Each spot is a unique experiment that edits or silences a single
gene in cells growing above the RNA spot.
Not exact matches
Using the
gene - editing tool CRISPR - Cas9 to turn off certain
genes in a mouse zygote as well as other new techniques to enrich the pluripotent stem
cells of a rat, the group managed to
grow various rat organs (a pancreas, heart, and eyes)
in a mouse embryo.
Where is the clear line
in a progression from (1) using animal insulin to treat diabetes, to (2) using
gene remodeling techniques to
grow insulin
in a host bacterium that will reproduce rapidly and from which a plentiful supply of insulin can be harvested, to (3) genetic surgery to replace the defective
gene in a person diagnosed as diabetic, to (4) genetic surgery immediately after fertilization
in order to replace the defective
gene and alter the germ
cells which would otherwise have transmitted the disease to one's offspring?
«
In addition, changes in how the genes are expressed (turned on or off) could be used in the future to predict how and when the cancer cells will spread to other parts of the body and how fast they will grow.&raqu
In addition, changes
in how the genes are expressed (turned on or off) could be used in the future to predict how and when the cancer cells will spread to other parts of the body and how fast they will grow.&raqu
in how the
genes are expressed (turned on or off) could be used
in the future to predict how and when the cancer cells will spread to other parts of the body and how fast they will grow.&raqu
in the future to predict how and when the cancer
cells will spread to other parts of the body and how fast they will
grow.»
The most promising chemical — sulforaphane, a naturally occurring compound found
in cruciferous vegetables — tamped down glucose production by liver
cells growing in culture, and shifted liver
gene expression away from a diseased state
in diabetic rats.
Bloch's colleagues at the National Institute of Environmental Health Sciences tested the oils
in gene expression studies on lab -
grown human breast cancer
cells and found that they could mimic estrogens, the primary female sex hormones, and inhibit androgens, the primary male sex hormones.
So far, researchers have mostly turned on
genes with CRISPRa
in cells growing in lab dishes, says Charles Gersbach, a biomedical engineer at Duke University not involved
in the new study.
Already, researchers have used CRISPR / Cas9 to edit
genes in human
cells grown in lab dishes, monkeys (SN: 3/8/14, p. 7), dogs (SN: 11/28/15, p. 16), mice and pigs (SN: 11/14/15, p. 6), yeast, fruit flies, the worm Caenorhabditis elegans, zebrafish, tobacco and rice.
High
in the Cederberg Mountains of South Africa
grows a bristly shrub that embodies the tug - of - war taking place between industrialized and developing nations over the value of genetic resources — the
genes found
in plant, animal or microbial
cells used for research as well as
in commercial products, such as enhanced seeds and naturally derived cosmetics and pharmaceuticals.
By studying infected
cells grown in a laboratory, the team found that a large number of CMV's
genes help it hide from the immune system by allowing it to destroy many of the proteins produced by the body during virus infection and preventing them from activating immune
cells to destroy the virus.
As
cells divide and
grow, mutations may crop up
in cancer - associated
genes.
The embryos lacking functional BRCA2
genes probably stopped
growing because molecular «checkpoints»
in the developing embryo either halt the division of
cells with damaged DNA, so that the damage can be repaired, or kill the
cells outright.
Genes with increased activity are
in metabolic pathways that allowed cancer
cells to bypass BRAF altogether and continue to
grow and divide.
Previous studies of genetic alterations
in lymphoma and lung cancer have found that certain genetic mutations — specifically when part of a
gene breaks off and gets fused to another — can inappropriately switch on ALK, driving cancer
cells to
grow and divide.
PTEN prevents tumor
cells from
growing uncontrollably, and mutations
in the
gene encoding this protein are commonly found
in many different types of cancer.
It isn't clear exactly why the differences fade, Hochedlinger says, but it may be that the expression of embryonic
genes is strengthened as the
cells grow in culture, gradually overwriting the
cells» old
gene - expression patterns.
«Signaling pathways and
gene expression profiles are very different
in cells that
grow in 2D and 3D cultures,» says Oksana Sirenko, a research scientist at Molecular Devices
in Sunnyvale, California.
«Scientists identify proteins crucial to loss of hearing: Proteins play key role
in genes that help auditory hair
cells grow.»
To test whether the new spheroids were a better mimic for functional dermal papilla
cells than those that had been
grown in typical dishes, Christiano and her team determined what
genes were turned on and off
in different sets of dermal papilla
cells.
They tested these drugs one at a time for lethal interaction with 112 different tumor - suppressor
gene mutations
in human cancer
cells growing in the lab.
The team reports that the adenomas
grow from
cells that express a
gene called Lgr5 +, which is also active
in normal intestinal stem
cells.
In cells grown on flat culture dishes, the expression of thousands of
genes didn't match up with their normal patterns, explaining why the
cells from those dishes had been unable to generate new hair follicles.
Then De Luca and colleagues used a retrovirus to insert a healthy copy of the LAMB3
gene into DNA
in the lab -
grown skin stem
cells.
It plays an important role
in how
cells sense their neighbors and, by controlling
gene expression, determines which
cells should develop into different types and how much they should
grow - like a master controller.»
When researchers inserted the LAMB3
gene, it landed
in different places
in each lab -
grown stem
cell.
From there it's a matter of getting the hybrid
cell to
grow in a surrogate, hoping all the
genes work harmoniously together, bringing the hybrid to term, and hoping it acts like the extinct species even though it was raised by a modern relative.
When the researchers used
gene engineering techniques to knock out DDX3 expression
in laboratory -
grown cell cultures that highly expressed this protein,
cell proliferation was half that of
cell cultures with high DDX3 expression.
In BRIC 17 - 1, cell cultures derived from thale cress plants are grown in Petri dishes and later examined to determine which genes are involved in certain cellular change
In BRIC 17 - 1,
cell cultures derived from thale cress plants are
grown in Petri dishes and later examined to determine which genes are involved in certain cellular change
in Petri dishes and later examined to determine which
genes are involved
in certain cellular change
in certain cellular changes.
A year later, researchers corrected the faulty
gene in lab -
grown lung
cells and felt it wouldn't be long before
gene therapy could be used to implant correct versions of the
gene into people with CF.
In 2006, Japanese biologist Shinya Yamanaka found a solution: He reprogrammed skin
cells from a mouse, turning them back into embryo - like
cells, with the potential to
grow into any tissue, simply by adding four
genes.
Traditionally, researchers then disable or «knock out» the
gene in lab -
grown cells or animals to test their hypothesis, a time - consuming and laborious process.
Ultimately, these signals change the expression of
genes in the
cell nucleus, causing the
cell to
grow abnormally.
«Because the primary Small Intestine Chip recapitulates the physical microenvironment that
cells experience inside the human body, such as fluid flow and cyclic peristalsis - like stretching motions, it exhibits a genome - wide
gene expression profile that comes closer to its
in vivo counterpart than that of the same intestinal
cells grown as 3D organoids,» said first - author Magdalena Kasendra, Ph.D., a former Postdoctoral Fellow on Ingber's team and now Principal Scientist at Emulate, Inc.
in Boston.
But when physiologist H. Lee Sweeney of the University of Pennsylvania School of Medicine
in Philadelphia and his colleagues put this faulty
gene into embryonic quail muscle
cells growing in lab dishes, the
cells made a shortened version of the protein and incorporated it into their contractile machinery.
To treat hereditary blood diseases, doctors could take a sample of bone marrow
cells from a patient, correct the faulty
gene, and then
grow healthy
cells in the bioreactor and transplant them back into the patient.
«Having a supply of these
cells could be a starting point to
grow functional organs
in the laboratory as well as a way to begin applying
cell therapy to kidneys with malfunctioning
genes.»
If the
cells grew on culture plates, the team inferred that the human
gene could fill
in for its yeast equivalent.
He showed
in 2010 that by adding rat stem
cells to mice embryos lacking a pancreas
gene, he could
grow a rat pancreas
in a mouse.
HXR9 targets the HOX
gene family, which includes 39 fairly similar
genes that help enable the remarkably rapid
cell division
in growing embryos.
They tagged a dozen
genes that turn on when the bacteria
grow inside clusters of immune
cells in the frog, the same spot where TB hides
in humans.
To find methods for stemming the tide of liver - damaging microbes, Schnabl and team tried experimentally bumping up copies of the REG3G
gene in intestinal lining
cells grown in the lab.
The
cells with the normal
gene grew significantly longer dendrites — the portions of the
cell that reach out to receive nerve impulses — than did neurons with the mutated
gene, the team reports 14 October
in Science.
In the new research, Prins and Liau used a technique called adoptive
cell transfer, which involves extracting and growing immune cells outside of the body, then reprogramming them with a gene known as New York Esophageal Squamous Cell Carcinoma, or NY - ESO
cell transfer, which involves extracting and
growing immune
cells outside of the body, then reprogramming them with a
gene known as New York Esophageal Squamous
Cell Carcinoma, or NY - ESO
Cell Carcinoma, or NY - ESO - 1.
The team, led by Eggan and Christopher Henderson of Columbia University Medical Center,
grew iPS
cells by introducing the four
genes used
in the earlier studies into about 30,000 skin
cells from the patient.
From directing the fate of stem
cells to determining how tall we
grow, the
genes in our body act
in complex networks.
IPS
cells are
grown in culture from body
cells, through the addition of
genes that cause them to revert to pluripotency — the stage
in which they can potentially develop into any type of body
cell.
Without this primer, researchers had to first
grow the bacterial
cells in a laboratory before extracting their DNA and amplifying the
gene.
In recent years, scientists have grown new retinal cells from stem cells and shown progress in developing an effective gene therap
In recent years, scientists have
grown new retinal
cells from stem
cells and shown progress
in developing an effective gene therap
in developing an effective
gene therapy.
More broadly, this landmark discovery has illuminated an unexplored avenue
in scientists» understanding of how
cells control
gene expression, and will indubitably incite a fresh wave of innovation
in this ever
growing field.
We are investigating the
genes that are the target of this pathway, how it influences the
cells of
growing worms, the size differences between the sexes (hermaphrodite worms are larger than males), and the way
in which it mediates signals from the environment.