Researchers at the University at Buffalo and the Jackson Laboratory discovered that humans' ability to digest starchy foods is linked to ancient duplications of a gene called AMY1. This gene produces the enzyme amylase which breaks down starch into glucose. The researchers analyzed the genetics of 68 ancient human bodies, the oldest of which was from 45,000 years ago. However they believe the gene duplications could date back to 800,000 years ago. The gene was even shown to be present in Neanderthals. This all suggests human bodies adapted to starch very early on in their evolution. The research shows that as farming became more popular, the copying of the AMY1 copy increased, which further enhanced starch digestion. Humans adaptation to starchy foods greatly contributed to human survival because they would not have been able to digest all of the food coming from the farming without it. Researchers also believe the AMY1 gene's role in starch digestion could provide new insights into research on metabolic health, obesity, and type 2 diabetes.
Monday, December 9, 2024
The Gene that Helps Us Digest Bread
Sunday, December 8, 2024
Can We Blame Our Love for Carbs on Genetics?
In humans, the salivary amylase gene (AMY1) has been found to break down starches in our mouths, which is the first step to properly digesting starches and carb-rich foods. Humans carry a varied number of AMY1 on our first chromosome. Moreover, amylase is an enzyme that breaks starch down into glucose, so the more amylase genes you have actively producing, the more starch you can break down. Therefore, the AMY1 gene has been credited with shaping humans adaptation to starchy foods, ultimately diversifying our diet and allowing us to use more food resources.
Within their study of AMY1, researchers looked into 68 ancient human bodies (even one who lived 45,000 years ago) to see how far back these genetic variations went. The researchers noted that the hunter-gatherers had four to eight copies of AMY1. Curiously, this was before humans began to farm their foods, so we had already began to adapt to starches before growing wheat/potatoes. From the findings of this study, it is now argued that the different amounts are attributed to duplications made over 800,000 years ago (before humans split from Neanderthals and Denisovans). As we spread out globally, the amount of AMY1s began to be distinctly different between locations, for the amount is dependent on the environment around them (Thompson, 2024). Also, the average number of AMY1 copies have dramatically increased in the past 4,000 years because of our diet. Interestingly, because individuals with more AMY1 copies digest starches easier, they have been found to reproduce more and also may explain why the average amount has increased.
In all, this genetic variation opens up many opportunities for future research. Personally, I would be interested in looking at the amount of AMY1 copies in places that eat a lot of carbs (f.e. Italy and Japan). One researcher even said that our current understanding of metabolic health may change from these findings. She also noted that,"Future research could reveal its precise effects and timing selection, providing critical insights into genetics, nutrition and health” (Yilmaz, 2024). I look forward to seeing how these findings will be researched and if the metabolic effects of AMY1 could be replicated with other medications or fixed with new genetic editing.
Sources used:
https://humgenomics.biomedcentral.com/articles/10.1186/s40246-017-0097-3