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. [1] It is located on the X chromosome. [1] The gene is an ortholog of the human OTX1/OTX2 gene. [2]
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. [3] In Drosophila, the function of otd as an essential factor in anterior pattern formation has been replaced by Bicoid, another homeodomain protein [4] which is involved in anterior patterning such that bcd mRNA is sequestered at the anterior pole of the mature oocyte. In the absence of bcd, all anterior structures of the embryo including the cephalic and thoracic segments fail to develop, and duplications of posterior structures are observed instead. [4]
Additionally, otd is involved in development of all eight photoreceptors of adult Drosophila in each of their ~700 individual eye units, known as ommatidia [5] and their proximal-distal distribution in the eye. [6] The two types of photoreceptors, outer (OPRs) and inner (IPRs), are distinguished through their function and anatomy such that OPRs have six neurons that respond to dim light conditions and are important for motion detection, while IPRs have two neurons that differentiate colour. [5] OPRs possess light-gathering apical surfaces called rhabdomeres, and otd is required for rhabdomere morphogenesis. Rapid expression of otd in all OPRs and IPRs is found following neuronal cell specification in the late larval stage and persists through photoreceptor differentiation. In later development of pupation through to adulthood, otd activates light detecting rhodopsin proteins Rh3 and Rh5 in IPRs while repressing Rh6 in OPRs.
In the anterior cap region of the syncytial blastoderm, which has non-segregated nuclei along the periphery of the blastoderm, bicoid in low concentrations is sufficient to activate otd expression through an enhancer located upstream of the otd gene. [7] [8] [9] Later, in the cellular blastoderm, which has all nuclei along the periphery separated in individual cells with their own cell membrane, otd expression is limited to a dorsal and anterior band due to repression of bicoid by torso, hunchback, and dorsal. [7] [8] [9] Torso and hunchback expression represses otd expression in the anterior most region of the blastoderm while dorsal expression represses expression in the ventral region. [1] [7] Groucho-independent repression of otd by runt, a pair-rule gene, has also been observed in the anterior and posterior regions of the syncytial and cellular blastoderm. [10]
Ocelliless (oc) is a general mutation in the otd gene locus in Drosophila , [11] which results in a loss of ocelli: the three photoreceptor organs located on the anterior region of Drosophila heads [1] Two alleles oc1 and ocγa1, are caused by lesions downstream of the last exon in otd which showed enhancer activity. [11] Another characteristic of the oc phenotype is the abnormal or deleted bristles in the ocellus region, [12] which relates back to the wild type otd gene’s role in mediating anterior patterning. [4] The same oc phenotype is found in loss-of-function epidermal growth factor receptor (EGFR) alleles and RNAi knockdown pointed (pnt) mutants [13]
The effect of oc on ocelli can be complemented by otduvi, another hypomorphic allele of the otd gene. otduvi/oc heterozygotes shows no ocellar phenotype or photoreceptor (R cell) phenotype, a phenotype that is related with otduvi allele. [6]
The Ocelliless mutant phenotype is not limited to loss of ocelli only. It has a role in disrupting oogenesis, where the inner and outer layer of the chorion in oc mutant eggs separate from one another leaving space for debris that is not seen in wild type otd, and disrupting reproductive capabilities, where female flies homozygous for the oc mutation are sterile. [14]
Drosophila melanogaster is a species of fly in the family Drosophilidae. The species is often referred to as the fruit fly or lesser fruit fly, or less commonly the "vinegar fly" or "pomace fly". Starting with Charles W. Woodworth's 1901 proposal of the use of this species as a model organism, D. melanogaster continues to be widely used for biological research in genetics, physiology, microbial pathogenesis, and life history evolution. As of 2017, five Nobel Prizes have been awarded to drosophilists for their work using the insect.
A genetic screen or mutagenesis screen is an experimental technique used to identify and select individuals who possess a phenotype of interest in a mutagenized population. Hence a genetic screen is a type of phenotypic screen. Genetic screens can provide important information on gene function as well as the molecular events that underlie a biological process or pathway. While genome projects have identified an extensive inventory of genes in many different organisms, genetic screens can provide valuable insight as to how those genes function.
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Drosophila embryogenesis, the process by which Drosophila embryos form, is a favorite model system for genetics and developmental biology. The study of its embryogenesis unlocked the century-long puzzle of how development was controlled, creating the field of evolutionary developmental biology. The small size, short generation time, and large brood size make it ideal for genetic studies. Transparent embryos facilitate developmental studies. Drosophila melanogaster was introduced into the field of genetic experiments by Thomas Hunt Morgan in 1909.
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A gap gene is a type of gene involved in the development of the segmented embryos of some arthropods. Gap genes are defined by the effect of a mutation in that gene, which causes the loss of contiguous body segments, resembling a gap in the normal body plan. Each gap gene, therefore, is necessary for the development of a section of the organism.
The zona limitans intrathalamica (ZLI) is a lineage-restriction compartment and primary developmental boundary in the vertebrate forebrain that serves as a signaling center and a restrictive border between the thalamus and the prethalamus.
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white, abbreviated w, was the first sex-linked mutation discovered, found in the fruit fly Drosophila melanogaster. In 1910 Thomas Hunt Morgan and Lilian Vaughan Morgan collected a single male white-eyed mutant from a population of Drosophila melanogaster fruit flies, which usually have dark brick red compound eyes. Upon crossing this male with wild-type female flies, they found that the offspring did not conform to the expectations of Mendelian inheritance. The first generation produced 1,237 red-eyed offspring and three white-eyed male flies. The second generation produced 2,459 red-eyed females, 1,011 red-eyed males, and 782 white-eyed males. Further experimental crosses led them to the conclusion that this mutation was somehow physically connected to the "factor" that determined sex in Drosophila. This led to the discovery of sex linkage, in which the gene for a trait is found on a sex chromosome. Morgan named this trait white, now abbreviated w. Flies possessing the white allele are frequently used to introduce high school and college students to genetics.
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Faint little ball (flb) is a Drosophila gene that encodes the Drosophila epidermal growth factor receptor (DER) homolog. The gene is also called torpedo and Ellipse. The gene is located at 3-26 of the Drosophila melanogaster genome. It is named faint little ball because when the gene is mutated the embryo forms a ball of dorsal hypoderm. flb is necessary for several processes to occur during embryonic development, specifically in central nervous system development. It is expressed as quickly as 4 hours after fertilization of the egg. The peak of expression of the flb gene is between 4–8 hours into development. In all processes that are facilitated by flb the same signal transduction pathway is used. Drosophila EGF receptor is involved in the development of embryos as well as larvae/pupae's wings, eyes, legs and ovaries.
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.
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Homeobox protein OTX1 is a protein that in humans is encoded by the OTX1 gene.
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