This is pretty much the underpinning question of the entire field of evolutionary developmental biology, so naturally any answer is going to be a bit surface level, and I get out of my depth fairly rapidly to be honest. Still, it is quite interesting.

One of the central ideas is that as an embryo grows, its cells go from being all equivalent multipotent stem cells into being different from each other - at first more specialized types of stem cell that can only turn into certain tissues and gradually specializing more and more. Since these cells are differentiated and expressing different genes from one another, they can then start to co-ordinate with each other using chemical markers and gradients of concentration of those markers across space to regulate what types of cells should be growing/dividing, where in the embryo they should be doing it and at what time they should be doing it.

That signaling is in turn controlled by some often complicated networks of regulatory genes - ones which when they are expressed make proteins that selectively attach to other bits of the DNA in that cell and make the genes there more or less likely to be expressed themselves. A lot of evolutionary variation is actually focused on these regulatory systems rather than on the genes which they are switching on and off.

So to my knowledge, something like nose shape likely comes down to some of those regulatory genes controlling where the cells that will eventually be forming the cartilage get placed relative to the skull etc.

I’ll focus on a side question, that I’m more prepared to answer.

Truthfully, everything besides that (including ‘what are proteins’) mostly wooshes over my head

At the end of the day, proteins are biiiiig arse molecules. Mostly composed of carbon, hydrogen, oxygen, and nitrogen. For example, here’s a protein called “myoglobin”, that carries oxygen within your blood:

Blue = nitrogen, red = oxygen, grey = carbon, white = hydrogen, salmon = iron, yellow = sulphur. Disregard the mix of sticks and balls in the model, they’re both representing atoms.

If you pay close attention to the model, you’ll notice a repetitive pattern: 1) nitrogen, 2) carbon connected to some large junk, 3) carbon connected to a “dangling” oxygen. That is not just in the myoglobin, but in all proteins.

If you flattened that pattern and removed the hydrogens (to simplify it), you’d get something like this:

That happens because the bodies of living beings don’t build those huge molecules out of nowhere; they do it with smaller molecules called “aminoacids”. That pattern there is the amide group, you could see it as the “solder” between aminoacids.

Here’s the representation of a few “free” aminoacids:

The fun part is that R, the “side chain”. I called it “junk” but it’s actually a big deal - because it’s what gives each protein a different shape and property. For example, it’s thanks to that junk that the myoglobin has a specific shape, that forms a “ring” of nitrogens, just at the right size to host an iron cation, but still leaves one of the sides of the iron cation free - so it could connect to something else. (Hopefully diatomic oxygen. As in, it’s how myoglobin transports that oxygen within your body. But if you get poisoned with carbon monoxide or cyanide, it gets stuck there, and it’s hard to take it off so the protein stops transporting oxygen.)

Good question. Might do better in a dedicated science community though. Also might just get answered with links to textbooks, since the actual explanation, to get to full understanding, is probably at least a years worth course of study that cannot be easily summarized. It likely involves a whole bunch of different individual chemical interactions, starting with “how proteins make structures”.

Not everything is summarizable, unfortunately.

There are a lot of missing steps people don’t really understand yet R.E. how this all amounts to something complicated like “a liver”. But we think that the basic building block of it is that there are gradients of chemical concentration that some cells set up, and then other cells react to the level of the chemical and decide to different things. There’s a famous analogy of the French Flag Model, where the different stripes of the French flag are imagined to emerge from how far you are from the left edge where a “morphogen” chemical is coming from, because cells detect and react to different concentrations of the chemical in different ways.

And the cells do these things because the DNA programs them to do it. Some genes produce proteins that can turn around and bind to the DNA that encodes other genes, and make those other genes produce more or fewer proteins of their own. Proteins can be made so that they bind or unbind DNA in the presence of other proteins, or particular chemicals, or which can function to turn one chemical into another. So you can have little logic circuits made out of genes that measure chemicals and turn other genes on and off. And you can have little memory circuits based on which genes have things bound to them and which ones are currently on or off, so the cells can remember what it is they decided to be. And so the cells are programmed to differentiate into progressively more specific cell types over time depending on what signals they see, with the morphogen gradients or combinations of them allowing the cells to have some idea of where they are in the body.

And the proteins are these little squishy clicky things, like long strings of magnets that will snap into certain shapes, or that can swap between a few shapes. They can be shaped so they fit really nicely against certain shapes of DNA sequence or other proteins, or so that they fit really nicely against small molecules with a piece pushing on the molecule in just the right place to make it easy for an atom to break off the end of it or whatever. And because they live in this weird tiny world where everything is constantly vibrating around and banging against everything else (because of how tiny the volumes get when you shrink the lengths to cell size), this is enough for them to find and stick to the stuff they are shaped to stick to.

Then depending on genetic variation between people, the proteins involved can e.g. have different set points for the concentrations they react to, and that can translate into the threshold between cells deciding to do one thing or another moving around in the body, and in turn translate into people having e.g. a wider or narrower region of their face decide to be a nose.

Richard Dawkins has an entire chapter on this exact topic in his book “The Greatest Show on Earth”. I highly recommend reading it, even just that one chapter! It doesn’t feel like a text book, and his writing is very easy to follow in my opinion.

It’s chapter 8, “You did it yourself in 9 months”. To summarize, many people mistakenly think of genes as a “blueprint”, but he suggests it’s better to think of genes as instructions for origami paper folding. Genes don’t know the whole creature, they just know what to fold next, what to duplicate, what to bend, and so on, kind of like that. It’s been a while since I read it. 😅

But I do remember, humans are so complex, we may never fully understand the complete embryo-to-adult growth process, BUT the author points out that there IS a creature, a very small worm, that we are able to understand everything.

That may not seem like a big deal at first, but think about it. Scientists understand the complete growth process of a living creature, from a single cell, every gene, every cell, everything, up to when it’s fully formed. So cool.

Like you said, there’s a metric ton of steps involved in the overall process, and our understanding of each of these ‘levels’ of organization varies quite a bit. Closest to my personal expertise is the sub-cellular and cellular level, for which I would refer you books or papers in developmental biology, developmental genetics, and epigenetics. I can give you a couple bloopers to get you excited though:

When it comes to deciding where different organs will form (again, from a sub-cellular level), it essentially starts from a concentration gradient of certain proteins/chemicals inside the zygotic cell. This gradient then determines the level of activation of other proteins, each level then leading to different biochemical cascades which, once more cells have formed from the zygote, determine which organ systems will come from them. Messing around with this concentration gradient can, thus, dramatically affect an organism’s development, leading to, for example, a body with just ‘left’ organs on both halves, just ‘top’ organs on both halves, missing an entire organ system (like circulatory system and heart) and so on.

A more or less similar process occurs to determine the shape of organs. As a simple example, when some animals with regenerative capabilities (like axolotls) lose a limb, they are able to regrow the limb to the exact same length as before. Turns out, each cell on the periphery of their limb has a certain concentration of receptor proteins on its surface, which acts as a molecular ‘signature’ of that cell’s position in the limb. These signatures provide information on how far to grow the limb for regeneration, and some chemicals, lile retinol, can even override these signatures and fool the organism’s body into regrowing the limb from scratch on top of the place of regeneration.

I hope these examples give you an introduction to the mechanisms involved. There’s obviously a lot more involved, so I would again highly recommend textbooks and research papers if you’re interested.

Genes!

We all start as a single cell that gets fertilized by a sperm. That single cell creates a copy of itself to become 2 cells. The 2 do the same to become 4, 4 become 8, and so on. At a certain point, you have enough cells to start differentiating and giving the cells a “job”. Your cells know where they are in your body by communicating with the cells around it, and that influences what job the cell should have.

Genes are a sequence of DNA, and certain genes serve as a “recipe” for proteins which do a lot of important work in the cell. The cell’s job determines which genes are used and therefore which proteins are made. The genes provide the information needed for the cells to form a certain way (look like a nose) and function a certain way (behave like a nose) and proteins help facilitate that.

Two people have different noses because they have different genes (different instructions for how it should look). Your family has a mole on the left side of their face because that gene continues to be passed down with each generation and instructing the cells in the face to form a mole.

I tried to simplify as much as I could without losing the integrity of the information. I hope this makes sense and is helpful!

to add to what others wrote: cells also signal a bit with each other. they tell each other when they are ready or it’s time to do something, like detach or self destruct, so a flipper can split into fingers.

AFAIK all signals for the formation of a human body are chemical, even though some cells can also produce electricity and light.

A good introductory explanation: https://coldbloodedscience.com/the-art-of-shape/

https://youtu.be/ydqReeTV_vk?si=ZvLCP_YhY-OsB_Zs General overview in an entertaining wrapping