Sex-linked genes involve genes on sex chromosomes (X or Y) and results differentiate between male and female.
Heterogametic means 2 different types of gametes. Usually male: X,Y chromosome.
Homogametic means 1 type of gamete. Usually in females, X chromosomes only.
X-linked recessive are traits controlled by recessive genes on the X chromosome. They are mostly common in males, 1X chromosome. Females need to inherit 2copies on the recessive allele.
X-linked dominant is expressed in both male and female. Males may show different expressitivity and females if they inherit 1 copy of the dominant allele.
Y-linked inheritance are genes on the Ychromosome are passed on from father to son and not expressed in females. Y chromosome is infertility disorder.
A father with the specific trait will transmit the mutantallele to all daughters, but no sons. This is because the mother is a dominanthomozygote. The daughters will have a normalphenotype, but will have carriers of mutation.
A carrier who mates with a normal male will pass the mutation to her half sons and half daughters. The half sons will have a mutation and the half daughters will be carriers like the mother.
A carrier mates with a male with trait, there is a 50% chance that each child will have the trait. Daughters without the trait will be carriers. Males without the trait will be free from all the harmfulrecessive allele.
There are 20,000 genes in humans, 23pairs of chromosomes, (1000 linked genes).
When genes are close together on a chromosome, the alleles on the same chromosome tend to be inherited, so it show non-independent assortment and are linked.
We can determine the order and location of genes within a chromosome using recombination.
Getting a double heterozygote means we know which alleles are together on the chromosome.
By finding recombinant events, we look at the gametes made by the heterozygous parent.
Parental types results are obtained by morgan.
We can combinants from crossing over in meiosis called recombination.
During crossing over, twochromatids on a gene tetrad cross over at randompoints and swap geneticmaterial when only 1 chiasmata is formed.
From getting combinants, we are able to calculate the recombinant frequency.
RF = recombinants / total offspring x 100
RF of the gametes contain a chromosome that has formed a chiasma between the 2genes.
The smaller the distance of 2 genes, less likely a chiasma will be formed, called unlinked genes.
Unlinked genes will have a RF of 50%, 1/2 recombinant and 1/2 parental. There is a linear relationship between distance and RF
Fewer recombinants means the 2genes must be linked (on the same chromosome).