We have 46 chromosomes (23 pairs). The bands on the
chromosomes show different GENES- genes come in
pairs
Chromosomes are made out of DNA- double helix - shows how
organism should be constructed, how each cell should function
Genes are sections of DNA, genes control development of diff
characteristics- issues instruction to cell- carries this out by
producing proteins.
Structural protein- structure in the body eg collagen in ligaments.
Functional- how the body works eg enzymes
Sex cells contain single chromosomes eg 23
chromosomes. 23-sex determining gene.
Differences between individuals of same species- variation.
Can be caused by genes: eye colour and dimples or
environment:scars, dyed hair or both: height, weight.
GENETIC MODIFICATION
All organisms have DNA- possible to introduce genetic
information from one organisms to another. Produces a new
combination of genes and characteristics.
GENETIC VARIATION & INFORMATION.
ALLELES
Genes have different versions- alleles eg
eye colour B and b- inherit one from each
parent.
Dominant- controls characteristics. Recessive need 2.
Heterozygous- 2 different alleles eg Bb. Homozygous 2 of same
allele eg BB or bb.
Female- XX lack of Y produce ovaries. Male- Xy- produce
testes & androgens
Poor diet can lead to disease eg fatty can lead to heart
disease. Possible to limit certain diseases by making
LIFESTYLE CHOICES.
Cystic fibrosis- affects cell membranes- thick mucus
round lung, guts. SYMPTOMS- chest infections, salty
sweat, weight loss. HAVE 2 HAVE 2 RECESSIVE ALLELES TO
HAVE IT. Ff- carrier FF NO ff have
GENETIC DISORDERS
GENETIC TESTING
Amniocentesis- needle into uterus amniotic fluid carrying cells from fetus. 14-16 weeks-
0.5% miscarriage. Chorionic villus- 8-10 weeks. Forceps through cervix- placenta- which
holds chorionic villi fetal cells. 2% miscarriage.
False positive- don't have disease tests says
you do, false negatively etc
Implications- right to interfere with nature?
what can be done/should be done. Could
be used to have info: your ethnicity,
susceptible to certain conditions. Babies
should be screened at birth: tailor
healthcare problems, stop g disorders
being passed on.
Less money- less suffering on treatment. Other
hand, diseases are natural wrong to eliminate.
Storing genetic information questions
confidentiality eg discrimination turned down
for jobs if higher risk of illness.
Embryo selection
Other way of preventing babies having genetic disorders- IVF 1/ ova harvested
from mother and feritilised 2. embroys tested for faulty allele. 3/ healthy
implanted in uterus
Pre implantation genetic diagnosis- 1/ after fertlisation embryo allowed divide to 8
cell before single cell is removed fro each one- testing.2/ testing if carry alleles for
specific g disorder.
CONTROVERSIAL- unnatural- concerns that ppl could select
characteristics- reduce variation eg blue eye, brown eye disappear.
Gene therapy - potential treatment for genetic disorders, involves
healthy genes inserted. Genes inserted into modified virus infecting
patient becoming part of cells correcting faulty allele.
Raises questions: is it safe?- potential risks and side effects. some can't be answered by science- right to
manipulate genes?, can we decide for future generations. Address same ethical issue- is it acceptable?-
based on if benefit majority.
ARGUMENTS FOR: 1/ Acceptable procedure vs vaccination not invasive. 2/ people with g conditions need lifetime of
treatment. It improves lives & free up resources. 3/ Some conditions reduce life expectancy- allows normal life.
ARGUMENTS AGAINST: 1/ It's unnatural and morally wrong to change people's genes & DNA. 2/
Experimental don't know long term effects. 3/ Need to be tested on humans- not safe- side effects?
ASEXUAL REP
Bacteria & single cell organisms can reproduce dividing individuals- clones (genetically identical to
parent). - plants&animals reproduce like this. Variation in organisms that reproduce asexually ONLY
caused by environment.
Clones can occur naturally: cells embryo separate, 2 new embryos- identical twins. Produced artificially: animal- nucleus
from adult body cell transferred to empty egg cell (without nucleus) into a surrogate animal- same genetics as donor.
CELL DIVISION- 1/ Parental cell with 2 pairs of chromosomes. 2/ Each chromosome replicates itself. 3/ Copies are pulled
apart. Cell divides for only times. 4/ Each daughter cell has same number of chromosomes & contain same genes as
parental cell.
STEM CELLS
Most organisms made up of various specialised cells- different structures. In
early stages of development, cells aren't specialised= stem cells.
They have potential develop into any cells. Can be used to replace damaged tissues eg Parkinson's. Clone embryos- enough cells.
Collected at 8 cell stage- cells are unspecialised- 16 cell specialisation begins. Possible to use up to 150 cell stage- not effective.
ETHICS OF STEM CELLS- is it right to clone embryos & s cells- are they
seen as people? IVF disused embryo? - acceptable to use parental
consent.
Could be cloned from patient's cells- reproductive cloning (new individ identical to donor) illegal UK.
GOVERNMENTS made laws on issues special advisory committees explore ethics of procedures such as cloning & stem cell use.