genomer
Joined 11 years ago
Joined 11 years ago
The most recent literature that I'm seeing is showing the most pronounced time of thymus involution occurring around puberty, suggesting a programmed switch from a growing to reproductive phase of life.
"Regardless of the seemingly crucial role of the thymus in preserving homeostasis, its involution in humans and other mammals begins in childhood and peaks around puberty, resulting in an almost completely non-functional organ in aging." https://www.sciencedirect.com/science/article/pii/S156816372...
In this light the following makes sense (stopping or suppressing the switch to a reproductive life). "Castrating rodents before puberty or reducing the levels of sex hormones [e.g., by using Lupron, which desensitizes the luteinizing hormone-releasing hormone (LHRH) receptors] can attenuate or markedly recover the involution process in aging mice."
I was in line for the Terminator ride at Universal Studios when I stumbled onto this article a few years back. Couldn't stop thinking about it the rest of the trip.
https://www.scientificamerican.com/article/scientists-surpri... “The idea is something that 10 years ago would have been science fiction,” says biochemist James Eberwine of the University of Pennsylvania. “We were taught that every cell has the same DNA, but that’s not true.”
Edit:
Reading into this more again for the first time in a while. I'm amazed at how large some of these differences are. Many having 1 million base pair copy number variants.
"Single cell sequencing of endogenous human frontal cortex neurons revealed that 13%-41% of neurons have at least one megabase-scale de novo CNV, that deletions are twice as common as duplications, and that a subset of neurons have highly aberrant genomes marked by multiple alterations." https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3975283/
Couple this with...
"Megabase-scale copy number variants (CNVs) can have profound phenotypic consequences. Germline CNVs of this magnitude are associated with disease and experience negative selection. However, it is unknown whether organismal function requires that every cell maintain a balanced genome. It is possible that large somatic CNVs are tolerated or even positively selected." https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4772019/
I can't imagine our brains are just accumulating mutations of this size for no reason.
My favorite theory so far is that it has to do with memory indexing. https://www.frontiersin.org/articles/10.3389/fgene.2020.0037...
Here's some supporting research from a quick search. https://journals.aai.org/jimmunol/article/192/6/2689/1552
Edit: some fun but possibly pontificating tangents
This seems to be part of the reason why vaccines have had relatively poorer efficacy in elderly populations. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3901832/ https://www.nature.com/articles/s41586-021-03739-1
I'm hopeful that cancer and immune profiling will be able to be used in tandem to (1) identify cancer early and (2) identify gaps in the immune repertoire to facilitate (3) design of antibodies that specifically target the cancer.
https://investors.adaptivebiotech.com/news-releases/news-rel...
Edit: that isn’t to say that this result isn’t exciting for human welfare. We’ll see if it translates…
It seems like the physician shortage will only continue to worsen. https://www.aamc.org/news-insights/press-releases/new-findin...
Edit: Basically, I think a lot of people will still be left without adequate health care in minor cases, but at least the most urgent cases will be taken care of without leaving people bankrupt.
An example of a different class: "Researchers have shown, for example, that aminoglycoside antibiotics can cause deafness by damaging mitochondria in the hair cells of the ear."
More general statement: "They reported that antibiotics in several classes triggered oxidative stress — a build-up of reactive, oxygen-containing molecules — in mitochondria, inhibiting their function across a range of mammalian cells, as well as in mice."
I interpreted the article as saying that quins are the most obvious example of antibiotics causing harm, but one example for where they cause harm (mitochondria) is a problem shared by other antibiotics. Unfortunately there isn't a test for evaluating mitochondrial damage in the body. Since we can't test, we don't know the real extent of damage done by any antibiotic to human cells. More research is needed.
"Until recently, investigations into the side effects of antibiotics have focused on how the drugs disrupt the human microbiome, says James Collins, a medical engineer at the Massachusetts Institute of Technology in Cambridge."
https://nanoporetech.com/products/sequence/minion
Sequencing DNA with nanopores: Troubles and biases https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8486125/
Based on what I'm seeing from 23andMe's website they only do genotyping, not sequencing.
https://customercare.23andme.com/hc/en-us/articles/227968028...
"23andMe uses genotyping, not sequencing, to analyze your DNA. Sequencing technology has not yet progressed to the point where it is feasible to sequence an entire person’s genome quickly and cheaply enough to keep costs down for consumers. It took the Human Genome Project, a consortium of multiple research labs, over 10 years to sequence the whole genomes of just a few individuals."
Edit: https://www.23andme.com/total-health
I guess they started providing whole exome sequencing, but I can't find information about what depth they're doing it at.