverse Transcriptase first converts the RNA into 1-stranded DNA, and afterwards into double-stranded DNA ? (a 2-steps conversion) Moreover, using host’s nucleotides ? :)))))))) How the non-living virus knows, that there will be some free nucleotides floating around which can be used for RNA->DNA conversion ? :)))))))))
And as i asked before, how a non-living viruses know, that there will be the incompatibility problem, to bring with its own and suitable data-conversion tool (REVERSE TRANSCRIPTASE)?
Pater
You are throwing numbers like a genuine Darwinist. You don’t think, you just throwing numbers.
But i have a question, perhaps you can help me:
Was a particular retrovirus’s insertion found in human DNA more than once ? I was unable to google this information …
If these retroviruses have billions of other places to insert to, as you claim, i would expect, to see the same virus DNA to be inserted many times across the human genome or any other genome …
As I read it, the paper notes that the choice of integration sites is non-random and proposes three possible molecular mechanisms by which this might happen. There is no mention of conscious purpose or intention.
Pater
“can only be explained by common ancestry.”
Right!
I like how you Darwinian guys suddenly don’t believe in huge coincidences :)))))))
I bet you heard of convergent evolution.
So, for you guys, convergent evolution is not a problem for common descent …, you guys BELIEVE in crazy absurd examples of convergent evolution even on molecular level, but suddenly, a ERV which obviously prefers some DNA locations to insert to, so suddenly, the only explanation is common descent :))))))))
We are talking about very similar species with a very similar DNA. Could have the virus CONVERGED to insert into the same location in human /chimp ?
Pater
another question:
what if the possible /preferred site for a particular virus insertion were already taken by insertions of other viruses, and the virus had no other option than to insert into the preferred location which left ? And the one left was the same in human and chimp … you said there are millions of locations available for the insertion, but you don’t know how many … NOBODY KNOWS … you just throwing numbers …
Pater
and my very first question about ERVs once again:
How would you explain, that tons of random ERV insertions do not do harm when even a single mutation can cause a serious genetic disease (so far we know 6000 of such mutations).
Any explanation or speculation ?
,,, to emphasize Martin_r’s point at 19
Seversky at 14,
Did you miss the numerous posts here about Design? Viruses are doing what they are designed to do. And one more thing. Something I’m sure you will ignore because it refers to a being you like to rant about. Before The Fall, a literal event, all viruses were beneficial, after, all of Creation was corrupted and changed.
ERVs are another nonsense fantasy of darwinists that is built on assumption that darwinian evolution is true(is not) and then is brought as evidence for darwinian evolution. Circular reasoning. This nonsense is expired even before junk DNA expired. Don’t bother…
Martin_r @16,
Thanks, I just watched the video segment on reverse transcriptase that you provided. I also watched this video introduction on ERVs which raised as many questions as it answered. It’s screams with design engineering.
https://www.youtube.com/watch?v=EGfMRVBDxaY
Question: Assuming everything else in an ERV is intact, how long would it take to evolve reverse transcriptase? What part of an ERV was the last to evolve? How is the DNA segment of the ERV isolated from the rest of the DNA and how long did that take to evolve?
Assuming that ERV segments in our DNA are indeed remnants of viruses (apparently inactive due to transcription errors), I found the following fascinating papers on the subject. They were also helpful, since my understanding of ERVs is still very basic.
Nomenclature for endogenous retrovirus (ERV) loci (2018)
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6114882/
So, our DNA incorporates the ERV RNA and it’s not “junk DNA” after all . . .
The idea that this is to preserve virus RNA assigns a Lamarckian “goal” to a virus. In addition to creating new copies of the retrovirus (an engineering miracle in itself), that DNA from ERV RNA is “exapted” (repurposed) by the host is the practical and useful outcome. I know that this is quite a stretch, but In this way, the virus acts as FOOD for our DNA (but only in certain locations in the DNA strand) analogously to cells absorbing, metabolizing, and repurposing glucose! But there’s more.
Endogenous retroviruses in the origins and treatment of cancer (2021)
https://pubmed.ncbi.nlm.nih.gov/33971937/
Endogenous retrovirus expression in testis and epididymis (2007)
https://pubmed.ncbi.nlm.nih.gov/17511667/
First of all, it’s delightful and refreshing to read honest admissions of cluelessness rather than arrogant assurances of full understanding minus a few, miniscule details.
Second, the naked facts are that the RNA of ERVs are absorbed into DNA where they are then somehow repurposed by the DNA. I find this amazing and profound! This process is analogous to taking a vacuous comment by a trollbot here and, by some automatic process, reusing the words to create a coherent and relevant thought!
If I had enough blind faith to be a Darwinist, I’d examine the possibility that ERVs are a degraded and literally pathological mechanism of a primary cause of evolution. The obvious inspiration is that ERVs are a profoundly more prolific source of random transcription errors than random mutations in an organism.
-Q
Querius @25
when i heard of viruses capable of inserting chunks of DNA into host genome, the first thing which came to my mind was, that this could be some sort of Creator’s backdoor, and/or, a way how to REMOTELY update species “software”. All what is needed, is to deliver the virus with “software update” close to the species. Basically, the same are trying to achieve (using retroviruses) medical doctors when treating cancer or other disorders like you mentioned in the post above.
PS: like i mentioned above, it is fascinating, that you insert huge amount of new data into human genome and the human is still working … this is not easy to believe …
Querius @25
How long would it take to evolve reverse transcriptase….
This is an excellent question.
But i see another problem … how can a Reverse Transcriptase evolve when the virus can’t reproduce without the Reverse Transcriptase ?
Also, where exactly did the Reverse Transcriptase evolve? Inside the virus? Or inside the host ?
Martin_r @27,
Yes, all these virus capabilities, as Athena, “musta” sprung fully formed from the brow of Zeus. The problem of prohibitive probabilities (haha) has also never been explained.
I just watched an interesting video on such macro-evolutionary probabilities:
Mathematical challenges to macroevolution
https://www.youtube.com/watch?v=i8Y8ZqzXeXU
This also raises the question of whether extant viruses aren’t degraded forms of either the equivalent of software patches (as you suggested) or originally had a significant role in adaptation and transfer of various features (echolocation of both bats and whales comes to mind).
-Q
Querius,
thanks for the link. I am aware of this channel/author, only few days ago i have watched a similar video from him.
However, this particular video discusses author’s paper on mathematical probability of evolution, published in a peer-reviewed journal !
… not sure you have noticed, but there was a pretty funny comment below the video:
:)))))
The probability of him being right is fairly small, too, I’d guess.
Seversky @30
i doubt that he counted in all the examples of convergent evolution … so he is right like 1000 more times :)))
https://www.stuffhappens.info
Martin_r @29,
Haha! No, I missed the comment.
Much of mathematical probability estimates must be taken in context of Baysian inference. However, back-of-the-envelope calculations can lead to some surprising confirmations. I’m thinking specifically of Michael Behe’s book, The Edge of Evolution, where he was able to accurately predict the amount of time it took for the malaria pathogen to evade a novel human genetic defense by random mutation.
-Q
Querius
i like Dr. Andelin. Yesterday, before i gone to sleep i listened to same of his videos. I very like how he is choosing words. Some of his thoughts it is like he is reading my mind. Unfortunately, this is not the case with some other creationists/ID proponents. Most of them repeating the same things over and over again, no new ideas /insights. This guy is pretty special, no wonder he has been a medical doctor for 40 years. Salem hypothesis confirmed again.
PS: off topic. Recently i came across a very interesting article on earwigs’ wing folding. This is something.
Earwig wing expands 10x larger than when closed.
I didn’t know (like many other people don’t), that earwigs have wings. But the way they fold/unfold their wings, this is really something … how could a rational educated 21st century person with some technical background believe that no engineer was involved in designing this …
Make sure you don’t miss this 1:37 mins video, our Creator is laughing in Darwinists’ faces.
https://www.youtube.com/watch?v=oNQ_nn3VLiY&t=2s
Martin_r @33,
Thanks–loved the earwig video! It absolutely blows apart magical step-wise evolution!
-Q
Querius,
let me finish this part with the following:
after seeing this video, any rational Darwinian scientist should make a statement – we got it all wrong … creationists were right. I know it will hurt a lot, and i doubt it will ever happen, but this has to be done one day …
And don’t forget, there is also the puffer fish … this is my favorite one …
https://www.youtube.com/watch?v=B91tozyQs9M
When divers discovered this ‘3D art’ for the first time, they thought that humans did it :)))) but i doubt, that humans are capable to do something like that, underwater, with naked hands, using no tools … with such a precision … I really doubt it …
Yes, I’ve seen this amazing behavior. Also the elaborate “courtship rituals” of some birds that musta/coulda/mighta evolved for some obscure reason in some animals but not in others . . .
But the origami wings of earwigs is absolutely fascinating!
-Q
Thanks to Martin_r for that video and also the puffer fish.
The origami wings are amazing.
That video is like a test of a person’s honesty. A fair-minded person needs to say something.
Silver Asiatic @37,
So far, we hear only the sound of crickets . . .
-Q