How do cDNA sequences facilitate gene annotation? Describe how the use of full-length cDNAs facilitates discovery of alternative splicing.
Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
15. Genomes and Genomics
Sequencing the Genome
Problem 11
Textbook Question
When comparing genes from two sequenced genomes, how does one determine whether two genes are orthologous? What pitfalls arise when one or both of the genomes are not sequenced?

1
Understand the concept of orthologous genes: Orthologous genes are genes in different species that evolved from a common ancestral gene through speciation. They typically retain similar functions across species.
Compare the sequences of the two genes: Use sequence alignment tools (e.g., BLAST) to compare the nucleotide or amino acid sequences of the genes. High sequence similarity is often indicative of orthology.
Analyze the phylogenetic relationship: Construct a phylogenetic tree using the sequences of the genes and their homologs from other species. Orthologous genes should cluster together based on their evolutionary history.
Consider synteny: Examine the genomic context of the genes (e.g., neighboring genes or conserved regions). Orthologous genes often reside in similar genomic locations across species.
Address pitfalls with incomplete genome sequencing: If one or both genomes are not fully sequenced, missing data can lead to incorrect identification of orthologs. Additionally, fragmented assemblies may obscure synteny or phylogenetic relationships, requiring careful interpretation and validation using additional data or methods.

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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Orthologous Genes
Orthologous genes are genes in different species that evolved from a common ancestral gene through speciation. They typically retain the same function across species, making them crucial for comparative genomics. Identifying orthologs helps in understanding evolutionary relationships and functional conservation.
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Genome Sequencing
Genome sequencing is the process of determining the complete DNA sequence of an organism's genome. Accurate sequencing is essential for identifying genes and their relationships. If one or both genomes are not sequenced, it can lead to incomplete data, making it difficult to accurately determine orthology.
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Sequencing Difficulties
Pitfalls in Comparative Genomics
Pitfalls in comparative genomics include misidentifying orthologs due to incomplete or erroneous genome data. Factors such as gene duplication, horizontal gene transfer, and sequencing errors can complicate the analysis. These issues can lead to incorrect conclusions about evolutionary relationships and gene functions.
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