Introduction to Variation Video
dominant
recessive
variation
continuous
discontinuous
distinct
discrete
allele
genes
mutation
meiosis
reproduction
zygote
gamete
qualitative
quantitative
somatic
germinal
phenotype
genotype
frequency
crossing over
independent
assortment
recombinant
Natural selection requires variation among members of a species in order to differentiate survival (variation needed for selection)
With dominant and recessive alleles of a single gene, the number of possible phenotypes is limited.
For example, a person either has cystic fibrosis or not. When multiple alleles are introduced, the number of possibilities for a single trait increases accordingly. For example, the ABO blood type has three alleles and four possible phenotypes. When a second gene is introduced, the number of possible genotypes increases dramatically. With three, four or five genes determining the phenotype, the number of possibilities is so big that it is impossible to see the difference between certain genotypes in the phenotype.
When an array of possible phenotypes can be produced, it is called continuous variation. The colour of skin in humans is an example of continuous variation and it is thought that the intensity of pigment in skin is the result of the interaction of multiple genes. In humans, continuous variation can also be seen in the genetic components of traits such as height, body shape, and intellectual aptitude. Each of these is also influenced by environmental components. A person’s height, for example, is determined by whether he or she inherits genes for tallness, but it also depends on the person’s nutrition as he or she is growing.
To help you decide whether or not a trait shows continuous variation, imagine a questionnaire to record phenotypes. In general, if it is possible to tick ‘yes’ or ‘no’ for a trait, that trait does not show continuous variation, for example dry versus wet earwax. The same is true for a trait whose possibilities can be represented by just a few choices, such as blood type (A, B, AB, or O). When variation is not continuous, it is referred to as discontinuous variation. The data for discontinuous variation can be displayed as bar charts . An unbroken transitional pattern from one group to another is not present.
There are three main mechanisms by which genetic variation between individuals in a species may occur:
A gene mutation is a change in the nucleotide sequence of a section of DNA coding for a specific trait
Gene mutations can be beneficial, detrimental or neutral
A gene mutation is a change to the base sequence of a gene that can affect the structure and function of the protein it encodes
Meiosis promotes variation by creating new gene combinations via either crossing over or independent assortment
1. Crossing Over
Crossing over involves the exchange of segments of DNA between homologous chromosomes during prophase I
As a consequence of this recombination, all four chromatids that comprise the bivalent will be genetically different
2. Independent Assortment
When homologous chromosomes line up in metaphase I, their orientation towards the opposing poles is random
The orientation of each bivalent occurs independently, meaning different combinations of maternal / paternal chromosomes can be inherited when bivalents separate in anaphase I
The fusion of two haploid gametes results in the formation of a diploid zygote
As meiosis results in genetically distinct gametes, random fertilisation by egg and sperm will always generate different zygotes
Variation in our species.
Look at these amazing humans.
Great similarities, greater differences.
Exhibiting some extreme cognitive features.