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Ingrida Domarkienėstudies ancient DNA , weaving together fragment of genetic material from modern human and our foresightful - extinct human relative to retell their stories .
From a background in molecular biology and aesculapian genetic science , Domarkienė now spearhead Lithuania ’s first ancientDNAlab , headquartered at theMedical Science Centreat Vilnius University . Along with outside collaborators , the lab is studying the remains of people in mediaeval spate tomb in Poland to learn about social practices that were prevalent in the region at the time , as well as the migrations of Iron Age individuals in Lithuania .
Ingrida Domarkienė, pictured above, and her team at Vilnius University in Lithuania conduct research on ancient DNA.
They ’re also revealing insights into the backwash of the 1986 disaster at theChernobyl atomic power plant . depend at the desoxyribonucleic acid of Lithuanian doer involve in the cleanup after the disaster , the research worker identifiedgenes that aid protect against the upshot of radiation .
Live Science speak with Domarkienė , who is also an associate professor at Vilnius , demand about her research , the singular challenges associate with study ancient DNA , and how delving into our genetic history can pass to aesculapian advances today .
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Studying ancient DNA comes with a whole host of challenges, Domarkienė says.
Emily Cooke : What is it about ancient DNA that you find interesting ?
Ingrida Domarkienė : It ’s fascinating , how you may reassemble stories from DNA piece , you bonk : You just succession DNA ; it ’s kind of the technological affair .
And for me , coming from molecular biological science , it ’s so fascinating that you learn the biochemical sherd , organic molecule , and then you liken it with other samples , and you get a moving-picture show of how people moved , where they hail from , where they fit , how they endure . you could get " admixture signal " — that means that people [ from different population ] mixed , and you may get an estimate of who met whom and how they went on and on , and you may retell [ their ] stories .
DNA from our extinct, distant cousins, the Neanderthals can reveal new insights about our health today.
EC : What are the unique challenges consort with studying ancient DNA ?
ID : The most decisive challenge is that you have to adopt uncertainty and unsuccessful person here . Why is that ? Because you are never quite sure if you will get the quality and amount of deoxyribonucleic acid to work on further .
That ’s because , when an organism give-up the ghost , desoxyribonucleic acid starts to decay , and there ’s nothing there to repair the deoxyribonucleic acid as it is in living cells . So it take off to fragment , and changes in authorship . What ’s more , it intermix with all otherenvironmental DNA , which , when evoke , appears as taint . So , in this event , I care an analogy of a confetti — or what is left of it after a Brobdingnagian celebration .
EC : Can you let the cat out of the bag a bit about your research on Chernobyl survivors ?
ID : Chernobyl survivors — cleanup workers or liquidator , they ’re also call .
It was our project with fellow at the Department of Human and Medical Genetics , and in the group , we had the mind to study the genomes of Chernobyl liquidators , and we invited them to enter in the subject . And when they started come , we heard their stories , and we infer that — you recognize , those the great unwashed hold up through a lot , but still , there were so many of them who were aging quite healthy , without cancers . You could expect the worst upshot after what they ’ve been through , but they were quite OK .
And then we incur this guess : that maybe there is something in the genome of those survivors that protects them from all that bad that happened , let ’s say — also , psychological stress , which was huge back then , when they were hire from where they were at the moment and brought to Chernobyl without articulate a news . They were tell stories of how they were woken up , and they were just there on a gearing going to God get laid where .
And then that was a hard metre , of course , there , and they had not only to work hard through liquidation study , but also attempt to keep reasonable in that kind of place .
So , we started analyzing their genomes , and we find some potential signal of protective variation . And then we also have this new [ as of yet unpublished ] paper write by our scholarly person , which is onmitochondrial DNA . So , those Chernobyl receiver might have protective variants also in the mitochondrial genome and atomic genome [ DNA in the core group ] that keep going mitochondrial subroutine . So perhaps that ’s the approximation .
Related : Chernobyl ’s liquidator did n’t go along on radioactivity damage to their small fry
EC : How can learn our familial chronicle help us address aesculapian challenges today ?
ID : analyse the past through ancient DNA is fundamental inquiry and take time to agnize what the determination are and how they can be enforce in praxis . Perhaps the most crucial ingredient would be a strong interdisciplinary team that you’re able to intrust , and you ca n’t do anything alone , really .
I findSvante Pääbo ’s work as a benchmarking example : How can you babble out about ancient desoxyribonucleic acid without mentioning Svante ’s name ?
He and his team developed the whole field of paleogenomics and generated thereference genome of Neanderthals . They start to give us explanations of what the differences between human and oafish sequences are and what they mean in a useable way . For example , one of Svante Pääbo ’s mathematical group scientist , Dr. Hugo Zeberg , with colleague , found that the Neanderthal variance in the progesterone sense organ is associate with preterm birth , but alsoprotective against stillbirth , and resultant role in more live births . That knowledge can be translate into real help for fair sex to save their gestation .
Or , another making love tale : metagenomics [ the cogitation of genetic cloth from all organisms in an surroundings ] , which is [ an ] even more challenging field . But it can help with infectious diseases , as we just witnessed one of the pandemics — and with the change climate , there might be even more . So while retrace genomes of pathogens and construct phylogenetic trees [ diagram of evolutionary relationships between metal money ] , we can understand the ways pathogens evolve and spread .
With those analyses , we can even start new narration . For example , a long meter ago , it was thought that the Spaniards introduced tuberculosis to the New World . But professorJohannes Krause ’s squad [ at the Max Planck Institute for Evolutionary Anthropology ] showed that the bacteria was there before Columbus was , and evidently it wasbrought and shift to humans by seals , which were a alimentary food for thought for the multitude live there in Peru .
So you’re able to see that , with this field , we can give science and medicine even more .
EC : What do you believe the future of ancient DNA research will take care like ?
ID : From my period of view , I think that with the fast - evolving technology , we will be able to go deeply in the sequences , wider in the datasets , and more diverging marker that we take apart .
Because now , we usually analyze single base polymorphisms , or SNPs [ pronounced " snipping , " which are variations in exclusive edifice blocks of DNA ] , as we call them . But my dream would be to remodel written matter bit variation , which are the huge lump of [ repeated ] DNA , and it ’s not potential to do that now , but there are initiatives to do that .
We can also go for psychoanalysis of epigenomic mark [ change to DNA across the genome that alter the bodily function of cistron without affecting the underlying sequence ] , which are very good markers for analysis of how the genome is regulated — to understand how it was back then . Those epigenomic marker also would be of great value .
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And besides analytic thinking of sociocultural structures of ancient internet site , I would say research will definitely be direct towards understand the working meaning of the DNA variance that we analyze .
And in the grand finale , we would be integrate the whole data of theholobiome . That means all genomic information from the environment — not only humans , but also bacteria , computer virus , plants , animals , everything who hold up there . And integrating this information not only from the unlike field , but also with different method acting we have . Because the data come using different methods , and that would be nice to integrate everything . And perhaps then we will have the concluded picture .
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