Friday, September 9, 2022

Key Genetic Differences Between Humans And Other Hominins

We are starting to reach the point where comparisons of modern human DNA and ancient DNA can tell us fairly precisely how we differed from archaic hominins and which differences mattered the most. The New York Times explains the latest development on this front:

Scientists have discovered a glitch in our DNA that may have helped set the minds of our ancestors apart from those of Neanderthals and other extinct relatives.

The mutation, which arose in the past few hundred thousand years, spurs the development of more neurons in the part of the brain that we use for our most complex forms of thought, according to a new study published in Science on Thursday.

“What we found is one gene that certainly contributes to making us human,” said Wieland Huttner, a neuroscientist at the Max Planck Institute of Molecular Cell Biology and Genetics in Dresden, Germany, and one of the authors of the study.
The most obvious feature of the human brain is its size — four times as large as that of chimpanzees, our closest living relatives.

Our brain also has distinctive anatomical features. The region of the cortex just behind our eyes, known as the frontal lobe, is essential for some of our most complex thoughts. According to a study from 2018, the human frontal lobe has far more neurons than the same region in chimpanzees does.

But comparing humans with living apes has a serious shortcoming: Our most recent common ancestor with chimpanzees lived roughly seven million years ago. To fill in what happened since then, scientists have had to resort to fossils of our more recent ancestors, known as hominins.

Inspecting hominin skulls, paleoanthropologists have found that the brains of our ancestors dramatically increased in size starting about two million years ago. They reached the size of living humans by about 600,000 years ago. Neanderthals, among our closest extinct hominin relatives, had brains as big as ours. . . .

But Neanderthal brains were elongated, whereas humans have a more spherical shape. Scientists can’t say what accounts for those differences. One possibility is that various regions of our ancestors’ brains changed size. . . .

In recent years, neuroscientists have begun investigating ancient brains with a new source of information: bits of DNA preserved inside hominin fossils. Geneticists have reconstructed entire genomes of Neanderthals as well as their eastern cousins, the Denisovans.

Scientists have zeroed in on potentially crucial differences between our genome and the genomes of Neanderthals and Denisovans. Human DNA contains about 19,000 genes. The proteins encoded by those genes are mostly identical to those of Neanderthals and Denisovans. But researchers have found 96 human-specific mutations that changed the structure of a protein.

In 2017, Anneline Pinson, a researcher in Dr. Huttner’s lab, was looking over that list of mutations and noticed one that altered a gene called TKTL1. Scientists have known that TKTL1 becomes active in the developing human cortex, especially in the frontal lobe
. . .

For their final experiment, the researchers set out to create a miniature Neanderthal-like brain. They started with a human embryonic stem cell, editing its TKTL1 gene so that it no longer had the human mutation. It instead carried the mutation found in our relatives, including Neanderthals, chimpanzees and other mammals.

They then put the stem cell in a bath of chemicals that coaxed it to turn into a clump of developing brain tissue, called a brain organoid. It generated progenitor brain cells, which then produced a miniature cortex made of layers of neurons.

The Neanderthal-like brain organoid made fewer neurons than did organoids with the human version of TKTL1. That suggests that when the TKTL1 gene mutated, our ancestors could produce extra neurons in the frontal lobe. While this change did not increase the overall size of our brain, it might have reorganized its wiring.

As a post-script, it is hard to understate the incredibly advanced the work is to extract ancient DNA samples, and to make sense of the DNA.

10 comments:

neo said...

extra neurons in the frontal lobe = high iq?

Darayvus said...

neo, these subspecies diverge so deeply I'm unsure how much sense "IQ" even makes.
I would guess at abstract thought over memory. Neanders would have to own good memory simply to survive a Pleistocene winter. On the other hand, once they learn (or physically evolve) how to survive in (say) a Pyrenees valley, a Neander tribe has little incentive to innovate. Innovation takes time away from hunting and gathering.
Modern East African TKTL1 perhaps arose where the enemy wasn't "General Winter", a vicious enemy but a predictable one; but where the enemy was other humans and also cunning beasts like the jackal, the lion, and the baboon.

DDeden said...

But no other animal which had humans and/or cunning beasts around developed super brains.

DDeden said...

https://pubmed.ncbi.nlm.nih.gov/17342325/
TKTL1 overexpressed in numerous cancer tumors.
Chimps & neanderthals : tumors rare?

Ryan said...

I wonder if damage to this gene is implicated in ADHD. I think less neurons in the frontal cortex is implicate as a cause?

Maybe I should have shared my vyvanse with Neanderthals...

andrew said...

@Ryan

ADHD is primarily a failure of executive function, which is often attributed to the pre-frontal cortex, which isn't so far departed (although its several distinct subtypes suggest that it isn't really even a true single condition with a single cause). https://www.nature.com/articles/s41386-021-01132-0 It isn't obvious that the frontal cortex impacts of TKTL1 extend to the pre-frontal cortex.

I also suspect that the derived version of this gene is at fixation in modern humans.

It is further fairly well established that ADHD is not, in almost any of its forms, a single gene condition. It is a syndrome (i.e. a condition characterized by symptoms rather than a common cause) with multiple distinct causes (including more than one distinct genetic causes) and does not behave hereditarily like a single gene or predominantly single gene condition.

It is almost surely a multi-gene condition, with none being dominant in effect, in almost all cases where it has a genetic cause.

andrew said...

A 2008 review paper on the genetics of ADHD did not identify this as a candidate ADHD gene. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2854824/

andrew said...

@DDeden

A classic illustration of the need to be careful in genetic engineering. A gene modification to reduce cancer risk might expose people so treated to tremendously diminished cognitive function.

DDeden said...

Yes, or a gene modification to increase cognitive function might expose individuals to increased cancer risk.

Ryan said...

@Andrew - "It is further fairly well established that ADHD is not, in almost any of its forms, a single gene condition. It is a syndrome (i.e. a condition characterized by symptoms rather than a common cause) with multiple distinct causes (including more than one distinct genetic causes) and does not behave hereditarily like a single gene or predominantly single gene condition."

It's 80% heritable. There can't be very many genes involved at that level of heritability. It's as heritable than eye colour.

"A 2008 review paper on the genetics of ADHD did not identify this as a candidate ADHD gene."

Appreciate the paper.

This is one I found neat too: https://www.sciencedirect.com/science/article/abs/pii/S0924977X17306582#:~:text=The%20analysis%20of%20the%20genetic,ADHD%20susceptibility%20in%20current%20populations.

It implicates other Neanderthal genes in ADHD, and suggests the ADHD genes were under positive selection until the advent of agriculture.