Bivalent marking of loci encoding lineage
specific transcription factors in ES cells is thought to prepare these genes for rapid activation of transcription once the pluripotency network is extinguished [4].
Not exact matches
However, each time a cell divides the
specific binding pattern of the
transcription factors is erased and has to be restored
in both mother and daughter cells.
Glk1 is a
transcription factor, meaning it binds to
specific regions of DNA and activates genes involved
in cell death and other plant immune responses.
Thus, this cDNA derives from a gene (oct - 2) that specifies an octamer binding protein expressed preferentially
in B lymphocytes, proving that, for at least one gene, a cell -
specific transcription factor exists and its amount is controlled through messenger RNA availability.
«Many thyroid diseases will be impacted by changing the expression levels of the thyroid -
specific transcription factor, so we want to investigate FOXE1 more carefully
in future work.»
It is situated just next to a thyroid -
specific transcription factor, a protein that regulates the rate of gene expression
in the thyroid.
Gray and cyan ribbons, Mtb RNAP; yellow and orange ribbons,
transcription initiation
factor sigma; red and pink ribbons, DNA (
specific sequence elements
in blue).
The predictors include «Online Mendelian Inheritance
in Man» (OMIM, a list of genetically caused diseases), receptors, kinases, growth
factors,
transcription factors, tissue
specific, plasma membrane localization, nuclear localization and conversation index.
The activity of each gene then was analyzed
in an attempt to find the
specific transcription factor responsible for regulating the conversion of sugar to starch
in the above - ground portions of the plant, primarily the grains.
«Our research revealed how small RNA molecules can work with other cell signals called
transcription factors to generate
specific types of neurons,
in this case motor neurons.
Previously,
in the region that controls the function of the
transcription factor that promotes differentiation from ES cells to a
specific cell type, bivalent modifications of histones such as the accelerator and brake histone marks for
transcription were thought to have coexisted.
«We know that
transcription factors bind to
specific sites
in the genome and when they misfire they drive many diseases, including cancers,» explains lead study author Graham Erwin, a former graduate student
in the lab of Aseem Ansari, a professor
in the Department of Biochemistry and the Genome Center of Wisconsin.
What they found was that when they overexpress
transcription factors that drive the specification of
specific subtypes of neurons
in other cells
in C. elegans, these do not by themselves cause the cell to convert into neurons.
So what we think is that probably
in many cells
in this section, all cells, the chromatin is encountered
in a
specific state, and
in order to render the cell is permissive to reprogramming, you have to overcome these certain epigenetic modifications that block, for example, the binding of Ascl1 to its target chains, or the binding of other
transcription factors to its target chains, then this way interfere with the possibility of reprogramming.
For example, his group looked at
specific signaling pathways and
transcription factors expressed
in their pre-HSCs.
Finally, I will show how we have combined our results to generate a model of hematopoietic differentiation where
specific transcription factors control lineage regulatory regions; our model predicts many already known lineage - controlling
factors as well as finds new potential regulators of hematopoietic differentiation such as ATF3
in monocytes and Tcf7l2 and Runx2
in NK cells.
This,
in turn, because the scientists did not know which DNA sequences are functional, and bind to the
specific proteins called
transcription factors that regulate gene expression.
In response to signals from inside and outside cells,
transcription factors attach to the DNA and cause
specific genes to be more or less activated, producing more or less of the corresponding protein.
Using chromatin accessibility and gene expression measurements, we present clear evidence that lineage
specific enhancer dynamics
in hematopoiesis is the result of lineage
specific transcription factor activity.
A famous example of how
transcription factor expression can be used to alter a cell's identity is the creation of iPSCs, where adult cells were forced to express
transcription factors normally expressed
in ESCs, which made the adult cells express genes
specific to ESCs, and consequently become nearly identical to ESCs.
These include molecular evolution of
transcription factors or changes
in transcriptional regulation (Enard et al., 2002; Konopka et al., 2009), accelerated evolution of small non-coding RNAs (Pollard et al., 2006), changes
in the tissue - specificity of enhancer elements (McLean et al., 2011; Prabhakar et al., 2008), or changes
in patterns of alternative splicing of
specific genes (Calarco et al., 2007).
The GDDS laboratory was responsible for first identifying the
transcription factor SOX10 as a key lineage -
specific regulatory
factor in melanocytes that is mutated congenitally
in individuals with Waardenburg syndrome IV.
In contrast, many scientists consider that chromatin does not form an independent epigenetic layer of the genome and that chromatin modifiers do not operate independently of a DNA sequence
specific targeting mechanism, such as
transcription factors.
In addition, well - characterized expression profiles for melanoma cells have been identified that correlate highly proliferative cell states with increased expression for pathways regulated by the lineage -
specific transcription factors SOX10 and MITF; conversely, migratory / invasive cell states have been correlated with TGFβ1 signaling pathways.
In particular, understanding how transcription factors (TFs) bind in a sequence specific manner to the DNA and how the alteration of transcriptional regulation contributes to cance
In particular, understanding how
transcription factors (TFs) bind
in a sequence specific manner to the DNA and how the alteration of transcriptional regulation contributes to cance
in a sequence
specific manner to the DNA and how the alteration of transcriptional regulation contributes to cancer.
Dmrt1 (Doublesex and mab - 3 related
transcription factor 1) was a testis -
specific positive control
in chicken [82] and Bnd (Bindin) was a testis -
specific positive control
in the sea urchin [83].
The 1500
transcription factors (TFs) within the human genome perform a key role
in determining the set of active genes within a
specific cell, as well as the magnitude of activity.
Here we measure allele -
specific transcription factor binding occupancy of three liver -
specific transcription factors between crosses of two inbred mouse strains to elucidate the regulatory mechanisms underlying
transcription factor binding variations
in mammals.
These 45 variants are significantly enriched for protein - coding changes (n = 13), direct disruption of
transcription -
factor binding sites (n = 3), and tissue -
specific epigenetic marks (n = 10), with the last category showing enrichment
in specific immune cells among associations stronger
in Crohn's disease and
in gut mucosa among associations stronger
in ulcerative colitis.
To be more
specific, we searched for
transcription factors that were changed
in NSCs after exposure to amiodarone HCl but showed no change
in differentiated cells after treatment with equivalent amounts of the drug.
The overall goal of the core is to provide support to investigators interested
in characterizing the interactions of post-translational modifications of histones (epigenetic marks that define a chromatin state or Epigenome) or
transcription factors at
specific genomic loci or genome - wide (Cistrome).
The pluripotent population is characterized by a high degree of plasticity
in chromatin structure [3], and lineage
specific transcription factors show bivalent chromatin epigenetic marks characteristic of both suppression and inactivation [4].
Specifically, we have generated clusters of transcripts that behave the same way under the entire spectrum of the sixty - seven experimental conditions; we have assembled genes
in groups according to their time of expression during successive days of ES cell differentiation; we have included expression profiles of
specific gene classes such as
transcription regulatory
factors and Expressed Sequence Tags; transcripts have been arranged
in «Expression Waves» and juxtaposed to genes with opposite or complementary expression patterns; we have designed search engines to display the expression profile of any transcript during ES cell differentiation; gene expression data have been organized
in animated graphs of KEGG signaling and metabolic pathways; and finally, we have incorporated advanced functional annotations for individual genes or gene clusters of interest and links to microarray and genomic resources.