Author Topic: Genetics, genetic manipulation, genetic harvesting, genetic targeting, etc  (Read 2843 times)


Body-by-Guinness

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Body-by-Guinness

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Genetically Modified Pig Heart Keeping End Stage Patient Alive
« Reply #3 on: October 24, 2023, 10:18:32 PM »
Lotsa implications if other transplantable organs can be grown in pigs.

Wait a sec, maybe we could put Hamas out of business tomorrow by using the threat of transplanted pig’s testicles as a punishment….

https://science.slashdot.org/story/23/10/23/1853210/one-month-after-experimental-pig-heart-transplant-doctors-say-they-see-no-signs-of-rejection-or-infection?utm_source=rss1.0mainlinkanon&utm_medium=feed

ccp

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that is great medical news

hope it keeps up

I know they were starting to do this with kidneys

had  no idea they are beginning to use for hearts too




Crafty_Dog

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Truly extraordinary!

Body-by-Guinness

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Manufacturing New Proteins to Solve Old Problems
« Reply #6 on: January 25, 2024, 01:51:04 PM »
I dunno, this piece embraces a very excited tone, but given the likely lab release of Covid one wonders if the brave new world these capabilities suggest are a net boon. IIRC Mad Cow Disease is caused by some sort of left handed protein or something; imagine creating a harmful and perhaps self replicating protein and pointing it at the food supply etc:

https://singularityhub.com/2024/01/23/scientists-coax-bacteria-into-making-exotic-proteins-not-found-in-nature/

Body-by-Guinness

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Uses of Artificial Chromosones
« Reply #7 on: March 28, 2024, 07:53:26 PM »
Another one from SingularityHub that’s interesting on its face, but scary in its implications:

Human Artificial Chromosomes Could Ferry Tons More DNA Cargo Into Cells

Novel method creates stable HACs

•Singularity Hub / by Shelly Fan / Mar 26, 2024 at 4:50 PM

The human genetic blueprint is deceptively simple. Our genes are tightly wound into 46 X-shaped structures called chromosomes. Crafted by evolution, they carry DNA and replicate when cells divide, ensuring the stability of our genome over generations.

In 1997, a study torpedoed evolution’s playbook. For the first time, a team created an artificial human chromosome using genetic engineering. When delivered into a human cell in a petri dish, the artificial chromosome behaved much like its natural counterparts. It replicated as cells divided, leading to human cells with 47 chromosomes.

Rest assured, the goal wasn’t to artificially evolve our species. Rather, artificial chromosomes can be used to carry large chunks of human genetic material or gene editing tools into cells. Compared to current delivery systems—virus carriers or nanoparticles—artificial chromosomes can incorporate far more synthetic DNA.

In theory, they could be designed to ferry therapeutic genes into people with genetic disorders or add protective ones against cancer.

Yet despite over two decades of research, the technology has yet to enter the mainstream. One challenge is that the short DNA segments linking up to form the chromosomes stick together once inside cells, making it difficult to predict how the genes will behave.

This month, a new study from the University of Pennsylvania changed the 25-year-old recipe and built a new generation of artificial chromosomes. Compared to their predecessors, the new chromosomes are easier to engineer and use longer DNA segments that don’t clump once inside cells. They’re also a large carrier, which in theory could shuttle genetic material roughly the size of the largest yeast chromosome into human cells.

“Essentially, we did a complete overhaul of the old approach to HAC [human artificial chromosome] design and delivery,” study author Dr. Ben Black said in a press release.

“The work is likely to reinvigorate efforts to engineer artificial chromosomes in both animals and plants,” wrote the University of Georgia’s Dr. R. Kelly Dawe, who was not involved in the study.

Shape of You

Since 1997, artificial genomes have become an established  biotechnology. They’ve been used to rewrite DNA in bacteria, yeast, and plants, resulting in cells that can synthesize life-saving medications or eat plastic. They could also help scientists better understand the functions of the mysterious DNA sequences littered throughout our genome.

The technology also brought about the first synthetic organisms. In late 2023, scientists revealed yeast cells with half their genes replaced by artificial DNA—the team hopes to eventually customize every single chromosome. Earlier this year, another study reworked parts of a plant’s chromosome, further pushing the boundaries of synthetic organisms.

And by tinkering with the structures of chromosomes—for example, chopping off suspected useless regions—we can better understand how they normally function, potentially leading to treatments for diseases.

The goal of building human artificial chromosomes isn’t to engineer synthetic human cells. Rather, the work is meant to advance gene therapy. Current methods for carrying therapeutic genes or gene editing tools into cells rely on viruses or nanoparticles. But these carriers have limited cargo capacity.

If current delivery vehicles are like sailboats, artificial human chromosomes are like cargo ships, with the capacity to carry a far larger and wider range of genes.

The problem? They’re hard to build. Unlike bacteria or yeast chromosomes, which are circular in shape, our chromosomes are like an “X.” At the center of each is a protein hub called the centromere that allows the chromosome to separate and replicate when a cell divides.

In a way, the centromere is like a button that keeps fraying pieces of fabric—the arms of the chromosome—intact. Earlier efforts to build human artificial chromosomes focused on these structures, extracting DNA letters that could express proteins inside human cells to anchor the chromosomes. However, these DNA sequences rapidly grabbed onto themselves like double-sided tape, ending in balls that made it difficult for cells to access the added genes.

One reason could be that the synthetic DNA sequences were too short, making the mini-chromosome components unreliable. The new study tested the idea by engineering a far larger human chromosome assembly than before.

Eight Is the Lucky Number

Rather than an X-shaped chromosome, the team designed their human artificial chromosome as a circle, which is compatible with replication in yeast. The circle packed a hefty 760,000 DNA letter pairs—roughly 1/200 the size of an entire human chromosome.

Inside the circle were genetic instructions to make a sturdier centromere—the “button” that keeps the chromosome structure intact and can make it replicate. Once expressed inside a yeast cell, the button recruited the yeast’s molecular machinery to build a healthy human artificial chromosome.

In its initial circular form in yeast cells, the synthetic human chromosome could then be directly passed into human cells through a process called cell fusion. Scientists removed the “wrappers” around yeast cells with chemical treatments, allowing the cells’ components—including the artificial chromosome—to merge directly into human cells inside petri dishes.

Like benevolent extraterrestrials, the added synthetic chromosomes happily integrated into their human host cells. Rather than clumping into noxious debris, the circles doubled into a figure-eight shape, with the centromere holding the circles together. The artificial chromosomes happily co-existed with native X-shaped ones, without changing their normal functions.

For gene therapy, it’s essential that any added genes remain inside the body even as cells divide. This perk is especially important for fast-dividing cells like cancer, which can rapidly adapt to therapies. If a synthetic chromosome is packed with known cancer-suppressing genes, it could keep cancers and other diseases in check throughout generations of cells.

The artificial human chromosomes passed the test. They recruited proteins from the human host cells to help them spread as the cells divided, thus conserving the artificial genes over generations.

A Revival

Much has changed since the first human artificial chromosomes.

Gene editing tools, such as CRISPR, have made it easier to rewrite our genetic blueprint. Delivery mechanisms that target specific organs or tissues are on the rise. But synthetic chromosomes may be regaining some of the spotlight.

Unlike viral carriers, the most often used delivery vehicle for gene therapies or gene editors, artificial chromosomes can’t tunnel into our genome and disrupt normal gene expression—making them potentially far safer.

The technology has vulnerabilities though. The engineered chromosomes are still often lost when cells divide. Synthetic genes placed near the centromere—the “button” of the chromosome—may also disrupt the artificial chromosome’s ability to replicate and separate when cells divide.

But to Dawe, the study has larger implications than human cells alone. The principles of re-engineering centromeres shown in this study could be used for yeast and potentially be “applicable across kingdoms” of living organisms.

The method could help scientists better model human diseases or produce drugs and vaccines. More broadly, “It may soon be possible to include artificial chromosomes as a part of an expanding toolkit to address global challenges related to health care, livestock, and the production of food and fiber,” he wrote.

Image Credit: Warren Umoh / Unsplash

https://singularityhub.com/2024/03/26/human-artificial-chromosomes-could-ferry-tons-more-dna-cargo-into-cells/

Crafty_Dog

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We are headed places beyond my comprehension , , ,

Body-by-Guinness

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Mammoth Genome Reconstructed
« Reply #9 on: July 11, 2024, 05:34:12 PM »
Perhaps my grandkids will be able to see a live one:

First Woolly Mammoth Genome Reconstructed in 3D Could Help Bring the Species Back to Life
Ancient woolly mammoth genome preserved
•Singularity Hub / by Shelly Fan / Jul 11, 2024 at 5:19 PM
Roughly 52,000 years ago, a woolly mammoth died in the Siberian tundra. As her body flash froze in the biting cold, something remarkable happened: Her DNA turned into a fossil. It wasn’t only genetic letters that were memorialized—the cold preserved their intricate structure too.

Fast forward to 2018, when an international expedition to the area found her preserved body. The team took little bits of skin from her head and ear, hairs still intact.

From these samples, scientists built a three-dimensional reconstruction of a woolly mammoth’s genome down to the nanometer. The results were published in Cell today.

Like humans, the mammoth’s DNA strands are tightly packed into chromosomes inside cells. These sophisticated structures are hard to analyze in detail, even for humans, but they contain insights into which genes are turned on or off and how they’re organized in different cell types.

Previous attempts to reconstruct ancient DNA only had tiny snippets of genetic sequences. Like trying to put together a puzzle with missing pieces, the resulting DNA maps were incomplete.

Thanks to the newly discovered flash-frozen DNA, this mammoth project—pun intended—is the first to assemble an enormous ancient genome in 3D.

“This is a new type of fossil, and its scale dwarfs that of individual ancient DNA fragments—a million times more sequence,” said study author Erez Lieberman Aiden at Baylor College of Medicine in a statement.

Aiden’s team heavily collaborated with Love Dalén at the Center of Palaeogenetics in Sweden. In a separate study, Dalén’s team analyzed 21 Siberian woolly mammoth genomes and charted how the species survived for six millennia after a potentially catastrophic genetic “bottleneck.”

The mammoth genomes weren’t that different than those of today’s Asian and African elephants. All have 28 pairs of chromosomes, and their X chromosomes twist into unique structures unlike most mammals. Digging deeper, the team found genes that were turned on or off in the mammoth compared to its elephant cousins.

“Our analyses uncover new biology,” wrote Aiden’s team in their paper.

DNA Serendipity

Ancient DNA is hard to come by, but it offers invaluable clues about the evolutionary past. In the 1980s, scientists eager to probe genetic history showed ancient DNA, however fragmented, could be extracted and sequenced in samples from an extinct member of the horse family and Egyptian mummies.

Thanks to modern DNA sequencing, the study of ancient DNA “has subsequently undergone a remarkable expansion,” wrote Aiden’s team. It’s now possible to sequence whole genomes from extinct humans, animals, plants, and even pathogens spanning a million years.

Making sense of the fragments is another matter. One way to decipher ancient genetic codes is to compare them to the genomes of their closest living cousins, such as woolly mammoths and elephants. This way, scientists can figure out which parts of the DNA sequence remained unchanged and where evolution swapped letters or small fragments.

These analyses can link genetic changes to function, such as identifying which genes made mammoths woolly. But they can’t capture large-scale differences at the chromosomal level. Because DNA relies on the chromosome’s 3D structure to function, sequencing its letters alone misses valuable information, such as when and where genes are turned on or off.

Chromosome Puzzle Master

Enter Hi-C. Developed in 2009 to reconstruct human genomes, the technique detects interactions between different genetic sites inside the cell’s nucleus.

Here’s roughly how it works. DNA strands are like ribbons that twirl around proteins in a structure resembling beads on a string. Because of this arrangement, different parts of the DNA strand are closer to each other in physical space. Hi-C “glues” together sections that are near one another and tags the pairs. Alongside modern DNA sequencing, the technique produces a catalog of DNA fragments that interact in physical space. Like a 3D puzzle, scientists can then put the pieces back together.

“Imagine you have a puzzle that has three billion pieces, but you don’t have the picture of the final puzzle to work from,” study author Marc A. Marti-Renom said in the press release. “Hi-C allows you to have an approximation of that picture before you start putting the puzzle pieces together.”

But Hi-C can be impossible to use in ancient samples because the surviving fragments are so short they’ve erased any chromosome shapes. They’ve literally withered away over time.

In the new study, the team developed a new technique, called PaleoHi-C, to analyze ancient DNA specifically.

Scientists immediately treated samples in the field to reduce contamination. They generated roughly 4.4 billion “pairs” of physically aligned DNA sequences—some interacting within a single chromosome, others between two. Overall, they painted a 3D snapshot of the woolly mammoth’s genetic material and how it looked inside cells with nanoscale detail.

In the new reconstructions, the team identified chromosome territories—certain chromosomes are located in different regions of the nucleus—alongside other quirks, such as loops that bring pairs of distant genomic sites into close physical proximity to alter gene expression. These patterns differed between cell types, suggesting it’s possible to learn which genes are active, not just for the mammoth but also compared to its closest living relative, the Asian elephant.

Roughly 820 genes differed between the two, with 425 active in the mammoth but not in elephants, and a similar number inactivated in one but not the other. One inactive mammoth gene that’s active in elephants has a human variant that is also shut down in the Nunavik Inuit, an indigenous people who thrive in the arctic. The gene “may be relevant for adaptation to a cold environment,” wrote the team.

Another inactive gene may explain how the woolly mammoth got its name. In humans and sheep, shutting down the same gene can result in excessive hair or wool growth.

“For the first time, we have a woolly mammoth tissue for which we know roughly which genes were switched on and which genes were off,” said Marti-Renom in the release. “This is an extraordinary new type of data, and it’s the first measure of cell-specific gene activity of the genes in any ancient DNA sample.”

Crystalized DNA

How did the mammoth’s genome architecture remain so well preserved for over 50,000 years?

Dehydration, often used to preserve food, may have been key. Using Hi-C on fresh beef, beef after 96 hours sitting on a desk, or jerky after a year at room temperature, the jerky took the win for resiliency. Even after getting run over by a car, immersed in acid, and pulverized by a shotgun (no joke), the dehydrated beef’s genomic architecture remained intact.

Dehydration could also partly be why the mammoth sample lasted so long. A chemical process called “glass transition” is widely used to produce shelf-stable food such as tortilla chips and instant coffee. It prevents pathogens from taking over or breaking down food. The mammoth’s DNA may also have been preserved in a glassy state called “chromoglass.” In other words, the sample was preserved across millennia by being freeze-dried.

It’s hard to say how long DNA architecture can survive as chromoglass, but the authors estimate it’s likely over two million years. Whether PaleoHi-C can work on hot-air-dried specimens, such as ancient Egyptian samples, remains to be seen.

As for mammoths, the next step is to examine gene expression patterns in other tissues and compare them to Asian elephants. Besides building an evolutionary throughline, the efforts could also guide ongoing studies looking to revive some version of the majestic animals.

“These results have obvious consequences for contemporary efforts aimed at woolly mammoth de-extinction,” said study author Thomas Gilbert at the University of Copenhagen in the release.

Image Credit: Beth Zaiken

https://singularityhub.com/2024/07/11/first-woolly-mammoth-genome-reconstructed-in-3d-could-help-bring-the-species-back-to-life/

Crafty_Dog

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Utterly extraordinary!!!