Not exact matches
Others have
normal chromosomes but poorly developed genitals, often caused by the wrong hormones being present
in the womb at a critical stage.
Both mouse and human males typically die early from the mutation
in Mecp2, because their Y
chromosome does not supply a
normal copy of the gene.
Some of the neochromosomes had three times as much DNA
in them as the largest
normal chromosomes.
Dr Paul Waters, an ARC fellow
in the School of Biotechnology and Biomolecular Sciences at UNSW Australia, says that the X and Y
chromosomes started their existence as
normal autosomes (non-sex
chromosomes) harbouring the same genes.
Fragile X occurs when a segment
in the FMR1 gene on the X
chromosome called the CGG triplet repeat is lengthened from the
normal 5 to 40 repeats to 200 repeats
in people with full mutation FXS.
Other researchers had linked the ank mutation to mouse
chromosome 15;
in this week's Science, Kingsley's team reports that it's a single typo
in a previously unknown gene, which they called ank, that led to a protein about 10 % shorter than the
normal version.
«But fruit flies have all their histone genes
in one place on the
chromosome; this makes it feasible to delete the
normal genes and replace them with designer genes.»
For Dr. Christophe Dufresnes from the University of Lausanne, first author of the common study just published
in Scientific Reports, this «suggests that the undifferentiated sex
chromosomes in these tree frogs contribute more to the evolution of new species than other,
normal chromosomes.»
They frequently find that
in both types of disease the region of the «healthy» copy of
chromosome 17 that should carry the
normal copy of the BRCA1 gene is missing, leaving only one copy of the gene — the one with the cancer - causing mutation.
As a result of this careful debugging, yeast cells with the synthetic
chromosomes grow just as quickly
in the lab as
normal, wild yeast, despite the wholesale alterations (Science, DOI: 10.1126 / science.aaf4557).
The best example of this occurs
in what's called gene imprinting, where for example, females have two X
chromosomes and one of those two X
chromosomes must be inactivated
in a cell
in order for the cell's
normal function.
For a decade, Mignot and his colleagues have scrutinized the dogs» dna, bit by bit, comparing it with that of
normal littermates until,
in 1998, they narrowed the defect down to a single
chromosome.
Comparing the damaged sites
in normal cells before and after infection with H. pylori revealed that genes located close to the margins of the
chromosomes, the so - called sub-telomeric regions, are more likely to be damaged after infection, as are genes that are active
in gastric cells.
Dysfunction
in these skills was highest
in two groups — Turner's females with a maternal X
chromosome and
normal males.
The culprit emerged as a gene, RCAN1, which
in Down syndrome appears
in three times the number that would be found
in normal chromosomes.
Perera's paper
in Cancer Epidemiology Biomarkers and Prevention linked the chromosomal aberrations, which were somewhat higher than
normal, to air pollution: On average, the higher the hydrocarbons
in the mothers» air, the more frequent the abnormalities seen
in the infants»
chromosomes.
The finding that
normal fertilization can result
in embryos containing cells with different parental sets of
chromosomes is a new mechanism for chimerism, which was previously thought to occur only as the result of fertilization errors, for example, the fusion of multiple sperm or eggs to form an embryo.
The other marker is an aberrant pattern
in the
chromosomes; the DNA shows a greater number of abnormalities than
normal, including DNA that is missing or moved.
He points out that
in normal cell division,
chromosomes line up near the center of the cell, where a structure called the spindle aligns two copies of each
chromosome and helps to separate them.
This phenomenon almost never happened
in sets of control cells that were pre-malignant but still had a
normal chromosome number.
Although the researchers only sequenced about 2 % of the mother's and fetus's genome, this was enough data to distinguish levels of
chromosome 21
in mothers carrying a Down syndrome baby from those with a
normal fetus as early as 14 weeks.
Viewed under a microscope,
normal human cells can be seen to have 46
chromosomes, arranged
in 22 pairs plus the two sex
chromosomes.
Under
normal circumstances, genes
in this region are inactive, or silenced, on maternal
chromosome 15 but active on paternal
chromosome 15.
An article by MIT Technology Review describes project «Boys Only,»
in which Alison Van Eenennaam of the University of California aims to create a bull that will father only male offspring: either
normal bull calves or ones with two X
chromosomes but also the male - making SRY.
Since genes
in our
chromosomes are very, very much better protected from mutations than the mitochondrial DNA is, we can rely on the chromosomal copies carrying on working
in very nearly all our cells for much longer than a currently
normal lifetime.
Cell type specific
chromosome territory organization
in the interphase nucleus of
normal and cancer cells.
Kinesins klp5 + and klp6 + are required for
normal chromosome movement
in mitosis.
LA JOLLA, CA — Rapidly dividing cancer cells are skilled at patching up damage that would stop
normal cells
in their tracks, including wear and tear of telomeres, the protective caps at the end of each
chromosome.
They discovered that extra
chromosome 21 - a genetic state known as trisomy 21 - disturbs a key regulating gene called NRSF or REST, which
in turn disturbs the cascade of other genes that control
normal development at the embryonic stem cell stage.
Variations
in the
normal ploidy are referred to as aneuploidy (gain or loss of whole
chromosomes) and polyploidy (gain of multiple sets of
chromosomes).
In their analysis, the research team found that a process called compensatory uniparental disomy (UPD) was responsible for the complete replacement of the ring
chromosome with a
normal copy of
chromosome 17.
These segments can get placed back at another spot
in the
chromosome and interrupt the
normal flow of information.
Swanton's new lab set out to identify specific genes that, when inhibited, result
in the death of tumor cells that displayed aneuploidy, meaning they had more or less than the
normal set of 46
chromosomes.
Normal male cats only inherit one X
chromosome so this is active
in all skin cells as there is nothing equivalent on the Y
chromosome which could «switch off» the O gene.