In today’s BioNews, I talk about two recent studies that show how most Neanderthal DNA has been purged from our genomes but their genes we kept may well have proven beneficial. Have a read.
BioNews just published my review of The DNA Journey — a video produced as part of an advertising campaign for travel comparison site momondo. Have a read here.
I’ve written a review of Adam Rutherford’s radio documentary, ‘The Business of Genetic Ancestry’ for BioNews. Have a read: http://www.bionews.org.uk/page_533193.asp
I reviewed last November’s Crick Lecture at the Royal Society on behalf of BioNews. Dr Duncan Odom spoke about mammals, genes, a branch of biology called ‘comparative functional genomics’ and how we all owe everything to tiny shrews. I also took the opportunity to have a moan about simplistic sloganeering and the rights of marginalised forest-dwelling people. Have a read.
The roof of the world, north of the Himalayas, stretches over two and a half million square kilometres. It is inhospitable, arid and permafrosted. When it rains, it mainly hails. It’s the highest place on the planet where you can stand on flat ground and be near the heavens, and standing there will thicken your blood. Unless you carry the EPAS1 gene.
This gene stops you over-producing haemoglobin – the oxygen-carrier in red blood cells. Too much haemoglobin raises blood pressure and, with it, the risk of stroke, among other bloody things.
This gene came from an ancient, extinct subspecies of human called the Denisovans. We know this because scientists sequenced Denisovan DNA four years ago. This DNA came from a fragment of a pinky and two teeth found in a cave.
The ancestors of today’s Tibetans had sex with Denisovans. Genes were passed around. The useful ones remained. This allows Tibetan people to survive on the roof of the world.
I wrote about the science for this week’s BioNews. Have a read.
I tried to make insurance interesting on behalf of the Progress Educational Trust (PET) and the Wellcome Trust. Have a read.
The piece comes from PET’s recent event ‘Risk Management: Breast Cancer, Business and Patents’ — the third of their four-part project ‘Breast Cancer: Chances, Choices and Genetics’.
Simon Hazelwood-Smith reviewed the night for BioNews.
James Heather covered the second event — Risk Assessment: Breast Cancer, Prediction and Screening.
The final event — Breast Cancer Risk: Facts, Fictions and the Future — is taking place on Thursday 3rd July. See PET’s website for more details.
Following last week’s post about a recently-published genetic ancestry test called Geographic Population Structure, BioNews kindly offered me the chance to witter on at greater length about it. In my comment piece, I dig in to some flaws in the concept, the problems with genetic ancestry testing in general, and some juicy gossip.
Have a read: So many genes, so close to home
This week for BioNews, I report on a genetic astrology ancestry test that claims to “tell you where your DNA was forged, and is accurate to home village with a time resolution of the past 1,000 years.” Researchers named the test Geographic Population Structure, or GPS, presumably to convey a sense of satnav-esque accuracy.
The method was published to a fanfare of overblown press releases and uncritical media coverage.
“What we have discovered,” spun one of the press releases, “is a way to find not where you were born – as you have that information on your passport – but where your DNA was formed up to 1,000 years ago by modeling these admixture processes.”
At the same time, the researchers founded a company called Prosapia Genetics which tells you your supposed ancestral homes in exchange for money.
But it doesn’t work so well. Some customers found their ancestral genomes stuck slap-bang in an ocean:
This is because the tool averages between the locations of genomes for which it has geographical data. Apparently it’s meant to work this way. Dr Eran Elhaik – one of the study’s co-authors – wrote on Prosapia’s forum: “when you have British and Chinese parents you will be predicted to Iraq, as it is in the middle of the two gene pools.”
Many in the know have dismantled the science far better than I ever could. Debbie Kennett writes a wonderfully comprehensive account. Pseudonymous blogger Dienekes Pontikos explains some of the wrongness in the tool amid hints of plagiarism. And Joe Pickrell – who peer-reviewed the study – posted a summary of his problems with the paper.
According to the Prosapia website, the scientists are developing an extended tool – GPS2 – that will apparently show two parent groups that formed your DNA, rather than just one. (If you trace back 10 generations – around 300 years, for sake of argument – you have up to 1,024 genealogical ancestors but you contain DNA from only maybe 120 of them. See Luke Jostins’ blog for an explanation.)
Anyhow, I’m writing a longer comment piece for BioNews that will be out next Monday and will go into more detail there.
In the meantime, have a read: http://www.bionews.org.uk/page_416034.asp
Last week, the Progress Education Trust launched a new project called ‘Breast Cancer: Chances, Choices and Genetics’, inspired by Angelina Jolie’s risk-reducing mastectomy surgery. It’s a topic I was previously keen on avoiding. I hoped to get through an entire science-writing career without using the ‘C’ word, but alas. I’ve reviewed the first of the four events for BioNews (have a read then come back here).
By dint of deadlines and word counts, I had to leave out so much I wanted to say about the evening. The rest of this post contains a hodgepodge of offcuts from my review.
This week for BioNews, I report on a thorough and thoroughly cool study that weaved its way down a biological pathway from exposure to pesticides to the death of nerve cells linked to Parkinson’s disease.
The researchers found how a genetic mutation can interact with toxins produced from pesticides to disrupt the functioning of neurons involved in movement and coordination. The mutation lies in a gene encoding a protein that is the main ingredient of Lewy bodies — the clumps found among neurons of people with Parkinson’s or certain forms of dementia.
They looked at the problem from all sorts of angles and involved patient-derived lines of induced pluripotent stem cells and embryonic stem cells and a lot of tweaking, coming to firm causal conclusions about a very particular interaction between genetics and environmental factors.