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57 Cards in this Set

  • Front
  • Back
Mitochondria (singular- mitochondrion)
Organelles contained within the cytoplasm of eukaryotic cells that convert energy, derived from nutrients, into a form that is used by the cell.
Ribosomes
Organelles located in the cell's cytoplasm that are essential to the manufacture of proteins.
Centrioles
Organelles located in the cell's cytoplasm that help to organize the assembly of microtubules during cell division.
Chromosomes
Nuclear organelles made of DNA and other proteins; in eukaryotic cells they are found only in the nucleus. They are the carries of genetic information in the cell.
Centromere
The constricted portion of a chromosome. After replication the duplicated chromosome are joined at the centromere.
Somatic cells
Body cells (muscle, brain, blood, or bone cells, for example); basically all cells in the body except reproductive cells (gametes)
Gametes
Cells produced through meiosis that carry a haploid set of chromosome to the next generation
Zygote
Diploid fertilized egg formed by union of haploid egg and sperm
Homologous chromosomes
Matching pairs of chromosomes, one member of the pair is inherited from each parent
Sex chromosomes
Chromosomes that determine sex (and some other traits)
Autosomes
All the chromosomes except the pair that determines sex
Diploid set
The full set of 23 homologous pairs of chromosomes (2 or each kind or 46)
Haploid set
Set formed when there is only one from each of the homologous pairs of chromosomes (one of each kind or 23)
Gene
Segment of a chromosome. Genes code for all or part of a specific protein (or other functional product).
Locus/loci
Fixed position or location of the gene on the chromosome
Allele
Alternate form of a gene
Deoxyribonucleic acid (DNA)
Two-stranded molecule made of chains of nucleotides twisted into a double helix
Molecules
Structures made up of two or more atoms. Molecules can combine with other molecules to form more complex structures
Nucleotide
Basic units of the DNA molecule, composed of a sugar, a phosphate, and one of four DNA bases.
Complementary
Referring to the fact that DNA forms base pairs in a precise manner. Since adenine and thymine can only bond with each other, they are said to be complementary to each other. Cytosine and guanine are another complementary pair.
Protein
Molecules made of chains of amino acids; they serve a wide variety of functions through their ability to bind to other molecules.
Protein synthesis
A process, directed by DNA, in which chains of amino acids are assembled into functional protein molecules.
Amino acids
Small molecules that are the building blocks of proteins
Ribonucleic acid (RNA)
A molecule similar to DNA, but it is single stranded, with a different sugar, and with uracil replacing thymine. RNA is essential to the production of proteins
Messenger RNA (mRNA)
A form of RNA that is assembled on a sequence of DNA bases. It carries the DNA code to the ribosomes during protein synthesis.
Transfer RNA (tRNA)
The type of RNA that binds to specific amino acids and carries them to the ribosome during protein synthesis
Replicate
To duplicate. DNA replication takes place prior to any type of cell division.
Mitosis
Cell division that leads to the production of somatic cells
Meiosis
Cell division that leads to the production of gametes
Mutation
A change in DNA bases, number, or structure (see point mutation and nondisjunction)
Nondisjunction
The failure of homologous chromosomes or chromosome strands to separate during cell division; results in a cell with an abnormal number of chromosomes
Point mutation
A change in the DNA base sequence of a gene that can lead to the production of a new protein
Genotype
The actual genetic makeup of an individual; the actual alleles that are present
Phenotype
The observable, measurable, physical expression of the genotype as affected by the environment
Dominant
An allele that masks the effect of another
Recessive
An allele whose expression can be masked by another
Codominant
The expression of two alleles in heterozygotes. Because neither allele is dominant or recessive, both influence the phenotype
Heterozygous
Having 2 different alleles at a given locus on a pair of homologous chromosomes
Homozygous
Having 2 of the same alleles at a given locus on a pair of homologous chromosomes
Principle of Segregation
Genes (alleles) occur in pairs (because chromosomes occur in pairs). During gamete production, the members of each gene pair separate, so that each gamete contains one member of each pair. During fertilization, the full number of chromosomes is restored, and members of gene or allele pairs are reunited.
Principle of Independent Assortment
The distribution of one pair of alleles into gametes does not influence the distribution of another pair. The gene controlling different traits are inherited independently of one another.
Mendelian or monogenic traits
Traits that are influenced by alleles at only one locus
Discrete distribution
Mendelian or monogenic traits, coded for by one gene, fall into clearly defined categories. For example, each human has either type A, B, AB or O blood.
Polygenic traits
Traits that are influenced by genes at two or more loci.
Continuous distribution
Polygenic traits, coded for by two or more genes, show continuous variation, from one extreme to another. Traits are measured in units on a scale with even increments (feet and inches, for example), and every person falls somewhere on the continuum for that trait.
Species
A group of organisms that can interbreed and produce fertile offspring; a reproductively isolated group of organisms.
Population
Within a species, an interbreeding group of individuals; the group among which an organism is most likely to find a mate; a group of organisms sharing a gene pool.
Gene pool
The total complement or store of genes in a population; described by allele frequency.
Allele frequency
Proportion (expressed as percentage) of different alleles in the gene pool of a population
Evolution
A change in the allele frequency in the gene pool of a population through time
Mutation
A change in allele frequency of a population can occur due to a change or alteration in genetic material in the gametes. A mutation is the only way to produce new variation that can then be acted upon by natural selection.
Gene flow
The exchange of genes between populations. A change in allele frequency of a population can take place due to movement of alleles into or out of populations.
Genetic Drift
A change in allele frequency of a population due to chance or random factors.
Founder effect
A type of genetic drift in which allele frequencies are altered in small populations that are taken from, or are remnants of, larger populations
Natural selection
A change in allele frequency of a population can take place due to differential individual net reproductive success
Microevolution
Small-scale changes in allele frequencies that can take place from generation to generation within a species.
Macroevolution
Large-scale evolutionary changes that lead to speciation, the development of a new species