Defect that causes Huntington's disease has been corrected for the first time
bbc.com
bbc.com
edit: Never mind, although the research took place at the University of London, it was funded by Ionis Pharmaceuticals (US) and further by Roche (Swiss multinational). The Guardian article relegates that bit of info to the very last line, as if they were just a minor part of the effort. http://markets.businessinsider.com/news/stocks/Ionis-Pharmac...
https://www.economist.com/news/science-and-technology/216457...
Something that may be related... The same unstable repeat that causes the disease is ancient and is conserved throughout mammals! So other mammals can get a similar disease driven by the same mutations. This is useful for generating models of the disease in other mammals (e.g. mice). Such conservation of repeats is exceptionally rare.
Huntington's is caused by an error in a section of DNA called the huntingtin gene. Normally this contains the instructions for making a protein, called huntingtin, which is vital for brain development. But a genetic error corrupts the protein and turns it into a killer of brain cells. The treatment is designed to silence the gene.
One fear was the injections could have caused fatal meningitis. But the first in-human trial showed the drug was safe, well tolerated by patients and crucially reduced the levels of huntingtin in the brain.
The UCL scientist, who was not involved in the research, says the same approach might be possible in other neurodegenerative diseases that feature the build-up of toxic proteins in the brain. The protein synuclein is implicated in Parkinson's while amyloid and tau seem to have a role in dementias. Off the back of this research, trials are planned using gene-silencing to lower the levels of tau.
It's clearly maladaptive, isn't it?
Of course, same question could be asked for BRCA.
Huntington's is caused by an expanded repeat composed of (CAG)n with n>40 repeats. Due to the instability of repeat regions, new mutations arise in this gene at a relatively high rate. So, even if there were strong selection against expanded repeats the disease would continue to exist. However, as mentioned by others here, strong selection is unlikely due to the late age of onset of the disease. So mutation continues to introduce the disease and selection has been too weak to remove it.
In contrast, BRCA mutations differ from the Huntington mutations. BRCA mutations are single "point" changes in the sequence, known as SNPs, that disrupt the protein function. Novel point mutations are exceptionally rare.
So, unlike with BRCA, when investigating why Huntinton's disease exists, one must consider BOTH mutation and selection.
I wish I could find the excerpt, but the book The Gene talks about the original research and it's an interesting story.
The book is worth reading in general (Siddhartha Mukherjee is a great writer and it's really good).
http://www.simonandschuster.com/books/The-Gene/Siddhartha-Mu...
Orphans are not a very good evolutionary tactics. But you definitely have a point otherwise. Had it earlier onset age, it would have no way to propagate.
I'm not arguing that this is necessarily the case, but it is not clearly maladaptive.
It's a trojan horse, and the clever thing about it is that there are valid medical reasons for it.
I can't edit or remove my comment because Hacker News believes they know better than me if I should have the ability to edit or remove my own comments.
https://www.sciencenews.org/article/car-t-cell-gene-therapy-...
https://geneticliteracyproject.org/2017/11/17/fda-likely-to-...
You effectively can't trust the regulators of something so potentially disruptive of the balance of power.
In Blade Runner, Replicants were not robots. They were genetically modified human beings designed to make them perfect slaves.
I don't expect perfection, but I expect an attempt at forcibly modifying people to make them healthier and satisfied in an increasingly unhealthier society.
No need to reform society if you can change human nature.