Orthodenticle
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Orthodenticle
Orthodenticle (otd) is a homeobox gene found in Drosophila that regulates the development of anterior patterning, with particular involvement in the central nervous system function and eye development. It is located on the X chromosome. The gene is an ortholog of the human OTX1/OTX2 gene. Function During embryonic Drosophila development, otd is required for the head and ventral midline to develop correctly. In the larval stage, otd is expressed in specific sac-like epithelial structures known as imaginal discs that later give rise to external structures of the head and thorax. Particularly, otd is required for the development of the dorsal region of the adult ''Drosophila'' head, that forms from the fusion of two eye-antennal discs. Distribution of the otd protein occurs along a concentration of the imaginal disc primordia for these head structures such that different levels of otd expression are required for differential mediolateral subdomains to be established. In ''Drosophila' ...
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OTX2
Homeobox protein OTX2 is a protein that in humans is encoded by the ''OTX2'' gene. Function This gene encodes a member of the bicoid sub-family of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and play a role in brain and sensory organ development. A similar protein in mice is required for proper forebrain development. Two transcript variants encoding distinct isoforms have been identified for this gene. Other alternative splice variants may exist, but their full length sequences have not been determined. Otx2 is a group of homeobox genes that are typically described as a head organizer in the primitive streak stage of embryonic development. Otx2, which is an encoded protein that plays the role of a transcription factor, has also been shown to be involved in the regional patterning of the midbrain and forebrain. This group of genes demonstrates later in progression to have an influence on the formation of the sensory organs, p ...
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Ocelli
A simple eye (sometimes called a pigment pit) refers to a form of eye or an optical arrangement composed of a single lens and without an elaborate retina such as occurs in most vertebrates. In this sense "simple eye" is distinct from a multi-lensed "compound eye", and is not necessarily at all simple in the usual sense of the word. The structure of an animal's eye is determined by the environment in which it lives, and the behavioural tasks it must fulfill to survive. Arthropods differ widely in the habitats in which they live, as well as their visual requirements for finding food or conspecifics, and avoiding predators. Consequently, an enormous variety of eye types are found in arthropods. They possess a wide variety of novel solutions to overcome visual problems or limitations. Use of the term ''simple eye'' is flexible, and must be interpreted in proper context; for example, the eyes of humans and of other large animals such as most cephalopods, are ''camera eyes'' and ...
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Homeotic Protein Bicoid
Homeotic protein bicoid is encoded by the ''bcd'' maternal effect gene in ''Drosophilia''. Homeotic protein bicoid concentration gradient patterns the anterior-posterior (A-P) axis during ''Drosophila'' embryogenesis. Bicoid was the first protein demonstrated to act as a morphogen A morphogen is a substance whose non-uniform distribution governs the pattern of tissue development in the process of morphogenesis or pattern formation, one of the core processes of developmental biology, establishing positions of the various .... Although bicoid is important for the development of ''Drosophila'' and other higher dipterans, it is absent from most other insects, where its role is accomplished by other genes. Role in axial patterning ''Bicoid'' mRNA is actively localized to the anterior of the fruit fly egg during oogenesis along microtubules by the motor protein dynein, and retained there through association with Cell cortex, cortical actin. Translation of ''bicoid'' is regula ...
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OTX1
Homeobox protein OTX1 is a protein that in humans is encoded by the ''OTX1'' gene In biology, the word gene (from , ; "...Wilhelm Johannsen coined the word gene to describe the Mendelian units of heredity..." meaning ''generation'' or ''birth'' or ''gender'') can have several different meanings. The Mendelian gene is a ba .... Function This gene encodes a member of the bicoid sub-family of homeodomain-containing transcription factors. The encoded protein acts as a transcription factor and may play a role in brain and sensory organ development. The Otx gene is active in the region of the first gill arch, which is related to the upper and lower jaw and two of the bones of the ear.Shubin, Neil "Your Inner Fish" 2009 A similar protein in mice is required for proper brain and sensory organ development and can cause epilepsy. References Further reading * * * * * * * External links * Transcription factors {{gene-2-stub ...
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Bicoid
Homeotic protein bicoid is encoded by the ''bcd'' maternal effect gene in ''Drosophilia''. Homeotic protein bicoid concentration gradient patterns the anterior-posterior (A-P) axis during ''Drosophila'' embryogenesis. Bicoid was the first protein demonstrated to act as a morphogen. Although bicoid is important for the development of ''Drosophila'' and other higher dipterans, it is absent from most other insects, where its role is accomplished by other genes. Role in axial patterning ''Bicoid'' mRNA is actively localized to the anterior of the fruit fly egg during oogenesis along microtubules by the motor protein dynein, and retained there through association with cortical actin. Translation of ''bicoid'' is regulated by its 3′ UTR and begins after egg deposition. Diffusion and convection within the syncytium produce an exponential gradient of Bicoid protein within roughly one hour, after which Bicoid nuclear concentrations remain approximately constant through cellulariza ...
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Homeobox
A homeobox is a DNA sequence, around 180 base pairs long, that regulates large-scale anatomical features in the early stages of embryonic development. For instance, mutations in a homeobox may change large-scale anatomical features of the full-grown organism. Homeoboxes are found within genes that are involved in the regulation of patterns of anatomical development (morphogenesis) in animal Animals are multicellular, eukaryotic organisms in the Kingdom (biology), biological kingdom Animalia. With few exceptions, animals Heterotroph, consume organic material, Cellular respiration#Aerobic respiration, breathe oxygen, are Motilit ...s, fungus, fungi, plants, and numerous single cell eukaryotes. Homeobox genes encode homeodomain protein products that are transcription factors sharing a characteristic protein fold structure that binds DNA to regulate expression of target genes. Homeodomain proteins regulate gene expression and cell differentiation during early embryonic dev ...
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Blastoderm
A blastoderm (germinal disc, blastodisc) is a single layer of embryonic epithelial tissue that makes up the blastula. It encloses the fluid filled blastocoel. Gastrulation follows blastoderm formation, where the tips of the blastoderm begins the formation of the ectoderm, mesoderm, and endoderm. Formation The blastoderm is formed when the oocyte plasma membrane begins cleaving by invagination, creating multiple cells that arrange themselves into an outer sleeve to the blastocoel. In oviparous In chicken eggs, the blastoderm represents a flat disc after embryonic fertilization. At the edge of the blastoderm is the site of active migration by most cells.{{cite book, last1=Bellairs, first1=Ruth, last2=Osmond, first2=Mark, title=Atlas of Chick Development, publisher=Atlas Press, page=15–28, edition=3 See also * Blastodisc *Embryology * Cleavage *Gastrulation Gastrulation is the stage in the early embryonic development of most animals, during which the blastula (a single-layered ho ...
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Cell Nucleus
The cell nucleus (pl. nuclei; from Latin or , meaning ''kernel'' or ''seed'') is a membrane-bound organelle found in eukaryotic cells. Eukaryotic cells usually have a single nucleus, but a few cell types, such as mammalian red blood cells, have no nuclei, and a few others including osteoclasts have many. The main structures making up the nucleus are the nuclear envelope, a double membrane that encloses the entire organelle and isolates its contents from the cellular cytoplasm; and the nuclear matrix, a network within the nucleus that adds mechanical support. The cell nucleus contains nearly all of the cell's genome. Nuclear DNA is often organized into multiple chromosomes – long stands of DNA dotted with various proteins, such as histones, that protect and organize the DNA. The genes within these chromosomes are structured in such a way to promote cell function. The nucleus maintains the integrity of genes and controls the activities of the cell by regulating gene expres ...
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Enhancer (genetics)
In genetics, an enhancer is a short (50–1500 bp) region of DNA that can be bound by proteins ( activators) to increase the likelihood that transcription of a particular gene will occur. These proteins are usually referred to as transcription factors. Enhancers are ''cis''-acting. They can be located up to 1 Mbp (1,000,000 bp) away from the gene, upstream or downstream from the start site. There are hundreds of thousands of enhancers in the human genome. They are found in both prokaryotes and eukaryotes. The first discovery of a eukaryotic enhancer was in the immunoglobulin heavy chain gene in 1983. This enhancer, located in the large intron, provided an explanation for the transcriptional activation of rearranged Vh gene promoters while unrearranged Vh promoters remained inactive. Locations In eukaryotic cells the structure of the chromatin complex of DNA is folded in a way that functionally mimics the supercoiled state characteristic of prokaryotic DNA, so although the en ...
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Cell Membrane
The cell membrane (also known as the plasma membrane (PM) or cytoplasmic membrane, and historically referred to as the plasmalemma) is a biological membrane that separates and protects the interior of all cells from the outside environment (the extracellular space). The cell membrane consists of a lipid bilayer, made up of two layers of phospholipids with cholesterols (a lipid component) interspersed between them, maintaining appropriate membrane fluidity at various temperatures. The membrane also contains membrane proteins, including integral proteins that span the membrane and serve as membrane transporters, and peripheral proteins that loosely attach to the outer (peripheral) side of the cell membrane, acting as enzymes to facilitate interaction with the cell's environment. Glycolipids embedded in the outer lipid layer serve a similar purpose. The cell membrane controls the movement of substances in and out of cells and organelles, being selectively permeable to ions a ...
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Mutation
In biology, a mutation is an alteration in the nucleic acid sequence of the genome of an organism, virus, or extrachromosomal DNA. Viral genomes contain either DNA or RNA. Mutations result from errors during DNA or viral replication, mitosis, or meiosis or other types of damage to DNA (such as pyrimidine dimers caused by exposure to ultraviolet radiation), which then may undergo error-prone repair (especially microhomology-mediated end joining), cause an error during other forms of repair, or cause an error during replication (translesion synthesis). Mutations may also result from insertion or deletion of segments of DNA due to mobile genetic elements. Mutations may or may not produce detectable changes in the observable characteristics (phenotype) of an organism. Mutations play a part in both normal and abnormal biological processes including: evolution, cancer, and the development of the immune system, including junctional diversity. Mutation is the ultimate source o ...
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Pair-rule Gene
A pair-rule gene is a type of gene involved in the development of the segmented embryos of insects. Pair-rule genes are expressed as a result of differing concentrations of gap gene proteins, which encode transcription factors controlling pair-rule gene expression. Pair-rule genes are defined by the effect of a mutation in that gene, which causes the loss of the normal developmental pattern in alternating segments. Pair-rule genes were first described by Christiane Nüsslein-Volhard and Eric Wieschaus in 1980. They used a genetic screen to identify genes required for embryonic development in the fruit fly ''Drosophila melanogaster''. In normal unmutated ''Drosophila,'' each segment produces bristles called denticles in a band arranged on the side of the segment closer to the head (the anterior). They found five genes – ''even-skipped, hairy, odd-skipped, paired'' and ''runt'' – where mutations caused the deletion of a particular region of every alternate segment. For example, ...
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