Not exact matches
This permits high - resolution mapping
of genes and chromosomal regions on
single fibers
of DNA, and it targets the physical location
of mitochondrial DNA probes down to a resolution
of 1,000 base
pairs.
In these and other inherited diseases, 10 to 15 percent
of the
single - base
pair mutations that cause the disease create a misplaced, premature «stop» codon in the middle
of the
gene — causing the machinery
of the cell to prematurely halt synthesis
of the protein, which destroys its ability to function.
Such plants have two mutant copies
of a
gene called hothead, which differ from the normal
gene by a
single base
pair.
In the U.S., this behavioral division follows a genetic one: workers bearing two copies
of one form, or allele,
of the Gp - 9
gene live in nests governed by a
single matriarch, whereas those that have one copy or a
pair of a second allele take orders from a female oligarchy.
Reviewing thousands
of genome wide associate studies (GWAS) to identify genetic variants in
single nucleotide polymorphisms (SNPs), investigators at Dartmouth's Norris Cotton Cancer Center found that some alleles (one
of a
pair of genes located on a specific chromosome) are more frequently risk - associated with disease than protective.
The team found that a mutation in a
single pair of nucleotides in the
gene causes seed coat permeability — that is, a change in one
pair out
of the approximately 1 billion base
pairs that make up the soybean genome.
But in
genes, differences as small as a point mutation — the alteration
of a
single base
pair — can lead to disease.
They found up to seven variations
of the
gene — some differing by as much as 25 %
of their base
pairs — in a
single snail.
They found a point mutation in the
gene (a
single altered base
pair) in one
of 91 randomly selected short individuals, and no such mutations in 300 people
of average height — suggesting that about 1 %
of all short people may carry a SHOX mutation.
Most
of the afflicted family members, but none
of those who sleep normally, carry a
single base -
pair mutation in a
gene called hPer2, the researchers report 12 January in a paper published online in Science.
A
single gene can be hundreds or thousands
of base
pairs long.
The most radical news at the conference was the first reported use
of CRISPR / Cas9 to generate precise genome edits (changing only a
single base
pair) in two
genes, not only in cell lines in vitro, but also in specific tissues
of embryos in ovo.
A
single DNA base -
pair of the PRKAG2
gene was edited using the method developed by Drs. Miyaoka and Conklin.
Forms
of variation include
single DNA base
pair alterations, duplications or deletions
of genes or sets
of genes, and translocations, a chromosomal rearrangement in which a segment
of genetic material from one chromosome becomes heritably linked to another chromosome.
In the first paper, utilizing genomic analysis
of nearly 8,500 Icelandic and Dutch participants, the deCODE team identified a novel, tightly - linked
pair of single - letter variants (SNPs) near the ASIP (agouti signaling protein)
gene on chromosome 20 that greatly increase the likelihood
of an individual being prone to freckles and sunburn.
Results: We confirmed the Gallus Gallus v5 consensus except for two insertions
of 5 and 1 base
pair within the chIFITM3 and B4GALNT4
genes, respectively, and a
single base
pair deletion within the B4GALNT4
gene.
The mode
of inheritance is unknown, but since the blue eyes can be
single or a
pair and an individual eye may be half - and - half, there probably are either more than one
gene involved or there is regulatory DNA that influences the function
of the
gene (s) that cause this type
of blue eye.
Not nearly as simple as those due to a
single pair of defective recessive
genes that some offspring inherit from their parents.