Inheritance, Variation And Evolution Flashcards
what is DNA
- polymer
- made up of 2 strands forming a double helix
- contained in structures called chromosomes
What is a gene
-small section of DNA on a chromosome
-each gene codes for a particular sequence of amino acids, to make a specific protein
What is a genome
-the entire genetic material of that organism
Importance of understanding human genome
1) It allows scientists to identify genes in the genome that are linked to different types of disease.
2) Knowing which genes are linked to inherited diseases could help us to understand them better and could help us to develop effective treatments for them.
3) Scientists can look at genomes to trace the migration of certain populations of people around the world. All modern humans are descended from a common ancestor who lived in Africa, but humans can now be found all over the planet. The human genome is mostly identical in all individuals, but as different populations of people migrated away from Africa, they gradually developed tiny differences in their genomes. By investigating these differences, scientists can work out when new populations split off in a different direction and what route they took.
How many pairs of chromosomes in a human
23
How many chromosomes control characteristics and how many control gender
22 control characteristics
1 controls gender
Female chromosomes
XX
Male chromosomes
XY
Gamete
A reproductive cell of an animal or a plant
Chromosome
A thin strand of DNA
Allele
A different version of the same gene
What is the dominant
The allele which is expressed in the phenotype when only 1 copy is present (the one that decides the phenotype)
What is the recessive
allele that only expresses itself when there are two copies of the allele present in an individual
Homozygous
2 of the same alleles (AA, aa)
Heterozygous
2 different alleles (Aa)
Genotype
The two alleles for a characteristics (for an organism it’s ALL the DNA for that organism)
Phenotype
The physical characteristics (blonde hair)
Polydactyl
Having extra fingers or toes, caused by dominant allele
Cystic fibrosis
Disorder of cell membranes, caused by recessive allele
Economic issues with embryo screening
- High Costs: Embryo screening can be very expensive, making it inaccessible to many families. This limits its availability mainly to wealthier people.
- Healthcare Spending: Public healthcare systems might need to allocate substantial funds to cover embryo screening, potentially taking resources away from other medical needs.
- Future Cost Savings vs. Immediate Cost: While screening could help prevent costly genetic diseases, the immediate costs are high, making it challenging to justify for public funding.
Ethical issues with embryo screening
- “Designer Babies”: Screening could be used to select traits beyond health, like appearance or intelligence, raising concerns about choosing babies’ characteristics and ethical boundaries.
- Value of Life: Deciding which embryos to keep based on genetics raises questions about whether all lives are valued equally, potentially stigmatizing certain conditions.
- Consent: Embryos can’t consent to screening or selection, leading to ethical debates on making such significant choices on behalf of a future person.
Social issues with embryo screening
- Increased Inequality: If only wealthier families can afford embryo screening, it could deepen social inequalities and create divides based on genetic “advantages.”
- Discrimination: Emphasizing genetic “normality” may foster discrimination against people with disabilities, suggesting that only certain types of people are desirable.
- Pressure on Parents: Social norms could develop, pressuring parents to screen embryos or risk being judged for not doing everything to ensure a “healthy” child.
5 steps of IVF
- Stimulating the Ovaries: Medicine is given to help the ovaries produce multiple eggs (usually, only one egg is released each month, but IVF aims to get several).
- Retrieving Eggs and Sperm: Doctors collect the eggs from the ovaries and also get a sperm sample from the partner or a donor.
- Fertilization in the Lab: The eggs and sperm are combined in a lab, where hopefully some eggs become fertilized and turn into embryos.
- Selecting and Transferring Embryos: Once the embryos grow for a few days, a healthy one (or sometimes more) is chosen and placed into the uterus.
- Waiting for Pregnancy: If the embryo attaches to the uterus lining, pregnancy begins, and the process continues like any typical pregnancy.
Explain meiosis
- before cell starts to divide, it duplicates its genetic information, forming 2 armed chromosomes: one arm of chromosomes is an exact copy of the other arm
- after replication, the chromosomes arrange themselves into pairs
- in the first division in meiosis the chromosome pairs line up in the centre of the cell
- the pairs are ten pulled apart so each new cell only has 1 copy of each chromosome. Some of the father’s chromosomes and some of the mother’s chromosomes go into each new cell
- in the second division, the chromosomes line up again in the centre of the cell
- the arms of the chromosome e pulled apart
- you end up with 4 gametes, each with only a single set of chromosomes in it
- each gamete is genetically different from the others because the chromosomes al get shuffled up during meiosis and each gamete only gets half of them at random