• Shuffle
    Toggle On
    Toggle Off
  • Alphabetize
    Toggle On
    Toggle Off
  • Front First
    Toggle On
    Toggle Off
  • Both Sides
    Toggle On
    Toggle Off
  • Read
    Toggle On
    Toggle Off
Reading...
Front

Card Range To Study

through

image

Play button

image

Play button

image

Progress

1/168

Click to flip

Use LEFT and RIGHT arrow keys to navigate between flashcards;

Use UP and DOWN arrow keys to flip the card;

H to show hint;

A reads text to speech;

168 Cards in this Set

  • Front
  • Back
Recombination
Formation of new genetic combinations by exchange of parts between homologs
Linkage
When two loci recombine at less that 50% of gametes
Chi-Square Test
A statistical method for testing the fit between observed and expected data
Chiasma
Structure formed at the spot where crossing-over occurs between homologs
Tetratype
A tetrad carrying four kinds of haploid cells; two different parental classes, and two recombinants
Locus
The relative chromosomal location of a gene
Coefficient of Confidence
The ratio of observed double-crossovers to expected crossovers
Interference
One crossover along a chromosome makes a second one nearby less likely
Parental ditype
An Ascus containing only two non-rcombinant kinds of spores
First-order segregation
When two alleles of a gene are separated into different cells at the first meiotic division
ascospores
Fungal spores contained in a sac
mosaic
Individual composed of cells with different genotypes
Transformation
Griffith Experiment
Pyrimidine
A nitrogenous base containing a single ring
Dexyribose
The sugar within the nucleotide subunits of DNA
Hydrogen bonds
Noncovalent bonds that hold the strands of the double helix together
Complementary bases
Two nitrogen bases that can pair via hydrogen bonds
Origin
A short sequence of bases where unwinding of the double helix for replication begins
Okazaki fragments
Short DNA fragments formed by discontinuous replication of one of the strands
Purine
A nitrogenous base containing a double-ring
Topoisomerases
Enzymes involved in uncoiling DNA
Semiconservative replication
Meselson - Stahl Experiment
lagging strand
The strand that is synthesized discontinuously during replication
telomeres
Structures at ends of eukaryotic chromosomes
Transition
Substitution that exchanges a purine for a purine (A ↔ G) or a pyrimidine for a pyrimidine, (C ↔ T)
Base Substitution
replacement of a single base nucleotide with another nucleotide
Transversion
Substitution that exchanges a purine for a pyrimidine or a pyrimidine for a purine (C/T ↔ A/G)
Inversion
180-degree rotation of a segment of the DNA molecule
Translocation
large-scale mutations in which part of one chromosome becomes attached to a nonhomologous chromosome
Deletion
the loss of a segment of the genetic material from a chromosome
Insertion
the gain of a segment of new genetic material into the a chromosome
Deamination
Hydrolysis changes a normal base to an atypical base containing a keto group in place of the original amine group.
X-ray irradiation
Substitution that exchanges a purine for a pyrimidine or a pyrimidine for a purine (C/T ↔ A/G)
Intercalator
Molecules that can sandwich between base pairs, disrupting ordering
Unequal crossing-over
crossing over between nonallelic sequences on nonsister chromatids in a pair of homologues.
codon
A group of three mRNA bases signifying one amino acid
colinearity
Linear sequence of amino acids in the polypeptide corresponds to the linear sequence of nucleotide pairs in the gene
reading frame
The grouping of mRNA bases in threes to be read as codons
degeneracy of genetic code
Most amino acids are not specified by a single codon
nonsense codon
Stop codons - UAA, UGA, UAG
initiation codon
AUG in a particular context
template strand
The strand of DNA having the base sequence complementary to that of the primary transcript
transcription
The conversion of DNA-encoded information to its RNA-encoded equivalent
intron
A sequence of base pairs within a gene that is not represented by any bases in the mature mRNA
Reciprocal Translocation
Exact exchange of parts of two non-homologous chromosomes
Gynandromorph
organism that contains both male and female characteristics
Pericentric
chromosome rearrangement that includes the centromere
Paracentric
inversions that do NOT include the centromere and both breaks occur in one arm of the chromosome
Euploids
having complete sets of chromosomes
Polyploidy
having more than two sets of homologous chromosomes
Transposition
Movement of short DNA elements
Aneuploids
state of not having euploidy
Deficiency
When a Block of one of more nucleotide pairs is lost from a DNA molecule
Base Analogs
Mutagens that are similar enough in chemical structure to the normal nitrogenous bases that they can be incorporated into DNA in place of normal bases
Acrocentric
A chromosome in which the centromere is close to one end
Allele Frequency
The proportion of all copies of a gene in a population that are of a given allele type
Allosteric proteins
Proteins that undergo reversible changes in conformation when bound to another molecule
Anaphase
The stage of mitosis in which sister chromatids are separated and pulled to opposite spindle poles
Anaphase I
Phase of Meiosis I in which the chiasmata joining homologous chromosomes dissolve, allowing parental homologs to move toward opposite spindle poles
Anaphase II
Phase of Meiosis II in which coheson joining sister chromatids is removed, allowing sister chromatids to move toward opposite spindle poles
Ascus
Saclike structure in some fungi that houses all four haploid products of meiosis
Attenuation
A type of gene regulation in which transcription of a gene terminates in the regulatory region before a complete mRNA transcript is made
Autotroph
An organism that is nutritionally self-sufficient, e.g. plants produce their own food by photosynthesis
Auxotroph
A mutant microorganism that can grow on minimal medium only if it has been supplemented with one or more growth factors not required by the wild-life strain
Bacteriophage (Phage)
A virus that attacks bacteria
Biochemical Pathway
An orderly series of reactions that allows an organism to obtain simple molecules from the environment and convert them step-wise into successively more complicated structures
Bivalent
A pair of synapsed homologous chromosomes during prophase of meiosis I
Catabolite repression
Repression of expression in sugar-metabolizing operons like the lac operon when glucose or another preferred catabolite is present
Centromere
Region of chromosome at which sister chromosomes are connected
Chiasmata
Observable regions in which non-sister chromatids of homologous chromosomes cross over.
Chromosome
Self-replicating genetic structure of cells that carries a linear array of genes in its nucleotide sequence
Codominant
Expression of heterozygous genotype resulting in hybrid offspring that resemble both parents equally for a particular trair
Codon
Nucleotide triplet that represents an amino acid to be inserted in a specific positionin the growing amino acid chain during translation
Conjugation
A mechanism of gene transfer in bacteria in which a donor connects to a recipient using a pilli, and transfers genetic material through the pilli.
Constitutive expression
A state of gene activation that remains at constant high level and is not subject to repression
Criss-cross inheritance
Inheritance pattern in which males inherit a trait from their mothers, while daughters inherit the trait from their fathers
Cross
The deliberate mating of selected parents based on particular genetic traits desired in the offspring
Crossing over
During Meiosis, the breaking of one maternal and one paternal chromosome, resulting in the exchange of corresponding sections of DNA and the rejoining of the chromosome. Can result in the exchange of alleles between chromosomes
Dihybrid
An individual that is heterozygous for two genes
Thymine Dimer
Bonding between two adjacent Thymines in a nucleotide sequence
Alleles
Alternatives forms of a single gene
Complementation test
Method of discovering whether two mutations are in the same or separate gene
Dominant allele
An allele that expresses its phenotype in a heterozygote
epistatis
When an allele hides the effects of another allele on the same gene
expressivity
The degree to which a genotype is expressed in a phenotype
F plasmid
A conjugative plasmid that carries many genes required for the transfer of DNA
F⁺ plasmid
Cell carrying the F plasmid
F⁻ plasmid
Cell without the F plasmid
F' plasmid
F plasmid variant that carries most plasmid genes plus some bacterial genes
Frameshift mutation
Insertion or deletion of base pairs that alter the grouping of nucleotides into codons
Gametes
Specialized haploid cells that carry genes between generations
gene
Basic unit of biological information; specific segment of DNA in a discrete region of a chromosome that serves as a unit of function by encoding a particular RNA or protein
Genetics
The science of heredity
genome
The sum total genetic information of a cell or organism
genotype
The actual alleles present in an individual
haploid
a single set of chromosomes present in gametes
Hemizygous
Describes the genotype for genes present in only one copy in an otherwise diploid organism, e.g. X-linked genes in males
Heterozygous
A genotype in which the two copies of the gene that determine a particular trait are different alleles
Hfr
Bacteria that produce a High Frequency of Recombinants for chromosomal genes because their chromosomes contain an integrated F plasmid
Homologous chromosomes (homologs)
A pair of chromosomes containing the same linear gene sequence, each derived from one parent
Homozygous
A genotype in which the two copies of the gene that determine a particular trait are the same allele
Incomplete dominance
Expression of heterozygous phenotype resulting in offspring whose phenotype is intermediate between those of the parents
Independent assortment
The random distribution of different genes during gamete formation
Lateral gene transfer
The introduction and incorporation of DNA from an unrelated individual or from a different species
Mendel's First Law - Law of Segregation
The two alleles for each trait separate during gamete formation and then unite at random, one from each parent, at fertilization
Mendel's Second Law - Law of Independent Assortment
During gamete formation, different pairs of alleles segregate independently of each other
Metaphase
Stage of meisosis/mitosis when the chromosomes line upalong the equatorial line of the cell
Missense mutation
Change in the nucleotide sequence of a gene that change the identity of an amino acid in the polypeptide encoded by that gene
Mitotic disjunction
The failure of two sister chromatids to separate during mitotic anaphase generates reciprocal trisomic and monosomic daughter cells
Monosomic
Individual lacking chromosome from the diploid number for the species
Monohybrid cross
Cross between parents that differ in only one trait
Monomorphic
A gene with only one wild-type allele
Mutagen
Any physical or chemical agent that raises the frequency of mutations above the spontaneous rate
Mutation
Heritable alteration in DNA sequence
Nondisjunction
Failure of chromosome segregation during meiosis
Non-Parental Ditype (NPD)
A tetrad containing four recombinant spores
Nonsense mutation
Mutational change in which a codon for an amino acid is altered to a stop codon
Null hypothesis
A statistical hypothesis to be tested and either rejected or accepted in favor of an alternative
Open Reading Frame (ORF)
DNA Sequence with long stretches of codons in the same reading frame uninterrupted by stop codons, suggesting the presence og genes
Operator site
DNA Sequence near the promoter that can be bound to by a repressor protein
Operon
A unit of DNA composed of specific genes, plus a promoter and/or operator, that acts in unison to regulate the response of the structural genes to environmental changes
Origin of replication
Sequence of nucleotides at which the initiation of DNA replication begins
Parental classes
Combination of alleles present in the original parental generation
Parental ditype
A tetrad that contains four parental class haploid cells
Penetrance
Indication of how many members of a population with a particular genotype show the expected phenotype
Phenotype
An observable characteristic
Pilus
Hollow protein tube that protrubes from F+, Hfr or F` bacterial cells and binds to the cell wall of an F- cell; used for gene transfer during conjugation
Plaque
A clear area on a bacterial lawn, devoid of living bacterial cells
Plasmid
Small circle of doube-stranded DNA that can replicate in bacterial cells independently of the bacterial chromosome
Polymerase (DNA/RNA)
Enzymes that catalyze the synthesis of nucleic acids on preexisting nucleic acid templates
Promoter
DNA Sequence near the beginning of a gene that signal RNA polymerase where to begin transcription
Prototroph
A microorganism that can grow on minimal medium in the absence of one or more growth factors
recessive allele
Allele whose phenotype is not expressed in the heterozygote
Recessive Lethal gene
An allele that prevents the birth or survival of homozygotes
Recombinant classes
Reshuffled combinations of alleles that were not present in the parental generation
Recombinant
Chromosome that carries a mix of alleles derived from different homologous chromosomes
Recombination frequency
The percentage of recombinant progeny
Repressor
A type of transcription factor that can bind to specific cis-acting elements such as operator sites preventing transcription
RNA Polymerase
Enzyme that transcribes a DNA sequence into an RNA transcript
semi-conservative replication
A pattern of double helix duplication in which complementary base pairing followed by the successive linkage of two nucleotides yields two daughter double helices that each contain one of the original strands intact, and one completely new strand
Sister chromatids
The two identical copies of a chromosome that exist immediately after DNA replication
Substitution
Occurs when a base at a certain position in one strand of the DNA molecule is replaced by one of the other three bases
Segregation
Equal separation of alleles for each trait during gamete formation, in which one allele of each gene goes to each gamete
Silent mutation
Mutation with no effect on phenotype
Temperate bacteriophages
After infecting the host, these phages can enter either the lyic or kysogenic cycle
Tetratype
A fungal ascus carrying four kinds of haploid cells; two different parental classes, and two recombinants
testcross
A cross used to determine the genotype of an individual showing a dominant phenotype by mating with an individual showing the recessive phenotype
tetrad
The four products of a meiotic division
Transduction
Bacterial gene transfer mechanism in which donor DNA is packaged with the protein coat of a bacteriophage and transferred to the recipient when the phage particle infects it
Translation
The process in which codons carried by mRNA direct the synthesis of a polypeptide from amino acids according to the genetic code
Transposable Elements (TEs)
All DNA segments that move about the genome, regardless of mechanism
Vector
A specialized DNA sequence that can enter a living cell, signal its presence to an investigator by conferring a detectable property on the host cell, and provide a means of replication for itself and the foreign DNA inserted into it. A vector must also possess distinguishing traits by which it can be purified away from the host cell's genome
Virulent bacteriophage
After infecting the host, these phages always enter the lytic cycle, multiply rapidly, and kill the host.
Virus
A noncellular biological entity that can reproduce only within a host cell. Viruses consist of nucleic acid convered by protein
Wild-type allele
An allele whose frequency is more than 1% in a population
Complete Dominance
A kind of dominance wherein the dominant allele completely masks the effect of the recessive allele in the heterozygote
Complementation Group
A collection of mutants that do not complement each other
Competent
Cells able to take up DNA from their environment
Corepressor
A molecule that binds to transcription factors rather than DNA and prevents transcription above basal levels
Episome
Plasmid that can integrate into the host chromosome
Induction
Gene activation by a molecule that inactivates a repressor protein, activating transcription of one or more structural genes
Inducer
Molecule that acts by binding either to an activator or to a repressor protein to stimulate gene expression.
Lysogenic cycle
viral DNA or RNA enters the cell and integrates into the host DNA as a new set of genes
Lytic cycle
Bacterial cycle resulting in cell lysis and release of progeny phage
Point Mutation
Mutation of one base pair
Prophage
Phage genome inserted as part of the DNA of a bacterium
Reporter Gene
Protein-encoding gene whose expression in the cell is quantifiable
Merodiploid
Partially diploid (having a second copy of only part of its genome)