Lifeboat Foundation: Safeguarding Humanity
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Category: genetics

Researchers at Umeå university in Sweden have published a new study showing that the gut bacteria can carry information of past experiences of an altered environment from parents to offspring. Eggs and sperm are not the only information carriers from one generation to the next.

Eggs and transmit genetic from one generation to the next. The genetic information contains the blueprint for how to assemble a functional offspring. Most of this information is hardcoded in DNA and cannot be altered by experiences such as changes to the environment.

However, in the last decades, it has been shown that some effects of various lifestyles can be transmitted from to offspring through both the egg and the sperm. This study shows for the first time that also the , which are in general also transmitted from parents to offspring, are capable of transmitting information about what environment the parents were exposed to, to the offspring.

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A new study by Calico found that our genes determine our lifespan much less than previously accepted and lifespan heritability is less than seven percent.

Although long life tends to run in families, genetics has far less influence on life span than previously thought, according to a new analysis of an aggregated set of family trees of more than 400 million people. The results suggest that the heritability of life span is well below past estimates, which failed to account for our tendency to select partners with similar traits to our own. The research, from Calico Life Sciences and Ancestry, was published in Genetics.

“We can potentially learn many things about the biology of aging from human genetics, but if the heritability of is low, it tempers our expectations about what types of things we can learn and how easy it will be,” says lead author Graham Ruby. “It helps contextualize the questions that scientists studying aging can effectively ask.”

Ruby’s employer, Calico Life Sciences, is a research and development company whose mission is to understand the biology of aging. They teamed up with scientists from the online genealogy resource Ancestry, led by Chief Scientific Officer Catherine Ball, to use publicly available pedigree data from Ancestry.com to estimate the heritability of human life span.

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“There was something else, too – something weirder. Of all the non-human DNA fragments the team gathered, 99 percent of them failed to match anything in existing genetic databases the researchers examined. We found a whole new class of human-infecting ones that are closer to the animal class than to the previously known human ones, so quite divergent on the evolutionary scale.”

A landmark Stanford 2017 study indicates that more than 99 percent of the microbes inside us are unknown to science. The survey of DNA fragments circulating in the blood suggests the microbes living within us are vastly more diverse than previously known. In fact, 99 percent of that DNA has never been seen before.

A new survey of DNA fragments circulating in human blood suggests our bodies contain vastly more diverse microbes than anyone previously understood. What’s more, the overwhelming majority of those microbes have never been seen before, let alone classified and named, Stanford researchers reported in the Proceedings of the National Academy of Sciences.

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Almost half of our DNA sequences are made up of jumping genes—also known as transposons. They jump around the genome in developing sperm and egg cells and are important to evolution. But their mobilization can also cause new mutations that lead to diseases, such as hemophilia and cancer. Remarkably little is known about when and where their movements occur in developing reproductive cells, the key process that ensures their propagation in future generations, but can lead to genetic disorders for the hosts.

To address this problem, a team of Carnegie researchers developed new techniques to track the mobilization of jumping genes. They found that during a particular period of , a group of jumping-genes called retrotransposons hijacks special called nurse cells that nurture the developing eggs. These jumping genes use nurse cells to produce invasive material (copies of themselves called ) that move into a nearby egg and then mobilize into the egg’s DNA. The research is published in the July 26 on-line issue of Cell.

Animals have unwittingly developed a powerful system to suppress jumping gene activity that uses small, non-coding RNAs called piRNAs, which recognize jumping genes and suppress their activity. Occasionally, jumping genes still manage to move, suggesting that they employ some special tactics to escape piRNA control. However, tracking the mobilization of jumping genes to understand their tactics has been a daunting task.

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An ambitious effort to sequence the genome of every complex organism on Earth was officially launched on 1 November in London.

“Variation is the fount of all genetic knowledge,” says project member and evolutionary geneticist Jenny Graves of La Trobe University in Melbourne, Australia. “The more variation you have the better — so why not sequence everything?”

The Earth BioGenome Project aims to sequence the genomes of the roughly 1.5 million known animal, plant, protozoan and fungal species — collectively known as eukaryotes — worldwide over the next decade. The initiative is estimated to cost US$4.7 billion, although only a small proportion of that money has been committed so far.

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New research shows how police could use forensic DNA to track down a suspect’s relatives in genealogy databases that store a different kind of genetic data—and that were never intended for use in police investigations.

In other words, if your sibling leaves DNA at a crime scene, it could lead detectives to your door. That suggests new investigative possibilities for police—and also new concerns about genetic privacy and whether authorities who use forensic DNA in creative ways might be overstepping their bounds, says Noah Rosenberg, a professor of biology at Stanford University and senior author of a study, which appears in Cell.

“The potential to link people’s genotypes across databases has been developing for some time. It is both of interest and concerning, depending on one’s point of view,” says Rosenberg, who is also a member of Stanford Bio-X.

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