DOC PREVIEW
UGA BIOL 1107 - Types of Mutations
Type Lecture Note
Pages 4

This preview shows page 1 out of 4 pages.

Save
View full document
View full document
Premium Document
Do you want full access? Go Premium and unlock all 4 pages.
Access to all documents
Download any document
Ad free experience
Premium Document
Do you want full access? Go Premium and unlock all 4 pages.
Access to all documents
Download any document
Ad free experience

Unformatted text preview:

BIOL 1107 1nd Edition Lecture 22Outline of Last Lecture I. Central DogmaII. Three Stages of TranscriptionIII. Prokaryote vs. Eukaryote IV. MutantsOutline of Current Lecture I. Mis-sense mutationII. Non-senseIII. SilentIV. FrameshifV. DeletionCurrent LectureI. Mis-sense mutation (substitution) - Substitutions that change one amino acid to another one- May have little effect on protein: new amino acid may have properties similarto those of amino acid it replaces, or it may be in a region of protein where exact sequence of amino acids is not essential to protein’s functionThese notes represent a detailed interpretation of the professor’s lecture. GradeBuddy is best used as a supplement to your own notes, not as a substitute.II. Non-sense mutation (truncation) - point mutation can change a codon for an amino acid into a stop codon- It causes translation to be terminated prematurely; the resulting polypeptide will be shorter than the polypeptide encoded by the normal gene.- Nearly all nonsense mutations lead to nonfunctional proteins.III. Silent- Some substitutions have no effect on the encoded protein, owing to the redundancy of the genetic code.- For example, if 3’-CCG-5’on the template strand mutated to 3’-CCA-5’, the mRNA codon that used to be GGC would be-come GGU, but a glycine would still be inserted at the proper location in the protein- A change in a nucleotide pair may transform one codon into another that is translated into the same amino acid.- Such a change is an example of a silent mutation, which has no observable effect on the phenotype.IV. Frameshif- Will occur whenever the number of nucleotides inserted or deleted is not a multiple of three.- All the nucleotides that are downstream of the deletion or insertion will be improperly grouped into codons, and the result will be extensive missense, usually ending sooner or later in nonsense and premature termination- Unless the frameshif is very near the end of the gene, the pro-tein is almost certain to be nonfunctional.V. Deletion- Mutation (a genetic aberration) in which a part of a chromosome or a sequence of DNA is missing- Deletion is the loss of genetic material. - Any number of nucleotides can be deleted, from a single base to an entire piece of chromosome. - Deletions can be caused by errors in chromosomal crossover during meiosis. This causes several serious genetic diseases. - Deletion also causes


View Full Document

UGA BIOL 1107 - Types of Mutations

Type: Lecture Note
Pages: 4
Documents in this Course
Load more
Download Types of Mutations
Our administrator received your request to download this document. We will send you the file to your email shortly.
Loading Unlocking...
Login

Join to view Types of Mutations and access 3M+ class-specific study document.

or
We will never post anything without your permission.
Don't have an account?
Sign Up

Join to view Types of Mutations 2 2 and access 3M+ class-specific study document.

or

By creating an account you agree to our Privacy Policy and Terms Of Use

Already a member?