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Chapter 1 - Genetics and the Organism

Terms

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Gene
the fundamental physical and functional unit of heredity, which carries information from one generation to the next;
a segment of DNA composed of a transcribed region and a regulatory sequence that makes transcription possible
Deoxyribonucleic Acid (DNA)
a double chain of linked nucleotides (having dexyroibose as their sugars);
the fundamental substance of which genes are composed
Protein
macromolecule composed of one or more amino acid chains;
main component of phenotypic expression
Alleles
one of the different forms of a gene that can exist at a single locus
Genome
the entire complement of genetic material in a chromosome set
Diploid
a cell having two chromosome sets or an individual organism having two chromosome sets in each of its cells
Haploid
a cell having one chromosome set or an organism composed of such cells
Homologous chromosomes
chromosomes that pair with each other at meiosis or chromosomes in different species that have retained most of the same genes during their evolution from a common ancestor
Nucleotides
a molecule composed of a nitrogenous base, a sugar, and a phosphate group; the basic building block of nucleic acids
Zygote
a cell formed by the fusion of an egg and a sperm;
the unique dipoid cell that will divide mitotically to create a differentiated diploid organism
Structural Proteins
a protein whose function is in cellular organism structure
Enzyme
a protein that functions as a catalyst
Polypeptide
a chain of linked amino acids;
a protein
Transcription
the synthesis of RNA from a DNA templete
Ribonucleic Acid (RNA)
a single-stranded nucleic acid similar to DNA but having ribose sugar rather than deoxyribose sugar and uracil rather than thymine as one of the bases
Transcript
the RNA molecule copied from the DNA template strand by RNA polymerase
messenger RNA
an RNA molecule transcribed from the DNA of a gene;
a protein is translated from this RNA molecule by the action of ribosomes
Translation
the ribosome- and tRNA-mediated production of a polypeptide whose amino acid sequence is derived from the codon sequence of an mRNA molecule
Codon
a section of DNA, three nucleotide pairs in length, that encodes a single amino acid
Ribosomes
a complex organelle that catalyzes the translation of messenger RNA into an amino acid sequence;
composed of proteins plus rRNA
transfer RNA
a class of small RNA molecules that bear specific amino acids to the ribosome in the course of translation;
an amino acid is inserted into the growing polypeptide chain when the anticodon of the corresponding tRNA pairs with a codon on the mRNA being translated
Introns
an intervening sequence;
a segment of largely unknown function within a gene;
this segment is intially transcribed, but the transcript is not found in the functinoal mRNA
Exons
any nonintron section of the coding sequence of a gene;
together, the exons correspond to the mRNA that is translated into protein
Discontinuous Variation
variation having distinct classes of phenotypes for a particular character
Phenotype
the form taken by some character (or group of characters) in a specific individual;
the detectable outward manifestations of a specific genotype
Genotype
the specific allelic composition of a cell, either of the entire cell or, more commonly, of a certain gene or a set of genes
Polymorphism
the occurence in a population (or among populations) of several phenotypic forms associated with alleles of one gene or homologs of one chromosome
Morph
one form of a genetic polymorphism;
may be either a phenotype or a molecular sequence
Mutant
an organism or cell carrying a mutation
Wild type
the genotype or phenotype that is found in nature or in the standard laboratory stock for a given organism
Continuous variation
Variation showing an unbroken range of phentoypic values
Active site
the part of a protein that must be maintained in a specific shape if the protein is to be functional - for example, in an enzyme, the part to which the substrate binds
Null allele
an allele whose effect is the absence either of normal gene product at the molecular level or of normal function at the phenotypic level
Nucleotide-pair substitution
the replacement of a specific nucleotide pair by a different pair; often mutagenic
Deletion
the removal of a chromosomal segment from chromosome set
Duplication
more than one copy of a particular chromosomal segment in a chromosome set
Frameshift mutation
the insertion or deletion of a nucleotide pair or pairs, causing a disruption of the translational reading frame
Genomics
the cloning and molecular characterization of entire genomes
Bioinformatics
computational information systems and analytical methods applied to biological problems such as genomic analysis
Probe
Labeled nucleic acid segment that can be used to identify specific DNA molecules bearing the complementary sequence, usually through autoradiography or fluorescence
Restriction enzymes
an endonuclease that will recognize specific target nucleotide sequences in DNA and break the DNA chain at those points;
a variety of these enzymes are known, and they are extensively used in genetic engineering
Southern blot
the transfer of electrophoretically separated fragments of DNA from a gel to an absorbent sheet such as paper; this sheet is then immersed in a solution containing a labeled probe that will bind to a fragment of interest
Northern blot
the transfer of electrophoretically separated RNA molecules from a gel onto an absorbent sheet, which is then immersed in a labeled probe that will bind to the RNA of interest
Western blot
Membrane carrying an imprint of proteins separated by electrophoresis, can be probed with a labeled antibody to detect a specific protein
Model organisms
a species chosen for use in studies of genetics because it is well suited to the study of one or more genetic processes
Norm of reaction
the pattern of phenotypes produced by a given genotype under different environmental conditions
Developmental noise
variation in the outcomes of development as a consequence of random events in cell division, cell movement, and small differences in the number and location of molecules within cells

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