Brain gene expression associated with depression differed markedly between men and women.
In addition to hinting at a link between depression and
brain gene expression during development, there was also evidence of overlap between the genetic basis of depression and other mental illnesses.
Not exact matches
There's better communication,» she told Inc.com in an interview, citing science that shows meditation changes the
brain, immune system, and even
gene expression.
Neuroscientists have over the past decade uncovered evidence, both in rodent and human studies, that parental caregiving, especially in moments of stress, affects children's development not only on the level of hormones and
brain chemicals, but even more deeply, on the level of
gene expression.
Procured from algae, algal oil is source of DHA, an important long - chain omega - 3 that supports
brain development, immune balance, and healthy
gene expression.
Because this imprinting affects hundreds of
genes that are non-coding, including microRNAs and non-coding RNAs, it's a very interesting fine - tuning mechanism for the dosage of
gene expression in the
brain and elsewhere in the body.»
By identifying
gene expression signatures common to sight, touch and hearing, neuroscientists at the University of Geneva (UNIGE), Switzerland, discovered a sensory «lingua franca» which facilitates the
brain's interpretation and integration of sensory input.
The activity of four transcription factors — proteins that regulate the
expression of other
genes — appears to distinguish the small proportion of glioblastoma cells responsible for the aggressiveness and treatment resistance of the deadly
brain tumor.
«Our work suggests that fine - tuning messenger stability is an important mechanism orchestrating
gene expression changes during normal
brain development.»
They did this by testing tissue concentrations of fatty acids in liver, muscle and
brain tissue, along with the
expression of
genes involved in regulating EPA status and its physiological benefits.
«We used the Allen Human
Brain Atlas data to quantify how consistent the patterns of expression for various genes are across human brains, and to determine the importance of the most consistent and reproducible genes for brain function.&r
Brain Atlas data to quantify how consistent the patterns of
expression for various
genes are across human
brains, and to determine the importance of the most consistent and reproducible
genes for
brain function.&r
brain function.»
Research published this month in Nature Neuroscience identified a surprisingly small set of molecular patterns that dominate
gene expression in the human
brain and appear to be common to all individuals, providing key insights into the core of the genetic code that makes our
brains distinctly human.
«It is exciting to find a correlation between
brain circuitry and
gene expression by combining high quality data from these two large - scale projects,» says David Van Essen, Ph.D., professor at Washington University in St. Louis and a leader of the Human Connectome Project.
Despite the anatomical complexity of the
brain and the complexity of the human genome, most of the patterns of
gene usage across all 20,000
genes could be characterized by just 32
expression patterns.
They compared the resulting
gene expression patterns in all the parrot
brains with neural tracing experiments in budgerigars.
By examining
gene expression patterns, the new study found that parrot
brains are structured differently than the
brains of songbirds and hummingbirds, which also exhibit vocal learning.
Ronald Kahn and his colleagues at Harvard Medical School in Boston compared
gene expression in
brain samples from mice with type 1 or type 2 diabetes against those of healthy mice.
The researchers then compared the
expression of all
genes in six parts of the
brain of the two bird species using state - of - the - art molecular techniques, including next - generation sequencing — the first time these tools have been used to find
brain properties related to innovation and problem - solving in wild birds.
Scientists at The Scripps Research Institute (TSRI) have identified a molecule in the
brain that triggers schizophrenia - like behaviors,
brain changes and global
gene expression in an animal model.
To find out, the duo decided to compare
gene expression in astrocytes in the adult
brain versus the aged
brain in mice.
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.
To develop a comprehensive view of astrocyte
gene expression, the duo used the technique in four very different areas of the mouse
brain: two regions of the cortex and the hypothalamus and cerebellum.
«The
genes which these miRNAs regulate also had increased levels, indicating that these
gene expression, indicating that these
gene products were likely targeted for storage and for possible future use within the
brain cell, rather than for destruction.
The researchers investigated 16 groups of female and male mice offspring exposed to maternal diet - induced obesity and male hormone excess and studied how these environmental factors affected the mice's behaviour as well as
gene expression in the
brain.
The environmental factors also affected
gene expression in the
brain.
The significance of the new model, according to Grange, is that «it enables us to now have a biological understanding of the patterns, the co-
expression profiles, seen in the Allen
Gene Expression Atlas of the Mouse
Brain.»
If the
gene expression profile of a neuronal type is measured, then the model predicts where in the
brain that type of neuron can be found.»
Such a treatment might be combined with a
gene therapy approach, also being pursued by her team and other groups, delivered directly to the
brain to curtail mHTT
expression.
The researchers discovered that this receptor mutation profoundly altered
gene expression in neurons receiving dopamine at distal sites in the
brain, specifically in the prefrontal cortex.
A molecule in cells that shuts down the
expression of
genes might be a promising target for new drugs designed to treat the most frequent and lethal form of
brain cancer, according to a new study by researchers at The Ohio State University Comprehensive Cancer Center — Arthur G. James Cancer Hospital and Richard J. Solove Research Institute (OSUCCC — James).
By comparing
gene expression in the
brains of resilient and avoidant mice, Berton and colleagues discovered that bullying in avoidant mice puts GABA neurons in a state where they become more excitable and the mice exhibit signs of social defeat.
Further, investigation of these CpG associations revealed nearby
genes whose RNA
expression was altered in
brain samples with Alzheimer's disease: ANK1, CDH23, DIP2A, RHBDF2, RPL13, RNF34, SERPINF1 and SERPINF2.
Booij and her colleagues hope that this study will shed more light on the specific role of early environmental influences on
brain development,
gene expression and emotional regulation.
While previous investigations into the protein's effects have used either mice in which
gene expression was knocked out or transgenic animals that expressed human
gene variants throughout their lifetimes, the MGH - MIND - led study used a different approach to investigate the effects of introducing the variant forms of the protein into
brains in which plaque formation had already begun.
It also remains unclear how knocking down
expression of certain
genes in zygotes via sperm miRNA leads to altered stress response in adult animals and altered
gene expression in the
brain.
We even did
gene -
expression studies in flies showing that
genes in their
brains change their level of activity in waking and in sleep.
The new research focused on just nine
genes, those most strongly associated with autism in recent sequencing studies, and investigated their effects using precise maps of
gene expression during human
brain development.
«Using a technique developed by our collaborators at the University of Iowa, we were able to get long - term
expression of these human
gene variants in the fluid that bathes the entire
brain,» says Bradley Hyman, MD, PhD, of the MassGeneral Institute for Neurodegenerative Disease (MGH - MIND), senior author of the report in the Nov. 20 Science Translational Medicine.
What we found is that the ability of this chronic social stress to produce maladaptive changes in
brain and behavior — loss of pleasure, inability to sleep normally and so on — are mediated through epigenetic modifications of
gene expression, in particular, emotional centers of the
brain.
Nestler: The ability of this chronic social stress to produce maladaptive changes in
brain and behavior are mediated through epigenetic modifications of
gene expression in particular emotional centers of the
brain.
During development, as an embryo forms differentiated tissues, liver cells,
brain cells, muscle cells, the cells in those tissues begin to allow for the selective
expression of
genes contained in those same 3 billion nucleotides.
The
brain attempts to adapt and respond to those challenges and that occurs in large part through changes in
expression of
brain genes through epigenetic mechanisms.
«TIA - 1 is known for its ability to regulate
gene expression during cellular stress,» says Hewett, who studies the processes that suppress the severe electrical storms in the
brain, leading to seizures.
However, the study showed the one area of the
brain with the most human - specific
gene expression is the striatum, a region most commonly associated with movement.
Despite differences in
brain size, the researchers found striking similarities between primate species of
gene expression in 16 regions of the
brain — even in the prefrontal cortex, the seat of higher order learning that most distinguishes humans from other apes.
Finally they looked at
gene expression in autopsied
brains of individuals with Rett.
The article «A gestational diet high in fat soluble vitamins alters
expression of
genes in 1
brain pathways and reduces sucrose preference, but not food intake, in Wistar male rat offspring» by Sanchez - Hernandez et al. was published in the journal Applied Physiology, Nutrition, and Metabolism.
In post-mortem
brains of 15 controls and 15 MDD subjects, the MDD group showed significant increase in the
expression of miR -124-3p, and
expression of three of the potential target
genes was significantly lower.
The researchers in the Greenberg lab found that across all analyzed datasets, and in studies of different mouse
brain regions, in the absence of MECP2 the
expression of long
genes is increased.
Then, they compared the patterns of
gene expression in the resulting neurons with cells taken from autopsied
brains.