Epigenetics is one of those things that seems wild until you pull the camera back a bit. A cell is affected by and responds to its surroundings - this is not controversial. In eukaryotes, this is usually done by way of altering gene expression - up- or down-regulation by means of chemical markers on the cell’s DNA which are created or removed by enzymes which are activated or deactivated by certain substances in the cell or its environment - in other words, the cell’s environment affects gene regulation within the cell by traceable mechanisms*. All cells, save at least one, are descendent of other cells, and cells split by meiosis, in which the chemical environment within and without the cell is shared by the “descendent” cell - so of course this happens with human embryos as well. Of course the expression of your genes is affected by what happened to your parents (well, your mother, at least), because gene expression is affected by what happens to a cell and you are made up of a lineage of cells descended from your mother’s cells. If you ask how one organism could be affected by something it didn’t experience, sure, that could be a quandary, but looking at a line of cells and wondering how later ones could be affected by environmental pressures on earlier ones isn’t nearly as much of a mystery, and we’re all just extended cell lineages.
(As if first time mothers didn’t have enough to worry about - stop stressing so much, it could lead to long-lasting irreversible changes to your fetus!)
* Standard biology disclaimers: this is not the only way this happens, this varies across species and time, nature has no master plan. “Some of the time some genes have some amount of their expression modified somewhat by some mechanisms that are somewhat responsive to some part of the cell’s environment sometimes.”
Being confused about how 2 environments could produce different individuals even though they are given the same DNA is like being confused about how 2 compilers could produce different binaries even though they are given the same source code.
The problem with this perspective is that you would expect the effect of a past environmental influence to be overwritten by a future environmental influence. The idea that the effect of the past influence would persist is what is questionable.
What I don't like when people bend over backwards to hype epigenetics:
1. the lack of historical context and opinion lock-in once expressed: before the human genome project many geneticists thought the number of "genes" (yes its an oversimplification) would be much much larger than what was eventually discovered to be the case. It was a shock to many biologists, that there were just about tens of thousands of genes in the genome, basically "a handful" in terms of control theory. The miracle of life started to look marginal and banal, just like many protested the earth not being the center of the solar system...
2. no highlighting the difference between single-cellular species and multi-cellular species: generational memory effects are obviously observable for single-cell organisms. For multi-cellular organisms, like humans, the concept of generation is ambiguous: is one talking about cellular generations (fertilized egg cell, dividing and the daughter cells dividing again, ...), or about organism-level generations (human parents of human children)? It becomes immediately apparent that the cell lineage from fertilized egg cell, to either sperm cell of the son or egg cells of the daughter, would involve lots of divisions, and the final sperm or egg cell would only have access to vague general variables: blood sugar levels, temperature, some hormonal levels, ...
3. Just like one can not truly study physics, without learning mathematics, and then formulating claims and observations mathematically, to truly study biology and the homeostasis it implements, you need systems biology: a mathematical description of biology. To understand multicellular organisms, one needs to understand the concept of cell types mathematically, and to summarize it in natural language cell types are the stable attractors forcing the cell contents to return to the closest state of the cell type. To make a rough analogy (cell/human, cell type/profession) then in contrary to humans, cell's don'
t have any memory which is independent of their cellular content. So apart from the content of the cell, a cell is amnesiac. Imagine humans without memory, but upon seeing the room in which they work, they can constantly re-understand what role they perform, and any deviation from what is ingrained in your local DNA copy of the genome is responded to. If you find yourself in a room with ovens and lots of dough, and some of the ovens have bread, but for some reason there's a cop's badge on the table, then you know you are a baker, and you throw out the cop's badge. If you are in a special car with red and blue lights, and you are behind the wheel, but there is for some reason an oven sitting on the passenger seat, then you are a cop, and you take the oven out of your police car.
Once you understand how cell types implement the memory necessary so that a neuron in your brain doesn't start to behave like a skin cell on your anus or vice versa, you understand the ridiculous proposition of epigenetics, a quest for the holy grail of all the missing information that the human genome project failed to find... Euhm well sure there is some modulation of transcription by histone modifications etc... but all of that can be modeled in the same language of reactions that is currently used to model Gene Regulatory Networks, with Gillespie simulators etc. Instead of wishing to vindicate ones old (and wrong) forgotten statements from before the human genome project due to psychological lock-in effects, it would be more productive to point out that in practice a lot of known useful data is ignored, so why not first make use of information we know exists before ingraining vague ideas about epigenetics in the next generation of students? stop ignoring the promotor regions and consensus sequences etc when sequencing genomes, there is a wealth of information to be had there, and personalized DNA-driven medicine will never take off until these are by default sequenced as well, as they directly relate to transcription rates! you know, good old classical gene regulatory network data.
1) epigenetic inheritance is just if a horse stretches its neck to reach up high, so to do that horses children and their children, and so on, until you end up with a giraffe
2) yes methylation and epigenetics resets, not so much at meiosis as at conception zygote formation
3) it doesn't 100% reset more like 98.3% resets, the remainder does NOT reset, thus, epigenetic inheritance. Sometimes that reset process fails, thusly, (epi)genetic disease. Also all this process called "imprinting" is why it was hard to clone various organisms including until recently humans - you can "reset" a skin cell 100% but that's not the ticket, you need to reset it 98.3% and leave the imprinting regions. Oh. And the specific imprinting regions are different for the chromosome that come from mom, vs, the chromosome come from dad
So the big takeaway is that DNA no longer is the main mechanism of inheritance as Darwin taught but actually epigenetic, and the basis is along the lines of horses stretching their necks and becoming giraffes. There's a lot of getting into the weeds as to how this all works molecularly is that's it's really complicated but it is inherited
no, no it does not strip protien complexes away from the DNA strand.
it involves a localized progression along the DNA surrounded by histones, and regulatory enzymes, displaced from proximity, until the replication fork zooms on through, and it all snaps back together.
the process is error prone, strands may cross over, chromosomes may fail to migrate properly.
>>> (As if first time mothers didn’t have enough to worry about - stop stressing so much, it could lead to long-lasting irreversible changes to your fetus!)
This is plainly not plausible. "Irreversible" doesn't play well with the length of time humans have been a thing.
Ask a parent what they hear when they hear “irreversible” in conjunction with their child. I promise nobody mistook that for “until the heat death of the universe,” but I can add a note if you really think it’s warranted.
But even reversible changes aren’t always “reversed”. They aren’t necessarily minor.
Sure, breaking an arm or skipping high school can be a “reversible” change. But not often not fully “reversed” and/or not done so in a negligible time frame. There are costs. Seems like biological development could be similar.
For whatever reason, epigenetics is somehow considered by a great many people to be some whackadoodle conspiracy theorist woo-woo.
When I posit the following explanation-question that helped me to understand at least that epigenetics does akshually come from science, either the light bulb goes on over one's head or it's seething hate:
How come all of the cells in our bodies have the same DNA, but they can be so different? In other words, why are we not comprised of an amorphous blob of identical cells?
Cells specialize based on the presence of certain chemical gradients, for example. These types of 'signals' that guide specialization already become apparent in a very early stage of embryonic development. I don't think that's part of the realm of epigenetics.
(As if first time mothers didn’t have enough to worry about - stop stressing so much, it could lead to long-lasting irreversible changes to your fetus!)
* Standard biology disclaimers: this is not the only way this happens, this varies across species and time, nature has no master plan. “Some of the time some genes have some amount of their expression modified somewhat by some mechanisms that are somewhat responsive to some part of the cell’s environment sometimes.”