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58 Cards in this Set

  • Front
  • Back
synapse
pairs of homologous chromosomes
bivalent
two sister chromatids
Tetrad
four sister chromosomes together
dyad
half of a tetrad
monad
a single chromosome
Leptonema
Stage in prophase 1 where chromatin material begins to condense and form chromomeres
chromomeres
localized condensations that resemble beads on a string. Used in homology search later in prophase
Zygonema
a continuation of the shortening and thickening process. Chromomeres undergo initial alignment. Synaptonemal complex begins to form
Pachynema
synaptonemal complex continues to develop, leading to synapsis. Evidence of the double structure is visually apparent now.
Diplonema
Within each tetrad, each pair of sister chromatids begins to separate. Some areas remain in contact, called chiasma. This is thought to be where crossing over occurs.
Diakinesis
chromosomes pull farther apart, but still loosly associated at chiasmata. Chiasmata move closer to the ends of the tetrad. Terminalization begins in late diplonema and is completed during diakinesis. Nucleolus and nuclear membrane begins to dissolve and spindle fibers begin to attach to kinetochores
Karyotype
a pictorial representation of all of an organisms chromosomes lined up and with homologous pairs together if diploid.
Interphase
the phase of cell growth and development. DNA replicated in the middle of interphase. Three checkpoints are passed during interphase: G1/S, G2/M, and M checkpoints
Kinetochore
The point at which spindle fibers attach to chromosomes. An assembly of multilayered proteins associated with the centromere.
Spindle checkpoint
AKA M checkpoint. Point that makes sure DNA has been copied faithfully and that spindle fibers have been associated with kinetochores. Controlled by spindle checkpoint genes.
Sister chromatids
Replica chromatids which are bound by a centromere
Cell Cycle Checkpoint
Set of checkpoints designed to ensure that certain replication processes are complete before the cell cycle is allowed to continue. Proteins known as cyclins along with cyclin-dependent kinases work to control the cell cycle by their concentration values.
Homologs
A pair of chromosomes which encode for the same function, each originating from one parent
Bivalents
one of a pair of synapsed homologous chromosomes
Tetrad
During meiosis, two pairs of sister chromatids which have been synapsed. Four chromatids in total
Chiasmata
Occurs durring Diplonema. An area in a synapse where chromatids remain intertwined
Nondisjunction
Occurs when one or more chromatids are not separated during mitosis or meiosis, resulting in more or less than normal chromosomes in a cell. Can cause genetic diseases in embryos when occurring during meiosis.
Synaptonemal complex
Forms during Zygonema. The ultrastructural component of the sunapse
Synapsis
A more intimate pairing of chromosomes during Pachynema. Chromosomes are separated by only 100nm
Somatic Cell
A cell which is part of the regular body. Usually already determined to become one kind of tissue type.
Gamates
haploid sex cells
Gene classes important in cell division (name at least 5)
Spindle checkpoint genes
kinetochore structure genes
spindle formation genes
DNA damage genes
Cyclins
Chromatin condensation genes
Centriole formation genes
Nuclear membrane breakdown/formation genes
Cytokinesis genes
Monohybrid Cross
A cross between two true-breeding individuals, selecting for a single inheritable trait
Dihybrid Cross
A cross between two true-breeding individuals, selecting for two inheritable traits
Test Cross
a method to determine the hetero or homozygocity of an individual expressing a dominant trait
Dominant trait
A trait which only requires one allele to be expressed that prevents the recessive allele from being expressed
Recessive trait
A trait which requires a homozygous set of alleles in order to be expressed
Unit Factor
Mendel thought that there must be some kind of discrete unit of heredity, which he called a Unit Factor, which allowed the inheritance traits to be inherited in the manner which he saw in his pea plant experiments
Complementation analysis
Allows for researchers to see if two independently isolated mutations are in the same gene. Two mutant strains are crossed. If the F1 generation does not exhibit the recessive mutant trait, then the genes are located on two different loci. If they still exhibit the trait, the gene is on the same loci
Pleiotropy
a single gene that affects several phenotypic traits
Epistasis
Interaction between genes such that one gene or gene pair masks or modifies the effect of another gene or gene pair (Example hh masks the expression of IA and IB)
Spontaneous mutation
The occurrence of mutations in the absence of known mutagens
Conditional allele
An allele who's expression depends on environmental factors
Lethal allele
An allele which, if present and active, results in the acute or eventual death of the organism
Locus heterogeneity
A single disorder, trait, or pattern of traits caused by mutations in genes at different chromosomal loci
nucleotide
Building blocks of DNA. Consists of a nitrogenous base, pentose sugar, and a phosphate group. Or a nucleoside attached to a phosphate group
nucleoside
purine or pyrimidine covalently linked to a ribose or deoxyribose
Hydrogen Bond
a polar bond formed between an highly electronegative atom on one molecule and a hydrogen on another molecule.
Phosphodiester bond
bonds that form the backbone of a single strand of DNA. Forms between the 5' end of one molecule (phosphate group) and the 3' end of the sugar on the next molecule
Pyrimidine
A single ring nitrogenous base
purine
a two ringed nucleotide base
haploid
only one set of chromosomes present
diploid
two sets of chromosomes present
autosome
a non-sex chromosome
gene
a heredity unit which encodes for a particular trait or set of traits
allele
a version of a gene which codes for one version of a trait
phenotype
the physical manifestation of a genotype
mutation
a random change in a gene producing a new allele which may or may not affect phenotype
denature
the unfolding of a protein due to unfavorable conditions
recombinant
genes which can be cut apart and rejoined in new ways
genetic map
a measure of where genes are on chromosomes with relation to each other
interference
the inhibition of one crossover event by a nearby crossover event
map unit
a relative measure of distance between two genes, measured by their percent of crossovers