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Protein Syn and Mut.
Protein synthesis and Mutations
| Question | Answer |
|---|---|
| The molecule that stores genetic instructions for building proteins | DNA |
| A segment of DNA that contains the code to make one protein. | Gene |
| a single-stranded copy of a gene that carries the instructions from the nucleus to the ribosome. | mRNA |
| Process in the nucleus where a gene’s DNA sequence is copied into mRNA. | Transcription |
| Process at the ribosome where the mRNA code is read and amino acids are linked to form a protein. | Translation |
| A three-base sequence on mRNA that codes for a specific amino acid. | Codon |
| brings the correct amino acid to the ribosome based on the codon. | tRNA |
| Cell organelle made of RNA that reads mRNA and assembles proteins. | Ribosome |
| The building block of proteins. | Amino Acid |
| A–T, C–G. | DNA Base Pairing |
| A–U, C–G. | RNA Base Pairs |
| Site where DNA is stored and transcription occurs. | Nucleus |
| A change in a single nucleotide (base) in DNA. | Point Mutation |
| A change in the DNA sequence that can alter a protein. | Mutation |
| One base is swapped for another; may change a single amino acid or have no effect. | Substitution |
| A substitution that does not change the amino acid coded for. | Silent Mutation |
| A substitution that changes one amino acid in the protein. | Missense Mutation |
| A substitution that creates a stop codon, causing the protein to be shorter. | Nonsense Mutation |
| Insertion or deletion of a nucleotide that shifts the reading frame, altering many amino acids. | Frameshift Mutation |
| Disease from a Point Mutation caused by a single base change in hemoglobin gene. | Sickle cell anemia |
| A change in the number or structure of entire chromosomes. | Chromosomal Mutation |
| Part of a chromosome is missing. | Deletion |
| A segment of a chromosome is repeated. | Duplication |
| A chromosome segment breaks off, flips, and reattaches in reverse order. | Inversion |
| A segment of one chromosome attaches to a different, non-homologous chromosome. | Translocation |
| Example of a Chromosomal Disorder | Down syndrome (trisomy 21) |