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This section explores how DNA sequence data provides powerful evidence for evolutionary relationships between species. By comparing the DNA sequences of different organisms, scientists can infer their evolutionary history and construct phylogenetic trees.
All living organisms use DNA as their genetic material. The sequence of nucleotides (Adenine, Guanine, Cytosine, Thymine) within DNA encodes the instructions for building and maintaining an organism. The universality of DNA provides a common basis for comparing genetic information across species.
Over time, mutations occur in DNA. These are changes in the nucleotide sequence. Mutations can be:
These mutations accumulate over generations, leading to differences in DNA sequences between species. The rate of mutation can vary between different regions of the genome.
Many mutations have no significant effect on an organism's phenotype. These are called neutral mutations. Because neutral mutations accumulate randomly, they are particularly useful for inferring evolutionary relationships. The more neutral mutations two species share, the more closely related they are likely to be.
To compare DNA sequences, they must first be aligned. This involves arranging the sequences so that homologous (similar) regions are in the same columns. Alignment algorithms are used to maximize the similarity between sequences.
Once sequences are aligned, phylogenetic analysis is used to determine the evolutionary relationships between species. This involves comparing the number of differences (mutations) between sequences and using these differences to build a tree-like diagram (a phylogenetic tree) that represents the evolutionary history of the species.
The molecular clock hypothesis suggests that mutations accumulate at a relatively constant rate over time. This allows scientists to estimate the time of divergence between species by calibrating the mutation rate using fossil evidence or known events in the geological record.
Comparing the DNA sequences of humans and other primates has revealed their close evolutionary relationship. DNA evidence supports the theory that humans evolved from a common ancestor with chimpanzees.
The rapid mutation rate of viruses, such as HIV and influenza, makes DNA sequence data particularly useful for tracking their evolution and understanding their adaptation to new hosts and environments. This information is crucial for developing effective antiviral drugs and vaccines.
Analyzing the DNA sequences of bacteria can reveal their evolutionary history, track the spread of antibiotic resistance genes, and understand the evolution of bacterial virulence factors.
While DNA sequence data is a powerful tool for studying evolution, it has some limitations:
Feature | Description |
---|---|
DNA Sequence | The sequence of nucleotides (A, T, C, G) in a DNA molecule. |
Mutations | Changes in the DNA sequence, including point mutations, insertions, and deletions. |
Sequence Alignment | Arranging DNA sequences to identify homologous regions. |
Phylogenetic Trees | Diagrams that represent the evolutionary relationships between species. |
Molecular Clock | The concept that mutations accumulate at a constant rate over time. |