Unit 3 Revision Biology
Across
- 1. abnormal chromosome number
- 9. DNA/chromosome section copied twice
- 10. mutation with no protein change in the phenotype
- 11. insertion/deletion shifts reading frame
- 12. extra copy of one chromosome
- 14. DNA that does not code for proteins
- 15. one base changed in DNA
- 19. chromosome piece moves to another chromosome
- 21. short DNA fragments on lagging strand
- 22. coding section kept in mRNA
- 24. agent that causes mutations
- 25. chromosome segment flips around
Down
- 2. type of point mutation that may lead to a frameshift mutation
- 3. region upstream of DNA where RNA polymerase binds
- 4. enzyme that separates DNA strands
- 5. mRNA end helping stability/export
- 6. mutation in this cell type will not be inherited to offspring
- 7. one nucleotide is swapped for another
- 8. tRNA bases matching mRNA codons
- 13. stage where chromosomes separate
- 16. permenant change in DNA sequence
- 17. second most common outcome of a mutation
- 18. chromosomes fail to separate properly
- 20. enzyme that seals DNA
- 23. type of physical mutagen that damages DNA