Not exact matches
When looking into mechanisms that might affect the levels
of SMN
protein in neurons, the researchers scanned a genomic database called the UCSC Genome Browser and identified two genetic
sequences that matched the opposite DNA strand
of the SMN
gene.
Gene discovery was greatly facilitated by a new exome
sequencing technology, which analyzes all
protein - coding regions
of the genome at once.
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.
To derive an evolutionary tree
of the TRIM5
gene, they analyzed and compared its complete
protein - coding DNA
sequences from 22 African primate species.
With the successful completion
of genome -
sequencing projects, science's knowledge
of genes and
proteins has increased exponentially.
Project members also catalogued
sequences that mark areas where DNA unwinds from the round histone
proteins that maintain the shape
of chromosomes, allowing the cell's transcription machinery to activate
genes in those areas.
In this standard view, the genetic differences between any two individuals are due to slight differences in the
sequence of their
genes that mean that the
genes «spell out» slightly different
proteins.
Sequencing the genome
of one such organism, King and her colleagues found
genes that code for pieces
of the same
proteins used for the binding
of cells and communication between cells in animals — functions that would be unexpected in such an organism.
These retroviral
gene sequences make up about 8 per cent
of the human genome, and are part
of what is called non-coding DNA because they don't contain genetic instructions to make
proteins.
In germline cells PIWI
proteins silence the RNA from jumping
genes by cutting them in
sequences of ~ 30 nucleotides that will become piRNAs.
The growth
of publicly accessible data troves on genome
sequences,
gene activity, and
protein structures and interactions has opened new territory for biologists.
The pilot project tested a dozen or so
of the most commonly used
gene promoters (regions
of DNA that facilitate
gene transcription) and segments
of DNA that encode ribosome - binding sites (
sequences of messenger RNA that control
protein translation) to determine whether they behave consistently in different cellular contexts.
«The total
sequence was needed, I think, to allow us to see that our one
gene - one
protein model
of genetics was much too simplistic,» wrote one respondent.
One aspect
of gene regulation involves enzymes placing chemical tags or modifications on histone
proteins — which control a cell's access to the DNA
sequences that make up a
gene.
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).
By comparing proteomic and RNA -
sequencing data from people on different exercise programs, the researchers found evidence that exercise encourages the cell to make more RNA copies
of genes coding for mitochondrial
proteins and
proteins responsible for muscle growth.
Berninger and others have previously shown that Sox2, Ascl1, and other transcription factors —
proteins that bind to specific DNA
sequences to control the activity
of genes — can induce the nonneuronal «support cells» known as glia to turn into neurons.
By deleting some
of these «ultraconserved elements», researchers have found that these
sequences guide brain development by fine - tuning the expression
of protein - coding
genes.
The team integrated three, complementary
gene sequencing approaches to look for mutations in tumor cells from SS patients: whole - genome
sequencing in six subjects,
sequencing of all
protein - coding regions (exomes) in 66 subjects, and comparing variation in the number
of copies
of all
genes across the genome in 80 subjects.
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.
Conventional genetic screening looks for specific mutated
sequences of DNA, but the Dutch test simply searches for
proteins which are shorter than those produced by healthy
genes.
Moreover, because they had an idea
of what cells the
genes came from and what kinds
of gene sequences produce what kinds
of proteins, they were able to draw some conclusions about what all those
genes are good for.
For most known
genes this «messenger» or mRNA is then shuttled off to a ribosome
of a cell where its translation into a
protein sequence occurs.
«The fact that the genetic code can simultaneously write two kinds
of information means that many DNA changes that appear to alter
protein sequences may actually cause disease by disrupting
gene control programs or even both mechanisms simultaneously,» said Stamatoyannopoulos.
Nucleic acid and
protein sequences, as well as three - dimensional structures
of proteins, are frequently the objects
of study, but
gene expression as well as the simulation
of pathways and biochemical networks are attracting more and more attention.
Fortunately only about 3 percent
of that is actual genetic information that gets translated into
proteins; the rest is regulatory
sequences, old, nonfunctioning
genes, or outright nonsense.
For this reason, their finding — that nearly half
of the unmapped
sequences contained in available genomic reference libraries, including many
protein - coding
genes, were located in the centromeres — was unexpected.
The 3 angstrom resolution crystal structure
of the Escherichia coli catabolite
gene activator
protein (CAP) complexed with a 30 - base pair DNA
sequence shows that the DNA is bent by 90 degrees.
Our
genes can be thought
of as packets
of information written in
sequences of DNA bases, which encode
proteins that perform the functions necessary for life.
As scientists began to
sequence human
genes in the 1990s, sorting out the cellular locations
of each
gene's
proteins became a priority, says Mathias Uhlén, a microbiologist at the Royal Institute
of Technology in Stockholm, Sweden, and director
of the
Protein Atlas effort.
«
Genes code for the sequence of amino acids in proteins, and some are involved in the regulation of the expression of other genes,» he
Genes code for the
sequence of amino acids in
proteins, and some are involved in the regulation
of the expression
of other
genes,» he
genes,» he says.
Previous work had shown that two variations in the COX - 2
gene, with either a guanine (G) or a cytosine (C) molecule at a particular spot in the
gene's DNA
sequence, lead to different levels
of COX - 2
protein.
His specific mutation subtly affects the slicing
of the
gene and doesn't affect the amino acid
sequence that synthesizes the ZAP70
protein.
«By
sequencing all
of the DNA that codes for mRNA and ultimately,
proteins, Dr. Amin and colleagues found a single
gene that may account for as much as 4 %
of the heritable risk for depression,» said Doctor John Krystal, Editor
of Biological Psychiatry.
They can insert in the middle
of a
gene, knocking out the structural
sequence for a
protein.
Still unclear is how the methuselah
gene mutation makes flies more stress - resistant, but the amino acid
sequence of the
protein it makes may be part
of a signaling pathway that controls how well cells resist or repair these stresses.
Certain
sequences of DNA make up
genes, which are the «instructions» for making
proteins that do most
of the heavy lifting within a cell.
But the primary
sequences of the human, mouse, and rat genomes are also tools from which we can derive the
protein sequence for each
gene.
Since the successful
sequencing of the human genome, interest in the group
of genes encoding
proteins responsible for DNA remodeling has grown exponentially.
The
gene that codes for this clotting
protein has a very similar
sequence across many plant species, and the researchers showed that the microRNA from dodder targets regions
of the
gene sequence that are the most highly conserved across plants.
Now that the
sequence of the PfEMP1
genes and
proteins is known, it may be possible to screen for drugs to block the production
of the
proteins, and so prevent infected cells sticking to capillaries.
Although aneuploidy does not bring in new genetic
sequences, it does make possible another kind
of genetic diversity — in which the extra
genes produce extra
proteins, resulting in an organism that differs from its parents.
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.
From these efforts, we identified a high - quality orthologous
gene set across avian species, consisting
of exons from 8251 syntenic
protein - coding
genes (~ 40 %
of the proteome), introns from 2516
of these
genes, and a nonoverlapping set
of 3769 ultraconserved elements (UCEs) with ~ 1000 bp
of flanking
sequences.
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.
To answer the question, the group performed «whole exome
sequencing»
of family members to, effectively, take snapshots
of each
protein - producing
gene in the chromosomes
of these people predisposed to ALL.
In brown bears, the
sequence of this
gene varies from one bear to another, but all the polar bears surveyed have an identical version, with the exact same genetic code at nine variable spots in the
gene, about half
of which should change the function
of the APOB
protein.
In the jargon, they are building the mouse «connectome», named in line with the term «genome» for the
sequence of all
of an organism's
genes, «proteome» for all its
proteins, and so on.
The tomato (left) shares all but 8 %
of its more than 34,000
protein - coding
genes with its close relative, the recently
sequenced potato.
DNA
sequencing of the ladybird's
protein - coding
genes revealed roughly 50 that help manufacture antimicrobial peptides, compared with 16 such
genes identified in the red flour beetle, which the researchers examined for comparison.