We have been looking for the mysterious ancestor town of the Indo -Europeans. We have a new track in DNA

We know that Latin languages ​​have their common origin in Latin peoples such as the one that ended up forging the Roman Empire. We know that Germanic languages ​​had their origin in the Germanic tribes that at that same time inhabited northern Europe. But these two language families have a common trunk that goes back to prehistory, the language protoindoeuropeo. Now, who spoke this language? CLV. A new study He has discoveredthrough a genetic analysis in several archaeological sites in Europe, a new prehistoric group, an archaic society that they have called people of the Caucasus-Bajo Volga or CLV (Caucasus-Lower Volga). As the study concludes, this town could be linked to the protoindo -European language and with Its expansion. The protoindoeuropeo. The protoindoeuropeo (foot) language is the “common ancestor” of numerous contemporary languages, including Spanish and the rest of languages ​​spoken in the Peninsula (except Basque). A list that includes from English to Persian, through Russian and Greek. It is estimated that about half of the world population speaks languages ​​with this origin. This language would have been the speech of one or more prehistoric peoples of the border region between Europe and Asia. The migrations starring this group would have given rise to the speakers of this language ending their linguistic imprint in much of Eurasia. And more than linguistics, also genetics. From Yamnaya to Clv. Genetics had already given us important clues about these peoples, allowing us The so -called Yamnaya culturea population that would have inhabited the steppes north of the Caspian between the years 3,300 and 2,600 before our era. These analyzes had focused on this culture as probable vector of Indo -European expansion around the year 3,100 aec But there was a problem with its own name: the Anatolias languages, a group of languages ​​already extinct among which was included, for example, the hitita. These languages ​​would have been the first to break down from the common Indo -European trunk, before acquiring “steppe features.” This implied that this separation would have occurred before the arrival of Yamnaya culture and that there should be a protoindo -European group prior to this from which both anatolias languages ​​arose and those that would later derive in the Greek, Latin or Celta. Now, the new Study points to the people of the CLV as possible common ancestors of both. More than 4,000 years ago. All thanks to genetics. The new work studied the DNA of 435 individuals found in various archaeological sites in Eurasia, covering a period between the years6,400 and 2,000 AEC the details of the study were broken down In an article Posted in the magazine Nature. Missing link. Genetic analysis pointed out that Yamnaya’s group would have inherited about 80% of its ancestry of the CLV population, which in turn would have legacked about 10% of its ancestry to the anatolians. This makes this mysterious group the common ancestors of the populations that initiated the expansion of Indo -European languages ​​during the Copper Age. In Xataka | Looking for money, they found gold: this was Dmanisisis Gora, the megafortiness of the Caucasus built 3,000 years ago Image | XVODOLAZX / Denis Vitchenko

Europe has the highest rate of multiple sclerosis in the world. The explanation lies in the DNA of the steppe shepherds

First there were hunter-gatherers about 45,000 years ago. The first modern humans arrived in a Europe where the Neanderthals still reigned. Then there were the farmers of the Middle East about 11,000 years ago and finally, about 5,000 years ago they were the nomadic pastoralists of the steppes of Central Asia. That is, according to research published in the journal Naturethe common genetic heritage of Europeans. A heritage that explains why, in an incredible historical twist, multiple sclerosis affects us more. A DNA mutating in the middle of the great steppe. While agriculture gained weight in the world, the great Eurasian steppe continued doing its thing. The culture yamnaa group of pastoral towns that arose in the enormous plains south of the Urals and east of the Black Sea, generations and generations passed living with livestock. Variant. It was there that it emerged (and was selected) a small genetic variant that strengthened natural immunity against zoonoses; that is, against livestock infections that could easily jump to the human communities that raised them. 5,000 years later, this genetic variant is behind the fact that Europeans have a higher risk of suffering from Multiple Sclerosis. The deep origins of current diseases. The study led by the Universities of Cambridge and Copenhagen (but with the participation of many more) analyze in detail from the DNA of almost 5,000 individuals spread throughout history. Some studied remains date back to about 34,000 years ago. The reconstruction. Reconstructing humanity’s immense genetic tree, researchers found numerous keys to understanding why there are specific geographic areas or ethnic groups that suffer from some diseases more than others. They realized that southern Europeanswith a greater genetic legacy from the agricultural people of the Middle East, have a greater predisposition to develop bipolar disorders; that people from the East had a higher genetic risk of developing Alzheimer’s or diabetes; and those from the northwest had a heightened risk of sclerosis. A medical enigma. For years, scientists have tried to understand why Europe has, with about 143 cases per 100,000 inhabitants, one of the highest incidence rates of sclerosis in the world. As I said in the previous paragraph, as you go south and east those differences fade, but (even so) the greater risk of developing this disease It is a European ‘differential fact’. Understanding better. The most interesting thing about all this is that the idea that the answer lies in the genetic history of its inhabitants It is not only a historical curiosity. On the contrary, thinking about this from an evolutionary point of view allows us to understand the disease in a new way. In Xataka | Where genes, do what you see: the surprising genetic differences (and similarities) within the Iberian Peninsula Image | Charlotte Venema *An earlier version of this article was published in January 2024

We are wrong about the origin of sunburn

We all know that if we spend a lot of time exposed to the sun without protection we will burn The skin becomes red, hot and inflamed and hurts with a simple touch. Then it peels off and for days we can barely touch each other. That’s clear, we don’t need science to explain it to us because practically all of us have experienced it at some point. However, we were wrong about the origin of those sunburn. We have always thought it was due to DNA damage. That’s what the textbooks say. Now, however, an international team of scientists has shown that, in reality, they are the RNA damage those that give rise to that unpleasant effect. These researchers, coming from the University of Copenhagen and Nanyang Technological Universityin Singapore, they carried out their experiments both in mice as in human skin cell cultures. This is very important, since not everything that is studied in mice can be extrapolated to humans, but cell cultures can help understand the effects on our species. With both types of experiments they observed that the response to RNA damage is much faster. At least, it is the one that seems to be closely related to sunburn. It may seem that this does not give us any interesting information. What does it matter if it’s DNA or RNA? Sunburns hurt just the same! And yes, that’s true, but this seemingly trivial fact It can help us a lot in the future. DNA or RNA? DNA is the instruction book of an organism. It contains all the information about who we are and what we need to stay alive. Our DNA contains the instructions to synthesize insulin when glucose builds up in the blood or to help us sleep through melatonin when night falls. They also include data about the color of our eyes or the way our hair grows. Everything we are is in DNA. All our cells have the same DNA, but not all DNA is used in all cells. For example, the gene with the instructions to synthesize insulin is in the cells of the eye, but it is not necessary there. It will never be used. Yes, it is necessary in the cells of the pancreas, since it is the organ that is responsible for synthesizing it. It is used there. This use of a specific gene is what is known as gene expression. The gene turns on where and when it is needed. In this case, in the cells of the pancreas (where), when glucose accumulates in the blood (when). Differences between DNA and RNA. Credit: Sponk (Wikimedia Commons) We already know what DNA is. Something more or less immutable. It can undergo mutations, but it remains more or less fixed throughout our lives. On the other side we have RNA. This is another nucleic acid. DNA is deoxyribonucleic acid and RNA is ribonucleic acid. It differs in the presence of a different sugar within the molecule: ribose In the case of RNA and deoxyribose in the case of DNA. There are many types of RNA: transfer RNA, ribosomal RNA, messenger RNA… Each one has a function, but in this case we are going to focus on the messenger, since it is the one mentioned in the study of sunburn. We have already seen that DNA is used only when and where it is necessary. This use consists of using the information contained in a gene to build a protein, which will carry out the desired function. These proteins are synthesized in cellular organelles called ribosomes. But there is a problem. Ribosomes are unable to read DNA. said very roughly speaking, It is a language they do not understand. They understand the language of messenger RNA. Therefore, when a gene is to be expressed, its information is transcribed into messenger RNA. Like when we translated a page from an instruction book that was in English into Spanish so that our grandmother knew how to use the washing machine. That is the function of messenger RNA. With this well learned, we can move on to the next thing. What does all this have to do with sunburn? Sunburn is caused by exposure to the Sun’s radiation. Specifically, ultraviolet raysespecially type B (UVB). This generates DNA damage, it is totally true. In fact, these DNA damages can accumulate and eventually lead to a melanoma. None of that has changed. However, we usually think that sunburns are that first warning that DNA has been damaged and, in reality, it turns out that it has not. It is the messenger RNA the one who gets upset. How UVB affects ZAK signaling pathways to cause sunburn symptoms. (Lind et al., Molecular Cell, 2025) After reading the literature and carrying out several experiments, the authors of the study that has just been published thought that sunburn could be related to a protein called ZAK-alpha. This is involved in the response to something known as ribotoxic stress. That is, when a failure is detected in the messenger RNA, this protein starts the immune system to attack the cells in which this damage is found, so that the altered messenger RNA not translated on the ribosome. If that happened, you would get failed proteins and could be dangerous. This immune system response also launches an inflammatory response. The skin turns red, becomes hot, swells… What does it sound like to you? Indeed, sunburn! This entire cascade of reactions to ultraviolet radiation was detected in human skin cell cultures. But what would happen in a living organism? The scientists tried to genetically modify a group of mice so that the gene with the instructions for synthesizing the ZAK-alpha protein was not present. If there was no ZAK alpha, when the mice were exposed to ultraviolet B radiation They did not experience burns. On the other hand, with ZAK-alpha intact they did. What is the use of knowing all this? The authors of the research believe that this new … Read more

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