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Sounds like the genesis for a new sci-fi movie.
I don't understand why an identical twin was needed to learn this.

Couldn't an astronaut's DNA be sampled before and after a mission and compared?

Sure, but everyone is accumulating mutations all the time, so you need a control on the ground to see if space itself is affecting the mutation rate.
Some accounting for a year of aging. Though the news press is probably more scientifically significant.
Well, consider the counterfactual of what would have happened to the astronaut's DNA if he hadn't gone to space. We don't know how it would have changed, so we can't compare it directly. Since we needed to do the experiment I'm guessing our knowledge DNA was not sufficient to predict that, so it makes sense to use a twin to get the closest proxy to the counterfactual that we can.
How would you rule out age-related changes since this specific astronaut was in space for a year? DNA is not fixed, they change all the time.

It is always better to have more data points to rule out several variables, especially considering that it is rare to have an astronaut with a twin sibling.

So how did it ever match his twin? Not being facetious but echoing the parent comments confusion. Do the age related changes occur the same way in identical twins?
This article may explain better than I can: https://arstechnica.com/science/2018/03/scott-kellys-medical...

> As a result, the more relevant comparison (and one NASA did) is Scott's DNA before and after his time in space. That can tell us how many changes were picked up while in space. But as noted above, he would have probably picked up some mutations even if he sat here on Earth. And that's where his twin Mark, who did sit here on Earth, comes in. Mark's before and after gives us a sense of the normal background rate of mutation on Earth. Comparing that rate to Scott's tells us the important number: the degree to which this rate is elevated in the environment of low-Earth orbit.

That really clever they put the ask for notifications button over the top of the close ad button.
"Answer a question in this survey to continue reading this content" Really? no thanks
> 93% of Scott's genetic expression returned to normal once he returned to Earth,

How much was abnormal during the trip?

The article headline is practically fake news. The article isn't very clear on it either. It's not someone's DNA that changes, that would be astounding if all the trillions of cells in your body underwent the same genetic mutations. No, this is a change in epigenetics. The things that change what parts of your DNA are expressed and are much easier to coordinate, change, and adapt in the short-term.

Epigenetics are not that foreign a concept that people should assume the average reader won't understand them or will find it any less amazing.

I consider myself to be very armchair scientifically literate (zero real applied knowledge but I have consumed just about all of the pop culture created on the subject in the last 30 years).

I have never heard the word epigenetics until now and am still confused about what exactly happened to this guy.

You might enjoy reading Seveneves
Great book, another rec here too!
Epigenetics is the idea that genes can express themselves differently based on the environment they are put in.

It is how you can have the same genetic code in your brain as you skin, but the cells the genes are part of are completely different.

It's how you can have a hard drive with a ton of information on it, but choose to read only small portions at a time

It has started to come up a lot recently in order to produce the above-like click-bait headlines. Here's my standard copy-pasta quoting myself from when it shows up around here:

Epigenetics. It's the make-file for your genetic source code. Certain conditions can cause certain parts of your genetic code to be uncommented or commented-out within any given cell or set of cells. There are actually a number of different kinds of 'comments' (histone modifications [1]) - each set of marks are particular to a different compiler, in different contexts. And these comments/marks are copied with some fidelity to daughter-cells/children along with a high-fidelty copy of the underlying genetic code itself.

So the genes (DNA) themselves are not being heritably altered, rather the recipe for which gene is produced, when, and where can be subtly changed. But again, the same mechanisms that permit the change in expression of those genes during a lifetime (of an organism, or a cell) can be subsequently changed in the next just as easily.

In this way you can store the code for some trait or capability over many generations without having it always be running. It can manifest itself in individual organisms or cells as having very different phenotypes even while possessing the same underlying genetic code.

[1] https://en.wikipedia.org/wiki/Histone_code

Thanks for the analogy, I’m actually copying & pasting for future references ;)
It's arguably much closer to RAM than a make file.

Picture a Glucose detector wrapped around a DNA segment that encodes something to break down Glucose. If you zero Glucose inside the nucleus you stop producing stuff to deal with it.

The difference for this analogy is cells never stop compiling. On the other hand if you think of cell division as a reboot it's a better fit.

Your epigenetic state very much starts off inherited from your parents. Also, it's not just a gene switch, and in fact that probably is it's least relevant role, if any. Rather, and besides being a hereditary factor, it determines the structure/packing of your nucleosomes, and therefore determines the integrity of your cell as a whole, not just your gene expression levels.
Genes are the data, epigenetics talks about the program instructions, notably proteins called transcription factors. The latter are of course also encoded for in genes.

The similarities to Von Neumann architecture are .. unsettling.

Every gene can have a tag attached to it which prevents the gene from being used to create RNA (the tag is a methyl group, so this is called "methylation"). Since the RNA would then be used as instructions for creating a protein molecule, inactivating a gene by tagging it generally causes the cell to stop producing particular proteins. Since each protein has one or more specific jobs to do in the cell, this causes the behavior of the cell to change. There are a huge number of known proteins (millions maybe? I don't actually know), and a vast potential number of proteins (if you just consider all possible ways of arranging the 20 amino acids into a chain), so there are a vast number of ways that cell behavior can change over time. Indeed, this is how we manage to have different types of tissues at all, including our very complicated immune system with cells that act autonomously to protect against disease.

Also, it's well established that there are plenty of feedback loops here. An active gene can code for the production of a protein that activates or inactivates other genes. There are numerous pathways by which external stimuli can amplify or inhibit all of these feedback loops, so external conditions often result in changes to which genes are tagged.

As you can imagine, the state-space of all of this is immense; far larger than just the number and type of genes that you have. Mapping it all is a vast project that might easily take thousands of years.

The well goes deeper still. Another mode of epigenetic regulation involves histones, the proteins around which DNA is wrapped, and the many ways they can be modified (by methylation, acetylation, ubiquitiylation, sumoylation, etc.). Both DNA methylation and histone modifications modulate how DNA wraps around histones, and thus how readily any given segment can be accessed and transcribed into RNA (and eventually translated into a given protein).

This barely scratches the surface. This process, along with others that modify how DNA is folded, brings certain genes closer together (while moving others farther apart), increasing (or decreasing) the likelihood of all sorts of first, second, and third order (...) interactions between them and their products.

And we've only just begun...

> This well goes deeper still

> This barely scratches the surface. This process, along with others that modify how DNA is folded, brings certain genes closer together (while moving others farther apart), increasing (or decreasing) the likelihood of all sorts of first, second, and third order (...) interactions between them and their products.

> And we've only just begun...

Horribly vague, care to elaborate mathematically or at least provide some study links? The 'DNA folding' you propose begs resolution from some study using quaternions or attractors, or ... ?

I see your username is accurate.
Epigenetics are fascinating. In my D&D headcanon, the reason Drow Elves are so obsessed with spiders is because they picture DNA as a three dimensional web whose spatial arrangement is central to gene expression.
This view that epigenetics is a gene switch is actually pretty misleading at least, and probably just plain wrong, as recent research published this year has shown. It is far more a structural and inheritance guiding factor, as it was conclusively shown that methylated promoters very much do still allow for gene expression, contrary to "popular" belief.
That doesn't surprise me in the least; practically everything in biology has turned out to be more complicated than it first looked.
I know about epigenetics because of many articles in Popular Science or Discovery.
I think the issue for the article is that identical twins are not epigenentically identical to begin with, time in space and life in general will only tend to magnify that. In essence, the headline is doubly misleading.
While I think it’s important to disagree with news that might be less than factual and better yet - think with a skeptical mindset, I think it’s rather anti-intellectual to blanket misleading or factually lacking news as ‘fake news’.
Good thing he didn't do that!
> would be astounding if all the trillions of cells in your body underwent the same genetic mutations.

spoiler: they won't all undergo the same epigenetic changes either.

Are you sure? Might there be a coordination mechanism of sorts?
Ok, that explains a lot, because my imagination was going wild with these 2 things:

According to the article: Preliminary results from NASA's Twins Study reveal that 7% of astronaut Scott Kelly's genes did not return to normal after his return to Earth two years ago.

According to my memory, and now looked it up: Chimps and bonobos in particular take pride of place as our nearest living relatives, sharing approximately 99 percent of our DNA, with gorillas trailing at 98 percent.

Good thing they put a picture in the article of the guy, haha.

> According to my memory, and now looked it up: Chimps and bonobos in particular take pride of place as our nearest living relatives, sharing approximately 99 percent of our DNA, with gorillas trailing at 98 percent.

I thought of that as well while reading about the 7% they mention, but then I assumed they were talking about 7% of the genes that are specific to human kind.

Indeed. If 7% of your genome were replaced with something else, it would be incredibly unlikely that you would still be alive.
Though now that I think about it, if 7% of the human-specific genome was changed, then it must mean that 7% of the rest was changed too. I mean it's not like cosmic particles specifically target human genes, is it?
Exactly, I would expect this person to perhaps have some additional mutations (in his superficial tissues so no body wide mutation of course) due to radiation, or perhaps due to selective pressures working differently on them in 0 G. Also I'd expect expression changes (RNA quantity changes), also related to 0 G or maybe to his diet. Also, it is often claimed that chimp DNA is only 1% different from ours. Which is also bull of course, it depends, (as here) on how difference is defined. The telomere story is interesting but from the text it sounds like we already expect that from radiation and calorie restriction.
Anyone else getting the “Congratulations you are a winner” ad spam / malware which takes over the page and forces a redirect?

I run into this on news sites several times a week. I assume these are ads which are sneaking by the ad networks filter and running scripts on the page, just not sure how they are so damn pervasive?

If these ads aren’t being paid for with stolen credit cards, then why aren’t they people buying them getting slammed with CFAA charges? Is it that hard to track these clowns down?

Are you sure you don't have malware on your system? I haven't experienced a redirect ad in basically forever.
It's super rare in Chrome for me, but I've seen it happen the first day on a new iPad / Safari just a few weeks ago.
I get these frequently too, especially on IOS devices. If you wipe your browser history it stops happening, so I assume they are doing some checks against Ad Network filters.
Yes, this was on my iPhone. I always hav Safari set to Private mode so I think there is no history.
The article is muddled.

> To better understand the genetic dynamics of each twin, Mason and his team focused on chemical changes in RNA and DNA. Whole-genome sequencing revealed that each twin has more than expected unique mutations in his genome -- in fact, hundreds.

So both experienced hundreds more unique mutations? But OK, let's say that it was Scott Kelly who experienced more mutations. But which tissues did they sample? Sperm?

> Preliminary results from NASA's Twins Study reveal that 7% of astronaut Scott Kelly's genes did not return to normal after his return to Earth two years ago.

This is about gene expression, not necessarily mutations. And it's the key take home. Given that we've known for some decades that radiation causes mutations.

More likely aliens have replaced him with a pod person to infiltrate NASA.
[I'll copy my comment from dupe story that didn't get any traction.]

The article avoids all the interesting technical details. In case you are wondering if this is possible and how much of this is an exaggeration, the title of the research article is "The Landscape of DNA and RNA Methylation Before, During, and After Human Space Travel (Twins Study - Mason) - 09.27.17" https://www.nasa.gov/mission_pages/station/research/experime...

Methylation is an usual process that the cells use for enabling and disabling genes expression. It's reversible, somewhat permanent and somewhat inheritable. If you like a bad analogy, it's like making a change in the bios setup of your computer or updating the configuration of the wifi-router. It's not a firmware upgrade or a hardware modification. More info: https://en.wikipedia.org/wiki/DNA_methylation

Oh heck, me too - since I was responding to your only comment just minutes ago, here is again :)

Maybe, but what is really causing the DNA methylation? The article pins it mostly on epigenetics or environment, the 'stress of space travel', including dietary constraints and oxygen levels all of which are valid.

- https://theconversation.com/epigenetics-can-stress-really-ch...

- http://sitn.hms.harvard.edu/flash/2017/stress-induced-dna-mo...

- https://www.scientificamerican.com/page/sponsored/nestle/how... ooh, sponsored article, didn't catch that the first time.

However, the CNN article only briefly mentions 'radiation' as a factor and likely is lumping that into the 'stressful environment' case repeated several times.

Realistically, cosmic rays or radiation are far more likely to the be prevailing indicator for DNA disruption but are not plainly disclosed here. Despite much research having been done on this specific topic.

Wikipedia states: https://en.wikipedia.org/wiki/Health_threat_from_cosmic_rays "The potential acute and chronic health effects of space radiation, as with other ionizing radiation exposures, involve both direct damage to DNA, indirect effects due to generation of reactive oxygen species, and changes to the biochemistry of cells and tissues, which can alter gene transcription and the tissue microenvironment along with producing DNA mutations."

From this paper: https://arxiv.org/abs/1406.6641 "In the present paper, we suggest the BNR as a cause of genetic “fails” in living cells, that is one of the possible origins of the so called spontaneous mutations. Cells exposed to the shower of electrons and ions, caused by the collision of a neutron and a proton of water, could be annihilated or experience a permanent damage, in particular, a damage in the DNA."

Cosmic radiation detrimental effects to DNA confirmed by NASA in this study: https://ntrs.nasa.gov/archive/nasa/casi.ntrs.nasa.gov/200800...

And more poignantly, from https://www.vencoreweather.com/blog/2017/6/26/1200-pm-cosmic... ( do not read full link if you are easily panicked ): "... there are other consequences of increasing cosmic rays according to “Spaceweather.com” including the penetration of commercial airlines, dosing passengers and flight crews enough that pilots are classified as occupational radiation workers. [Dose rates are expressed as multiples of sea level. For instance, we see that boarding a plane that flies at 25,000 feet exposes passengers to dose rates ~10x higher than sea level. At 40,000 feet, the multiplier is closer to 50x]"

Sorry for the data dump, I just happened to be researching cosmic ray effects the past few evenings and have collected many interesting facts on the topic. The most I have concluded at this point is that humans, as currently derived, are not made for space travel.

I am not a biologist, so my answer may have a mistake ...

Radiation and cosmic rays produce random mutations, where one of the bases of the DNA is changed by another base. (IIRC the radiation breaks the old base, and when the copy or correction enzymes see the mess, they may make a mistake and use the wrong base.)

Methylation is on purpose. Some part of the cell "decides" to enable or disable a gen, and send the correct enzymes to add or remove the methyles in the bases of the specific part of the gene.

(There are also some arm races between bacteria and virus that attack bacteria. The bacteria has an enzyme that split the DNA at points with some specific patterns, to try to kill the virus that enter the cell. The parts of the DNA of the bacteria with this pattern are methylated, so the enzyme doesn't attack the DNA of the owner. https://en.wikipedia.org/wiki/Restriction_modification_syste... )