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Artificial Life One Step Closer: Scientists Clone And Engineer Bacterial Genomes In Yeast And Transplant Genomes Back Into Bacterial Cells
ScienceDaily (Aug. 22, 2009) — Researchers at the J. Craig Venter Institute (JCVI), a not-for-profit genomic research organization, have just published results describing new methods in which the entire bacterial genome from Mycoplasma mycoides was cloned in a yeast cell by adding yeast centromeric plasmid sequence to the bacterial chromosome. Researchers modified it in yeast using yeast genetic systems. This modified bacterial chromosome was then isolated from yeast and transplanted into a related species of bacteria, Mycoplasma capricolum, to create a new type of M. mycoides cell.
See also:
Health & Medicine
* Human Biology
* Gynecology
* Genes
Plants & Animals
* Bacteria
* Microbiology
* Biology
Reference
* Vector (biology)
* Yeast
* Prokaryote
* Human Genome Project
This is the first time that genomes have been transferred between branches of life—from a prokaryote to eukaryote and back to a prokaryote. The research was published by Carole Lartigue et al in the journal Science on August 21.
Hamilton Smith, M.D., one of the leaders of the JCVI team said, “I believe this work has important implications in better understanding the fundamentals of biology to enable the final stages of our work in creating and booting up a synthetic genome. This is possibly one of the most important new findings in the field of synthetic genomics.”
The research published today was made possible by previous breakthroughs at JCVI. In 2007 the team published results from the transplantation of the native M. mycoides genome into the M. capricolum cell which resulted in the M. capricolum cell being transformed into M. mycoides. This work established the notion that DNA is the software of life and that it is the DNA that dictates the cell phenotype.
In 2008 the same team reported on the construction of the first synthetic bacterial genome by assembling DNA fragments made from the four chemicals of life—ACGT. The final assembly of DNA fragments into the whole genome was performed in yeast by making use of the yeast genetic systems. However, when the team attempted to transplant the synthetic bacterial genome out of yeast into a recipient bacterial cell, all the experiments failed.
The researchers had previously established that no proteins were required for chromosome transplantations, however they reasoned that DNA methylation (a chemical modification of DNA that bacterial cells use to protect their genome from degradation by restriction enzymes, which are the proteins that cut DNA at specific sites) might be required for transplantation. When the chromosome was isolated direct from the bacterial cells it was likely already methylated and therefore transplantable due to it being protected from the cells restriction enzymes.
In this study, the team began by cloning the native M. mycoides genome into yeast by adding a yeast centromere to the bacterial genome. This is the first time a native bacterial genome has been grown successfully in yeast. Specific methylase enzymes were isolated from M. mycoides and used to methylate the M. mycoides genome isolated from yeast. When the DNA was methylated the chromosome was able to be successfully transplanted into a wild type species of M. capricolum. However, if the DNA was not first methylated the transplant experiments were not successful. To prove that the restriction enzymes in the M. capricolum cell were responsible for the destruction of the transplanted genome the team removed the restriction enzyme genes from the M. capricolum genome. When genome transplantations were performed using the restriction enzyme minus recipient cells, all the genome transplantations worked regardless of if the DNA was methylated or not.
“The ability to modify bacterial genomes in yeast is an important advance that extends yeast genetic tools to bacteria. If this is extendable to other bacteria we believe that these methods may be used in general laboratory practice to modify organisms,” said Sanjay Vashee, Ph.D., JCVI researcher and corresponding author on the paper.
The team now has a complete cycle of cloning a bacterial genome in yeast, modifying the bacterial genome as though it were a yeast chromosome and transplanting the genome back into a recipient bacterial cell to create a new bacterial strain. These new methods and knowledge should allow the team to now transplant and boot up the synthetic bacterial genome successfully.
The research published August 21 by JCVI researchers was funded by the company Synthetic Genomics Inc., a company co-founded by Drs. Smith and Venter.
Journal reference:
1. Lartigue et al. Creating Bacterial Strains from Genomes That Have Been Cloned and Engineered in Yeast. Science, August 20, 2009; DOI: 10.1126/science.1173759
Adapted from materials provided by J. Craig Venter Institute.
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Yeast. The entire bacterial genome from Mycoplasma mycoides was cloned in a yeast cell by adding yeast centromeric plasmid sequence to the bacterial chromosome and modifying it in yeast using yeast genetic systems. This modified bacterial chromosome was then isolated from yeast and transplanted into a related species of bacteria, Mycoplasma capricolum, to create a new type of M. mycoides cell. (Credit: Wikimedia Commons. Public Domain Image)
Related Stories
On The Origin Of Subspecies (Feb. 21, 2009) — Scientists have sequenced over seventy strains of yeast, the greatest number of genomes for any species, bringing into focus the small branches of Darwin's Tree of ... > read more
How DNA Repairs Can Reshape Genome, Spawn New Species (Aug. 14, 2008) — Researchers have shown how broken sections of chromosomes can recombine to change genomes and spawn new species. The scientists used X-rays to break yeast chromosomes, and then studied how the damage ... > read more
Humans And Chimpanzees Genetically More Similar Than One Yeast Variety Is To Another (Feb. 15, 2009) — There may be greater genetic variation between different yeasts of the same species than between humans and chimpanzees. This is one of the findings of a new study. This study heralds a new era in ... > read more
DNA Clues To Reproductive Behavior (May 27, 2008) — A species of wild yeast goes through a cycle of sexual reproduction once in every 1,000 asexual generations, according to new research. The study focused on the wild yeast Saccharomyces paradoxus, ... > read more
New Yeasts Could Help Fast-Track Biofuel Production (Aug. 4, 2009) — A new yeast that makes ethanol from both five-carbon and six-carbon sugars without needing oxygen has now been developed. This could be an important breakthrough in industrial ethanol production, ... > read more
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Artificial Life One Step Closer: Scientists Clone And Engineer Bacterial Genomes In Yeast And Transplant Genomes Back Into Bacterial Cells
ScienceDaily (Aug. 22, 2009) — Researchers at the J. Craig Venter Institute (JCVI), a not-for-profit genomic research organization, have just published results describing new methods in which the entire bacterial genome from Mycoplasma mycoides was cloned in a yeast cell by adding yeast centromeric plasmid sequence to the bacterial chromosome. Researchers modified it in yeast using yeast genetic systems. This modified bacterial chromosome was then isolated from yeast and transplanted into a related species of bacteria, Mycoplasma capricolum, to create a new type of M. mycoides cell.
See also:
Health & Medicine
* Human Biology
* Gynecology
* Genes
Plants & Animals
* Bacteria
* Microbiology
* Biology
Reference
* Vector (biology)
* Yeast
* Prokaryote
* Human Genome Project
This is the first time that genomes have been transferred between branches of life—from a prokaryote to eukaryote and back to a prokaryote. The research was published by Carole Lartigue et al in the journal Science on August 21.
Hamilton Smith, M.D., one of the leaders of the JCVI team said, “I believe this work has important implications in better understanding the fundamentals of biology to enable the final stages of our work in creating and booting up a synthetic genome. This is possibly one of the most important new findings in the field of synthetic genomics.”
The research published today was made possible by previous breakthroughs at JCVI. In 2007 the team published results from the transplantation of the native M. mycoides genome into the M. capricolum cell which resulted in the M. capricolum cell being transformed into M. mycoides. This work established the notion that DNA is the software of life and that it is the DNA that dictates the cell phenotype.
In 2008 the same team reported on the construction of the first synthetic bacterial genome by assembling DNA fragments made from the four chemicals of life—ACGT. The final assembly of DNA fragments into the whole genome was performed in yeast by making use of the yeast genetic systems. However, when the team attempted to transplant the synthetic bacterial genome out of yeast into a recipient bacterial cell, all the experiments failed.
The researchers had previously established that no proteins were required for chromosome transplantations, however they reasoned that DNA methylation (a chemical modification of DNA that bacterial cells use to protect their genome from degradation by restriction enzymes, which are the proteins that cut DNA at specific sites) might be required for transplantation. When the chromosome was isolated direct from the bacterial cells it was likely already methylated and therefore transplantable due to it being protected from the cells restriction enzymes.
In this study, the team began by cloning the native M. mycoides genome into yeast by adding a yeast centromere to the bacterial genome. This is the first time a native bacterial genome has been grown successfully in yeast. Specific methylase enzymes were isolated from M. mycoides and used to methylate the M. mycoides genome isolated from yeast. When the DNA was methylated the chromosome was able to be successfully transplanted into a wild type species of M. capricolum. However, if the DNA was not first methylated the transplant experiments were not successful. To prove that the restriction enzymes in the M. capricolum cell were responsible for the destruction of the transplanted genome the team removed the restriction enzyme genes from the M. capricolum genome. When genome transplantations were performed using the restriction enzyme minus recipient cells, all the genome transplantations worked regardless of if the DNA was methylated or not.
“The ability to modify bacterial genomes in yeast is an important advance that extends yeast genetic tools to bacteria. If this is extendable to other bacteria we believe that these methods may be used in general laboratory practice to modify organisms,” said Sanjay Vashee, Ph.D., JCVI researcher and corresponding author on the paper.
The team now has a complete cycle of cloning a bacterial genome in yeast, modifying the bacterial genome as though it were a yeast chromosome and transplanting the genome back into a recipient bacterial cell to create a new bacterial strain. These new methods and knowledge should allow the team to now transplant and boot up the synthetic bacterial genome successfully.
The research published August 21 by JCVI researchers was funded by the company Synthetic Genomics Inc., a company co-founded by Drs. Smith and Venter.
Journal reference:
1. Lartigue et al. Creating Bacterial Strains from Genomes That Have Been Cloned and Engineered in Yeast. Science, August 20, 2009; DOI: 10.1126/science.1173759
Adapted from materials provided by J. Craig Venter Institute.
Email or share this story:
| More
Need to cite this story in your essay, paper, or report? Use one of the following formats:
APA
MLA
enlarge
Yeast. The entire bacterial genome from Mycoplasma mycoides was cloned in a yeast cell by adding yeast centromeric plasmid sequence to the bacterial chromosome and modifying it in yeast using yeast genetic systems. This modified bacterial chromosome was then isolated from yeast and transplanted into a related species of bacteria, Mycoplasma capricolum, to create a new type of M. mycoides cell. (Credit: Wikimedia Commons. Public Domain Image)
Related Stories
On The Origin Of Subspecies (Feb. 21, 2009) — Scientists have sequenced over seventy strains of yeast, the greatest number of genomes for any species, bringing into focus the small branches of Darwin's Tree of ... > read more
How DNA Repairs Can Reshape Genome, Spawn New Species (Aug. 14, 2008) — Researchers have shown how broken sections of chromosomes can recombine to change genomes and spawn new species. The scientists used X-rays to break yeast chromosomes, and then studied how the damage ... > read more
Humans And Chimpanzees Genetically More Similar Than One Yeast Variety Is To Another (Feb. 15, 2009) — There may be greater genetic variation between different yeasts of the same species than between humans and chimpanzees. This is one of the findings of a new study. This study heralds a new era in ... > read more
DNA Clues To Reproductive Behavior (May 27, 2008) — A species of wild yeast goes through a cycle of sexual reproduction once in every 1,000 asexual generations, according to new research. The study focused on the wild yeast Saccharomyces paradoxus, ... > read more
New Yeasts Could Help Fast-Track Biofuel Production (Aug. 4, 2009) — A new yeast that makes ethanol from both five-carbon and six-carbon sugars without needing oxygen has now been developed. This could be an important breakthrough in industrial ethanol production, ... > read more
Search ScienceDaily
Number of stories in archives: 44,032
Find with keyword(s):
Enter a keyword or phrase to search ScienceDaily's archives for related news topics,
the latest news stories, reference articles, science videos, images, and books.
Just In:
Lightning's Mirror Image ... Only Much Bigger
Using Light To Teach Magnets New Tricks
Microchip Does 1,000 Chemical Reactions At Once
Naming Evolution's Winners And Losers
Inner 'Fingerprint' For Personal Medical Care
Why Sleep? To Boost Efficiency, Minimize Risk
Ultrathin LEDs: New Class Of Displays
Oxycholesterol: Greatest Heart Disease Risk?
Science Video News
Bacteria As Art
Biophysicists are growing Petri dishes of different species of bacteria in order to develop new antibiotics. The bacteria are subjected to different. ... > full story
* Doctors Combine Cell Biology, Endocrinology to Eliminate Insulin Implants
* Acoustical Engineers Reduce Hospital Noise with Fiberglass Panels
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* Gene swap experiment makes altering bugs easier
* more science news
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* Justice Dept advises pursuing CIA abuses: report
* Suspect in U.S. model murder found dead in Canada
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