By using multiple RNA guides, researchers are able to «knock out» — that is, effectively delete or turn off —
zebrafish genes with close to 90 % efficiency vs. about 5 % efficiency using earlier methods.
Study pursues the genes with which a zebrafish views its world Neuroscientist biologist Herwig Baier, PhD, UCSF assistant professor of physiology and formerly of the Max Planck Institute in Tubingen, is working to identify
zebrafish genes that play a role in visual perception.
However, to be able to do this, we need to have as complete as a list of
zebrafish genes as possible.
Some mouse and
zebrafish genes remain active for up to four days after the animals die, scientists reported in 2017 in Open Biology.
«We studied
a zebrafish gene that is analogous to a human gene that causes deafness, and here we show the defect is in the process of mechanotransduction.»
Because of the usefulness of this information, we set ourselves the goals of constructing
a zebrafish gene set based on RNA - Seq alone and then identifying the highest quality models.
Not exact matches
For the study, the researchers created a line of
zebrafish with defective immune systems by inserting a mutation into a
gene required for development of an important component of the immune system.
The centre will be structured around six technical platforms focusing on
zebrafish transgenesis and micromanipulation, bioimaging, mouse transgenesis, flow cytometry, stem cell culture, and
gene - expression analysis.
The study found that
zebrafish that failed to inherit specific genetic instructions from mom developed fatal defects earlier in development, even if the fish could make their own version of the
gene.
In the study, Burdine and two graduate students Jose Pelliccia and Granton Jindal used CRISPR / Cas9
gene editing to remove Vg1, known as Gdf3 in
zebrafish.
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.
Investigators at Duke University, led by Erica Davis, PhD, a co-senior author of the report, blocked the
gene's expression in
zebrafish, which resulted in abnormal facial cartilage, smaller eyes and structural abnormalities of neurons involved in the development of reproductive organs.
To gain more insights as to why
zebrafish are more successful at regenerating spinal tissue, the researchers analyzed the
gene expression of fish spinal tissue following injury, identifying seven
genes of interest.
Using a novel combination of technologies, including trio exome sequencing of patient / parental DNA and genetic studies in the tiny larvae of
zebrafish, the EuroEPINOMICS RES consortium found that mutations in the
gene CHD2 are responsible for a subset of epilepsy patients with symptoms similar to Dravet syndrome — a severe form of childhood epilepsy that is in many patients resistant to currently available anti-epileptic drugs.
Removing a single
gene from the brains of mice and
zebrafish causes these animals to become more anxious than normal.
«Although
zebrafish look quite different from humans, they share an astonishing 70 percent of their genetic material with humans, including
genes important for the formation of new heart muscle,» Yin said.
If you actually read the paper that launched a thousand offbeat tidbits, by one Emmanuel Mignot of Stanford University, you discover that those «mutant»
zebrafish with the defective
genes were engineered to be mutants, in bulk, purely for the purpose of research.
In the case of CHD2, scientists collaborating with the EuroEPINOMICS RES consortium used antisense technology to rapidly generate
zebrafish larvae with a partial loss of function of this
gene, and were then able to detect epileptic seizures in these animals using electrographic analysis (this method is very similar to electroencephalography, or EEG, which is used to analyze seizures in humans).
The
zebrafish larva is an ideal model to study
genes involved in epilepsy, and the methods necessary for such studies are now well - established in our laboratory.
Functional analyses indicate that MFSD12 encodes a lysosomal protein that affects melanogenesis in
zebrafish and mice, and that mutations in melanocyte - specific regulatory regions near DDB1 / TMEM138 correlate with expression of ultraviolet response
genes under selection in Eurasians.
The results from McCammon's initial screen with
zebrafish indicate that two
genes in the 16p11.2 region could be key for brain development: fam57ba and doc2a.
For the first time, Whitehead Institute scientists have documented a direct link between deletions in two
genes — fam57ba and doc2a — in
zebrafish and certain brain and body traits, such as seizures, hyperactivity, enlarged head size, and obesity.
Zebrafish also have the PSENEN
gene.
Like the human genome, the
zebrafish genome has two copies of each
gene, and scientists can remove the function of multiple
genes to produce phenotypes that are reminiscent of human symptoms.
«In order to be able to research more closely what effect PSENEN has, we, in collaboration with Prof. Odermatt, deactivated the
gene in some
zebrafish larvae and then compared these with normal larvae under the microscope,» explains Damian Ralser.
Humans and
zebrafish share most protein - coding
genes, and CTGF is no exception.
When Kaufman, Zon and colleagues looked to see what was different about these early cancer cells, they found that crestin and the other activated
genes are the same ones turned on during
zebrafish embryonic development — specifically, in the stem cells that give rise to the pigment cells known as melanocytes, within a structure called the neural crest.
Zebrafish can find a way to compensate for a mutated
gene, but artificial methods of inactivating the same
gene are not so readily overcome, a new study suggests.
When
zebrafish with the green fluorescing endothelial
gene matured, the researchers observed green FGPs on the surface of the fish's brains — confirming that these cells arose from endothelial tissue.
«In the future,
zebrafish will be used to identify new
genes and drugs that can influence myelin formation and myelin repair,» says Dr. Lyons.
When the scientists prevented the
genes from working in
zebrafish, they failed to develop fingerlike projections called fin rays — the fishes» «hands.»
Because these
genes have the same function in
zebrafish, humans, and other tetrapods, it should help researchers further understand how our ancestors left the water and evolved limbs from fins.
Scientists led by John Kuwada, professor of molecular, cellular and developmental biology at the University of Michigan, and Hiromi Hirata of the National Institute of Genetics in Japan originally identified the
gene in mutant
zebrafish that exhibited severe muscle weakness.
It is also known that
zebrafish and humans have very similar
genes, and these similarities extend to more than 80 % of the
genes associated with human disease.
To get a better idea of the
gene's role in development the researchers blocked the expression of the
gene in
zebrafish.
This is possible because the
zebrafish retina contains cells called Müller glia that harbor a
gene that allows them to regenerate.
Using
gene therapy to insert the
gene, they expressed the synthetic
gene in adult mice or in
zebrafish embryos, and witnessed remote activation of neurons the presence of a magnetic field through the altered behavior of the animals.
Blood vessels of a
zebrafish larva: if the
gene EGFL7 is lacking, the blood vessels (stained green) are not formed correctly.
The shared
gene allows
zebrafish to sense water flow direction, and it also helps cells inside the human ear sense a range of sounds.
McDermott's team discovered hair cells on the
zebrafish skin use different mechanotransduction
genes — like tmc2b — depending on their orientation.
GENE SCENE
Zebrafish experiments that didn't go as planned may help researchers find
genes that can fill in for others in a pinch.
Zebrafish share 70 percent of
genes with people and also share similar biological pathways that lead to addiction.
In late 2012, the pathologist at Massachusetts General Hospital in Boston assembled the components of the new
gene - editing technology and fiddled with the DNA of a
zebrafish embryo.
Researchers discovered a
gene also found in humans helps
zebrafish convert water motion into electrical impulses that are sent to the brain for perception.
«Variable
gene expression in
zebrafish.»
Using the CAGE (Cap Analysis of
Gene Expression) high - throughput method, the scientists determined the starting points of transcription of many thousands of
genes in various phases of embryonic development of
zebrafish.
For the first time, it is now found by a study that various mechanisms of transcribing DNA into RNA exist during
gene expression in the different development phases of
zebrafish.
Surprisingly, the researchers found a similar bimodal 3 - dimensional chromatin architecture in the Hoxd
gene region in
zebrafish embryos.
More than 200
genes in the germ - free
zebrafish showed levels of activity different than those in their bacteria - exposed cousins.
«Fish eyes to help understand human inherited blindness: Discovery of a
gene in
zebrafish that triggers congenital blindness could lead to a suitable cure for similar disease in humans..»