Monthly Archives: May 2013

Atmosphere – Wanessa @DNA TOUR live in BELO HORIOZONTE/MG – Video

Posted: May 22, 2013 at 9:49 pm


Atmosphere - Wanessa @DNA TOUR live in BELO HORIOZONTE/MG

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Atmosphere - Wanessa @DNA TOUR live in BELO HORIOZONTE/MG - Video

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DNA IC – Video

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DNA IC
just some crap IC I made in like an hour LOL I ended up not adding anything else to it cause this song was just difficult. only upload for le vicky to see XD...

By: HydroDiffusion

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Entrepreneurial DNA: Joe Abraham at TEDxBend – Video

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Entrepreneurial DNA: Joe Abraham at TEDxBend
Joe is the founder/CEO of bosiDNA.com, featured in the Wall Street Journal for its breakthrough technology and award-winning accelerator. Entrepreneurship ha...

By: TEDxTalks

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DNA – Little Mix (Guitar) – Video

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DNA - Little Mix (Guitar)
Me playing DNA by Little Mix on guitar 🙂

By: Adriiaana G

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BMS302 Oral Presentation- Genetic Screening

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BMS302 Oral Presentation- Genetic Screening DNA Sequencing

By: RIPkas1

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BMS302 Oral Presentation- Genetic Screening

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"DNA" Minecraft Oasis Ep 46 – Video

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"DNA" Minecraft Oasis Ep 46
Now they finally have some privacy! Submit YOUR Fan Art to the Cupquake Facebook Fan page and see it on the next episode!! Make sure to LIKE and COMMENT!!! /...

By: iHasCupquake

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"DNA" Minecraft Oasis Ep 46 - Video

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Man's rape conviction overturned after DNA testing

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OSHKOSH Joseph Freys conviction for a rape more than 20 years ago was overturned Wednesday by a Winnebago County Circuit Court judge based on DNA testing and other evidence that showed Frey, who was serving a 102-year sentence, was likely the wrong man.

In a subdued hearing, Judge Daniel Bissett agreed that Freys conviction must be vacated in the interest of justice.

However, the journey to freedom for Frey has not ended. He will remain in the Winnebago County Jail until prosecutors decide whether to retry him. Bissett ordered him held in lieu of $100,000 cash bail.

Frey, now 53, was charged with breaking into a UW-Oshkosh students apartment in 1991 and sexually assaulting her at knifepoint. He was convicted on Feb. 2, 1994, by a Winnebago County jury despite his claims of innocence, the victims dubious identification of him as the attacker, the lack of a DNA match and destruction by an Oshkosh Police detective of important evidence before the trial.

DNA found at the crime scene as a result of new testing requested by the Wisconsin Innocence Project matched a man who, after the 1991 attack, went on to sexually assault two sisters, ages 12 and 13, in Fond du Lac. He has since died.

Assistant District Attorney Adam Levin said the new evidence, including the DNA test and witness interviews, isnt significantly different from the old evidence, saying it was similar to what was used to convict Frey in 1994. That old evidence included a jailhouse informant, the victims identification of Frey in a live in-person lineup, prior sexual assault charges and DNA results from the victims bedsheet that excluded Frey as the source.

The jury knew that the DNA on the sheet did not match the defendant, Levin said.

But Levin said the new testing, which shows that DNA from convicted sex offender James E. Crawford was commingled with the victims DNA on her bedsheet, is a significant new fact that the jury did not know.

UW-Madison law student Micheal Hahn with the Innocence Project told Bissett there is no innocent explanation for the discovery of Crawfords DNA at the crime scene. He also pointed to a Winnebago County Sheriffs investigation requested by Levin last month that revealed Crawford may have been trying to confess to the attack in this case prior to his death in 2008.

Whether Frey is retried for the 1991 rape will hinge on the results of DNA testing of condoms collected from Frey as part of a Brown County case, Levin said.

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Man's rape conviction overturned after DNA testing

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DNA damage: The dark side of respiration

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May 22, 2013 Adventitious changes in cellular DNA can endanger the whole organism, as they may lead to life-threatening illnesses like cancer. Researchers at Ludwig-Maximilians-Universitaet (LMU) in Munich now report how byproducts of respiration cause mispairing of subunits in the double helix.

The DNA in our cells controls the form and function of every cell type in our bodies. The instructions for this are encoded in the linear sequence of the four subunits found in DNA, the bases adenine (A), cytosine (C), guanine (G) and thymine (T). Random changes in the sequence can lead to cell dysfunction, and may result in unrestricted cell proliferation and malignancies. Mutations can be induced by a variety of agents. For example, cellular respiration, i.e. the reduction of inspired oxygen to water, which powers cell function, also generates highly reactive oxygen species that can damage DNA, with the purine bases G and A being particularly susceptible to this kind of attack.

"Reactive oxygen species are responsible for two different sorts of DNA damage, as they induce formation of both 8-oxo-G and FaPy-G," says Professor Thomas Carell of the Department of Chemistry at LMU. In 2004, work done by Carell and his team defined how 8-oxo-G generates mutations. However, the basis for the mutagenic effect of FaPy-G has remained obscure -- until now. In their latest publication, Carell and his colleagues describe how FaPY-G leads to mispairing of bases in the double helix.

Pernicious partner swapping One G in one strand of the double helix normally matches up with a C on the other, forming a G:C pair. But as a consequence of damage by reactive oxygen species, the guanine base may be transformed into FaPy-G, so that we get a FaPy-G:C base pair. "We have now shown that, in the course of DNA replication prior to cell division, FaPy-G interacts with adenine, leading to the formation of FaPy-G:A base pairs. This partner swap is unusual, since unmodified guanine normally does not team up with adenine," Carell notes.

FaPy-G is subsequently recognized as abnormal and is removed by DNA repair enzymes. The missing base is replaced by a T -- which is the usual partner for A. The net result is that the original G:C base pair has been converted into an A:T pair, and the base sequence has undergone a potentially dangerous mutation.

This outcome is made possible by the fact that the cell's damage-control systems find it surprisingly difficult to distinguish the normal guanine base from its aberrant derivative FaPy-G during DNA replication. "That this defect then leads to mispairing with adenine is one of the main reasons for the spontaneous development of tumors," says Carell. "So with every breath we take, our risk of getting cancer goes up by a teeny-weeny bit." Further insights into the reasons why FaPy-G often eludes the cell's detection and correction systems could help to improve the treatment of cancer, as the inhibition of DNA repair processes in tumor cells increases their sensitivity to chemotherapeutic drugs.

The study was supported by DFG grants awarded to Collaborative Research Centers 646 and 749 and the Center for Integrated Protein Science Munich (CIPSM), an Excellence Cluster.

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The Norway spruce genome sequenced

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Public release date: 22-May-2013 [ | E-mail | Share ]

Contact: Pr Ingvarsson par.ingvarsson@emg.umu.se 46-708-485-977 Umea University

Swedish scientists have mapped the gene sequence of Norway spruce (the Christmas tree) a species with huge economic and ecological importance - and that is the largest genome to have ever been mapped. The genome is complex and seven times larger than that of humans. The results have been published in the prestigious journal Nature.

This major research project has been led by Ume Plant Science Centre (UPSC) in Ume and the Science for Life Laboratory (SciLifeLab) in Stockholm.

In addition to its scientific interest this new knowledge has immense importance to the forestry industry in many countries.

"Forest tree breeding is now entering a new era, and Sweden has the potential to be in the forefront of development," says Professor Ove Nilsson from UPSC. "Newer and more effective methods can begin to be used to ensure that the over 200 million tree seedlings planted each year in Sweden are as strong, healthy and well-adapted as possible for both poor and rich soil areas in different parts of the country."

The scientists have identified about 29,000 functional genes, marginally more than humans have, but the question arises: why is the spruce genome still seven times larger than ours? According to the study an explanation is "genome obesity" caused by extensive repetitive DNA sequences, which have accumulated for several hundred million years of evolutionary history. Other plant and animal species have efficient mechanisms to eliminate such repetitive DNA, but these do not seem to operate so well in conifers.

"It is remarkable that the spruce is doing so well despite this unnecessary genetic load," says Professor Pr Ingvarsson at UPSC. "Of course, some of this DNA has a function but it seems strange that it would be beneficial to have so very much. This appears to be something special for conifers."

The greatest challenge in the project has been to get the approximately 20 billion "letters" found in spruce's genetic code into the correct order, rather than obtaining the actual DNA sequences.

"Imagine a library with ten thousand books as thick as the bible, written in a language with only four letters," explains Professor Stefan Jansson at UPSC. "If someone took one hundred identical copies of each of the ten thousand titles, passed them all through a document shredder and mixed all the shreds, and you then were asked to piece together an accurate copy of each title, you can realize that it can be a bit problematic."

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The Norway spruce genome sequenced

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Pines punched a “one way ticket toward genome obesity”

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Relatives of the Norway spruce are some of the oldest living things on the planet. They haven't used all that time to tidy up their genomes, though.

Last week we heard about the genome of a plant that pushed the limits of compacting its DNA:the bladderwortseems to have done away with of most of the genetic material that typically makes plant and animal genomes so large without any apparent ill effects. This week, the genome of a different plant is in the spotlight:the Norway spruce (Picea abies), which also seems to suffer no ill effects, even though it has picked up an enormous amount of DNA. Each one of its chromosomes is nearly the size of the entire human genomeand it has a dozen of them. When researchers looked at what all that extra DNA might be doing, they came up with a simple answer: probably not anything useful.

If you're aware of the Norway spruce, it's probably because you have been shopping for a Christmas tree. But conifers (technically Gymnosperms, although the group includes gingkoes and a few other species) are some of the most phenomenally successful organisms on Earth. They've dominated forests for over 200 million years, and members of the group include the tallest, heaviest, and oldest things currently alive. All of them seem to have managed this despite having a staggeringly inefficient genome management style.

Unlike many groups that vary widely in the number of chromosomes their species carry, pretty much all the Gymnosperms have a dozen pairs of chromosomes. And pretty much all of these chromosomes are up in the area of two billion bases long, or a bit smaller than the human genome. That size is so consistent, in fact, that the authors think the trees might be pushing up against the limits of how much stuff you can put in a chromosome and still get it copied and shared between two cells when they divide. In other words, if firs wanted to carry any more DNA than they already do, they'd have to start making new chromosomes.

From an evolutionary fitness perspective, would the plants actually want more DNA? Probably not, if the new genome is anything to go by. Despite all the extra DNA, the Norway spruce has almost exactly the same number of genes28,354 in totalthat the bladderwort does, even though the latter has about 1/250th the DNA. But it has plenty of dead copies of genes that have been inactivated by mutation. All told, these pseudogenes take up over seven times as much space in the genome as the working genes do.

However, the pseudogenes are a small contributor to the size of the genome compared to mobile genetic parasites called transposons. The transposons have hopped into all sorts of places in the genomewithin the non-coding introns of genes, in between genesand just stayed there. In fact, the Norway Spruce has an unusually high number of large introns simply because so many of them have picked up one or more transposons. Based on looking at a number of other Gymnosperms, these transposons have just been slowly accumulating throughout the group's history and have just never gone away, "possibly owing to the lack of an efficient elimination mechanism. "

Inaccurate recombination between chromosomes can sometimes create deletions, which might get rid of some of the excess DNA once it's present. But the conifers don't undergo recombination very often in the areas where that DNA residesinstead, the exchange of DNA mostly happens where the genes are.All told, the authors call this a "one way ticket toward genome obesity."

Incidentally, all this stuff made sequencing the genome a nightmare. Normally, software is used to recognize when two stretches of sequence partly overlap because the sequence is identical, and it uses further overlaps to build ever-larger sequences. In this case, the frequency of transposons meant that there were nearly identical sequences scattered everywhere in the genome. Imagine trying to build a city map where every road that ran north-to-south had a name, but everything east-west was simply called "street." To cope with this, the team separated out chunks of the chromosome a few hundred thousand bases long, figured out the sequence of the chunk, and then looked for places where the chunks overlapped. This method got the job done, but there are still plenty of gaps and missing sequences.

There are a few other draft conifer genomes in the works and all of them pretty much look like this, although the exact details of which transposons are present and where they're located differ somewhat among the species. So far, the genomes only tell us a little about the origin of the features we commonly associate with trees. But they definitely tell us that a group of species don't have to be neat freaks in order to be phenomenally successful.

Nature, 2013. DOI: 10.1038/nature12211 (About DOIs).

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