ES cells can be described based on a characteristic morphology, the presence of cell surface markers such as SSEA - 1 and Pecam1, or the expression
of the key transcription factors such as Oct4, Sox2, Nanog, and a number of ES cell - specific transcripts (ECATs)[4]--[6].
We have identified a number
of key transcription factors that are deregulated during this process, and we are using this information to investigate mechanisms by which differentiation can be reprogrammed in tumour cells.
What are the direct targets
of key transcription factors that regulate cardiogenesis and cardiomyocyte differentiation and how do they function in networks?
While the process usually proceeds in a one - way direction, artificially inducing the activity
of key transcription factors can reprogram differentiated cells back into a stem - like state, a discovery honored with the 2012 Nobel prize.
Not exact matches
The investigators focused on studying the activity
of AHR, a
transcription factor that is known to play a
key role in regulating inflammatory and immune responses, and the effects
of two AHR ligands (ITE and FICZ).
In addition, when these
transcription factors lose their function, terminal differentiation into the vascular endothelium (completion
of differentiation) is completely suppressed, and genes that are
key to differentiation into vascular endothelial cells as well as
transcription factors that maintain the undifferentiated state are adversely induced.
In the March 24 issue
of the Proceedings
of the National Academy
of Sciences they explain that they were able to crystallize a
key protein called a
transcription factor and work out its structure.
Shimon Sakaguchi and colleagues report that the
transcription factor Foxp3 is a
key regulatory gene for the development
of regulatory T cells.
However, genome integrating viral vectors and oncogenic
transcription factors are still
key parts
of many reprogramming schemes, and many early differentiation studies need to be confirmed using iPSCs generated using safer non-integrating viral vectors.
June 2009 - The X
factors of stem cells Ian Chambers and Simon Tomlinson review the
transcription factor and pluripotency story so far Transcription factors are key proteins in c
transcription factor and pluripotency story so far
Transcription factors are key proteins in c
Transcription factors are
key proteins in cell identity.
A
key transcription factor involved in expression
of pro-inflammatory cytokines and senescence is Nuclear
factor - kB (NF - kB) 24.
The STAT3, in turn, goes into the nucleus and it binds to a number
of genes, and this is particularly happening in the hypothalamus and that we don't know all
of the mechanisms, but this activation
of the STAT3
transcription factor is
key in exerting the leptin signal, and leptin action.
This
transcription factor appears to be
key to the loss
of A9 subtype dopamine neurons
of the substantia nigra in PD.
These experimental data establish the retromer complex as a
key spatiotemporal regulator
of IFNAR endosomal sorting and a new
factor in type - I IFN - induced JAK / STAT signalling and gene
transcription.
The project will test the hypothesis that the SOXC
transcription factors have
key roles in these cells, similar to those
of SOX2 in pluripotent stem cells.
Searching for details on underlying mechanisms, the scientists found that tribbles was binding to ATF4, a «
transcription factor» protein that regulates the creation
of the
key docking proteins.
The bromodomain containing protein 9 (BRD9) has been reported as a component
of the switch / sucrose non-fermentable (SWI / SNF) brahma - related gene 1 - associated
factor (BAF) complex, which plays a
key role in chromatin remodelling and
transcription control [1] although the precise biological role is unknown.
We then found that the
transcription factors Smad1, Smad5 and Zeb2 were also experimentally validated targets
of miR - 181a [30,31,34], which are
key downstream regulators
of BMP / GDF signalling [32,33,35,36].
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.
Likewise, the expression pattern
of cdx - 2, a
key transcription factor in the trophoblast lineage, overlaps with that
of Oct - 4, but within any blastomere, cdx - 2 expression bears no consistent relationship to that
of Oct - 4 or nanog until after the trophectoderm lineage has been sorted [9].
Through a series
of genetic analyses, we have constructed a hierarchical map composed
of five
transcription factors that define the
key steps
of proliferation, survival, differentiation, and hormone expression
of the PVN and SON neurons during development.