We elucidated
the nucleotide sequence of a gene, and this was published in 1972.
Not exact matches
In 1972 he and his team were the first to publish the
nucleotide sequence of a complete
gene.
Fiers investigated the
nucleotide sequence of the hemagglutinin
gene of this duck virus and found that it was indeed very closely related to the strain that started the 1968 Hong Kong outbreak.
In the new study, the researchers
sequenced the entire genome
of mice that had undergone CRISPR
gene editing in the team's previous study and looked for all mutations, including those that only altered a single
nucleotide.
Which
genes are activated and which are turned off is in part determined by a second tier
of information which is superimposed on the
nucleotide sequences that provide the blueprints for protein synthesis.
In germline cells PIWI proteins silence the RNA from jumping
genes by cutting them in
sequences of ~ 30
nucleotides that will become piRNAs.
«By analysing the first
nucleotides we are able to identify which
sequence of gene starts the transcription.
A chromosome is, minimally, a very long, continuous piece
of DNA, which contains many
genes, regulatory elements and other intervening
nucleotide sequences.
A family
of neuropeptide
genes which includes the
gene encoding ELH along with two additional
genes encoding the A and B peptides thought to initiate the egg - laying process has been isolated and their
nucleotide sequence has been determined.
With the completion
of the first phase
of the Human Genome Project in 2000, and the advent
of sequencing technologies that can detect
gene variations such as single
nucleotide polymorphisms (SNPs), for the first time scientists have the tools in hand to find the key immune
genes and genetic networks that play roles in vaccine response.
By using random series
of 30
nucleotides — the building blocks
of RNA and DNA — he thought he could give neurons unique barcodes, linking the barcodes across synapses, then create maps
of their connections using high - throughput
gene sequencing technology.
His goal was to measure how the
sequence of nucleotides — the DNA building blocks
of genes — differed from animal to animal.
Extensive research has already examined the function
of microRNAs, a category
of small evolutionarily conserved noncoding RNAs about 22 to 24
nucleotides in length that target protein - coding
genes in a
sequence - specific manner.
Where the Neanderthal had
gene variants for a larger skull, for instance, Church would use MAGE to modify the
nucleotide sequences that constituted those
genes in one or more
of the chunks
of human DNA.
First the two researchers narrowed the possible location
of the lin - 4
gene to a
sequence of DNA 700
nucleotides long, about one - third the size
of a typical protein - coding
gene.
The study used whole - exome
sequencing to characterize genetic alterations that occur at the single
nucleotide level for all
genes in 25 cell lines commonly used as models
of bladder cancer.
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).
This study further investigated the impact
of nicotine use / smoking status and variation in the mu opioid receptor
gene (OPRM1), specifically, an A118G single
nucleotide polymorphism (SNP, or DNA
sequence variation), on the effects
of naltrexone on a range
of drinking outcomes.
The gRNA
sequence must complement a stretch
of 20
nucleotides on the segment
of the CD32
gene we want to cut.
Working with French composer Richard Krüll, the pair turned the complete
nucleotide sequences of several microbe
genes into compositions based on DNA bases: A (adenosine), C (cytosine), G (guanine), and Thymine (which they have translated to «Re,» or D).
Silent mutations occur when the change
of a single DNA
nucleotide within a protein - coding portion
of a
gene does not affect the
sequence of amino acids that make up the
gene's protein.
Much
of this DNA is no longer capable
of moving, but is likely «auditioning» perhaps as a regulator
of gene function or in homologous recombination, which is a type
of genetic recombination where the basic structural units
of DNA,
nucleotide sequences, are exchanged between two DNA molecules to repair breaks in the DNA strands.
Sequencing accelerates the analysis
of cancer associated alterations in genome
sequence such as insertions and deletions, CNVs, inversions, duplications, translocations and
gene fusions, as well as single
nucleotide variants.
The isolation and
nucleotide sequence of a cDNA encoding the T cell surface protein T4: a new member
of the immunoglobulin
gene family.
Comparisons between the
nucleotide makeup, or
sequence,
of particular
genes allows scientists to see how closely they are related, and thus, group the organisms accordingly.
Research interests: The biology
of pregnancy, Evolution
of genes X environment interactions, Mammalian phylogenetics, Rates
of nucleotide sequence evolution, The evolution
of the brain, Primate evolutionary genetics
In each case they checked tiny sites
of known DNA -
sequence variations — «single
nucleotide polymorphisms» — that mark common
gene variants.
Scott D. Collins, Ph.D., University
of Maine, Orono $ 850,000 (2 years) «High - speed Nanopore
Gene Sequencing» Skilled in silicon fabrication methods, this group will try to fabricate a nanopore with tiny electrodes and built - in circuits that will be used in experiments that attempt to measure differences in the electron tunneling
of individual
nucleotides in DNA molecules.
PULLMAN — Researchers at Washington State University have identified a new class
of DNA
sequence variation in
gene promoter regions that could help control the activity
of genes.The novel variations, dubbed «multiple
nucleotide length polymorphisms,» or MNLPs, altered transcription
of the
genes they were associated with as much as 11-fold.
Studying a specific type
of genetic variation in the DNA
sequences of wolves and domestic dogs - called Single
Nucleotide Polymorphisms (SNPs)- the scientists identified the transfer
of dog
gene variants into wolf genomes.
Input a DNA
sequence of up to 150,000
nucleotides to identify the
genes and transposons in it, and annotate (associate) the
sequence with this information.
This section invites manuscripts describing (a) Linkage, association, substitution or positional mapping and epigenetic studies in any species; (b) Validation studies
of candidate
genes using genetically - engineered mutant model organisms; (c) Studies focused on epistatis and
gene - environment interactions; (d) Analysis
of the functional implications
of genomic
sequence variation and aim to attach physiological or pharmacogenomic relevance to alterations in
genes or proteins; (e) Studies
of DNA copy number variants, non-coding RNA, genome deletions, insertions, duplications and other single
nucleotide polymorphisms and their relevance to physiology or pharmacology in humans or model organisms, in vitro or in vivo; and (f) Theoretical approaches to analysis
of sequence variation.
A conserved 11
nucleotide sequence contains an essential promoter element
of the maize mitochondrial atp1
gene
A normal version
of the FMR1
gene sequence, where the fragile X syndrome can develop, contains 5 - 55
nucleotide (CGG) repeats.
At the highest level
of resolution, the user can inspect the
nucleotide sequence of individual
genes.
To this end, we determined the susceptibility
of 38 NAPCR1 isolates to ten antibiotics from seven classes using E-tests or macrodilution tests and examined 31 NAPCR1 whole - genome
sequences to identify single
nucleotide polymorphisms and
genes that could explain the observed resistance phenotypes.
In DNA, each protein is encoded by a
gene (a specific
sequence of DNA
nucleotides that specify how a single protein is to be made).
NCBI provides
Gene, Online Mendelian Inheritance in Man, the Molecular Modeling Database (3D protein structures), dbSNP (a database
of single -
nucleotide polymorphisms), the Reference
Sequence Collection, a map
of the human genome, and a taxonomy browser, and coordinates with the National Cancer Institute to provide the Cancer Genome Anatomy Project.