8. Inheritance And Selection Flashcards
What does genotype describe?
Describes all the alleles an organism contains
-Sets the limits within the characteristics of an organism may vary
How can a change to the genotype be inherited by offspring?
If the mutation occurs in the formation of gametes
What does phenotype describe?
The observable characteristics of an organism
What is a modification? (In terms of inheritance and selection?)
A change to the phenotype that does not affect the genotype and is not inherited
What is the position of a gene on a chromosome called?
Locus
What is a homologous chromosome?
Homologous chromosomes are chromosome pairs, one from each parent, that are similar in length, gene position, and centromere location. The position of the genes on each homologous chromosome is the same, however the genes may contain different alleles.
What does co-dominant/incompletely dominant mean?
When both alleles appear in the phenotype- there is a blend of both features
What does multiple alleles mean?
When there are more than two alleles for a particular characteristic. However as there are only two chromosomes in a homologous pair, it follows that there can be only two of the multiple alleles present in any one organism
What is an example of multiple alleles? Which are recessive/ dominant in your example?
Blood groups where groups A B ad O are possible. A and B are co-dominant and O is recessive to both.
How are genetic crosses represented? What must you not forget to include?
Represented using punnet squares with genes represented as different letters (eg G for green seeds and Y for yellow seeds) and uppercase represents a dominant allele and a lower case represents a recessive allele
You must not forget to include:
- Phenotype of the parents
- Genotype of the parents
- What alleles their sperm and egg would include (during meiosis)
What is sex linkage of a gene?
A gene is said to be sex linked when carried on either the X or the Y chromosome
Why could some characteristics found on some parts of the X chromosome appear more frequently in males than in females?
- The X chromosome is much longer than the Y chromosome which means there is a part on the X chromosome which has no homologous portion on the Y chromosome
- Therefore if there is a recessive allele on the portion of the X chromosome with no homologous Y portion then there will be no dominant allele to mask the expression of the recessive allele
Why does haemophilia occur almost exclusively in males?
Haemophilia is caused by a recessive allele in which the nucleotides do not code for teh required protein for blood clotting. It occurs almost exclusively in males because it occurs on the portion of the X chromosome with no homologous Y section therefore if present in a male, there is no dominant allele to mask the effect. However as females have two X chromosomes, it is more likely that the other X will have a dominant allele so the recessive allele for the faulty protein would not be expressed.
What is a carrier? (In the context of inheritance and selection)
An organism that is heterozygous for a certain gene, perhaps for a genetic disease which is caused by a recessive allele- individuals do not express any characteristics/ symptoms of the disease/ disorder but may pass on the allele for the genetic disorder onto their offspring.
What is a pedigree chart and how are different individuals represented? (Using the example of tracking a genetic disease)
A chart similar to a family tree. Males represented as square, females represented as circles. Affected individuals have their circle/ square shaded in.