Not exact matches
An international team
of scientists has
sequenced the genome
of an octopus, bringing researchers closer to
discovering the
genes involved in the creature's unusual biology, including its ability to change skin color and texture and a distributed brain that allows its eight arms to move independently.
By characterising the DNA
sequence of these individuals, the project gained insight into the contribution
of rare variants to a broad range
of disease scenarios, and
discovered new genetic variants and
genes underpinning disease risk.
Publishing their findings in the open - access journal Nature Communications, the researchers
discovered DNA
sequences for «control dials» that consistently produce very high levels
of gene activity.
Douglas Thomas, associate professor
of medicinal chemistry and pharmacognosy at UIC, and co-workers
discovered that nitric oxide plays an important role in epigenetics — heritable alterations in
gene expression caused by mechanisms other than changes in DNA
sequence.
Using a battery
of comparative tests to study the genome
sequences of the giraffe and the okapi, the scientists
discovered 70
genes that showed multiple signs
of adaptations.
Significant differences were also
discovered between the centenarians and the two control groups when their genotype frequencies were compared, in other words, the proportion
of individuals with a specific
gene sequence.
He told the ESHG meeting that
of the 572 people he has
sequenced so far,
genes with strong links to cancer were
discovered in 10
of them.
By performing DNA
sequencing of more than 4,000 families affected by neurological problems, the two research teams independently
discovered that a disease marked by reduced brain size and sensory and motor defects is caused by a mutation in a
gene called CLP1, which is known to regulate tRNA metabolism in cells.
The evidence that the SWEET4c
gene was selected during domestication was
discovered by the team
of Jeff Ross - Ibarra at UC Davis, while comparing SWEET4
sequences from modern maize against its wild ancestor Teosinte.
One - hundred - ten
of the
genes had clear similarities in
sequence to known antibiotic - resistance
genes, the team
discovered, and 18
of those were 100 % identical to
genes found in human pathogens.
A new
sequencing technology based on longer
sequence reads allows missing
genes and missing forms
of genetic variation to be
discovered for the first time.
«We
discovered the existence
of a short DNA
sequence capable
of activating a specific Hox
gene, and which is present only in placental mammals and marsupials», explains Ruben Schep, the first author
of the article.
Other medical
sequencing projects will use DNA
sequencing to:
discover new
genes that are involved in common diseases; identify the
genes responsible for dozens
of relatively rare, single -
gene (autosomal Mendelian) diseases;
sequence all
of the
genes on the X chromosome from affected individuals to identify those involved in sex - linked diseases; and survey the range
of variants in
genes known to contribute to certain common diseases.
«This work compares the complete genome
sequences of all known species
of Leptospira to
discover which
genes make this bacterium a pathogen.
Reykjavik, ICELAND, 12 October 2011 — deCODE genetics today announced that it has entered into a research collaboration with Pfizer Inc., the objective
of which is to
discover sequence variants associated with specific clinical phenotypes related to Systemic Lupus Erythematosis by utilizing deCODE's expertise in
gene discovery.
After looking at 9 million genetic variants in those who were asparagus anosmic, they linked this deficiency to 871 individual
sequence variations they
discovered in chromosome 1, on
genes associated with our sense
of smell.
The SIGMA project aims to develop novel biomedical approaches to treat this devastating disease by applying powerful
sequencing technologies to
discover the
genes and key pathways underlying common varieties
of cancer.
Piroska Szabó
of the Van Andel Research Institute in Grand Rapids, Michigan, was once excited to think she'd
discovered a new
gene that expressed only the maternal allele — until she realized that the RNA
sequences she was looking at were from a
gene that had been misannotated as a nuclear
gene, explaining the maternal - only inheritance.
July 3, 2013 New mechanism for human
gene expression
discovered In a study that could change the way scientists view the process
of protein production in humans, University
of Chicago researchers have found a single
gene that encodes two separate proteins from the same
sequence of messenger RNA.
Although these regions have been heavily studied, their
sequences have led to unexpected observations; in the Bithorax complex for example, a glucose transporter
gene was
discovered in the midst
of the complex
of homeotic
genes.
His laboratory has also
discovered and characterized a significant number
of novel
genes contributing to autism and human neurodevelopmental disorders, and has recently applied whole - genome
sequencing technologies and large - scale genomics datasets to prenatal detection and interpretation
of structural variation in the genome.
The researchers then analyzed another 147 colorectal cancer cell lines in the same way for kinase - domain mutations in these
genes, and then
sequenced the entire coding region
of all kinases that were mutated, in all
discovering 46 new mutations.
By
sequencing the DNA
of different croc populations, the researchers
discovered that the Abanda cave crocs were inheriting their own unique haplotypes, the term for a group
of genes that one parent passes to its offspring, according to National Geographic.
With the completion and publication
of multiple fully
sequenced Woolly Mammoth genomes, the Church lab is
discovering potential cold climate adaptations in different
genes.
Genome Alberta announced C$ 25.2 million (US$ 22.2 million) in public / private funding over four years for two new genomic research projects, one targeted at enhanced recovery
of fossil hydrocarbon resources from oil sands and coal beds through biological processes, the other focused on
discovering plant
genes that can be
sequenced and used... Read more →
By zooming out
of the specific suspected regions, we
discovered differentially - methylated and acetylated regions that span large domains
of sequence in the vicinity
of the NR3C1
gene (Fig. 4a).