Most such research focuses on mutations in the DNA of chromosomes within
the cellular nucleus.
Up until now, however, it has been unclear what comes first during cardiomyocyte differentiation: the reorganization of the DNA's folding in
the cellular nucleus or the DNA's methylation — and whether these mechanisms are dependent on one another.
Systemic lupus erythematosus (SLE) is an immune reaction against material from the body's
cellular nuclei leaking out of dying cells.
Not exact matches
A magnified transmission electron microscopy view of the rat
nucleus accumbens neurons containing mitochondria in different
cellular compartments.
Previous research conducted at Mount Sinai found that the trafficking of protein molecules between the
nucleus (the
cellular compartment containing the genetic information of the cell) and the cytoplasm is altered in neurodegenerative disease.
Proteins called kinesins, for example, are natural nanomotors that support
cellular functions such as mitosis (the chromosomal process that creates two
nuclei from one parent
nucleus) and meiosis (when the number of chromosomes per cell is reduced by one half).
In response to
cellular stress that can cause cancer, the team found that LC3, chromatin, and laminB1 migrate from the
nucleus — via the nuclear blebs — into the cytoplasm and are eventually targeted for disposal.
Neurobiologists at Heidelberg University have identified calcium in the cell
nucleus to be a
cellular «switch» responsible for the formation of long - term memory.
But UL138, the viral protein, is actually located outside the
nucleus, at a
cellular component called the Golgi.
Our body's master clock — a collection of about 50,000 neurons in the brain's suprachiasmatic
nucleus — responds to external cues, such as light, and coordinates the
cellular clocks in our organs and muscles.
The
cellular proteins are located in the
nucleus of the cell, where the virus maintains its genetic material.
In the past decade, researchers have used mouse models to unravel how
cellular changes in the
nucleus accumbens (NAc), a brain structure involved in action selection associated with arousal and reward, may contribute to addiction - related behavior.
The viral protein outside the
nucleus is somehow preventing the
cellular proteins in the
nucleus from accessing the viral genome, which is also in the
nucleus.
Previous studies in the lab showed that once HCMV is inside the cell, it quickly becomes latent by entering the cell's
nucleus and co-opting a
cellular protein called Daxx — part of the intrinsic immune system — to shut down its own replication, the process of reproducing its genetic material to make more copies of itself.
The goal of the NIH program, as described on its website, is «to understand the principles behind the three - dimensional organization of the
nucleus in space and time (the fourth dimension), the role nuclear organization plays in gene expression and
cellular function, and how changes in the nuclear organization affect normal development as well as various diseases.»
Like jewels in a vault, our precious genetic material is stored in the
nucleus of a cell — sequestered away from potentially damaging
cellular components and toxins so that no harm can come to it.
Working with mouse, fly and human cells and tissue, Johns Hopkins researchers report new evidence that disruptions in the movement of
cellular materials in and out of a cell's control center — the
nucleus — appear to be a direct cause of brain cell death in Huntington's disease, an inherited adult neurodegenerative disorder.
Moreover, they suggest, laboratory experiments with drugs designed to clear up these
cellular «traffic jams» restored normal transport in and out of the
nucleus and saved the cells.
RNA was once thought to be a mere middleman, carrying genetic messages from the DNA in the
nucleus out to
cellular structures called ribosomes, where it directs the production of proteins.
The answer to this daunting biological riddle is central to understanding how the three - dimensional organization of DNA in the
nucleus influences our biology, from how our genome orchestrates our
cellular activity to how genes are passed from parents to children.
First, some microbes developed a
nucleus using
cellular membranes to contain their DNA («eukaryotes»), perhaps through endosymbiosis.
One view of the Phylogeny of Life on Earth (at the University of California at Berkeley's Museum of Paleontology) highlights the role of archeabacteria among prokaryotes — as a separate «Archaea domain» apart from Eubacteria — in the development of
cellular life with
nuclei (eukaryotes).
On
cellular stimulation by immune and proinflammatory responses, becomes phosphorylated promoting ubiquitination and degradation, enabling the dimeric RELA to translocate to the
nucleus and activate transcription.
This landmark revelation was the first definition of an entire
cellular signaling pathway from the cell surface to the
nucleus, providing an important paradigm for understanding intracellular signaling.
Cells are the units of organic life and store in their
nuclei what constitutes the instruction manual for proper
cellular functioning, the DNA molecule.
Scientists at the Pacific Northwest National Laboratory have added to the understanding of ERK with proof that ERK oscillates within cells; that is, it cycles continuously in and out of a cell's
nucleus in response to
cellular growth cues.
The Sarma laboratory is interested in the mechanisms of epigenetic gene regulation, or how the dynamic modifications of the architecture of chromatin, the complex of DNA and proteins within the
nucleus of our cells, impacts gene expression and
cellular function.
Whether a protein is found in the
nucleus, cell membrane, or mitochondria can provide clues to the protein's
cellular role.
Which is roughly where things stood until last year when Princeton bioengineers Marina Feric and Cliff Brangwynne published a paper in Nature Cell Biology describing their probing of
cellular inner space, the cell
nucleus, and their discovery that gravity could limit cell size.
With Cell Painting, a technique developed at the Broad, researchers tag eight
cellular components and organelles (actin, cytoplasmic RNA, endoplasmic reticulum, Golgi apparatus, mitochondria,
nucleus, nucleolus, and the plasma membrane) with fluorescent dyes.
The mRNA is released from the
nucleus and then enters another
cellular body known as a ribosome.
It has unique properties (a
nucleus, to be exact) that make it great for
cellular repair and generation.