Upon joining the lab, Lee chose a high - risk project — «it sounded like more fun,» she says — aimed at determining whether a key
gene in the yeast cell cycle, cdc2, was also present in human cells.
And researchers at the «Seattle project», an effort funded by the National Cancer Institute to find new anticancer drugs, are mutating
genes in yeast cells — such as the ATM gene or the mismatch repair genes — that often lead to cancer in humans.
Not exact matches
Yoshinori Ohsumi, the most recent prizewinner, used baker's
yeast to identify
genes crucial
in autophagy, the process by which
cells recycle their components.
The new compounds boost the activity of Sir2
in yeast and of an analogous
gene, SIRT1,
in human
cells.
A class of small molecules found
in grapes, red wine, olive oil, and other foods extends the life of
yeast cells by approximately 70 % and activates
genes known to extend life span
in laboratory animals.
To answer this question, the researchers created numerous premature stop signs, known as nonsense mutations,
in test
genes in human and
yeast cells.
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.
She still does not know why he considered her at the time — «Maybe it was just my enthusiasm,» she wonders — but he nonetheless became her mentor as she studied the transcriptional activation of the
cell - cycle regulated HO
gene in the
yeast Saccharomyces cerevisiae.
They found numerous
genes activated
in the XYL regulon - controlled
yeast that upregulated pathways involved
in growth, such as
cell wall maintenance,
cell division, mitochondrial biogenesis and adenosine triphosphate (ATP) production.
When Fishel and Kolodner heard of the accumulation of mutations
in cancer
cells from patients with familial colon cancer, they suspected that the
gene responsible would be similar to the bacterial and
yeast genes they had studied.
Dr Nadeau added «Our results are even more surprising because the cortex
gene was previously thought to only be involved
in producing egg
cells in female insects, and is very similar to a
gene that controls
cell division
in everything from
yeast to humans.»
But while this study has proved that the technique works
in a simple organism, it could also be applied to other bacterial species,
yeast or even human
cells to find useful information about how
genes are controlled and how they can be manipulated.
A
yeast retrotransposon called Ty3, the researchers have found, is especially judicious: it always inserts itself
in safe places, outside
genes rather than inside them, and only near
genes of which a
yeast cell has many copies.
The studies on autophagy by Yoshinori Ohsumi, which earned him the Nobel Prize
in Medicine
in 2016, and the discovery of
cell cycle regulatory
genes for which Leland Hartwell, Timothy Hunt and Paul Nurse received the same award
in 2001, including the research of Elizabeth Blackburn, Carol Greider and Jack Szostak on telomeres, telomerase and its protective effect on the chromosomes, were all made possible thanks to
yeast.
«Mapping the
genes that increase lifespan: Comprehensive study finds 238
genes that affect aging
in yeast cells.»
Light played a key role
in the experiment because it allowed the researchers to switch on
genes that they had added to the
yeast cells.
If the
cells grew on culture plates, the team inferred that the human
gene could fill
in for its
yeast equivalent.
In 2003 Sinclair's lab published a paper in Nature that described the discovery of a gene that switched on in the yeast cell in response to calorie restriction, which Sinclair calls a «master regulator in aging.&raqu
In 2003 Sinclair's lab published a paper
in Nature that described the discovery of a gene that switched on in the yeast cell in response to calorie restriction, which Sinclair calls a «master regulator in aging.&raqu
in Nature that described the discovery of a
gene that switched on
in the yeast cell in response to calorie restriction, which Sinclair calls a «master regulator in aging.&raqu
in the
yeast cell in response to calorie restriction, which Sinclair calls a «master regulator in aging.&raqu
in response to calorie restriction, which Sinclair calls a «master regulator
in aging.&raqu
in aging.»
Given his training
in developmental biology, Raman focused the team to seek a novel drug target on
genes important to the development of model organisms — fruit flies (Drosophila) and
yeast (Saccharomyces cerevisiae)-- rather than on oncogenes that transform a normal
cell into a cancer
cell.
The group took the first step toward their goal of a novel engineering strategy for
yeast by creating what is known as a cDNA library: a collection of over 90 % of the
genes from the genome of baker's
yeast (Saccharomyces cerevisiae), arranged within a custom segment of DNA so that each
gene will be,
in one version, overactive within a
yeast cell, and
in a second version, reduced
in activity.
An ambitious study
in yeast shows that the health of
cells depends on the highly intertwined effects of many
genes, few of which can be deleted together without consequence.
October 21, 1994 Immortalizing agent of tumor
cells found
in yeast Researchers at the University of Chicago Medical Center have isolated the
gene for a component of the elusive molecular machinery that plays a key role
in making cancer
cells immortal.
Simon's strategy is to compare the effects of a drug on a normal strain of
yeast and a strain with a mutation
in one of the many
genes that affect normal
cell division - a property that is disrupted
in cancerous
cells.
A dual
yeast and human stem
cell discovery platform for Parkinson's disease: Investigations
in simple baker's
yeast cells brought to light abnormalities
in Parkinson's patient neurons and identified
genes and small molecules that correct them.
These methods integrate single -
cell experiments and discrete stochastic analysis to predict complex
gene expression and signaling behaviors
in Saccharomyces cerevisiae — or
yeast, a scientific - lab standard since
yeast and human
cells share many
genes.
The research team identified predictive models of transcription — the first step
in gene expression — when the
yeast cell is responding to osmotic stress (salt), which greatly affects
cell growth.
Kennedy is interested
in understanding why reduced
gene expression
in ribosomes enhances longevity
in yeast and worms — ribosomes are tiny organelles that occur within the
cell and are involved
in the production of proteins.
The human microbiome — the diverse array of bacteria,
yeast, parasites, and other single -
celled organisms that live
in and on our bodies — is comprised of more microbes than there are stars
in the galaxy, and the
genes encoded
in microbiome DNA vastly outnumber our own
genes.
Large - scale targeted - deletions have been successful
in defining
gene functions
in the single -
celled yeast Saccharomyces cerevisiae, but comparable analyses have yet to be performed
in an animal.
Breeden, Prentice and Zhao, whose study appeared
in the May 8 Proceedings of the National Academy of Sciences, compared their new algorithm to other methods used to analyze microarray experiments designed to identify
cell cycle
genes in yeast.
We combine biochemical, structural, cellular and functional information using purified proteins, mutant and transgenic plants,
yeast and chemical genomic screening systems, transient
gene expression assays, confocal microscopy and
in silico data analysis to compare ROP - centered kinase signaling during
cell polarity (
in vitro pollen tubes), morphogenesis (whole plant) and pathogenesis (fungi - infected
cells).
This new research, conducted by scientists
in Belgium and published
in the journal Nature Communications, found that
in yeast, the presence of high levels of glucose (sugar) can activate a
gene called Ras — the role of which is to regulate
cell generation, both
in mammals and
in yeast — which is often found
in tumours.