Deciphering how
each human gene works is no easy undertaking.
Not exact matches
Nils Lonberg, a Harvard - trained molecular biologist who
worked at Medarex, had figured out not only how to engineer a mouse with
human immune
genes but also how to make antibodies from these
genes that were fully
human as well.
In April, Chinese researchers
working with non-viable
human embryos (those that would never end up turning into people) used it to try to tweak a
gene that would normally have caused a rare blood disorder.
During reproduction,
humans inherit two
working copies of most
genes — one copy, or allele, from each parent.
Like the per
gene, the new
genes — dubbed RIGUI in
humans and m - rigui in mice — are turned on and off in a daily cycle and may
work with other
genes to generate the oscillating mechanism that runs the internal clock.
The research builds upon the group's
work on «knockout
humans,» which are naturally occurring mutations that inactivate a certain
gene.
And researchers are already
working on identifying the
genes unique to modern
humans — at the most basic level, what unites and defines our species.
The findings of this
work will help scientists identify possible shortcomings of current animal models and construct a more accurate picture of how
genes work in
humans.
Several of the network
genes Volkan and her team identified have counterparts in
humans and other vertebrates, which suggests the same basic mechanism could be at
work in building the nervous system in other animals too.
In the current
work, they used a new variation of the
gene - editing system to repair the defect in both a mouse model and in
human cells.
«If this approach
works in
humans, it will really change the conversation that providers have with patients,» Scadden said, especially for those «who have these underlying genetic disorders and for who the new
gene - editing and
gene therapy techniques are being developed.»
Researchers
working in the Development and Growth Control Lab at IRB Barcelona reveal that the Dpp
gene (BMP in
humans) plays a double role in the structural organisation and growth of the wings of the fruit fly Drosophila melanogaster.
The research team from the Department of Biochemistry and Molecular Biology headed by Professor Susanne Mandrup are publishing a paper entitled «Browning of
human adipocytes requires KLF11 and reprogramming of PPAR super-enhancers» in the January 1 edition of the scientific journal
Genes & Development that describes their results from
working with «brite» fat cells.
PowderMed, based in Oxford, is developing a DNA - based vaccine that
works by spraying gold particles coated with avian flu
genes directly into
human skin with high - pressure helium.
«Our
work helps us to understand what causes
human diversity in appearance by showing how
genes involved in pigmentation subtly adapted to external environments and even social interactions during our evolution.
The study suggests that
human knockouts could prove valuable evidence for understanding how
genes work and for developing drugs.
«Understanding how
gene editing
works in
human embryos will require research in
human embryos,» because mouse embryos, for example, have species - specific developmental differences, notes Dana Carroll, a biochemistry professor at the University of Utah who researches CRISPR.
The researchers inserted the
genes for the 25 subtypes into
human kidney cells (an easier feat than
working with real taste cells).
Although the experiments were done in mice, Hertzano says that it is likely that these
genes work similarly in
humans.
Whether their
work is in
human genes, dwarf planets, or computer chips, many scientists have this in common: What they study is tangibly out there, somewhere.
After
working on the genetics of yeasts during a Ph.D. in pharmacy at the University of Valencia, Gil moved to the United States for a postdoc on
human suppressor
genes.
As when he
worked on the
human genome, Venter is relying on a radical technique called shotgun sequencing: He chops up vast amounts of DNA into tiny pieces and then uses sophisticated computer analyzers to piece them back together into intelligible
genes and chromosomes.
The researchers don't yet know how exactly these
genes influence social behavior in either bees or people, but manipulating the
genes in honey bees may shed light on what they do in
humans, says Alan Packer, a geneticist at the Simons Foundation in New York City, which funds autism research, including this bee
work.
«However, we were able to show for the first time that changes in this
gene primarily cause Dowling - Degos disease and around half of the mutation carriers develop acne inversa,» emphasizes Damian Ralser, who is currently
working on his doctorate at the Institute of
Human Genetics.
After years of studying yeast
genes in search of insights into how
human DNA
works, he was looking for a challenge.
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.
«The BDNF
gene has previously been linked to obesity, and scientists have been
working for several years to understand how changes in this particular
gene may predispose people to obesity,» said Jack A. Yanovski, M.D., Ph.D., one of the study authors and an investigator at NIH's Eunice Kennedy Shriver National Institute of Child Health and
Human Development (NICHD).
In the coming months, plummeting costs will allow
gene hunters to start routinely
working with complete
human genome sequences.
Previous
work has also shown that, following hybridization, many Neanderthal
gene variants were lost from the modern
human population due to selection.
After inserting more than 400
human genes into yeast cells, researchers found that almost half of the
human genes actually
worked and kept the yeast alive!
According to Kosik, this
work not only identifies a very critical
gene for
human brain development but also offers a clue about a component that likely contributed to brain expansion in
humans.
Further studies showed that very similar
genes controlled the process in animal and
human cells, and also helped piece together how the
genes work together to keep the cell's recycling centers running.
Human genes and friendly microbes
work together to control inflammation, he says.
Hox
genes are arranged in several clusters, and their order and spacing within the clusters — which varies little between insects and
humans — turns out to be central to the way they
work.
In 2013, CRISPR passed two important tests: It
works in
human cells, and it can target several
genes at once.
All organisms, including
humans, carry «extinct»
genes that no longer
work.
The first stumbling block was obtaining enough data to
work out how often
human genes are inherited together in families.
Alongside its soon - to - be — unveiled physical map, CEPH - Genethon is also leading the world with its efforts to build
human «genetic maps» — maps which show the relative positions of thousands of
genes, culled from careful genealogical
work on the way characteristics are passed on in
human families.
The embryo
work (done in China with nonviable embryos from a fertility clinic) even prompted an international summit this month to discuss
human gene editing.
Researchers at Oregon Health and Science University captured the development of
human embryos in images as part of their
work using a
gene - editing tool.
Greider and Ariel Avilion, a grad student
working in her lab toward a Ph.D. from the State University of New York, Stony Brook, were attempting to find and isolate the
gene for the RNA portion — dubbed hTR — of
human telomerase.
This in turn should help geneticists
work out the functions of
human genes, many of which are likely to have sequences similar to those found in the nematode.
A HD pig could be an opportunity to test if CRISPR - Cas9
gene editing can
work in larger animals before clinical applications in
humans.
• Evan Eichler
works on
genes and
human evolution at the University of Washington in Seattle; Washington State University is 500 kilometres away in Pullman (24 March, p 34).
Sabeti's
work is the latest to identify
genes that were important in the evolution of
humans, and our subsequent history.
Chimp Coordinators, on the other hand, easily turn on chimp
genes but don't
work as well for
human genes.
In 1991 he invented a quick way to find
human genes, using expressed sequence tags, after the senior scientists at the Human Genome Project had said it wouldn't
human genes, using expressed sequence tags, after the senior scientists at the
Human Genome Project had said it wouldn't
Human Genome Project had said it wouldn't
work.
Indeed, a close look at the chimp genome reveals an important lesson in how
genes and evolution
work, and it suggests that chimps and
humans are a lot more similar than even a neurobiologist might think.
Lanner will discuss the
work at a meeting on
human gene editing organized by the US National Academy of Sciences and National Academy of Medicine this month in Paris.
The first results of
gene editing in viable
human embryos reveals it
works better than we thought, but that there's another big problem blocking the way