So here’s my third video to the mini series, introducing the idea of genetic engineering in a way that hopefully won’t sound as scary as some people might find the idea.
Genetic engineering is a wonderful tool allowing us to take genes from a human and put them into bacteria. Because every organism’s genetic code is made up of the same As, Gs, Cs and Ts the bacteria can interpret the genes and make the protein products we need. Also, because bacteria are so small and multiply so often, we can have a bacteria factory making things like insulin that we can use to treat people.
I was able to have a go at genetic engineering at university to make bacteria produce a blood thinner and the fact that a whole class of 3rd year students could do this successfully without ever trying the technique before is incredible and shows how far we’ve come in using genetic tools to treat medical conditions successfully.
What’s also great is that the protein made from the gene is a human version, not a bacterial version, as the original gene is from humans. This cuts out a whole number of potential problems!
So have a look at my video and let me know what you think!
A quick additional note: if you do download the adobe voice app, they’ve selected my second video in the series as part of their inspiration feed on the homepage of the app! So you’ll be able to see that within the app as an example video!
This is the second video in my back to basics series, this time introducing the idea of genes being regulated differently in different cells. There’s more to it then just off or on but the concept is fundamental, especially in developmental biology (my broader field of work).
This time round with the video I decided to try and use the images that are readily available to any user to see how far I could stretch the app to my needs, and I think it worked out quite well for a non-specialised app!
Have a watch and let me know what you think. The video still stays along the ks4 science curriculum guidelines so hopefully it can be a useful resource.
I recently took part in the ‘I’m a scientist, get me out of here!’ outreach event. As soon as the school children found out I was a developmental geneticist and worked out what I did, one question I was repeatedly asked was: “what’s your favourite gene and why?” so for a bit of fun, I thought I’d share my thoughts and see what everyone else’s are too.
Now, I could have gone into detail about a gene of utmost importance in my work or one we literally couldn’t live without (although picking either of those would be tricky as that hardly narrows the list down). However, my first thought when picking my ‘favourite gene’ is always listing the funny-named ones that stuck out from my university lectures. That’s not to say these genes don’t also fit into the important and essential-to-life categories, but they have that added ‘pazzaz’ of an ear-catching name that would wake you from your university slumber, thinking “did he actually just say what I think he said…?”. So here is my shortlist, the top 5 genes based almost entirely on their names: Continue reading What’s your favourite gene?→
Unfortunately this is quite a delayed post so I’d like to apologise for that but suddenly things got very busy around here…
I took part in the I’m a scientist competition from 10th March until my eviction on the 18th (sad to say I didn’t win!). I will start with this – I was not prepared for the sheer onslaught of questions, hard questions from the kids. I took part in a handful of live chats and I’m pretty sure I’ve worn down a few letters on my keyboard! Continue reading I’m a Scientist, get me out of here!→
Yesterday, my evening was spent at Senate House in London for my first experience of a Crick Symposium run by the new/future Francis Crick Institute. Just so you know, The Francis Crick Institute is the developing giant biomedical research institute being built just by King’s Cross Station in London and will house researchers from Imperial College, King’s College, University College, The NIMR and the LRI. It’s huge, it’s a big deal and if (fingers crossed) everything goes to plan timing wise I will be finishing up my PhD there!
Now the symposium was about rare diseases, which weirdly enough are a big problem. Each individual rare disease is defined in the EU as affecting less than 5 in 10000 of the general population however with over 6000 recognised rare diseases that equates to a lot of people living with them. Rare diseases are often severe, chronic, life threatening, life debilitating and have large impacts on the patient and their families. Continue reading Crick Symposium: Rare Diseases→
Yesterday I went to a talk at UCL. The evening was a “beer and pizza science evening” led by the UCL Genetics Institute in population genetics. Anyone with some sort of knowledge in this field would also realise that the beer and pizza would bring in a crowd despite the amount of not so popular statistics and modelling that can be involved. This was very true as the large gathering of people to the event somewhat dwindled after the half-time break. I however did stay until the end and was pleasantly surprised both at my ability to understand the talks and the actual content. Here I’ll summarise each one and give my own take on the topics.
Prof Mark Jobling was first and spoke about Y chromosome analysis. The Y chromosome is the smallest of the bunch and is somewhat neglected in sequencing projects and medical genetics. It is present in just males and in many instances it isn’t even included in higher organism genome releases purely because the subject chosen is female as this gives the added benefit of twice the amount of X chromosome for your money. However the potential in this little guy shouldn’t be underestimated.
The Y chromosome itself actually has very little sequence diversity and through custom sequencing of just this chromosome it is possible to map all the chunks of DNA across it and where they come from. The contents of these chunks and order of variation inside them can be called the haplotype. The novelty of comparing haplotypes across the Y chromosome with inherited surname shows that many men who think they are unrelated (despite actually having the same surname) are in fact descendants of common ancestors. In fact, a relatively rare version of the Y chromosome is common in almost all ‘Attenborough’ men that were sequenced! The idea behind all of this is that the Y chromosome appears to be under some strong purifying selection, although what that exactly is we can only guess (but most people believe it is some sexual/social advantage i.e. successful men have successful sons who have successful sons etc.). The personal gain from this talk was the confirmation that the methods behind this sequencing are very similar to mine and they are facing very similar problems to me. Woohoo, I am not alone!
Dr Simon Myers was the second speaker and he described his lab’s work on chromosome painting. When we inherit our chromosomes (one from mum, one from dad) they undergo recombination. That is bits from one chromosome in dad have crossed over and replaced the same bit from the paired chromosome in dad and therefore we get a mixture of both chromosomes from dad in just one chromosome. The same thing happens with the chromosome from mum and suddenly we realise that we have a mix of bits from all 4 grandparents in the 2 chromosomes. The image below goes might help explain that…
Now what his lab have done is trace these bits of chromosome back across many generations and painted all the differently inherited bits in different colours. Well they haven’t manually done this; they have a big fancy computer algorithm to do the maths. But from this information you can look at a modern day person and see how ‘African’ they are or how ‘East Asian’ they are based on their inherited chromosome segments. What’s then nice to do is show that these descriptions of modern populations follow patterns of ancient large-scale and more modern small scale human migration patterns. Plus there are lots of pretty colours to look at…
Dr Daniel Lawson was the first speaker after the beer and pizza break so had a smaller audience to contend with. The talk was a lot more maths/statistics/programming/algorithm stuff that often goes over my head but at least I understood the reasoning behind the concept. I often talk about sequencing and whole genomes but what can be difficult to comprehend is the enormity of this data. The total length of the human genome is over 3 billion base pairs, now multiply that by however many people you are sequencing and your computer can get really slow! Now the genome can supposedly be sequenced in its entirety for $1000 we are going to get a lot more data, but how do we handle this? The current algorithms and models can’t be scaled up easily as the estimates of important parameters actually get worse with more data! We have to look for analytics rather than models to generate our data. Now the rest of the talk was describing the specific algorithm Dr Lawson has been working on which seems to iteratively select a samples to estimate off of but I’d be lying if I said I understood any more. I have a lot of reading to go and do!
Prof Mark Thomas was the final speaker and he works on detecting signals of recent selection using ancient DNA data. Again, I’d like to brush over the statistics and modelling and talk more about the applications and ideas. There are a few aspects of modern humans that have so obviously been strongly selected for. A key one is lactase persistence – the ability to digest lactose from milk. It is a western thing really and you may even know many East Asian descendants who are lactose intolerant. Oddly enough there are many known (and unknown) mutations that lead to the persistence of the enzyme lactase into adulthood. This shows convergent evolution: different pathways have led to the same outcome. The benefit of being able to drink milk and eat dairy was, at some point in the past, so strong in Western Europe that people who couldn’t effectively died out! The map below shows lactase persistence (people who can digest lactose in adulthood) in red and lactose intolerance in blue.
It can be shown that this emergence of lactase persistence did not occur from natural genetic drift and was definitely the result of high selection pressure.The same effect can be seen in the blue eye pigmentation in Western Europe and the development of lighter skin. The question of ‘why?’ is one I don’t think we can ever answer for sure but a lot of people have their own theories. A strong case is put forward for the change from a fishing diet to an agricultural farming one where vitamin D and calcium deficiencies left people needing to be able to drink milk and use UVB rays from the sun to make a form of vitamin D in their skin. However this doesn’t explain the blue eyes part, at all. No one can. I’d speculate that the sudden emergence of a child with blue eyes would either be seen as an outsider or someone special so I wouldn’t be surprised if it just so happened that people with blue eyes simply looked hotter and preferentially reproduced with each other in some form of blue eyed revolution! But like I said, sexual/social selection can only be guessed, but it is fun to do so, I mean, look at this fitty:
First note: the title of this post is the name of a book by Professor Tim Spector. Just thought I’d get that in quick before anyone throws around accusations of plagiarism! And on that same note, this is a post about a talk I went to at my old university (King’s College London – thanks to KCLA for organising it!) by Prof Spector about that same topic his book is about: epigenetics.
Epigenetics is another biologically defined layer to who we are. It sits ‘above’ the genes so to speak and, similar to regulatory elements, can control the amount a gene is expressed without actually being a genetic code that is itself transcribed. The difference is that epigenetics isn’t a genetic code in the same way our DNA is, it is a layer of other changes to the DNA without changing the actual bases written in our genome. Two key examples of these changes are methylation and histone modification. Both are effectively ‘structural’ changes. It is believed that our ‘epigenetic code’ is heritable (although there is some debate over that of histone modifications) and this is where Prof Spector’s talk focussed it’s attention.
Professor Tim Spector works with twins, thousands of them. And what better way to understand heritability of things, stuff, everything to do with who we are! Monozygotic twins have exactly the same DNA but we can tell (once we’ve got past the identical appearances) who is who in a pair through anything from favourite colour to taste in a partner. So how can two people derived from the same egg, the same sperm, the same ‘stuff’ be different? Prof Spector believes that much of this missing heritability lies in our epigenetics. This extra layer of ‘code’ (I’m not keen on calling it code but will use this for now until I think of a better word. It is not code like our DNA is, it is not comprised of bases or chains of molecules) can be affected by our diet, exercise regime and even maternal care. However Prof Spector goes on to suggest that the diet, exercise regime and even maternal care of our parents or even grandparents could affect our epigenetic pattern (possibly a better word?). He also spoke about how our epigenetic pattern (yes a much better word) could be altered, reversed or added to. Surely epigenetics is therefore transient? I therefore feel slightly uneasy at the idea that nurture could alter what we think of as nature in the great debate of who we are and how we become ourselves if it isn’t permanent however Prof Spector put forward some good valid points about family patterns of inheritance not found in the genes.
One thing that has certainly been shown is that our epigenetics do change over time, with MZ twins diverging from one another, a reasonable explanation for differences in identical twins as they get older (1). This leaves me with two questions really, how much of this missing heritability can we attribute to epigenetics? I don’t want to blame my grandparents’ generation for our current obesity epidemic just yet…! and secondly, a question that I’ll have to just read into more probably, could it be possible for epigenetic changes to cause subtle permanent changes to our genome in a way we don’t yet understand and cause a whole new way of creating variation within the population? Just speculation for now, I’ll have a read round and see what I can find but a layer of information on top of the genome (although limited to the possible information within it) surely has plenty of potential?
1) Fraga, Mario F., et al. “Epigenetic differences arise during the lifetime of monozygotic twins.” Proceedings of the National Academy of Sciences of the United States of America 102.30 (2005): 10604-10609.
Information about Professor Tim Spector’s book is found here.