Homeodomain Proteins
Genes, Homeobox
Transcription Factors
Antennapedia Homeodomain Protein
LIM-Homeodomain Proteins
Molecular Sequence Data
Gene Expression Regulation, Developmental
DNA-Binding Proteins
Base Sequence
Repressor Proteins
Amino Acid Sequence
Drosophila Proteins
Promoter Regions, Genetic
Binding Sites
Transcription, Genetic
Trans-Activators
Paired Box Transcription Factors
DNA
Drosophila
Goosecoid Protein
Nuclear Proteins
MSX1 Transcription Factor
Octamer Transcription Factor-1
Protein Binding
Otx Transcription Factors
Embryo, Nonmammalian
In Situ Hybridization
Sequence Homology, Amino Acid
Minichromosome Maintenance 1 Protein
Recombinant Fusion Proteins
Transcriptional Activation
Body Patterning
Two-Hybrid System Techniques
Mutation
POU Domain Factors
Fushi Tarazu Transcription Factors
Protein Structure, Tertiary
Enhancer Elements, Genetic
Host Cell Factor C1
Xenopus Proteins
Conserved Sequence
Consensus Sequence
Cell Differentiation
Transcription Factor Pit-1
Zebrafish Proteins
Gene Expression Regulation
Caenorhabditis elegans Proteins
Insect Hormones
Morphogenesis
Sequence Alignment
Hepatocyte Nuclear Factor 6
Animals, Genetically Modified
Zebrafish
Cloning, Molecular
Hepatocyte Nuclear Factor 1-beta
Phenotype
Hepatocyte Nuclear Factor 1
Drosophila melanogaster
Caenorhabditis elegans
Transfection
Genes, Reporter
Rhombencephalon
Regulatory Sequences, Nucleic Acid
Mesoderm
Dimerization
Basic Helix-Loop-Helix Transcription Factors
DNA Primers
Onecut Transcription Factors
Cell Nucleus
Genes, Mating Type, Fungal
Proto-Oncogene Proteins
Oligodeoxyribonucleotides
DNA, Complementary
Nervous System
Hepatocyte Nuclear Factor 1-alpha
Organizers, Embryonic
Octamer Transcription Factor-2
Nodal Signaling Ligands
Chick Embryo
Embryo, Mammalian
Meristem
Plant Proteins
RNA, Messenger
Zinc Fingers
Electrophoretic Mobility Shift Assay
Prosencephalon
Cell Lineage
Serum Response Factor
Gastrula
COS Cells
Mutagenesis, Site-Directed
TATA Box
LIM Domain Proteins
AGAMOUS Protein, Arabidopsis
Mutagenesis
Central Nervous System
Gene Expression
Neurons
Islets of Langerhans
Models, Biological
Multigene Family
Immunohistochemistry
Structure-Activity Relationship
Gene Library
Sequence Homology, Nucleic Acid
beta-Galactosidase
Neoplasm Proteins
Signal Transduction
Eye
Stem Cells
Arabidopsis Proteins
Luciferases
Precipitin Tests
Wnt1 Protein
Gene Expression Regulation, Plant
HeLa Cells
Arabidopsis
Glutathione Transferase
Xenopus
Amino Acid Motifs
Telencephalon
Spinal Cord
Interneurons
Polymerase Chain Reaction
Bone Morphogenetic Proteins
Hedgehog Proteins
Cells, Cultured
Protein Structure, Secondary
NIH 3T3 Cells
Gene Expression Regulation, Fungal
Tissue Distribution
Mice, Knockout
Response Elements
Models, Molecular
Saccharomyces cerevisiae Proteins
Retina
Plasmids
Sequence Homology
Helix-Loop-Helix Motifs
3T3 Cells
Chromatin Immunoprecipitation
Embryonic Induction
Reverse Transcriptase Polymerase Chain Reaction
T-Box Domain Proteins
Pancreas
Models, Genetic
Point Mutation
Saccharomyces cerevisiae
Oligonucleotide Probes
Larva
Plants, Genetically Modified
Introns
High Mobility Group Proteins
Pharynx
Xenopus laevis
Evolution, Molecular
DNA Probes
Blotting, Western
Down-Regulation
Repetitive Sequences, Nucleic Acid
Mice, Transgenic
Protein Isoforms
Caco-2 Cells
Blotting, Northern
Chromosome Mapping
Tumor Cells, Cultured
Green Fluorescent Proteins
RNA Interference
Carrier Proteins
Gene Deletion
Protein Conformation
Chromatin
Macromolecular Substances
Separation of shoot and floral identity in Arabidopsis. (1/15498)
The overall morphology of an Arabidopsis plant depends on the behaviour of its meristems. Meristems derived from the shoot apex can develop into either shoots or flowers. The distinction between these alternative fates requires separation between the function of floral meristem identity genes and the function of an antagonistic group of genes, which includes TERMINAL FLOWER 1. We show that the activities of these genes are restricted to separate domains of the shoot apex by different mechanisms. Meristem identity genes, such as LEAFY, APETALA 1 and CAULIFLOWER, prevent TERMINAL FLOWER 1 transcription in floral meristems on the apex periphery. TERMINAL FLOWER 1, in turn, can inhibit the activity of meristem identity genes at the centre of the shoot apex in two ways; first by delaying their upregulation, and second, by preventing the meristem from responding to LEAFY or APETALA 1. We suggest that the wild-type pattern of TERMINAL FLOWER 1 and floral meristem identity gene expression depends on the relative timing of their upregulation. (+info)Novel regulation of the homeotic gene Scr associated with a crustacean leg-to-maxilliped appendage transformation. (2/15498)
Homeotic genes are known to be involved in patterning morphological structures along the antero-posterior axis of insects and vertebrates. Because of their important roles in development, changes in the function and expression patterns of homeotic genes may have played a major role in the evolution of different body plans. For example, it has been proposed that during the evolution of several crustacean lineages, changes in the expression patterns of the homeotic genes Ultrabithorax and abdominal-A have played a role in transformation of the anterior thoracic appendages into mouthparts termed maxillipeds. This homeotic-like transformation is recapitulated at the late stages of the direct embryonic development of the crustacean Porcellio scaber (Oniscidea, Isopoda). Interestingly, this morphological change is associated with apparent novelties both in the transcriptional and post-transcriptional regulation of the Porcellio scaber ortholog of the Drosophila homeotic gene, Sex combs reduced (Scr). Specifically, we find that Scr mRNA is present in the second maxillary segment and the first pair of thoracic legs (T1) in early embryos, whereas protein accumulates only in the second maxillae. In later stages, however, high levels of SCR appear in the T1 legs, which correlates temporally with the transformation of these appendages into maxillipeds. Our observations provide further insight into the process of the homeotic leg-to-maxilliped transformation in the evolution of crustaceans and suggest a novel regulatory mechanism for this process in this group of arthropods. (+info)The Drosophila kismet gene is related to chromatin-remodeling factors and is required for both segmentation and segment identity. (3/15498)
The Drosophila kismet gene was identified in a screen for dominant suppressors of Polycomb, a repressor of homeotic genes. Here we show that kismet mutations suppress the Polycomb mutant phenotype by blocking the ectopic transcription of homeotic genes. Loss of zygotic kismet function causes homeotic transformations similar to those associated with loss-of-function mutations in the homeotic genes Sex combs reduced and Abdominal-B. kismet is also required for proper larval body segmentation. Loss of maternal kismet function causes segmentation defects similar to those caused by mutations in the pair-rule gene even-skipped. The kismet gene encodes several large nuclear proteins that are ubiquitously expressed along the anterior-posterior axis. The Kismet proteins contain a domain conserved in the trithorax group protein Brahma and related chromatin-remodeling factors, providing further evidence that alterations in chromatin structure are required to maintain the spatially restricted patterns of homeotic gene transcription. (+info)FGF8 induces formation of an ectopic isthmic organizer and isthmocerebellar development via a repressive effect on Otx2 expression. (4/15498)
Beads containing recombinant FGF8 (FGF8-beads) were implanted in the prospective caudal diencephalon or midbrain of chick embryos at stages 9-12. This induced the neuroepithelium rostral and caudal to the FGF8-bead to form two ectopic, mirror-image midbrains. Furthermore, cells in direct contact with the bead formed an outgrowth that protruded laterally from the neural tube. Tissue within such lateral outgrowths developed proximally into isthmic nuclei and distally into a cerebellum-like structure. These morphogenetic effects were apparently due to FGF8-mediated changes in gene expression in the vicinity of the bead, including a repressive effect on Otx2 and an inductive effect on En1, Fgf8 and Wnt1 expression. The ectopic Fgf8 and Wnt1 expression domains formed nearly complete concentric rings around the FGF8-bead, with the Wnt1 ring outermost. These observations suggest that FGF8 induces the formation of a ring-like ectopic signaling center (organizer) in the lateral wall of the brain, similar to the one that normally encircles the neural tube at the isthmic constriction, which is located at the boundary between the prospective midbrain and hindbrain. This ectopic isthmic organizer apparently sends long-range patterning signals both rostrally and caudally, resulting in the development of the two ectopic midbrains. Interestingly, our data suggest that these inductive signals spread readily in a caudal direction, but are inhibited from spreading rostrally across diencephalic neuromere boundaries. These results provide insights into the mechanism by which FGF8 induces an ectopic organizer and suggest that a negative feedback loop between Fgf8 and Otx2 plays a key role in patterning the midbrain and anterior hindbrain. (+info)The homeobox gene Pitx2: mediator of asymmetric left-right signaling in vertebrate heart and gut looping. (5/15498)
Left-right asymmetry in vertebrates is controlled by activities emanating from the left lateral plate. How these signals get transmitted to the forming organs is not known. A candidate mediator in mouse, frog and zebrafish embryos is the homeobox gene Pitx2. It is asymmetrically expressed in the left lateral plate mesoderm, tubular heart and early gut tube. Localized Pitx2 expression continues when these organs undergo asymmetric looping morphogenesis. Ectopic expression of Xnr1 in the right lateral plate induces Pitx2 transcription in Xenopus. Misexpression of Pitx2 affects situs and morphology of organs. These experiments suggest a role for Pitx2 in promoting looping of the linear heart and gut. (+info)The cardiac homeobox gene Csx/Nkx2.5 lies genetically upstream of multiple genes essential for heart development. (6/15498)
Csx/Nkx2.5 is a vertebrate homeobox gene with a sequence homology to the Drosophila tinman, which is required for the dorsal mesoderm specification. Recently, heterozygous mutations of this gene were found to cause human congenital heart disease (Schott, J.-J., Benson, D. W., Basson, C. T., Pease, W., Silberbach, G. M., Moak, J. P., Maron, B. J., Seidman, C. E. and Seidman, J. G. (1998) Science 281, 108-111). To investigate the functions of Csx/Nkx2.5 in cardiac and extracardiac development in the vertebrate, we have generated and analyzed mutant mice completely null for Csx/Nkx2.5. Homozygous null embryos showed arrest of cardiac development after looping and poor development of blood vessels. Moreover, there were severe defects in vascular formation and hematopoiesis in the mutant yolk sac. Interestingly, TUNEL staining and PCNA staining showed neither enhanced apoptosis nor reduced cell proliferation in the mutant myocardium. In situ hybridization studies demonstrated that, among 20 candidate genes examined, expression of ANF, BNP, MLC2V, N-myc, MEF2C, HAND1 and Msx2 was disturbed in the mutant heart. Moreover, in the heart of adult chimeric mice generated from Csx/Nkx2.5 null ES cells, there were almost no ES cell-derived cardiac myocytes, while there were substantial contributions of Csx /Nkx2.5-deficient cells in other organs. Whole-mount &bgr;-gal staining of chimeric embryos showed that more than 20% contribution of Csx/Nkx2. 5-deficient cells in the heart arrested cardiac development. These results indicate that (1) the complete null mutation of Csx/Nkx2.5 did not abolish initial heart looping, (2) there was no enhanced apoptosis or defective cell cycle entry in Csx/Nkx2.5 null cardiac myocytes, (3) Csx/Nkx2.5 regulates expression of several essential transcription factors in the developing heart, (4) Csx/Nkx2.5 is required for later differentiation of cardiac myocytes, (5) Csx/Nkx2. 5 null cells exert dominant interfering effects on cardiac development, and (6) there were severe defects in yolk sac angiogenesis and hematopoiesis in the Csx/Nkx2.5 null embryos. (+info)Requirement of a novel gene, Xin, in cardiac morphogenesis. (7/15498)
A novel gene, Xin, from chick (cXin) and mouse (mXin) embryonic hearts, may be required for cardiac morphogenesis and looping. Both cloned cDNAs have a single open reading frame, encoding proteins with 2,562 and 1,677 amino acids for cXin and mXin, respectively. The derived amino acid sequences share 46% similarity. The overall domain structures of the predicted cXin and mXin proteins, including proline-rich regions, 16 amino acid repeats, DNA-binding domains, SH3-binding motifs and nuclear localization signals, are highly conserved. Northern blot analyses detect a single message of 8.9 and 5.8 kilo base (kb) from both cardiac and skeletal muscle of chick and mouse, respectively. In situ hybridization reveals that the cXin gene is specifically expressed in cardiac progenitor cells of chick embryos as early as stage 8, prior to heart tube formation. cXin continues to be expressed in the myocardium of developing hearts. By stage 15, cXin expression is also detected in the myotomes of developing somites. Immunofluorescence microscopy reveals that the mXin protein is colocalized with N-cadherin and connexin-43 in the intercalated discs of adult mouse hearts. Incubation of stage 6 chick embryos with cXin antisense oligonucleotides results in abnormal cardiac morphogenesis and an alteration of cardiac looping. The myocardium of the affected hearts becomes thickened and tends to form multiple invaginations into the heart cavity. This abnormal cellular process may account in part for the abnormal looping. cXin expression can be induced by bone morphogenetic protein (BMP) in explants of anterior medial mesoendoderm from stage 6 chick embryos, a tissue that is normally non-cardiogenic. This induction occurs following the BMP-mediated induction of two cardiac-restricted transcription factors, Nkx2.5 and MEF2C. Furthermore, either MEF2C or Nkx2.5 can transactivate a luciferase reporter driven by the mXin promoter in mouse fibroblasts. These results suggest that Xin may participate in a BMP-Nkx2.5-MEF2C pathway to control cardiac morphogenesis and looping. (+info)Retinoids are produced by glia in the lateral ganglionic eminence and regulate striatal neuron differentiation. (8/15498)
In order to identify molecular mechanisms involved in striatal development, we employed a subtraction cloning strategy to enrich for genes expressed in the lateral versus the medial ganglionic eminence. Using this approach, the homeobox gene Meis2 was found highly expressed in the lateral ganglionic eminence and developing striatum. Since Meis2 has recently been shown to be upregulated by retinoic acid in P19 EC cells (Oulad-Abdelghani, M., Chazaud, C., Bouillet, P., Sapin, V., Chambon, P. and Dolle, P. (1997) Dev. Dyn. 210, 173-183), we examined a potential role for retinoids in striatal development. Our results demonstrate that the lateral ganglionic eminence, unlike its medial counterpart or the adjacent cerebral cortex, is a localized source of retinoids. Interestingly, glia (likely radial glia) in the lateral ganglionic eminence appear to be a major source of retinoids. Thus, as lateral ganglionic eminence cells migrate along radial glial fibers into the developing striatum, retinoids from these glial cells could exert an effect on striatal neuron differentiation. Indeed, the treatment of lateral ganglionic eminence cells with retinoic acid or agonists for the retinoic acid receptors or retinoid X receptors, specifically enhances their striatal neuron characteristics. These findings, therefore, strongly support the notion that local retinoid signalling within the lateral ganglionic eminence regulates striatal neuron differentiation. (+info)Some common types of eye abnormalities include:
1. Refractive errors: These are errors in the way the eye focuses light, causing blurry vision. Examples include myopia (nearsightedness), hyperopia (farsightedness), astigmatism, and presbyopia (age-related loss of near vision).
2. Amblyopia: This is a condition where the brain favors one eye over the other, causing poor vision in the weaker eye.
3. Cataracts: A cataract is a clouding of the lens in the eye that can cause blurry vision and increase the risk of glaucoma.
4. Glaucoma: This is a group of eye conditions that can damage the optic nerve and lead to vision loss.
5. Macular degeneration: This is a condition where the macula, the part of the retina responsible for central vision, deteriorates, leading to vision loss.
6. Diabetic retinopathy: This is a complication of diabetes that can damage the blood vessels in the retina and lead to vision loss.
7. Retinal detachment: This is a condition where the retina becomes separated from the underlying tissue, leading to vision loss.
8. Corneal abnormalities: These are irregularities in the shape or structure of the cornea, such as keratoconus, that can cause blurry vision.
9. Optic nerve disorders: These are conditions that affect the optic nerve, such as optic neuritis, that can cause vision loss.
10. Traumatic eye injuries: These are injuries to the eye or surrounding tissue that can cause vision loss or other eye abnormalities.
Eye abnormalities can be diagnosed through a comprehensive eye exam, which may include visual acuity tests, refraction tests, and imaging tests such as retinal photography or optical coherence tomography (OCT). Treatment for eye abnormalities depends on the specific condition and may include glasses or contact lenses, medication, surgery, or other therapies.
Transcription factor
Homeobox
ZEB2
Hox gene
ZEB1
Homeotic selector gene
PROP1
EN1 (gene)
HOXC8
HHEX
HOXA11
HOXB2
HOXD4
Homeobox A10
PCBD1
HOXB4
HOXB9
HOXD10
PITX2
HOPX
Homeobox protein SIX1
Evolutionary developmental biology
NOBOX
SIX5
VSX1
VSX2
PRRX1
HIPK1
PAX1
MEOX2
NKX-homeodomain factor
Sex-chromosome dosage compensation
Index of biochemistry articles
CLDN12
CUTL1
DLX gene family
Nuclear receptor 4A3
NKX2-3
DLX6-AS1
FGF15
POU4F1
WNT16
Myotonin-protein kinase
DNA-binding domain
DLX5
Pierre Gönczy
PECR
Alain Prochiantz
PAX3
HOXC4
LDB2
FLNA
Protein fold class
IRX5
Cajal-Retzius cell
Acute lymphoblastic leukemia
Neuromere
Tauopathy in the young autistic brain: novel biomarker and therapeutic target
PHOX2A gene: MedlinePlus Genetics
Lhx2 Balances Progenitor Maintenance with Neurogenic Output and Promotes Competence State Progression in the Developing Retina ...
Mapping of Structure-Function Peptide Sites on the Human Alpha-fetoprotein Amino Acid Sequence
LMX1A Antikörper
Interactive Fly, Drosophila
RCSB PDB - 5ME8: N-terminal domain of the human tumor suppressor ING5
IJMS | Free Full-Text | Recent Developments in Peptide-Based Nucleic Acid Delivery
Pediatric Atrial Septal Defects Clinical Presentation: History, Physical Examination
An adhesion code ensures robust pattern formation during tissue morphogenesis | bioRxiv
AG Schmitz - Biochemical Institute
WikiGenes - CYP7A1 - cytochrome P450, family 7, subfamily A,...
Sim1a and Arnt2 contribute to hypothalamo-spinal axon guidance by regulating Robo2 activity via a Robo3-dependent mechanism |...
Thyroid transcription factor-1 (TTF-1/Nkx2.1/TITF1) gene regulation in the lung | Clinical Science | Portland Press
HOXA1 Antibodies, ELISA Kits
YRC Public Data Repository - Protein Structure Prediction - Protein Overview
Finding the undiscovered roles of genes: an approach using mutual ranking of coexpressed genes and promoter architecture-case...
DeCS
High mobility group I/Y protein functions as a specific cofactor for Oct-2A: Mapping of interaction domains - Fingerprint ...
Search | VHL CLAP/WR-PAHO/WHO
Myeloid Ecotropic Viral Integration Site 1 Protein | Profiles RNS
Shibai Li | Sloan Kettering Institute
Barry Behr, Ph.D., H.C.L.D.'s Profile | Stanford Profiles
CoP: Co-expressed Biological Processes
Thyroid transcription factor-1
AREB6 Antibody - N-terminal region (P100657 T100) | Aviva Systems Biology | Aviva Systems Biology
Esther Landesman | Profiles RNS
Context-dependent HOX transcription factor function in health and disease. - Texas A&M University (TAMU) Scholar
Find Research outputs - Augusta University Research Profiles
Kinase4
- This study aimed to determine the role of the interleukin-4 (IL-4)/signal transducer and activator of transcription 6 (STAT6) signaling pathway and homeodomain-interacting protein kinase 2 (HIPK2) in aberrant IgA1 O-glycosylation production, and identify potential therapeutic targets in IgAN. (nih.gov)
- Protein kinase CK2 inhibition suppresses neointima formation via a proline-rich homeodomain-dependent mechanism. (nottingham.ac.uk)
- Serine/threonine-protein kinase involved in transcription regulation, apoptosis and steroidogenic gene expression. (nih.gov)
- Serine/threonine-protein kinase involved in transcription regulation, p53/TP53-mediated cellular apoptosis and regulation of the cell cycle. (nih.gov)
Genes8
- Here, we show that the CINCINNATA-like TEOSINTE BRANCHED1, CYCLOIDEA, PROLIFERATING CELL FACTORS (CIN-TCP) transcription factors activate the class II KNOTTED1-LIKE ( KNOX-II ) genes and the CIN-TCP and KNOX-II proteins together redundantly suppress leaflet initiation in simple leaves. (nature.com)
- Furthermore, we demonstrated that the reduction of KMT2D protein level in patients' lymphoblastoid and skin fibroblast cell lines carrying KMT2D-truncating mutations affects the expression levels of known KMT2D target genes. (nih.gov)
- 6. Target genes of homeodomain proteins. (nih.gov)
- NRL interacts with homeodomain protein CRX and numerous other regulatory factors to control expression of most rod-expressed genes. (nih.gov)
- The characterization of genes encoding the nodal-related factor, Squint, and homeodomain protein, Bozozok, both of which are expressed in the YSL, suggested that the YSL has a role in mesendoderm induction. (biologists.com)
- Most animal homeotic genes encode transcription factor proteins that contain a region called the homeodomain and are called Hox genes . (khanacademy.org)
- the proteins encoded by early genes regulate the expression of later genes. (khanacademy.org)
- Proteins encoded by homeobox genes ( GENES, HOMEOBOX ) that exhibit structural similarity to certain prokaryotic and eukaryotic DNA-binding proteins. (nih.gov)
Plant homeodomain2
- In this study, we identified plant homeodomain finger-containing protein 20 (PHF20) as a crucial epigenetic regulator for sustaining the stem cell-like phenotype of GBM. (frontiersin.org)
- Plant homeodomain-finger containing protein 20 (PHF20) has been previously identified as a novel antigen in glioma patients and named as glioma-expressed antigen 2 (GLEA2) ( 8 , 9 ). (frontiersin.org)
Specificity2
- Our work investigated the DNA binding specificity of the HPV E2 proteins and their effects on gene regulation and cell survival. (nottingham.ac.uk)
- Defining how homeodomain proteins achieve DNA binding specificity has therefore been a long-standing goal . (bvsalud.org)
Homeotic1
- 17. Cofactor-interaction motifs and the cooption of a homeotic Hox protein into the segmentation pathway of Drosophila melanogaster. (nih.gov)
Bozozok1
- 7. The role of the homeodomain protein Bozozok in zebrafish axis formation. (nih.gov)
Sequences3
- AFP AA sequences are further presented as peptide identification sites for growth factors, receptors, cytoskeletal proteins, and chemokines. (atlasgeneticsoncology.org)
- Approximately one third of the paired-like homeodomain proteins cooperatively bind palindromic sequences spaced 3 bp apart, whereas other homeodomain proteins cooperatively bind sites with distinct orientation and spacing requirements. (bvsalud.org)
- In addition, the binding site spacing requirements of select homeodomain proteins provide a mechanism by which seemingly similar AT-rich DNA sequences can preferentially recruit specific homeodomain factors. (bvsalud.org)
Regulate5
- Members of the E2 class of DNA binding proteins regulate human papillomavirus (HPV) gene expression and are required for HPV replication. (nottingham.ac.uk)
- Study of these proteins has provided several insights into how transcription factors find their binding sites and regulate gene expression. (nottingham.ac.uk)
- This protein acts early in development to help promote the formation of nerve cells (neurons) and regulate the process by which the neurons mature to carry out specific functions (differentiation). (medlineplus.gov)
- We investigate how external signals lead to the activation of protein kinases, which then transmit their signals into the nucleus where they regulate transcription factors and epigenetic events. (uni-giessen.de)
- Genetic studies have demonstrated that homeodomain proteins regulate many developmental processes. (bvsalud.org)
Serine1
- A discussion follows in which peptide epitopes, extracellular matrix proteins, serine proteases, extracellular matrix, and cellular adhesion AA identity sites on AFP are considered. (atlasgeneticsoncology.org)
Transcriptional3
- How do distinct transcriptional regulatory proteins coordinate their job with extrinsic factors and the microenvironment? (nih.gov)
- How do post-transcriptional events modulate the expression of functional macromolecules, including proteins and non-coding RNAs? (nih.gov)
- May act as a transcriptional corepressor for NK homeodomain transcription factors. (nih.gov)
Developmental1
- Homeodomain proteins are involved in the control of gene expression during morphogenesis and development ( GENE EXPRESSION REGULATION, DEVELOPMENTAL ). (nih.gov)
Apoptosis2
- Emphasis is further placed upon homeodomain and apoptosis AA sequence identities given that AFP serves as a fetal, phase-specific protein throughout embryogenesis, histogenesis, and organogenesis. (atlasgeneticsoncology.org)
- Inhibits cell growth and promotes apoptosis through the activation of p53/TP53 both at the transcription level and at the protein level (by phosphorylation and indirect acetylation). (nih.gov)
Sequence3
- Addition or deletion of nucleotides changes the sequence of amino acids in the PHOX2B protein. (nih.gov)
- The atlas further shows AFP as a protein consisting of multiple peptide-cassettes consisting of amino acid (AA) sequence stretches matched to peptide segments on prohormones and biological response modifier proteins. (atlasgeneticsoncology.org)
- The AFP molecule is also viewed as a carrier/transport protein based on AA sequence comparison of various proteins that bind hydrophobic ligands and heavy metals similar to AFP binding of such components. (atlasgeneticsoncology.org)
Ontology1
- Classes for this protein according to by Drug Target Ontology (DTO). (nih.gov)
UniProt1
- Description of the protein which includes the UniProt Function and the NCBI Gene Summary. (nih.gov)
Receptors2
- The multiple molecular variant forms of AFP are discussed in relation to published reports of AFP binding proteins and cell surface receptors. (atlasgeneticsoncology.org)
- Upon ligand binding, the receptors of the TGFbeta family phosphorylate Smad proteins, which then move into the nucleus where they activate transcription. (sdbonline.org)
Functional2
- To assess this, we performed a proof-of-principle study on 14 KMT2D and two KDM6A nonsense mutations using specific compounds that mediate translational readthrough and thereby stimulate the re-expression of full-length functional proteins. (nih.gov)
- Structural and functional studies of the MutS mismatch repair protein. (nih.gov)
Kinases2
- non-olfactory GPCRs, ion channels, and protein kinases. (nih.gov)
- We study these processes using the NF-κB transcription factor system and the family of stress-regulated homeodomain-interacting protein kinases (HIPKs) as model systems. (uni-giessen.de)
RNAs1
- Discovery of New Intronic Small Nucleolar RNAs (snoRNA) Associated with the Ribosomal Protein SA Gene in Fruit Fly, Chicken and Human. (nih.gov)
TGFbeta1
- Transforming Growth Factor-beta (TGFbeta) is up-regulated in many tumours and this protein can induce EMT and increase cell migration. (nottingham.ac.uk)
Amino acid2
- The protein produced from the PHOX2B gene contains two areas where a protein building block (amino acid) called alanine is repeated multiple times. (nih.gov)
- In some people with neuroblastoma, mutations in the PHOX2B gene change a single protein building block (amino acid) in the PHOX2B protein. (nih.gov)
Domains1
- The Enigmatic Origin of Papillomavirus Protein Domains. (nottingham.ac.uk)
Descriptor1
- Goosecoid Protein" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus, MeSH (Medical Subject Headings) . (harvard.edu)
Differentiation1
- The PHOX2B protein helps support the formation of nerve cells (neurons) and regulates the process by which the neurons mature to carry out specific functions (differentiation). (nih.gov)
Factors4
- The focus of my research is on transcription factors and the roles that these proteins play in tumourigenesis. (nottingham.ac.uk)
- Homeodomain proteins constitute one of the largest families of metazoan transcription factors . (bvsalud.org)
- Importantly, we found that 15 of 88 homeodomain factors form cooperative homodimer complexes on DNA sites with precise spacing requirements. (bvsalud.org)
- Acts as a corepressor of several transcription factors, including SMAD1 and POU4F1/Brn3a and probably NK homeodomain transcription factors. (nih.gov)
Interactions2
- Specific areas of expertise include RNA sequencing and ChIP sequencing and related bioinformatics, protein-DNA interactions, cell migration and cell invasion assays, and the analysis of signal transduction pathways. (nottingham.ac.uk)
- The E2 proteins are an excellent model system in which to study DNA-protein interactions. (nottingham.ac.uk)
Human1
- Our previous work looked at the human papillomavirus E2 proteins. (nottingham.ac.uk)
Class1
- Long, J. A., Moan, E. I., Medford, J. I. & Barton, M. K. A member of the KNOTTED class of homeodomain proteins encoded by the STM gene of Arabidopsis . (nature.com)
Data3
- We also present data that indicate the stability of existing proteins in the YSL is unaffected by RNase injection. (biologists.com)
- Prediction of cooperative homeodomain DNA binding sites from high-throughput-SELEX data. (bvsalud.org)
- Here, we developed a novel computational approach to predict cooperative dimeric binding of homeodomain proteins using High-Throughput (HT) SELEX data. (bvsalud.org)
Structural1
- SCOPe: Structural Classification of Proteins - extended. (berkeley.edu)
Targets2
- This page lists protein targets that have been identified by the IDG program for additional research. (nih.gov)
- These models are being used to systematically elucidate proteins required for cutaneous carcinogenesis and to test their potential role as therapeutic targets. (stanford.edu)
Function1
- Although the PHOX2A protein plays an important role in autonomic nervous system development, PHOX2A mutations do not seem to affect the function of this part of the nervous system. (medlineplus.gov)
Formation1
- The PHOX2A protein is also involved in the formation of certain nerves in the head and face (cranial nerves). (medlineplus.gov)
Control2
- A lack of this protein prevents the normal development of several cranial nerves and the extraocular muscles they control. (medlineplus.gov)
- Las proteínas de homeodominios participan en el control de la expresión génica durante la morfogénesis y el desarrollo (REGULACIÓN DE LA EXPRESIÓN GÉNICA, DESARROLLO). (bvsalud.org)
Specific1
- Cell identity and sexual development in Cryptococcus neoformans are controlled by the mating-type-specific homeodomain protein Sxi1alpha. (duke.edu)
Role1
- From these studies, it is clear that the protein plays a critical role in the development of the autonomic nervous system, which controls involuntary body functions such as breathing, blood pressure, heart rate, and digestion. (medlineplus.gov)
Found2
- The PHOX2A gene provides instructions for making a protein that is found in the nervous system. (medlineplus.gov)
- We found that a number of KMT2D truncating mutations result in mRNA degradation through the nonsense-mediated mRNA decay, contributing to protein haploinsufficiency. (nih.gov)
Cell3
- Our current focus is the Proline Rich Homeodomain protein (PRH/Hhex), an oligomeric transcription factor that regulates cell proliferation and cell migration in multiple contexts. (nottingham.ac.uk)
- 1) During Epithelial-Mesenchymal transition (EMT) epithelial cells begin to express different cell adhesion proteins and they start to become more migratory. (nottingham.ac.uk)
- The analysis of the noncanonical IKKs and their adaptor proteins is of special relevance for the lab, as their overexpression in pathophysiological conditions triggers oncogenic transformation of breast cancer cells and mediates chemoresistance of non-small cell lung cancer and HER2+ breast cancer cells. (uni-giessen.de)
Studies1
- Most of researchers' knowledge about the PHOX2A protein comes from studies in animals. (medlineplus.gov)
Early2
- During neuron development, the protein is active in the neural crest, which is a group of cells in the early embryo that give rise to many tissues and organs. (nih.gov)
- The LIM-Homeodomain transcription factor Lhx2 is an essential organizer of early eye development and is subsequently expressed in retinal progenitor cells (RPCs). (jneurosci.org)
Sites2
- It is unclear how brief protein-DNA contacts can mediate efficient transcription from enhancers containing low-affinity binding sites. (elifesciences.org)
- At the scale of a single enhancer over a few hundred base pairs long, multiple low-affinity binding sites for the same transcription factor in close proximity could increase the frequency of binding events by trapping the protein. (elifesciences.org)