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Biological Ontologies in Rice Databases. An Introduction to the
Biological Ontologies in Rice Databases. An Introduction to the

... (orange–red); each tree extends away from the center toward a different direction. All nodes are called ‘GO terms’ and each term has a unique GO-ID. All nodes except the root have a parent node and some nodes have child node(s). Each GO-ID is unique, and more than two nodes can share the same GO-ID ...
FINAL EXAM (50 pts)
FINAL EXAM (50 pts)

... 8. You are studying regulation of the AFP gene in humans. You discover that the AFP gene is only expressed in fetal liver, not in adult liver. You decide to measure the levels of Foxa1 protein in fetal and adult liver in humans (You know from your readings that Foxa1 activates AFP gene expression). ...
Clairvoyance and Caution
Clairvoyance and Caution

... disease from Iowa. He searched the DNA from these two families for a telltale marker, helping to develop what were to become standard laboratory procedures in such ventures. Jim sliced up each person's DNA with restriction enzymes. He then developed markers, RFLPs, which he made radioactive. These m ...
投影片 1
投影片 1

... Has chaperonins to help fold “tough” prtns Can handle S-S rich proteins ...
Gene Regulation
Gene Regulation

... arac muants are rare because the mutation must make AraC active without binding arabinose Inactivation of araC (unlike lacI) produces an ara- phenotype AraC must also be an antiactivator since... araCc mutations should be dominant (but they are not). ...
High-level transcription of large gene regions: a novel T7 RNA
High-level transcription of large gene regions: a novel T7 RNA

... A variety of genetic tools have been developed, which are suitable for genetic studies in R. capsulatus. In contrast, there are very few expression vectors available for this bacterium. Therefore we explored the possibility of using the T7 promoter for high-level expression in R. capsulatus. First, ...
Gene Regulation
Gene Regulation

... arac muants are rare because the mutation must make AraC active without binding arabinose Inactivation of araC (unlike lacI) produces an ara- phenotype AraC must also be an antiactivator since... araCc mutations should be dominant (but they are not). IV. The trp operon (Negative regulation and trans ...
See more scientific discussion on this here.
See more scientific discussion on this here.

... effect. It was not selected against by Natural Selection. What other explanation could there be? It is also a definite piece of evidence for evolution in the sense just described but also because this non-functional gene has the same missing parts in all of the anthropoid primates. ...
Gene Mapping using 3 Point Test Crosses: Outlined below are the
Gene Mapping using 3 Point Test Crosses: Outlined below are the

... has been backcrossed (test-cross), to a homozygous, recessive individual. Therefore the two groups in the NCO class represent the two chromosomes in the F1 parent. These should then be drawn out, such as below. F1 ...
1. Introduction to Molecular Biology
1. Introduction to Molecular Biology

... Identify the regulatory effects of genes on each other, independent of the underlying regulatory mechanism Can be inferred from correlations in gene expression data, time-series gene expression data, and/or gene knock-out ...
Features on Nucleic Acid Sequences, Gene Features and Coding
Features on Nucleic Acid Sequences, Gene Features and Coding

... is a sequence, there is a feature located on that sequence, and there is a span on that sequence where the feature is located. Each of these pieces, the sequence, the feature and the location will have sub-properties including. ` In GUS, location, feature and sequence are all stored in separate tabl ...
1. Introduction to Molecular Biology
1. Introduction to Molecular Biology

... Identify the regulatory effects of genes on each other, independent of the underlying regulatory mechanism Can be inferred from correlations in gene expression data, time-series gene expression data, and/or gene knock-out ...
Comment - The Journal of Cell Biology
Comment - The Journal of Cell Biology

... tion and death in the muscular dystrophies are poorly understood. For example, how does the absence of dystrophin lead to instability of the sarcolemma? Why do different disruptions of the DGC lead to different manifestations of the dystrophic process? The overall phenotypic manifestations of these ...
R and BioConductor
R and BioConductor

... Note: Genes with similar expression levels in two experiments will appear around the first diagonal of the coordinate system. ...
- Cal State LA - Instructional Web Server
- Cal State LA - Instructional Web Server

... /product="TCP1-beta" Descriptive free text must be in quotations /protein_id="AAA98665.1" Protein sequence ID # ...
Slide 1 - Montville.net
Slide 1 - Montville.net

... The objective of the Paper Plasmid lab is to have you create a paper recombinant plasmid, a plasmid with a new gene inserted. The plasmid will contain DNA from two different organisms. You will use colored paper, scissors and tape to do this. If you are successful, you will have a two colored paper ...
Bombay Phenotype
Bombay Phenotype

... genes to make the A or B antigen at one loci but lack the genes that produce the H substance produced at another loci. – No H antigen gives you the O phenotype! ...
Genes and Traits
Genes and Traits

...  Genetics is the study of how traits ...
Leukaemia Section t(6;14)(p25;q32) IRF4/IGH / t(2;6)(p12;p25) IRF4/IGK / t(6;22)(p25;q11) IRF4/IGL
Leukaemia Section t(6;14)(p25;q32) IRF4/IGH / t(2;6)(p12;p25) IRF4/IGK / t(6;22)(p25;q11) IRF4/IGL

... immunoglobulin heavy chain gene to the IRF4 gene have been shown to activate the transcription factor MUM1/IRF4 in multiple myeloma and in a subtype of mature B-cell lymphomas (Iida et al., 1997; Salaverria et al., 2011). The translocation leads to the overexpression of the MUM1/IRF4 gene. In multip ...
Polygenic Traits Lab
Polygenic Traits Lab

... weight, hair color, skin color (basically, anything that deals with size, shape and color). This allows for a wide range of physical traits. For example, if height was controlled by one gene A and if AA= 6 feet and Aa = 5 feet 7 inches and aa= 5 feet, then people would be one of three different heig ...
Genetic Defects
Genetic Defects

... of bad news. The financial losses associated with dead and nonviable calves are obvious; however, it is the seed stock producer(s) who suffers the most when his program is identified as the source. A lot of great cattle may be carriers and they will have produced many non-carriers, so it is unreason ...
Teacher`s Guide - Cornell Science Inquiry Partnerships
Teacher`s Guide - Cornell Science Inquiry Partnerships

...  How can we identify and annotate or describe the protein-coding sequences apart from the rest of the DNA in an organism’s genome?  Is the sequence of a newly discovered gene similar to that of another gene that is better understood, and can we use that information as an experimental starting poin ...
Chapter 18 Gene Expression and Protein Synthesis
Chapter 18 Gene Expression and Protein Synthesis

... A eukaryotic gene has two parts: • A structural gene that is transcribed into RNA; the structural gene is made of exons and introns. • A regulatory gene that controls transcription; the regulatory gene is not transcribed but has control elements, one of which is the promoter. A promoter is unique to ...
Livestock Judging Basic Genetics Terminology
Livestock Judging Basic Genetics Terminology

... PHA gene from both its sire and dam. Since the PHA gene is recessive, the lethal form of this condition is only expressed when the calf is homozygous for the PHA gene. PHA-affected calves are either aborted or stillborn. Because of the anasarca that is associated with this condition, the PHA-affecte ...
D - Protein Information Resource
D - Protein Information Resource

... thesaurus, BioThesaurus, which maps a comprehensive collection of gene/protein names from over 35 biological databases, including the major gene (e.g., Entrez Gene) and protein databases (e.g. UniProt), and the model organism databases (e.g. MGD, SGD). BioThesaurus currently contains 5.8 million gen ...
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Gene nomenclature

Gene nomenclature is the scientific naming of genes, the units of heredity in living organisms. An international committee published recommendations for genetic symbols and nomenclature in 1957. The need to develop formal guidelines for human gene names and symbols was recognized in the 1960s and full guidelines were issued in 1979 (Edinburgh Human Genome Meeting). Several other species-specific research communities (e.g., Drosophila, mouse) have adopted nomenclature standards, as well, and have published them on the relevant model organism websites and in scientific journals, including the Trends in Genetics Genetic Nomenclature Guide. Scientists familiar with a particular gene family may work together to revise the nomenclature for the entire set of genes when new information becomes available. For many genes and their corresponding proteins, an assortment of alternate names is in use across the scientific literature and public biological databases, posing a challenge to effective organization and exchange of biological information. Standardization of nomenclature thus tries to achieve the benefits of vocabulary control and bibliographic control, although adherence is voluntary. The advent of the information age has brought gene ontology, which in some ways is a next step of gene nomenclature, because it aims to unify the representation of gene and gene product attributes across all species.Gene nomenclature and protein nomenclature are not separate endeavors; they are aspects of the same whole. Any name or symbol used for a protein can potentially also be used for the gene that encodes it, and vice versa. But owing to the nature of how science has developed (with knowledge being uncovered bit by bit over decades), proteins and their corresponding genes have not always been discovered simultaneously (and not always physiologically understood when discovered), which is the largest reason why protein and gene names do not always match, or why scientists tend to favor one symbol or name for the protein and another for the gene. Another reason is that many of the mechanisms of life are the same or very similar across species, genera, orders, and phyla, so that a given protein may be produced in many kinds of organisms; and thus scientists naturally often use the same symbol and name for a given protein in one species (for example, mice) as in another species (for example, humans). Regarding the first duality (same symbol and name for gene or protein), the context usually makes the sense clear to scientific readers, and the nomenclatural systems also provide for some specificity by using italic for a symbol when the gene is meant and plain (roman) for when the protein is meant. Regarding the second duality (a given protein is endogenous in many kinds of organisms), the nomenclatural systems also provide for at least human-versus-nonhuman specificity by using different capitalization, although scientists often ignore this distinction, given that it is often biologically irrelevant.Also owing to the nature of how scientific knowledge has unfolded, proteins and their corresponding genes often have several names and symbols that are synonymous. Some of the earlier ones may be deprecated in favor of newer ones, although such deprecation is voluntary. Some older names and symbols live on simply because they have been widely used in the scientific literature (including before the newer ones were coined) and are well established among users.
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