Activation of these pathways further leads to the activation of
multiple transcription factors, pro- and antiapoptotic proteins, cell cycle check point proteins, etc. [4, 6, 8].
Not exact matches
When those same
transcription factors land on another part of the code, the risk of
multiple sclerosis appears to rise.
One encodes retinoid - related orphan receptor alpha (RORα), a
transcription factor that itself regulates
multiple other genes.
After much experimentation with
multiple combinations, the researchers found that adding two more signals to the mix —
transcription factors called ISL1 and LHX3 — turned the skin cells into spinal cord motor neurons in about 30 days.
The overall aim of this study was to determine if pluripotent cells overexpressing these
transcription factors could be intentionally driven toward retinal progenitors that differentiate into
multiple retinal cell classes and form a functional retina.
Ellen V. Rothenberg and Susan B. Ward report that the interleukin - 2 (IL - 2) transcriptional apparatus integrates
multiple types of biochemical information in determining whether or not the gene will be expressed, using
multiple diverse
transcription factors that are each optimally activated or inhibited by different signaling pathways.
XPD encodes one of the two helicase components of basal
transcription / DNA repair
factor IIH (TFIIH), a ten - subunit, multifunctional complex that is essential for
multiple processes, including basal
transcription initiation and DNA damage repair via the nucleotide excision repair (NER) pathway [6,7].
A major aspect of this process is the production of
multiple angiogenic cytokines and growth
factors in response to hypoxia / ischemia, which is mediated by the
transcription factor HIF - 1 (hypoxia - inducible
factor 1).
Additionally, ERK1 / 2 and AKT are known to cross talk with
multiple substrates including several kinases,
transcription factors, etc. which increase the complexity of the signaling network.
What they found was that there were two populations of
transcription factors — a diffuse set of smaller molecules and distinct, larger clusters made up of
multiple Mig1p's.
In the current study, the researchers found that EBNA2 and its related
transcription factors activate some of the human genes associated with the risk for lupus and several other autoimmune diseases, including
multiple sclerosis, rheumatoid arthritis, inflammatory bowel disease, type 1 diabetes, juvenile idiopathic arthritis and celiac disease.
This is in accordance with previous reports that decitabine and 5 - azacytidine produce a marked synergistic effect in combination with suberoylanilide hydroxamic acid and romidepsin in T - lymphoma cell lines by modulating cell cycle arrest and apoptosis.26, 27 As a mechanism of action, KMT2D mutations of B - lymphoma cells promote malignant outgrowth by perturbing methylation of H3K4 that affect the JAK - STAT, Toll - like receptor, or B - cell receptor pathway.28, 29 Here our study indicated that dual treatment with chidamide and decitabine enhanced the interaction of KMT2D with the
transcription factor PU.1, thereby inactivating the H3K4me - associated signaling pathway MAPK, which is constitutively activated in T - cell lymphoma.13, 30,31 The
transcription factor PU.1 is involved in the development of all hematopoietic lineages32 and regulates lymphoid cell growth and transformation.33 Aberrant PU.1 expression promotes acute myeloid leukemia and is related to the pathogenesis of
multiple myeloma via the MAPK pathway.34, 35 On the other hand, PU.1 is also shown to interact with chromatin remodeler and DNA methyltransferease to control hematopoiesis and suppress leukemia.36 Our data thus suggested that the combined action of chidamide and decitabine may interfere with the differentiation and / or viability of PTCL - NOS through a PU.1 - dependent gene expression program.
Working in Brennan's lab, she took on the challenge of understanding how a
transcription factor in soil bacteria regulates a transporter of
multiple drugs.
Also relevant are studies of the upstream mechanisms that regulate levels and function of those gene products, for example: how a
transcription factor regulates
multiple targets or how
factors can regulate translation or post-translational modification of
multiple proteins.
Thus, depending on arrangements of the octamer motif, and presence of DNA motifs for additional
transcription factors, Oct4 can form heterodimers with
multiple partners or homodimers in one of several unique conformations [17].
«There are
multiple interactive pathways and molecular mechanisms by which CR (calorie restriction) and IF (intermittent fasting) benefit neurons including those involving insulin - like signaling, FoxO
transcription factors, sirtuins and peroxisome proliferator - activated receptors.