This is the first study in human trials to identify genes driving acute peanut allergic reactions using a double - blind placebo - controlled approach with comprehensive
sequencing of genes expressed before, during, and after they ingested peanut.
Not exact matches
Biologists now know that the genome
sequence holds only a small part
of the answer, and that key elements
of development and disease are controlled by the epigenome — a set
of chemical modifications, not encoded in DNA, that orchestrate how and when
genes are
expressed.
The policy — in the form
of first Office Actions on a series
of applications for patents on
expressed sequence tags, ESTs — could greatly complicate basic
gene therapy research by substantially allowing patents for small
sequences of a
gene that may later be used by the patent holder to corner ownership and uses
of entire
genes.
Epigenetic modifications do not affect the DNA
sequence of genes, but change how the DNA is packaged and how
genes are
expressed.
But the benefits
of this technology for discerning the circuits
of the mind go much deeper, because the virus that carries the photoreceptor
genes can also carry promoter
sequences that
express their payload only in neurons with the appropriate molecular address.
Molecular geneticists dream
of having a similarly comprehensive view
of networks that control
genes: For example, they would like to identify rules explaining how a single DNA
sequence can
express different proteins, or varying amounts
of protein, in different circumstances (see p. 80).
RNA
sequencing of both single and clustered CTCs from breast cancer patients identified several
genes expressed at elevated levels in CTC clusters, one
of which — a protein called plakoglobin — also was overexpressed in the primary tumors
of patients with reduced survival.
They then used next generation
sequencing — a state -
of - the - art method to rapidly measure
gene expression — to
sequence and quantify the thousands
of genes that are
expressed in hair cells, in comparison with other cells in the ear.
The BBSRC - funded ARK - Genomics facility — which is part
of Edinburgh Genomics at the University
of Edinburgh — provided a substantial body
of sequence data, including information on which
genes are
expressed in a spectrum
of 40 different tissues.
SEATTLE — Apparently ending several years
of uncertainty, an official
of the U.S. Patent and Trademark Office (PTO) revealed here today that the government intends to grant patents on
expressed sequence tags (ESTs), human DNA
sequences of up to a few hundred base pairs in length that can be used to identify and detect the expression
of specific
genes.
The team, headed by OIST's Prof. Alexander Mikheyev
of the Ecology and Evolution Unit and Dr. Claire Morandin, post-doctoral scholar at the University
of Helsinki, collected queens and workers and
sequenced the transcriptome — the full range
of messenger RNA molecules
expressed by an organism —
of 16 species
of ants to create a co-expression network
of 36 sets
of genes, that represent groups
of similarly
expressed genes.
Single - cell RNA
sequencing allows researchers to determine the precise nature
of the total
gene transcripts, or all
of the
genes that are actively
expressed in a particular cell.
The human genome contains about 3 billion base pairs, but only about 2 percent
of these base pairs represent protein - coding
genes, meaning that whole - exome
sequencing measures the genetic alterations focused on a small but very important fraction
of the genome (as opposed to techniques
of whole genome
sequencing, which measures every nucleotide across the entire genome, regardless
of whether these
genes are
expressed or silent).
The Yale - led study performed whole exome
sequencing ¬ — a technique for
sequencing all the
expressed genes in a genome ¬ — on TNBC tumors to identify mutations in specific
genes or pathways that may indicate response or resistance to the standard
of care, which is anthracycline / taxane (ACT) chemotherapy.
By isolating strands
of complementary DNA (cDNA) that fit together with mRNA, researchers can figure out what
sequence was just translated into mRNA — that is, they can get a read on an
expressed gene.
But because the vinclozolin - induced fertility changes occurred in almost every male rat descended from a treated mother rather than in a small percentage
of offspring (as is seen in germ line mutations caused by radiation), Skinner suspects an epigenetic mechanism — a change that doesn't mutate the DNA
sequence of an animal, but rather affects how
genes are
expressed.
Seeking to understand how the cone snail springs its slow - motion trap, the Utah researchers searched the
gene sequences of all
of the proteins
expressed in the venom gland
of Conus geographus.
Epigenetics is the study
of changes to DNA packaging that influence which
genes are
expressed but don't affect the DNA
sequence itself.
Then, if you want only certain types
of cells to
express the protein they encode, you must add a «promoter», i.e. a small DNA
sequence which regulates expression, to this
gene.
Expressed sequence tag analysis of genes expressed in the bay scallop, Argopecten i
Expressed sequence tag analysis
of genes expressed in the bay scallop, Argopecten i
expressed in the bay scallop, Argopecten irradians.
To assess the speed with which both humans and chimpanzees accumulated many small differences in
gene sequences accurately, Wu and colleagues in Taiwan and Japan decided to
sequence several thousand
genes expressed in the brain
of the macaque monkey and compare them with available genomic
sequences from human, chimpanzee, and mice.
Although over 270,000 human
expressed sequence tags (ESTs) were available in public databases as
of October, 1995, it is still unclear how many
genes have been identified by this methodology (Jordan, 1996).
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.
We found 1,098
genes in the
sequence,
of which 99 encode proteins
expressed in testis and in various tumour types.
To find a solution to this, Marcel Martin at Bioinformatics Long - term Support (WABI) at SciLifeLab, in collaboration with the group
of Gunilla Karlsson Hedestam at Karolinska Institutet, has developed a practical, computational technique, IgDiscover, that enables rapid production
of individualized V
gene databases following deep
sequencing of expressed antibody repertoires.
has developed a practical, computational technique, IgDiscover, that enables rapid production
of individualized V
gene databases following deep
sequencing of expressed antibody repertoires.
This permissive expression includes lineage - specific and tissue - specific
genes, non-coding regions
of the genome that are normally «silent,» and repetitive
sequences in the genome, which comprise the majority
of the mammalian genome but are also normally not
expressed.
We are using a new technique, called single cell RNA
sequencing, to isolate thousands
of single neurons from human brain tissue, study all the
genes that are
expressed in each individual cell, and make cell - to - cell comparisons between normal, early stage and late stage AD.
Although the researchers found no change in the coding region
of the
gene, they did find that autistic children were much more likely to have inherited a shortened form
of the
genes promoter — the DNA
sequence that serves as the on ramp for the cellular machinery that will
express the
gene.
By comparing the promoter
sequences of expressed with non-
expressed OR and VR
genes and pseudogenes, it may now be possible to identify key genomic motifs that control receptor choice.
MicroRNAs are short
sequences of genetic material that play a role in regulating how
genes are
expressed.
Specifically, we have generated clusters
of transcripts that behave the same way under the entire spectrum
of the sixty - seven experimental conditions; we have assembled
genes in groups according to their time
of expression during successive days
of ES cell differentiation; we have included expression profiles
of specific
gene classes such as transcription regulatory factors and
Expressed Sequence Tags; transcripts have been arranged in «Expression Waves» and juxtaposed to
genes with opposite or complementary expression patterns; we have designed search engines to display the expression profile
of any transcript during ES cell differentiation;
gene expression data have been organized in animated graphs
of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual
genes or
gene clusters
of interest and links to microarray and genomic resources.
As part
of an ongoing functional genomic screening approach, we have been using microarray analysis and next generation
sequencing to identify mouse
genes that are specifically
expressed in meiosis, and are likely involved in aspects
of chromosome biology that are required for meiotic ploidy reduction.