specialized structure on centromere to which microtubular spindle fibers attach during mitosis/meiosis
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Chromatid
DNA strings, joined at the centromere
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Spindle fibers
attach to chromosomes & move them by pulling homologous pairs in opposite directions
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Centrioles
one pair of cellular organelles acting as anchor points for spindle fibers
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Microtubules
minute tubules that pull chromatids to the centrioles
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Nucleotides
Adenine, Guanine, Cytosine, & Thymine (make up DNA)
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Blastula stage
stage before specialization of cells
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Gastrula stage
after specialization
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Telomere
protects the ends of chromosomes from deterioration/fusion with other chromosomes by allowing ends to shorten (necessary in cell division), genetic info eventually lost (age limit on life)
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Apoptosis
cell suicide
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Histone
structural protein in chromosome
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Karyotype
complete set of chromosomes in a cell, 23 pairs homologous chromosomes, 22 pairs autosomes (not sex chromosomes)
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Homologous
one member of each pair acquired from gamete of each parent
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Mitosis cells
2 diploid cells result
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Meiosis cells
4 haploid cells result
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Unique meiosis processes
crossing over during Prophase 1, paternal & maternal chromosomes randomly assorted, different combinations of genes after fertilization
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Crossing over
must be the same chromosome
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Polar bodies
3 form with making of an egg, disintegrate & nutrients reabsorbed by body
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Prophase 1
nuclear membrane dissolves, centriole splits & moves to poles, spindle fibers form, chromosome pairs come together as homologous pairs (synapsis), crossing over may occur
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Metaphase 1
chromosomes attach themselves to the spindle, homologous pairs line up at the center
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Anaphase 1
homologous pairs segregate, 1 pair of each homologous pair found in each cell
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Telophase 1
nuclear membrane forms around each cell, nuclei not identical but have same traits
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Meiosis 2
same as mitosis
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Nondisjunction
1 pair of chromosomes doesn’t separate properly
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Polyploidy
organism has more than 2 sets of chromosomes
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Trisomy
organism has 3 homologous chromosomes in 1 pair
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Monosomy
organism has 1 homologous chromosome in 1 pair
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Down’s syndrome
aka Trisomy 21, extra chromosome at pair 21 \[almond shaped eye, flatter face, philtrum abnormalities, small ears, round/full face, short height, large forehead, flat nasal bridge, degree of cognitive impairment\]
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Turner syndrome
female with only 1 X chromosome \[infertile, short stature, underdeveloped sex features, broad chest, low set ears, webbed/wide neck, low hairline, drooping eyelids, dry eyes, no period\]
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Klinefelter syndromee
2 X & 1 Y chromosomes, appears male at birth, female hormones take over during puberty, infertile
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Gene
2 alleles
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Genotype
what’s in your genes: homozygous dominant/recessive, heterozygous
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Allelephenotype
visible traits, can be used to determine genotype
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Locus
physical location of a certain gene on a chromosome
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Heredity
mechanisms by which traits are passed on through genes
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Testcross
animal with unknown genotype is bred with known genotype to see offspring & determine genotype of unknown parent
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Dominant/Recessive
all offspring appear dominant
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Dominant/Heterozygous
all offspring appear dominant
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Recessive/Heterozygous
50/50 split in offspring appearance
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Dominant/Dominant
all offspring are dominant
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Recessive/Recessive
all offspring are recessive
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Heterozygous/Heterozygous
75/25 split in appearance, favoring dominant
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Dominant trait examples
free earlobe, brown eyes, freckles, dark hair, dimples, widow’s peak, cleft chin
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Recessive trait examples
attached earlobe, blue eyes, no freckles, blonde hair, no dimples, no widow’s peak, no cleft chin
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Incomplete dominance
trait shown is between that of parents, equally dominant (ex: red flower + white flower = pink flower)
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Genotypic ratio
expected ratio when certain phenotypes cross
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Phenotypic ratio
visible ratio
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Pleiotropic genes
effects more than 1 characteristic (ex: sickle cell anemia = higher malaria resistance)
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Epistatic genes
genes that mask the expression of another gene
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Multiple alleles
particular gene that exists in 3+ allelic forms, but individuals possess only 2 such alleles at same loci (ex: blood type/eye colour)
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Codominance
traits both show in different cells (ex: Dalmatians)
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Morgan
discovered that the farther from the centromere, the more often crossover happens, linked sex & genes using fruit fly eye colour
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Marker genes
easily identifiable phenotypes
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Gene mapping
distances based on frequency (process of elimination)
number of recombinations/total number of offspring x 100%
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Sex linked traits
some traits are found on the X chromosome, if mother carries 50% of children will be unaffected, 50% sons will have, 50% daughters will carry (ex: colour blindness, hemophilia) both parents must have it for a daughter to have it
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Sexual dimorphism
differences between sexes other than reproductive organs (ex: colour pattern in animals)
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Questions for pedigrees
1) is there anyone whose phenotype is different than both parents? (yes = both parents are heterozygous) 2) are there any girls with recessive phenotype who have a father or son with dominant phenotype? (yes = can’t be sex-linked)
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Polygenic
genotypes controlled by more than 1 gene (ex: chicken combs)
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Continuous traits
varying degrees of variation between dominant & recessive
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Continuity of Life
succession of offspring that share structural similarities with parents
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Isotope
atoms of the same element containing the same number of protons, but a different number of neutrons
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Radioisotope
isotope that decays spontaneously by emitting radiation
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Nucleotide
molecule having 5 carbon sugar with nitrogenous base attached at its 1’ carbon & a phosphate group attached to its 5’ carbon
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Deoxyribose sugar
sugar molecule containing 5 carbon
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Phosphate group
group of 4 oxygen atoms surrounding central phosphorus atom found in the backbone of DNA
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Complimentary pairs
Adenine-Thymine, Guanine-Cytosine
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Miescher
isolated nucleic acids from pus
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Griffith
Discovered that hereditary characteristics from dead bacteria could still be passed on and kill mice
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Hammerling
Discovered that hereditary material much be in the nucleus
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Avery & team
1944, isolated pneumococci → DNA = transforming principle. Proved Griffith’s findings on transformation
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Chargaff
Discovered that the amounts of A-T and C-G were always the same is all tested organisms
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Hershey & Chase
Confirmed that genetic material was carried in nucleic acid
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Franklin
Used X-ray photographs and deduced the structure of DNA from that
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Watson & Crick
Build a model of the double helix
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DNA side structure
made of a pentose sugar, deoxyribose bonded to phosphate groups by phosphodiester bonds (merely structural, they don’t contain DNA info)
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DNA center structure
made of nitrogen bases bonded together by weak hydrogen bonds
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Hydrogen bonds between C & G
3
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Hydrogen bonds between A & T
2
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Antiparallel strands
run in opposite directions (1’ to 5’ or 5’ to 1’)
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Double ring purines
Adenine & Guanine
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Single ring pyrimidines
Thymine & Cytosine
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Stage when DNA is copied
Synthesis stage of interphase
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Leading strand
continuously replicates, from origin to the fork opening
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Lagging strand
works backwards, gaps left, only a bit replicated at a time, from fork opening to the origin
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Topoisomerase
untwists DNA
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Helicase
cuts hydrogen bonds
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Single strand binding proteins
keep strands separated
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Primase
attach an RNA primer (starting point for DNA replication)