1 birds and the bees Flashcards
(40 cards)
Which types of cell-division exist and how do they differ?
somatic cells
gametes
meiosis 1
meiosis 2
Mitosis and Meiosis , differences
Mitosis: the process of cell duplication
Chromosomes duplicate and split into two cells
Contain the exact same information
New cells are daughter cells
Meiosis: cell division, but the end product is a sex cell
Meiosis 1: diploid cell to haploid cell
Meiosis 2: haploid cells to haploid cells
Only one of the four daughter cells become an ovum
What is DNA and how is DNA copied during cell division/can it change?
How does inheritance of traits in humans work? How do you calculate risks and what are
basis principles of inheritance?
Genotype: the actual games
Phenotype: the physical characteristics
Dominant alles: need only one to be that expressed
Recessive alles: need two in order to be expressed
Punnet squares: a way to calculate the likelihood of gene expression
Calculated using probability
Homozygous: the same alles, so it will have the trait
Heterozygous: gene expression decided by the relationship between the alleles
Codominance: if there is two dominant, they are both expressed fully(ex. Blood type A and blood type B, create blood type AB)
Polygenetic traits: some characteristics are influenced by multiple genes (intelligence, etc.)
Incomplete dominance: the allele are expressed in a mix
X-linked inheritance: males more likely to express, because they one have one x chromosome so there is no way to cancel out
Fragile x syndrome, asd, color blindness
Which periods of prenatal development are there, and what develops when?
Germinal stage – zygote
* First 2 weeks of life from fertilization
* Rapid cell division
* Implants itself in the wall of the uterus
* From this point on the zygotes becomes dependent on the mother
* Until this point, alcohol, drugs etc. won’t harm the organism
Embryonic stage – embryo
* 3
rd – 8
th week of gestation (carrying of the embryo/fetus)
* Development of
o Amniotic sac (filled with amniotic fluid which serves as a protective buffer against physical shock and
temperature changes)
o Placenta – transfers O2 and nutrients, removes CO2, does not permit direct blood exchange –
however some drugs, viruses and antibodies are able to pass to the embryo
o Umbilical cord – transmits between placenta and embryo
* Inner mass differentiates into
o Endoderm becomes – gastrointestinal tract, trachea, bronchi, glands, and vital organs (lungs,
pancreas, liver)
o Mesoderm – muscles, skeleton, circulatory and excretory systems, and inner skin layer
o Ectoderm – sensory cells, nervous system (and skin, nails, hair, teeth…)
* 4
th week → head begins to take shape, eyes, nose and mouth
o Blood vessels that will become the heart start to pulsate
* 5
th week → buds that will become limbs start to form
* End of embryonic stage – 8
th week (10th of pregnancy)
o Face, fingers, toes, external genitalia
o Most common miscarriages often unnoticed (1 in 4 pregnancies)
Development in directions
- Cephalocaudal: development starts at the brain and proceeds down to trunk and legs (from head to tail)
- Proximal-distal: development from center to more distant areas (from middle out)
The fetus
* From 3rd month of gestation to delivery
* Development of muscles and the nervous system
* By the 3rd month the fetus has all its body parts including organs and external genitalia
* 4
th months – starts moving
* 5 months – reflexes (suckling, swallowing, hiccupping)
* Develops nails, sweat glands, more adult-like skin
* 6 months – eyes open and close
* Age of viability (22-26 weeks → app. 6 months)
o Point at which the fetus has physically advanced systems to survive even if born prematurely
(reasonable chances not 100%)
o However, can have difficulties mainly depending on the environmental conditions
What possible external harm could the child suffer during pregnancy?
teratogens – environmental factors that may cause developmental deviations (most threatening in the embryonic
stage)
* Medications
* Drugs
* Environmental toxins
* Other factors: age, diet, emotional state affect the response of the mother to the teratogens
When do these affect the child? What are the effects?
What types of genetic disorders are there?
- Most genetic problems are recessive traits – does not appear unless both of the parents carry the harmful
allele and a child inherits it from each - Sex-linked defects are more common in males because the alleles are often on the X-chromosome which he
inherits from the mother and only owns one (if it is defected, does not have an extra X that could be healthy
as females do) - E.g. colorblindness = X-linked
- Sickle-cell anemia = 2 recessive alleles
- Dominant allele → the parent will display the disability e.g. Huntington’s disease (nervous system
degenerates but often displays late in life once the person already has children) - Mutations – change the genetical information into harmful, non-harmful, beneficial or fatal
o Occurs spontaneously
o Can be induced by environmental hazards – toxic waste, radiation, chemicals etc.
types of cell-division and differences
DNA
inheritance
teratogens
A teratogen exerts its effects largely during critical periods of development
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a. Embryonic stage
b. Each organ has a more specific period e.g. heart → 20-40 days after conception
2. Teratogens have specific effects → different teratogens influence different developmental processes
3. Maternal or fetal genotypes may counteract a teratogen’s effect (their vulnerability to a specific one or not)
4. Effects of one teratogen may intensify effect of another
a. Mothers physiological status, nutritional and hormonal balance modify the impact of a teratogen
b. E.g. nutritional deficiencies intensify effects of drugs ingested by the mother
5. Different teratogens may produce the same defect
6. The longer and the more intensely a fetus is exposed to a teratogen, the more likely it is to be harmed
somatic cells
for repair and growth
gametes
reproduction and its variety
meiosis
process of cell division into gamete production, diploid → haploid
diploid
haploid
booty hole
`
homologous chromosomes
fertilization
combination of 2 random gametes
crossing over
How is genetic material present in the body and how is it passed on?
In the nucleus → chromosomes → DNA → genes → alleles → sequences of base pairs
- DNA usually free in the nucleus, when cell divides → coils into chromosomes
- Homologous chromosomes: same genes but not always the same alleles
- Homozygous: 2 identical alleles of a gene (AA)
- Heterozygous: 2 different alleles of a gene (Aa)
- Diploid and haploid: diploid are all somatic cells (2n), haploid are gamete (n)
condominance
– two heterozygous alleles are equally powerful → phenotype fully and equally expressed e.g. bloodtype AB
polygenic traits
characteristics influenced by many genes not a single one e.g. weight, height, intelligence, skin
color
chromosomal abnormalities
Too many or too few – if meiosis or mitosis does not proceed well
2. Broken or damaged chromosomes
3. Sex or autosomal chromosomes
Sex chromosomes:
* Involve the 23rd pair = sex chromosomes
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* Turner’s syndrome (X0) – sterile, females but need more estrogen to look womanly, struggles with spatial
and verbal abilities
* Poly-X “superfemale” (XXX, XXXX or XXXXX) – female and fertile, somewhat below average intelligence,
developmental delays and intellectual problems the more X chromosomes
* Klinefelter’s syndrome (XXY or XXXY) – sterile male with some secondary sex characteristics of a female,
taller than XY males, intellectual problems the more X chromosomes
* Supermale syndrome (XYY, XYYY, XYYYY) – typically fertile, phenotypic males who are taller, and develop
more acne, intellectual characteristics similar to normal XY male
➔ Problems in meiosis (mostly anaphase), wrong attachment of spindle
➔ X chromosome is larger thus is more harm when there are more than 2 present (too much genetic
information being produced)
Autosomes:
* Problems with the 22 non-sex chromosomes
* Most commonly happens when an gamete carries an extra autosomal chromosome and combines with a
normal one = 47 chromosomes
o 3 chromosomes of one type =trisomy
o Most common = Down syndrome = trisomy-21
o Chromosome 21 is the smallest, trisomy’s of other chromosomes usually lead to death
* Down syndrome – trisomy-21
o Mentally retarded
o Average IQ around 55
o Congenital eye, ear, and heart defects
o Physiological features: almond eyes, protruding tongue, short stubby limbs, flattened nose
o Developmental progress is the greatest when they are included, with lots of emotional support