Thursday, 2 April 2015
Stem Cells Age-discriminate Organelles to Maintain Stemness
Posted by ZenMaster at Thursday, April 02, 2015
Labels: cell division, human, mammary, mitochondria, research, self-renewal, stem cells 0 comments
Thursday, 29 January 2015
Mitochondrial Donation: How Many Women Could Benefit?
Posted by ZenMaster at Thursday, January 29, 2015
Labels: chimera, cloning, designer baby, egg, ethics, human, mitochondria, oocyte, research, SCNT, sequence, sperm, UK 0 comments
Friday, 21 November 2014
Pluripotent Cells Created by Nuclear Transfer Can Prompt Immune Reaction
Posted by ZenMaster at Friday, November 21, 2014
Labels: California, embryonic, fibroblast, mitochondria, mouse, pluripotent, reprogramming, research, stem cells 0 comments
Wednesday, 18 June 2014
Three Parents and a Baby
![]() |
Already a
few dysfunctional mitochondria (in
yellow on
top of the picture) could cause a
disease by
overgrowing functional ones (in blue).
Credit: Illustration: Iain Johnston.
|
Posted by ZenMaster at Wednesday, June 18, 2014
Labels: cloning, designer baby, egg, human, mitochondria, mouse, research, SCNT 0 comments
Thursday, 5 December 2013
Oldest Hominine DNA Sequenced
![]() |
This is
a skeleton of a Homo heidelbergensis
from
Sima de los Huesos, a unique cave site in
Northern
Spain. Credit: Javier Trueba, Madrid
Scientific Films. |
![]() |
Matthias Meyer at work in the clean lab.
Credit: Max Planck Institute for Evolutionary Anthropology. |
The
Sima de los Huesos hominines lived
approximately
400,000 years ago during the
Middle
Pleistocene. Credit: Javier Trueba,
Madrid Scientific Films. |
![]() |
Prof. Juan Luis Arsuaga, Director of
the Centro
Mixto de Evolución and Compòrtamiento
Humanos in Madrid, Spain. Credit:
Javier
Trueba, Madrid Scientific Films. |
Posted by ZenMaster at Thursday, December 05, 2013
Labels: DNA, fossil, human, mitochondria, Neanderthal, research, sequence 0 comments
Tuesday, 17 August 2010
Mother of All Humans Lived 200,000 Years Ago
Rice statisticians confirm date of 'mitochondrial Eve' with new method
Tuesday, 17 August 2010
The most robust statistical examination to date of our species' genetic links to "mitochondrial Eve" — the maternal ancestor of all living humans confirms that she lived about 200,000 years ago. The Rice University study was based on a side-by-side comparison of 10 human genetic models that each aim to determine when Eve lived using a very different set of assumptions about the way humans migrated, expanded and spread across Earth.
The research is available online in the journal Theoretical Population Biology.
"Our findings underscore the importance of taking into account the random nature of population processes like growth and extinction," said study co-author Marek Kimmel, professor of statistics at Rice.
"Classical, deterministic models, including several that have previously been applied to the dating of mitochondrial Eve, do not fully account for these random processes."
The quest to date mitochondrial Eve (mtEve) is an example of the way scientists probe the genetic past to learn more about mutation, selection and other genetic processes that play key roles in disease.
"This is why we are interested in patterns of genetic variability in general," Kimmel said.
"They are very important for medicine."
For example, the way scientists attempt to date mtEve relies on modern genetic techniques. Genetic profiles of random blood donors are compared, and based upon the likenesses and differences between particular genes, scientists can assign a number that describes the degree to which any two donors are related to one another.
Using mitochondrial genomes to gauge relatedness is a way for geneticists to simplify the task of finding common ancestors that lived long ago. That is because the entire human genome contains more than 20,000 genes, and comparing the differences among so many genes for distant relatives is problematic, even with today's largest and fastest supercomputers.
But mitochondria — the tiny organelles that serve as energy factories inside all human cells — have their own genome. Besides containing 37 genes that rarely change, they contain a "hypervariable" region, which changes fast enough to provide a molecular clock calibrated to times comparable to the age of modern humanity. Because each person's mitochondrial genome is inherited from his or her mother, all mitochondrial lineages are maternal.
To infer mtEve's age, scientists must convert the measures of relatedness between random blood donors into a measure of time.
"You have to translate the differences between gene sequences into how they evolved in time," said co-author Krzysztof Cyran, vice head of the Institute of Informatics at Silesian University of Technology in Gliwice, Poland.
"And how they evolved in time depends upon the model of evolution that you use. So, for instance, what is the rate of genetic mutation, and is that rate of change uniform in time? And what about the process of random loss of genetic variants, which we call genetic drift?"
Within each model, the answers to these questions take the form of coefficients — numeric constants that are plugged into the equation that returns the answer for when mtEve lived.
Each model has its own assumptions, and each assumption has mathematical implications. To further complicate matters, some of the assumptions are not valid for human populations. For example, some models assume that population size never changes. That is not true for humans, whose population has grown exponentially for at least several thousand generations. Other models assume perfect mixing of genes, meaning that any two humans anywhere in the world have an equal chance of producing offspring.
Cyran said human genetic models have become more complex over the past couple of decades as theorists have tried to correct for invalid assumptions. But some of the corrections — like adding branching processes that attempt to capture the dynamics of population growth in early human migrations — are extremely complex. Which raises the question of whether less complex models might do equally well in capturing what is occurring.
"We wanted to see how sensitive the estimates were to the assumptions of the models," Kimmel said.
"We found that all of the models that accounted for random population size — such as different branching processes — gave similar estimates. This is reassuring, because it shows that refining the assumptions of the model, beyond a certain point, may not be that important in the big picture."
Source: Rice University
Contact: Jade Boyd
.........
ZenMaster
For more on stem cells and cloning, go to CellNEWS at
http://cellnews-blog.blogspot.com/
Posted by ZenMaster at Tuesday, August 17, 2010
Labels: DNA, evolution, genome, human, mitochondria, research, sequence 0 comments
Wednesday, 26 August 2009
Mitochondrial Gene Replacement in Primate Offspring and Embryonic Stem Cells
Breakthrough could help break the chain of several maternally-based diseases passed from generation to generation
Wednesday, 26 August 2009
Researchers at Oregon Health & Science University's Oregon National Primate Research Center (ONPRC) believe they have developed one of the first forms of genetic therapy – a therapy aimed at preventing serious diseases in unborn children. Specifically, the therapy would combat inherited diseases passed on from mothers to their children through mutated DNA in cell mitochondria. The research is published in the Aug. 26 advance online edition of the journal Nature.
"We believe this discovery in nonhuman primates can rapidly be translated into human therapies aimed at preventing inherited disorders passed from mothers to their children through the mitochondrial DNA, such as certain forms of cancer, diabetes, infertility, myopathies and neurodegenerative diseases," explained Shoukhrat Mitalipov, Ph.D.. Dr. Mitalipov is an associate scientist in the Division of Reproductive Sciences at ONPRC, the Oregon Stem Cell Center and the departments of Obstetrics and Gynecology and Molecular & Medical Genetics of Oregon Health & Science University (OHSU).
"Currently there are 150 known diseases caused by mutations of the mitochondrial DNA, and approximately 1 out of every 200 children is born with mitochondrial mutations."
Mitochondria are structures that are found in all cells that provide energy for cell growth and metabolism, which is why they are often called the cell's "power plant." The structures produce energy to power each individual cell. Mitochondria also carry their own genetic material.
When an egg cell is fertilized by a sperm cell during reproduction, the embryo almost exclusively inherits the maternal mitochondria present in the egg. This means that any disease-causing genetic mutations that a mother carries in her mitochondrial DNA can be passed on to her offspring.
The method developed by OHSU researchers transfers the mother's chromosomes to a donated egg that has had its chromosomes removed, but which has healthy mitochondria, thereby preventing the disease from being passed on to one's offspring.
How the OHSU researchers' method works
Scientists collected groups of unfertilized eggs from two female rhesus macaque monkeys (monkeys A and B). They then removed the chromosomes, which contain the genes found in the cell nucleus, from the eggs of monkey B, and then transplanted the nuclear genes from the eggs of monkey A into the eggs of monkey B. Then the eggs from monkey B, which now contained their own mitochondria but monkey A's nuclear genes, were fertilized. The fertilized eggs developed into embryos that were implanted in surrogate monkeys.
The initial implantation of two embryos resulted in the birth of healthy twin monkeys, nicknamed "Mito" and "Tracker" (in reference to the procedure used for imaging of mitochondria). These monkeys are the world's first animals derived by spindle transfer.
Follow-up testing showed that there was little to no trace of cross-animal mitochondrial transfer using this procedure. This demonstrates that the researchers were successful in isolating nuclear genetic material from mitochondrial genetic material during the transfer process.
"In theory, this research has demonstrated that it is possible to use this therapy in mothers carrying mitochondrial DNA diseases so that we can prevent those diseases from being passed on to their offspring," added Mitalipov.
"We believe that with the proper governmental approvals, our work can rapidly be translated into clinical trials for humans, and, eventually, approved therapies."
"This breakthrough is an excellent example of how OHSU's research findings can often be rapidly translated into health therapies that benefit residents of our state and the country as a whole," said Dr. Joe Robertson, M.D., M.B.A., president of OHSU.
"Recent findings suggest that mitochondrial disorders play a role in at least some proportion of many human disorders," said Duane Alexander, M.D, director of the Eunice Kennedy Shriver National Institute of Child Health and Human Development, which provided funding for the study.
"Pending further research, the findings hold the potential of allowing a couple to have a child who is biologically their own, but is free of any conditions associated with defects in maternal mitochondria."
Using the technique, the researchers created fertilized eggs and achieved three successful pregnancies in rhesus monkeys, which have resulted in four healthy newborns. Recent advances in the transfer of hereditary material and in microscopy facilitated the achievement, they wrote.
The researchers said that the technique did not appear to pose any risk of chromosomal damage. Analysis of 5-6-day-old embryos (blastocysts) resulting from the fertilized eggs, and of embryonic stem cell lines established from them, did not uncover any evidence of damage to the chromosomes. Analysis of cells from the infant monkeys born after the procedure failed to detect any mitochondrial DNA from the mother.
Reference:
Mitochondrial gene replacement in primate offspring and embryonic stem cells
Masahito Tachibana, Michelle Sparman, Hathaitip Sritanaudomchai, Hong Ma, Lisa Clepper, Joy Woodward, Ying Li, Cathy Ramsey, Olena Kolotushkina & Shoukhrat Mitalipov
Nature advance online publication 26 August 2009, doi:10.1038/nature08368
See also:
DNA swap could avoid inherited diseases
David Cyranoski
Nature News 26 August 2009, doi:10.1038/news.2009.860
.........
ZenMaster
For more on stem cells and cloning, go to CellNEWS
at http://cellnews-blog.blogspot.com/
Posted by ZenMaster at Wednesday, August 26, 2009
Labels: egg, embryonic, Gene Therapy, mitochondria, research, stem cells 0 comments
Thursday, 20 November 2008
Extinct Woolly-mammoth Genome Sequenced
Thursday, 20 November 2008

Scientists at Penn State are leaders of a team that is the first to report the genome-wide sequence of an extinct animal, according to Webb Miller, professor of biology and of computer science and engineering and one of the project's two leaders. The scientists sequenced the genome of the woolly mammoth, an extinct species of elephant that was adapted to living in the cold environment of the northern hemisphere. They sequenced four billion DNA bases using next-generation DNA-sequencing instruments and a novel approach that reads ancient DNA highly efficiently.
"Previous studies on extinct organisms have generated only small amounts of data," said Stephan C. Schuster, Penn State professor of biochemistry and molecular biology and the project's other leader.
"Our dataset is 100 times more extensive than any other published dataset for an extinct species, demonstrating that ancient DNA studies can be brought up to the same level as modern genome projects."

The researchers suspect that the full woolly-mammoth genome is over four-billion DNA bases, which they believe is the size of the modern-day African elephant's genome. Although their dataset consists of more than four-billion DNA bases, only 3.3 billion of them — a little over the size of the human genome — currently can be assigned to the mammoth genome. Some of the remaining DNA bases may belong to the mammoth, but others could belong to other organisms, like bacteria and fungi, from the surrounding environment that had contaminated the sample. The team used a draft version of the African elephant's genome, which currently is being generated by scientists at the Broad Institute of MIT and Harvard, to distinguish those sequences that truly belong to the mammoth from possible contaminants.
"Only after the genome of the African elephant has been completed will we be able to make a final assessment about how much of the full woolly-mammoth genome we have sequenced," said Miller.
The team plans to finish sequencing the woolly mammoth's genome when the project receives additional funding.
Ball of permafrost-preserved mammoth hair containing thick outer-coat and thin under-coat hairs. Credit: Stephan Schuster lab, Penn State University.
The team sequenced the mammoth's nuclear genome using DNA extracted from the hairs of a mammoth mummy that had been buried in the Siberian permafrost for 20,000 years and a second mammoth mummy that is at least 60,000-years-old. By using hair, the scientists avoided problems that have bedevilled the sequencing of ancient DNA from bones because DNA from bacteria and fungi, which always are associated with ancient DNA, can more easily be removed from hair than from bones. Another advantage of using hair is that less damage occurs to ancient DNA in hair because the hair shaft encases the remnant DNA like a biological plastic, thus protecting it from degradation and exposure to the elements.
Members of the team previously ruled out humans as a cause of extinction for at least one of the Siberian sub-populations — the group appears to have gone extinct at least 45,000 years ago at a time when there were no humans living in Siberia. However, much debate still remains regarding the causes of extinction for the other group and for those populations that lived in other places, such as North America. Currently, the team is searching the mammoth's genome for clues about its extinction.
Posted by ZenMaster at Thursday, November 20, 2008
Labels: DNA, evolution, genome, mammoth, mitochondria, research, sequence, US 0 comments
Wednesday, 13 August 2008
Casting a Security Net to Catch Harmful Bacteria
White Blood Cell Uses DNA 'Catapult' to Fight Infection
Wednesday, 13 August 2008
Swiss and US scientists have made a breakthrough in understanding how a type of white blood cell called the eosinophil may help the body to fight bacterial infections in the digestive tract, according to research published online this week in Nature Medicine.
Hans-Uwe Simon, from the University of Bern, Switzerland, Gerald J.Gleich, M.D., from the University of Utah School of Medicine, and their colleagues discovered that bacteria can activate eosinophils to release mitochondrial DNA in a catapult-like fashion to create a net that captures and kills bacteria.
“This is a fascinating finding,” says Gleich, professor of dermatology and internal medicine at the University of Utah and a co-author of the study.
“The DNA is released out of the cell in less than a second.”
Eosinophils, which comprise only 1 to 3 percent of human white blood cells, are known to be useful in the body’s defence mechanisms against parasites. However, their exact role in the immune system is not clear. Unlike other white blood cells, which are distributed throughout the body, eosinophils are found only in selected areas, including the digestive tract. Mitochondria – often referred to as the power plants of the cell – are components within cells that are thought to descend from ancient bacteria. Although most cellular DNA is contained in the nucleus, mitochondria have their own DNA.
Previous research has shown that eosinophils secrete toxic granule proteins during parasite infections and that these granule proteins kill bacteria.
Simon, Gleich, and their colleagues found that when eosinophils are stimulated by infection, such as E. coli, they rapidly secrete mitochondrial DNA. This DNA binds to the granule proteins and forms a net that is able to trap and kill bacteria. The researchers also found higher levels of eosinophils were linked to improved survival and lower numbers of bacteria in the blood of mice with widespread bacterial infections.
The toxic proteins released by eosinophils are not always helpful to the body, however, and can damage nearby tissues. The inflammation in some types of asthma and Crohn’s disease, a chronic inflammatory disease of the bowel, is attributed to eosinophils. In fact, Simon and his team first found evidence of these DNA-protein traps in tissue taken from the digestive tracts of people with Crohn’s disease.
Earlier studies suggested another type of white blood cell – the neutrophil – also expels DNA and granule proteins to kill bacteria. However, this DNA comes from the nucleus and its release causes the neutrophil to die. The eosinophil is able to survive after expelling its mitochondrial DNA.
The researchers hope to learn more about how eosinophils expel mitochondrial DNA. They speculate that the explosive mechanism might rely on stored energy, similar to the way plants release pollen into the air.
“We don’t know how eosinophils are capable of catapulting mitochondrial DNA so quickly,” says Gleich.
Future investigation may focus on how this energy is generated and how this new knowledge can be applied to the treatment of bacterial infections and inflammatory diseases related to eosinophils.
Reference:
Catapult-like release of mitochondrial DNA by eosinophils contributes to antibacterial defense
Shida Yousefi, Jeffrey A Gold, Nicola Andina, James J Lee, Ann M Kelly, Evelyne Kozlowski, Inès Schmid, Alex Straumann, Janine Reichenbach, Gerald J Gleich & Hans-Uwe Simon
Nature Medicine, 10 August 2008, doi:10.1038/nm.1855
.........
ZenMaster
For more on stem cells and cloning, go to CellNEWS
at http://cellnews-blog.blogspot.com/
Posted by ZenMaster at Wednesday, August 13, 2008
Labels: bone marrow, DNA, human, mitochondria, research 0 comments





