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The Evolutionary Perspective
Daily Archives: July 31, 2017
human Mars: Mars Colonization Timeline
Posted: July 31, 2017 at 9:50 am
Inspired from FutureTimeline.net and the Integrated Space Plan we have created a speculated timeline of human exploration and colonization of Mars. Predictions are based on a reasonably optimistic evaluation of technological and social progress of humanity. Only the most important and innovative events are mentioned. Timeline is regularly updated taking into account latest developments. Last update was made on 30th July, 2017.
The timeline will get a major update when SpaceX will reveal its updated plan for Mars later this year.
2036 The ISRU capabilities of Mars Base Alphaare extended not only to produce air, water and rocket fuel, but also steel, bricks, cement and basic fertilizers, plastics and silica products (as glass). Some industrial size 3D printers are also assembled, as well as equipment to make Martian soil usable in the greenhouse. First reality show on Mars is transmitted to Earth and called "Mars One" 🙂 2037 First child is born on Mars atMars Base Alpha. His voyage to Earth later in his life would be dangerous because of his bones and organs not being fit for Earth's gravity. 2037 NASA's 1st crew leaves Mars. 2037 Blue Origin's 1st crew leaves Mars. 2037 Second full-crew ITS spaceship with 100 human colonists and workers lands at Mars Base Alpha, which now has a population of more than 200. Among them is SpaceX's founder Elon Musk.
2040 Two moreITSspaceships with 200 human colonists, workers and somewealthy tourists landatMars Base Alpha.
2040 3rd Blue Origin's crew lands at Blue Mars base, which now has a population of ~50.
Mars becomes practically self-sufficient, having to import only the most complex goods and intellectual property.
The self-sufficiency results in Mars becoming an independent nation-state. The Martian government has to buy up the non-Martian governmental assets located on Mars.
As a technologically advanced frontier society Mars and orbital stations around it become the primary source of specialists and workers needed for human bases and missions further in Main asteroid belt and outer Solar system.
Air pressure and temperature on Mars is increased to the level where there is flowing water on the surface and simple plants can be introduced into newly created biosphere of the planet.
As one of the lower regions on Mars close to the equator Valles Marineris is seeing the most benefits from terraformation activities and Phobos space elevator; cities and farming communities are spreading throughout the valleys and at the end of the 22nd century there are nearly 5 million people living in Valles Marineris. It's the most populous urban area on Mars.
In the 22nd century the total human population on Mars increases 30-fold - to more than 30 million.
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Genetic engineering creates an unnaturally blue flower – Engadget
Posted: at 9:49 am
The approach is generic enough that you could theoretically apply it to other flowering plants. Blue roses, anyone? There are broader possibilities, too. While the exact techniques clearly won't translate to other lifeforms, this might hint at what's required to produce blue eyes or feathers. And these color changes would be useful for more than just cosmetics. Pollinating insects tend to prefer blue, so this could help spread plant life that has trouble competing in a given habitat.
Just don't count on picking up a blue bouquet. You need a permit to sell any genetically modified organism in the US, and there's a real concern that these gene-modified flowers might spread and create havoc in local ecosystems. The research team hopes to make tweaked chrysanthemums that don't breed, but that also means you're unlikely to see them widely distributed even if they do move beyond the lab. Any public availability would likely hinge on a careful understanding of the flowers' long-term impact.
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Genetic engineering creates an unnaturally blue flower - Engadget
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‘True blue’ chrysanthemum flowers produced with genetic … – Nature – Nature.com
Posted: at 9:49 am
Naonobu Noda/NARO
Giving chrysanthemums the blues was easier than researchers thought it would be.
Roses are red, but science could someday turn them blue. Thats one of the possible future applications of a technique researchers have used to genetically engineer blue chrysanthemums for the first time.
Chyrsanthemums come in an array of colours, including pink, yellow and red. But all it took to engineer the truly blue hue and not a violet or bluish colour was tinkering with two genes, scientists report in a study published on 26 July in Science Advances1. The team says that the approach could be applied to other commercially important flowers, including carnations and lilies.
Consumers love novelty, says Nick Albert, a plant biologist at the New Zealand Institute for Plant & Food Research in Palmerston North, New Zealand. And people actively seek out plants with blue flowers to fill their gardens.
Plenty of flowers are bluish, but its rare to find true blue in nature, says Naonobu Noda, a plant researcher at the National Agriculture and Food Research Organization near Tsukuba, Japan, and lead study author. Scientists, including Noda, have tried to artificially produce blue blooms for years: efforts that have often produced violet or bluish hues in flowers such as roses and carnations. Part of the problem is that naturally blue blossoming plants arent closely related enough to commercially important flowers for traditional methods including selective breeding to work.
Most truly blue blossoms overexpress genes that trigger the production of pigments called delphinidin-based anthocyanins. The trick to getting blue flowers in species that arent naturally that colour is inserting the right combination of genes into their genomes. Noda came close in a 2013 study2 when he and his colleagues found that adding a gene from a naturally blue Canterbury bells flower (Campanula medium) into the DNA of chrysanthemums (Chrysanthemum morifolium) produced a violet-hued bloom.
Noda says he and his team expected that they would need to manipulate many more genes to get the blue chrysanthemum they produced in their latest study. But to their surprise, adding only one more borrowed gene from the naturally blue butterfly pea plant (Clitoria ternatea) was enough.
Anthocyanins can turn petals red, violet or blue, depending on the pigments structure. Noda and his colleagues found that genes from the Canterbury bells and butterfly pea altered the molecular structure of the anthocyanin in the chrysanthemum. When the modified pigments interacted with compounds called flavone glucosides, the resulting chrysanthemum flowers were blue. The team tested the wavelengths given off by their blossoms in several ways to ensure that the flowers were truly blue.
The quest for blue blooms wouldn't only be applicable to the commercial flower market. Studying how these pigments work could also lead to the sustainable manufacture of artificial pigments, says Silvia Vignolini, a physicist at the University of Cambridge, UK, who has studied the molecular structure of the intensely blue marble berry.
Regardless, producing truly blue flowers is a great achievement and demonstrates that the underlying chemistry required to achieve 'blue' is complex and remains to be fully understood, says Albert.
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'True blue' chrysanthemum flowers produced with genetic ... - Nature - Nature.com
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Can genetic modification turn annual crops into perennials? – Genetic Literacy Project
Posted: at 9:49 am
The last several decades have witnessed a remarkable increase in crop yields doubling major grain crops since the 1950s. But a significant part of the world still suffers from malnutrition, and these gains in grains and other crops probably wont be enough to feed a growing global population.
These facts have put farmers and agricultural scientists on a quest to squeeze more yield from plants (and livestock), and how to make these yield increases more sustainable. The best land is already taken and could be altered by climate changes, so new crops may have to be grown in less hospitable locations, and the soils and nutrition in existing lands need to be better preserved.
Several methods are being used to boost yields with less fertilizer or pesticides, including traditional combination techniques, marker-assisted breeding, and, of course, trans- and cis-genic modifications.
One way to get more food from a plant is through another genetic switch. It may be possible to genetically, either through hybridization, mutagenesis, or genetic engineering to alter a plant so that it transforms from an annual (one you have to replant every year) to a perennial (which you plant once and can thrive for many years).
This video from Washington State University discusses some advantages of perennial crops:
Most staples, like corn, wheat, sorghum and other grains are annuals. About 75 percent of US and 69 percent of global croplands are cereal, oilseed and legumes, and all of those are annuals, said Jerry Glover, plant geneticist at the Land Institute in Salina, Kansas, and John Reganold, a geneticist at Washington State University. This means, they wrote:
They must be replanted each year from seed, require large amounts of expensive fertilizers and pesticides, poorly protect soil and water, and provide little habitat for wildlife. Their production emits significant greenhouse gases, contributing to climate change that can in turn have adverse effects on agricultural productivity.
Perennials, meanwhile, have longer growing seasons and more extensive roots, making them more productive, and more efficient at capturing nutrients and water from the soil. Replanting isnt necessary, reducing pesticide and fertilizer use, and reducing the need to use tractors and other mechanical planters in fields. Erosion also can be reduced. Its been estimated that annual grains can lose five times more water and 35 times more nitrate than perennial grains. All plants at one time were perennials, and breeders and farmers concentrated on breeding new annuals that could meet a farmers (and consumers) needs.
Now, the table has turned. Genetics may make the annual-to-perennial transformation easier. The switch to perennials is not a new avenue of research, but its been a rocky road. Scientists in the former USSR and the US tried to create perennial wheat in the 1960s, but the offspring plants were sterile and didnt deliver on desired traits. Since then, scientists worldwide have looked at deriving perennials from annual and perennial parents using molecular markers tied to desirable traits (and the genes responsible for them). This technique, and knowing the genotypes of more and more plants, has made it possible to combine desirable genes with traditional and genetic engineering methods to find these desirable perennial plants.
Glover has pointed out that molecular markers tied to desirable traits (higher yields, disease resistance, etc.) can allow for faster breeding by determining the sources of plant variation, and that plant genomics has facilitated the combination of genes without having to field test over years at a time. Genetic modifications can also help spur this along.
Andrew Paterson, head of the plant genome laboratory at the University of Georgia, has studied for years the development of perennial sorghum one of the top five cerealon the planet. Sorghums drought resistance has made it useful as a grain and biomass source in degraded soil, and a perennial version (which has happened spontaneously twice) could reduce drought losses even to other crops. Patersons genetic analysis of wild perennials and cultivated annuals has shown the genes involved in perennial ism and offered DNA markers for more precise breeding.
Techniques like CRISPR/Cas9, which can precisely edit, insert or delete genes at specific locations, are being studied for their possible role in transforming perennials, but a few challenges remain. Chung-Jui Tsai at the University of Georgia, recently showed that CRISPR could be used to alter genes in existing perennials (like fruit and nut trees, for example), once some hurdles like frequent polymorphisms and other variations could be overcome.
Still others are not so optimistic about using genetic modification to enact the perennial-annual switch. First, the whole field would require much more research funding than currently exists, Glover warns. Then, as Paterson told Brooke Borel in her article in Popular Science, perennial traits are much more complicated than those currently addressed by genetic engineering. We dont really know all of the genes involved, not yet:
We dont actually have any of the genes in hand. We know where they are in the genome and we are working on their locations more and more finely, but there arent any of these genes that we can yet point to the specific gene among the 30,000 or so in sorghum. Even if they did know the exact genes, most GMOs that are currently available only insert a single new trait rather than information from multiple genes. The technology isnt yet able to handle something so complicated as perennialism.
Andrew Porterfieldis a writer, editor and communications consultant for academic institutions, companies and non-profits in the life sciences. He is based in Camarillo, California. Follow@AMPorterfieldon Twitter.
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Can genetic modification turn annual crops into perennials? - Genetic Literacy Project
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Editing human embryos with CRISPR is moving ahead now’s the time to work out the ethics – Phys.Org
Posted: at 9:49 am
July 31, 2017 by Jessica Berg, The Conversation Theres still a way to go from editing single-cell embryos to a full-term designer baby. Credit: ZEISS Microscopy, CC BY-SA
The announcement by researchers in Portland, Oregon that they've successfully modified the genetic material of a human embryo took some people by surprise.
With headlines referring to "groundbreaking" research and "designer babies," you might wonder what the scientists actually accomplished. This was a big step forward, but hardly unexpected. As this kind of work proceeds, it continues to raise questions about ethical issues and how we should we react.
What did researchers actually do?
For a number of years now we have had the ability to alter genetic material in a cell, using a technique called CRISPR.
The DNA that makes up our genome comprises long sequences of base pairs, each base indicated by one of four letters. These letters form a genetic alphabet, and the "words" or "sentences" created from a particular order of letters are the genes that determine our characteristics.
Sometimes words can be "misspelled" or sentences slightly garbled, resulting in a disease or disorder. Genetic engineering is designed to correct those mistakes. CRISPR is a tool that enables scientists to target a specific area of a gene, working like the search-and-replace function in Microsoft Word, to remove a section and insert the "correct" sequence.
In the last decade, CRISPR has been the primary tool for those seeking to modify genes human and otherwise. Among other things, it has been used in experiments to make mosquitoes resistant to malaria, genetically modify plants to be resistant to disease, explore the possibility of engineered pets and livestock, and potentially treat some human diseases (including HIV, hemophilia and leukemia).
Up until recently, the focus in humans has been on changing the cells of a single individual, and not changing eggs, sperm and early embryos what are called the "germline" cells that pass traits along to offspring. The theory is that focusing on non-germline cells would limit any unexpected long-term impact of genetic changes on descendants. At the same time, this limitation means that we would have to use the technique in every generation, which affects its potential therapeutic benefit.
Earlier this year, an international committee convened by the National Academy of Sciences issued a report that, while highlighting the concerns with human germline genetic engineering, laid out a series of safeguards and recommended oversight. The report was widely regarded as opening the door to embryo-editing research.
That is exactly what happened in Oregon. Although this is the first study reported in the United States, similar research has been conducted in China. This new study, however, apparently avoided previous errors we've seen with CRISPR such as changes in other, untargeted parts of the genome, or the desired change not occurring in all cells. Both of these problems had made scientists wary of using CRISPR to make changes in embryos that might eventually be used in a human pregnancy. Evidence of more successful (and thus safer) CRISPR use may lead to additional studies involving human embryos.
What didn't happen in Oregon?
First, this study did not entail the creation of "designer babies," despite some news headlines. The research involved only early stage embryos, outside the womb, none of which was allowed to develop beyond a few days.
In fact, there are a number of existing limits both policy-based and scientific that will create barriers to implanting an edited embryo to achieve the birth of a child. There is a federal ban on funding gene editing research in embryos; in some states, there are also total bans on embryo research, regardless of how funded. In addition, the implantation of an edited human embryos would be regulated under the federal human research regulations, the Food, Drug and Cosmetic Act and potentially the federal rules regarding clinical laboratory testing.
Beyond the regulatory barriers, we are a long way from having the scientific knowledge necessary to design our children. While the Oregon experiment focused on a single gene correction to inherited diseases, there are few human traits that are controlled by one gene. Anything that involves multiple genes or a gene/environment interaction will be less amenable to this type of engineering. Most characteristics we might be interested in designing such as intelligence, personality, athletic or artistic or musical ability are much more complex.
Second, while this is a significant step forward in the science regarding the use of the CRISPR technique, it is only one step. There is a long way to go between this and a cure for various disease and disorders. This is not to say that there aren't concerns. But we have some time to consider the issues before the use of the technique becomes a mainstream medical practice.
So what should we be concerned about?
Taking into account the cautions above, we do need to decide when and how we should use this technique.
Should there be limits on the types of things you can edit in an embryo? If so, what should they entail? These questions also involve deciding who gets to set the limits and control access to the technology.
We may also be concerned about who gets to control the subsequent research using this technology. Should there be state or federal oversight? Keep in mind that we cannot control what happens in other countries. Even in this country it can be difficult to craft guidelines that restrict only the research someone finds objectionable, while allowing other important research to continue. Additionally, the use of assisted reproductive technologies (IVF, for example) is largely unregulated in the U.S., and the decision to put in place restrictions will certainly raise objections from both potential parents and IVF providers.
Moreover, there are important questions about cost and access. Right now most assisted reproductive technologies are available only to higher-income individuals. A handful of states mandate infertility treatment coverage, but it is very limited. How should we regulate access to embryo editing for serious diseases? We are in the midst of a widespread debate about health care, access and cost. If it becomes established and safe, should this technique be part of a basic package of health care services when used to help create a child who does not suffer from a specific genetic problem? What about editing for nonhealth issues or less serious problems are there fairness concerns if only people with sufficient wealth can access?
So far the promise of genetic engineering for disease eradication has not lived up to its hype. Nor have many other milestones, like the 1996 cloning of Dolly the sheep, resulted in the feared apocalypse. The announcement of the Oregon study is only the next step in a long line of research. Nonetheless, it is sure to bring many of the issues about embryos, stem cell research, genetic engineering and reproductive technologies back into the spotlight. Now is the time to figure out how we want to see this gene-editing path unfold.
Explore further: In US first, scientists edit genes of human embryos (Update)
This article was originally published on The Conversation. Read the original article.
For the first time in the United States, scientists have edited the genes of human embryos, a controversial step toward someday helping babies avoid inherited diseases.
(Phys.org)A team of researchers in China has announced that they have performed gene editing on human embryos. In their paper uploaded to the open access site Protein & Cell (after being rejected by Nature and Science) ...
(Medical Xpress)A team of researchers at Guangzhou Medical University in China has published a paper in the Journal of Assisted Reproduction and Genetics describing their efforts to genetically modify a human embryo using ...
This week, scientists gathered in Washington, DC for the International Summit on Human Gene Editing to discuss a technology called CRISPR-CAS9, which can insert, remove and change the DNA of basically any organism. It is ...
Scientists from The University of Texas at Austin took an important step toward safer gene-editing cures for life-threatening disorders, from cancer to HIV to Huntington's disease, by developing a technique that can spot ...
Don't expect designer babies any time soonbut a major new ethics report leaves open the possibility of one day altering human heredity to fight genetic diseases, with stringent oversight, using new tools that precisely ...
A transparent ranking system for measuring the socio-economic impact of plants and animals that are introduced by humans to areas where they do not naturally occur (termed "aliens") has been developed by an international ...
The field of medicine has come a long way from using heroine as a cough remedy or magnet therapy to improve blood flow. These outdated methods were put to bed decades ago. But there are plenty of ancient medicinal practices ...
The announcement by researchers in Portland, Oregon that they've successfully modified the genetic material of a human embryo took some people by surprise.
Methylation and nitric oxide (NO)-based S-nitrosylation are highly conserved protein posttranslational modifications that regulate diverse biological processes, including abiotic stress responses. However, little is known ...
Choosing between sex or sleep presents a behavioral quandary for many species, including the fruit fly. A multi-institution team has found that, in Drosophila at least, males and females deal with these competing imperatives ...
Cell division is an essential process in humans, animals and plants as dying or injured cells are replenished throughout life. Cells divide at least a billion times in the average person, usually without any problem. However, ...
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Biblical mystery solved: Ancient Canaanites DNA lives on in Lebanese – Genetic Literacy Project
Posted: at 9:49 am
The Canaanites lived at the crossroads of the ancient world. They experienced wars, conquests and occupations for millennia, and as a result evolutionary geneticists expected that their DNA would become substantially mixed with incoming populations.
Astonishingly, new genetic analysis shows that scientists were wrong. According to a new study in the American Journal of Human Genetics, todays Lebanese share a whopping 93% of their DNA with the ancient Canaanites.
One of five Canaanites found buried in present-day Lebanon from which scientists extracted and sequenced DNA. Photo by Dr. Claude Doumet-Serhal/the Sidon excavation
Archaeologists at the Sidon excavation site have been unearthing ancient Canaanite secrets for the last 19 years in the still-inhabited Lebanese port city
They sequenced the whole genomes of five individuals found in Sidon who lived about 3,700 years ago. The team then compared the genomes of these ancient Canaanites with those of 99 Lebanese people currently living in the country, along with the previously published genetic information from modern and ancient populations across Europe and Asia.
This evidence supports the idea that different Levantine cultural groups such as the Moabites, Israelites, and Phoenicians may have had a common genetic background, the authors said.
The findings have powerful cultural implicationsIn a country struggling with the ramifications of war and a society fiercely divided along political and sectarian lines, religious groups have often looked to an uncertain history for their identities.
The GLP aggregated and excerpted this article to reflect the diversity of news, opinion, and analysis. Read full, original post: The DNA of ancient Canaanites lives on in modern-day Lebanese, genetic analysis shows
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Biblical mystery solved: Ancient Canaanites DNA lives on in Lebanese - Genetic Literacy Project
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Scientists from US Have Successfully Edited Human DNA – News4C
Posted: at 9:49 am
Scientists from U.S Have Successfully Edited Human DNA By using CRISPR technology, a team of scientists from Oregon has edited the genes in human embryos and made huge steps in reaching new results. They tried to eradicate genetically transmitted diseases.
CRISPR isnt a new technology but it has started being used in human genetics recently. CRISPR is a DNA sequence that was found in bacteria and could protect the immune system, detecting and destroying invaders such as viruses that try to infect the bacteria. Scientists try to use CRISPS so that they target mutations that would cause diseases, this way treating them from the root of DNA encoding.
Major issues were solved using gene-altering technology.
The lead researcher Shoukhrat Mitalipov from the Oregan Health and Science University stated that they solved their previous problems they had with CRISPR gene-altering technology. In 2015 they faced a problem using this technology, resulting in embryos suffering a condition named mosaicism due to CRISPR that aligned edited and unedited cells.
In the early 2017 China went through a similar problem at the Hospital Guangzhou Medical University.
They tried to repair abnormal embryos and the results were not satisfying. They also used normal embryos resulted from immature eggs and fertilized them with sperm that carried genetic disease. Before the cell division started, they injected CRISPR and out of 6 embryos, half were repaired but with a problem: two of them were suffering from mosaicism.
New ground has been broken later by Mitalipov and his team.
In Oregon Mitalipov and his team were able to inject CRISPR into the eggs while they fertilized them with sperm and avoided moisaicism. They also solved the problem of genetic disease transmission, correcting the genes.
Were still waiting for official results from the Oregon Health and Science University and Shoukhrat Mitalipov through a published paper which will soon appear in a scientific journal.
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Scientists from US Have Successfully Edited Human DNA - News4C
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Wade genealogy info boosted by DNA test – Fairfield Daily Republic
Posted: at 9:49 am
My oldest brother Orvis recently submitted his DNA to Mountain View personal genomics and biotechnology company 23andMe. Hed been interested in finding out details of his genealogy for some time and finally bit the bullet.
Orvis submitted his saliva samples and got his results back in about six weeks. The cool thing is that he got a special deal where the regular $100 price was reduced to $80. The cooler thing is that brothers unless they are identical twins share 50 percent of the same DNA. Thats close enough for me to pay $0 and get a column out of it.
Here are Orviss test results:
Sub-Saharan African 72.7%European 23.4%East Asian & Native American 2.9%South Asian 0.5%Unassigned 0.6%
The fact that our ancestors were from Africa is not a surprise. The website breaks it down further. The lions share (68.9 percent) of our distant relatives came from West Africa. This is what the website says: Expanding from Senegal to Nigeria, West Africa composes about a fifth of the African continent. West Africans have a long shared history, and were united by large empires such as the Ghana Empire, dating as far back as the eighth century AD.
The great thing about the DNA results is that they can be combined with another chunk of information we already had, a 20-page document called The Wade Genealogy. I got it from a Texas Landman (an intermediary for an energy company) in 2010 whod used it to find me because of a parcel of land in the Lone Star state my late father had owned. Most of its information came from a file in (where else?) Salt Lake City called the wills of San Augustine (Texas, where both my parents were born and grew up).
The first part of the genealogy is rather detailed and the second part is less so, but lists six generations of my family. The names are just that to me, names, but then suddenly there is my grandfather whom I never met, Booker T. Wade. He married Corine Dennis and then it lists their children including my dad, Orvis T. Wade Sr.
I wish I knew more of my relatives, but I dont. One name that jumped out from the document was Carla Nicole Wade, my cousin, whom I know from Facebook.
The first time I saw the names of my brothers and myself in the document it was sort of like the part in the book Roots where Alex Haley changes the tense of the narrative as he entered into the history of his own book. The genealogy has errors and omissions. My youngest brother Scott was not listed and Kelvins name was misspelled as Kevin the story of his life.
I wrote a column about the genealogy in 2010 and here is a part:
My great-great-grandmothers name was . . . wait for it . . . Anarchy. Seriously. Ned and Anarchy Wade were listed together in the 1870 census. Her name sounds like a Marvel Comics Super Villain.
Ned and Anarchy had been the property of a man named Edward Teal and when he died in 1858 he left no will so the courts had to settle the estate. This is what it says in the genealogy:
The appointed commissioners of the courts ordered that the heirs of the estate separate the Negro property into two lots, 1 & 2, and place them in a hat and draw, and whichever one drew that lot would own those Negroes.
That is still horrifying for me to actually picture happening, but it did.
Orvis DNA test results showing our mixed heritage is boosted by the Wade Genealogy. In it, Ned was described as a Negro man of yellow complexion. Ned, Anarchy and their childrens race was listed as mulatto, meaning one-half negro blood.
The .6 percent unassigned made me scratch my head. Pod people? Borg? 23andMes explanation: There is a wide range of human diversity and sometimes our algorithm is unable to assign a region of DNA to a specific population. As we collect more data and update our algorithm, we expect that the amount of unassigned ancestry will decrease.
The ancestry DNA thing is very interesting and informative and I recommend that everyone have their sibling pay for it and then check out the results.
Reach Fairfield writer Tony Wade at toekneeweighed@gmail.com.
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How scientists redesign DNA codes – ABC News
Posted: at 9:49 am
Scientists are working to create yeast that operates with custom-made DNA.
They have long been able to make specific changes in an organism's DNA. Now, they're pushing into the more radical step of starting over, and building redesigned versions from scratch.
Their work is part of a bold and controversial pursuit aimed at creating custom-made DNA codes to be inserted into living cells to change how they function, or even provide treatments for diseases. It could also someday help give scientists the profound and unsettling ability to create entirely new organisms.
The genetic code is like a book written with an alphabet of only four letters: A, C, G, and T. Chemical building blocks that correspond to these letters line up in DNA molecules like links in a chain; genes are made up of specific sequences of those building blocks. These sequences tell the yeast cell how to build particular proteins.
The complete DNA code for yeast, called its genome, contains about 12 million letters. An international scientific team aims to add, delete or alter about a million of the DNA letters.
Yeast DNA is spread across 16 large chunks called chromosomes, which were parceled out among the team's labs to tackle.
So how do you redesign and build a chromosome? We asked Leslie Mitchell, a researcher at New York University. She created a 240,000-letter synthetic yeast chromosome, starting while she was at Johns Hopkins University in Baltimore.
Here's the recipe:
1. On a computer, start with the natural DNA sequence of the letters across a chromosome.
2. Tell the computer to make specific alterations, such as:
Every time it sees the letter series TAG at the end of a gene, change it to TAA. Both triplets deliver the same message to the yeast's machinery for making protein, so the change doesn't affect the yeast. But the TAG triplet could be used in a different place to make the yeast produce a protein from building blocks not found in nature, for example.
Delete a class of genes called 'tRNA genes' from their normal positions, where they can impair the process of duplicating the genome before a yeast cell divides. These genes will be relocated to their own, new chromosome, where they can do their jobs without causing trouble.
Insert bits of DNA code that will let researchers rearrange the order of genes on the chromosomes, like shuffling a deck of cards. This way, scientists can experiment with many different reshufflings to see which one makes yeast grow best, or perform best in some other way.
3. Once the alterations are done, break the redesigned code into lengths of about 10,000 letters apiece and have a company create chunks of DNA that reflect each of these segments. Chunks of that size can be easily manipulated in a laboratory.
4. In the test tube, use a chemical reaction to glue three to six of these chunks together into a "megachunk."
5. Take ordinary yeast and use this 30,000-60,000-letter megachunk to replace the corresponding segment of natural DNA. Yeast will do this without much coaxing.
6. If the yeast doesn't grow normally, identify and fix the problem in the megachunk. This is called debugging. If it's fine, add the next megachunk.
7. Repeat steps 4-6 until the entire chromosome has been replaced with megachunks of synthetic DNA.
Mitchell said it took her a couple months to build her chromosome but longer to debug. "The tiniest change in the code can have dramatic effect on growth," she said. "We are learning new rules about how cells operate by building from scratch."
Follow Malcolm Ritter at http://twitter.com/malcolmritter His recent work can be found at http://tinyurl.com/RitterAP
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Love Island fans spot Britain’s Got Talent stars DNA on reunion show but did you see them? – The Sun
Posted: at 9:49 am
LOVE Island fans noticed Kem Cetinays homecoming bash had two very special guests of honour waiting to welcome him back.
During tonights reunion show, eagle eyed viewers spotted Britains Got Talent double act DNA loitering in the background during a clip of Kem and Amber Davies visiting his salon in Essex.
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Some fans couldnt believe their eyes as they saw Darren, 29, and Andrew,43, mingling with the barbers friends and family.
One tweeted: Wtf! Was it just me who just saw DNA in Kems barbers shop?
Another wrote: Anyone know why DNA were in @KemCetinay barber shop on Love Island?
Darren and Andrew, who made it to the final of Britains Got Talent earlier this year, stayed pretty low key during Kems arrival and didnt speak during the short clip.
It turns out the pair are pretty chummy with Kem, and actually hinted they would be performing with them at a later date.
They told their Twitter followers: Great seeing Kem and Amber! So happy for them, worthy #LoveIsland winners!! Video of us performing on them coming soon! #KemandAmber.
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Tonight's reunion show had it's far share of surprises, with Chyna Ellis left stunned when Jonny Mitchell appeared to dump her live on air.
She got her revenge and later branded him a p***k - filming him secretly on her phone and uploading it to Instagram.
In another shot, she wrote over the smiling reality stars face, What a little p***k.
Jonny and Chyna had jetted off on a romantic break away to Budapest, giving fans the impression they were dating.
When Caroline Flack asked them what was happening however, Jonny denied they were dating leaving Chyna looking stunned.
As Caroline told them it was the most awkward moment of the night so far, Chyna blushed and said the pair were just having fun.
Caroline then quizzed Jonny on why hed taken Chyna on holiday which he had boasted cost 100,000 to which he replied: I just like holidays.
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The show became more awkward when Montana Brown and Alex Beattie tried to persuade Caroline they were still dating.
Since leaving the villa, the pair have tried to convince fans theyre dating despite The Sun revealing the couple had broken up.
A source told The Sun: Montana is keen to follow her dreams as a TV presenter and has been attending meetings this week to get the wheels in motion.
She doesnt like partying and isnt a big drinker so personal appearances in nightclubs arent really her thing.
Instead she is ambitious and very much a career woman her relationship with Alex is going to take a back seat.
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Love Island fans spot Britain's Got Talent stars DNA on reunion show but did you see them? - The Sun
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