genetics Flashcards
genetics
informationt hat shows genes that are passed down generations
somatic cell
body cells of plants and animals
chromosome
holds genes and its information
centromere
holds sister chromatids together
spindle fibers
helps sister chromatids move around, specifically move to opposite poles
centrosome
the things spindle fibres come out of
genome
complete dna sequence of an organism
sex chromosome
gender teller thing
autosome
the 1-22 pairs of chromosomes that represent traits
homologous chromosome
same sequence of genes as another
gene
part of a chromosome that contains traits, passable traits and DNA sequence
allele
part of a chromosome that contains dominant or recessive cells
karyotype
picture of stained chromosomes laid out to study gender and health
asexual reproduction
one parents making sisters (mitosis)
sexual reproduction
two parents and genetically distinct offspring (Meiosis)
gamete
cell with sperm and egg
zygote
cell formed by fusion of two gametes
fertilization
joining of male and female haploid gametes
haploid
cell that’s has half the # of chromosomes as parent cells
meiosis
produces cells containing half the # of chromosomes during prophase 1
diploid
pairs of homologous chromosomes
synapsis
aligning homologous chromosomes during prophase 1
crossing over
exchange of chromosomal segments between homogous
genetic reduction
produces daughter cells with half the # of the parent
genetic recombination
products of meiosis have different combinations of alleles (crossing over)
fraternal
unidentical twins from different eggs
identical twins
split zygote in first few days
deletion
piece of chromosome is lost
duplication
section of chromosome appears 2 or more times
inversion
segment of DNA is flipped (No lost info)
translocation
fragments of DNA from two different non-homologous exchange
Non disjunction
failure of proper serperation
monosomy
too few (Single pair in the place of homologous pairs)
Trisomy
too many (3 homogenous in place of 1 homologous)
Trisomy 21
down syndrome (Extra chromosome)
Trisomy 18
Edward syndrome (Trisomy at 18th)
Trisomy 13
Patau Syndrome (extra 13th)
XXY
Kilnefelter (Cannot produce sperm)
XYY
Jacobs (Taller than average)
XXX
Triple X (Tall and thin, irregular menstrual)
XO
turner (Short, webbed neck, sexually underdeveloped)
Multiple Marker screen
Blood test and ultrasound
Amniocentesis
needle in uterus and extract amniotic fluid (Tests all trisomy and gender)
Chorionic Villi sampling (CVS)
Chorionic Villi Sampled for placenta test (Tests everything)
the split down the cell called
cleavage furrow
selective breeding
select which genes are favourable and reproduce them
artificial insemination
transfer semen into females reproductive tract
embryo transfer
fertilizing an egg artificially and then transferring it into recipient female. No need to transfer an entire animal, just need to transfer the egg
in vitro fertilization (IVF)
For women with blocked fallopian tubes, immatures are taken and combined with sperm in a lab. When became an embryo, its back in the womb. (test tube babies)
cloning
produces identical genes, cells or organisms
gene cloning
the use of dna manipulation techniques to produce multiple copies of a single gene or segment of dna
recombinant dna
molecule of dna that includes genetic material from different sources
therapeutic cloning
produces genetically identical cells that are used to treat diseases. replaced egg cells nucleus with nucleus from somatic donor cell to produce a line of genetically identical cells.
reproductive cloning
producing genetically identical organims
zygote to embryo steps
zygote > dividing > mass of stem cells > embryo
Preimplantation Genetic Diagnosis
genetic testing done before embryo is implanted
spermatogenesis
testicals, two divisions produce 4 spermatids that mature into sperm, starting at mitosis, after puberty then meiosis. 250k are produced per day
Oogenesis
ovaries, two divisions make 3 polar bodies where 2 die and one turns into an egg. Polar bodies die due to uneven cytoplasm
oocyte Is a
immature egg
mitosis happens when in the body
thogughout life
meiosis happens when int he body
after puberty
deletion is
a piece of chromosome is lost
duplication is
a section of chromosome that appears two or more times in a row
inversion is
a segment of DNA in a chromosome flips upside down
translocation is
fragments of DNA from two different (non-homologous) chromosomes exchange places
Non-disjunction
failure of proper separation during meiosis anaphase
monosomy is
single pair of chromosome in the place of homologous pair
trisomy is
3 homologous pairs in a place of homologous pair
what is a test cross
tests if a person is homologous or heterozygous for a dominant trait, to see if they are a carrier or not
Incomplete dominance
when neither alleles completely conceal each other
codominace is
when both alleles have equal roles
sex linked inheritance is
controlled by genes on either x or Y chromosome
multiple alleles is
many traits resulted int he interaction of more than two alleles for one gene ( the chinchilla and himayalyan one)
Polygenic Inheritence
characteristic influenced by two or more genes (Mixed babies)
gonads
organisms that produce egg or sperm
loci is the
section in chromatids that genes occur in
who showed chromosome and meiosis
Walter sutton\
what is sickle cell anemia
normal red blood cells look elongated and c shaped and stubble to transport oxygen leading to blockages
tetrad
a group of four sister chromatids (2 chromosomes)