Comparison of observable features- not useful due to polygenetic characteristics.
Comparison of DNA base sequences- closely related organisms can be identified and mutations can be seen between distantly-related organisms.
Comparison of the base sequence of mRNA.
Comparison of the amino acid sequence in proteins.
DNA sequence can be used to find out the amino acids, but the amino acid sequence can't be used to find out the DNA sequence, because of the degenerate code.
DNA hybridisation:
Sections of DNA are used- whole strands are too long.
Heat is used to separate and mix the two strands- forming a hybrid.
The level of hybridisation indicates how related they are.
Complete hybridisation- organisms are identical, they have complementary bases
No hybridisation- organisms are unrelated, they have nocomplementary bases
The early days of estimating genetic diversity:
Scientists observed visual features in a population and the number of organisms with that particular feature.
Different alleles determine different characteristics, so a wide variety of each characteristic indicates high allele numbers and genetic diversity.
Gene technology can now measure genetic diversity directly:
Different alleles of the same gene have slightly different DNA base sequences which can be compared within individuals in a population to identify the number of those gene alleles.
Different alleles produce slightly differentmRNA base sequences and proteins with slightly different amino acid sequences- which are easy to compare.
Gene technologies can get more accurate estimates of genetic diversity within populations/ species than traditional ways of comparing observable characteristics and features.