Key Area 1.6 (a) and (b) Gene Mutations. Learning Outcomes.

Slides:



Advertisements
Similar presentations
12-4 & 5 Mutations.
Advertisements

Key area 6: Mutations.
Lesson Overview 13.3 Mutations.
Mutations. The picture shows a human genome Karyotype. Look at it carefully and discuss.
Section 1: Mutation and Genetic Change
12.4 MUTATIONS I. Kinds of Mutations
Lesson Overview Lesson OverviewMutations Lesson Overview 13.3 Mutations.
RNA and Protein Synthesis
RNA AND PROTEIN SYNTHESIS RNA vs DNA RNADNA 1. 5 – Carbon sugar (ribose) 5 – Carbon sugar (deoxyribose) 2. Phosphate group Phosphate group 3. Nitrogenous.
RNA Ribonucleic Acid. Structure of RNA  Single stranded  Ribose Sugar  5 carbon sugar  Phosphate group  Adenine, Uracil, Cytosine, Guanine.
MUTATIONS SC STANDARD B-4.9: The student will exemplify ways in which new characteristics are introduced into an organism or a population.
Gene Mutations Higher Human Biology Unit 1 – Human Cells.
Lesson Overview 13.3 Mutations.
Gene Regulations and Mutations
1. What are genetic disorders caused by. 2
Chapter 12 Section 4 Mutations. Mutations DNA contains the code of instructions for cells. Sometimes, an error occurs when the code is copied. - Such.
Mutation Chapter 16. Mutation A change in structure or amount of genetic material If phenotype is altered – affected organism is called a mutant Mutation.
Mutations Section Objectives for this section  Contrast gene mutations and chromosomal mutations.
Mutations Mutation  Now and then cells make mistakes in copying their own DNA They can insert an incorrect base or skip a base as the new strand.
Mutations.
Types of mutations Mutations are changes in the genetic material
12-4 MUTATIONS. I. KINDS OF MUTATIONS 1. Mutation- change in genetic material that can result from incorrect DNA replication 2. Point Mutations- gene.
Slide 1 of 24 Copyright Pearson Prentice Hall 12-4 Mutations 12–4 Mutations.
 During replication (in DNA), an error may be made that causes changes in the mRNA and proteins made from that part of the DNA  These errors or changes.
Genes in ActionSection 1 Section 1: Mutation and Genetic Change Preview Bellringer Key Ideas Mutation: The Basis of Genetic Change Several Kinds of Mutations.
Slide 1 of 24 VIII MUTATIONS Mutations Types of Mutations:
End Show Slide 1 of 24 Copyright Pearson Prentice Hall 12-4 Mutations Outline 12–4: Mutations.
Slide 1 of 24 Copyright Pearson Prentice Hall Biology.
Fantasy Mutations Reality. Mutations: a permanent and heritable change in the nucleotide sequence of a gene. Are caused by mutagens (x-rays and UV light)
13.3 Mutations KeyQuestions: 1)What are mutations? 2)How do mutations affect genes? The sequence of bases in DNA are like the letters of a coded message.
Name the 4 gene mutations that can occur State the effect of gene mutations on amino acid sequences.
Lesson Overview 13.3 Mutations. THINK ABOUT IT The sequence of bases in DNA are like the letters of a coded message. What would happen if a few of those.
Objective: To discuss different mutations Gene mutation Mutations: change in genetic material Gene Mutation: change is on one or a few nucleotides.
Lesson Overview 13.3 Mutations.
(4) Genes and proteins in health and disease
Wild-type hemoglobin DNA Mutant hemoglobin DNA LE Wild-type hemoglobin DNA Mutant hemoglobin DNA 3¢ 5¢ 3¢ 5¢ mRNA mRNA 5¢ 3¢ 5¢ 3¢ Normal hemoglobin.
Section 1: Mutation and Genetic Change
Lesson Overview 13.3 Mutations.
Lesson Overview 13.3 Mutations.
Copyright Pearson Prentice Hall
Chapter 14 GENETIC VARIATION.
Chapter 4 – proteins, mutations & genetic disorders
Mutations Chapter 12-4.
12- 4 Mutations.
PROTEIN SYNTHESIS AND MUTATIONS
Mutations TSW identify and describe the various types of mutations and their effects.
Human Cells Genes and proteins in health and disease
Types of mutations Mutations are changes in the genetic material
Lesson Overview 13.3 Mutations.
DNA and the Genome Key Area 6a & b Mutations.
Copyright Pearson Prentice Hall
Lesson Overview 13.3 Mutations Objectives:
DNA and the Genome Key Area 6a & b Mutations.
Higher Biology Unit 1: 1.6 Mutations.
Gene and Chromosomal Mutations
Copyright Pearson Prentice Hall
Copyright Pearson Prentice Hall
Copyright Pearson Prentice Hall
Copyright Pearson Prentice Hall
Gene Mutations.
Section 20.4 Mutations and Genetic Variation
Copyright Pearson Prentice Hall
Lesson Overview 13.3 Mutations.
Unit 1 Human Cells Higher Human Biology for CfE Miss Aitken
Copyright Pearson Prentice Hall
Lesson Overview 13.3 Mutations.
12–4 Mutations 12-4 Mutations Copyright Pearson Prentice Hall.
Lesson Overview 13.3 Mutations.
Copyright Pearson Prentice Hall
Copyright Pearson Prentice Hall
Presentation transcript:

Key Area 1.6 (a) and (b) Gene Mutations

Learning Outcomes

Genetic Variation Within the human population, there are many different types of variation in the genomes. These difference are the result of mutations and rearrangements of parts of the sequence of bases.

Mutations Mutations are changes in the genome that can result in no protein or an altered protein being expressed. Mutations arise spontaneously and at random but only occur rarely.

Single Gene (point) Mutations A single gene (point) mutation involves a change in one of the base pairs in the DNA sequence of a single gene. A point mutation can alter the expression of the gene.

Single Gene Mutations Three types of single gene mutation are: 1)Substitution 2)Insertion 3)Deletion Each of these results in one or more codons for one or more amino acids being altered.

Task Using the text book (page 61), add a diagram of each type of mutation into your notes. Ask your partner to check over it to make sure it is fully completed and to a high standard.

Impact of Protein Structure Single-nucleotide substitutions brings about only a minor change (one different amino acid). Single-nucleotide substitutions include: 1)Missense 2)Nonsense 3)Splice-Site

Missense Following a substitution, the altered codon codes for an amino acid which still makes sense but not the original sense.

Nonsense As a result of a substitution, a codon that used to code for an amino acid becomes changed into one that acts as a stop codon. It causes protein synthesis to be halted prematurely and results in the formation of a polypeptide chain which is shorter than the normal one.

Splice-Site A molecule of primary mRNA transcript is spliced to remove introns and seal exons together. A splice-site mutation substitutes, inserts or deletes one or more nucleotides at a site where introns are normally removed. Splice-site mutations can alter post- transcriptional processing.

Research Task Research reasons for geographical variation in incidence of post-weaning lactose tolerance or sickle-cell trait in humans.

Frame-shift Mutations Insertion and deletion both lead to major changes since each cause a large portion of gene’s DNA to be misread. The protein produced differs from the normal protein by many amino acids and it is usually non-functional. Frame-shift mutations can also result in an expansion of a nucleotide sequence repeat.

Starter/Task

Key Area 1.6 (c), (d) and (e) Chromosome Mutations

Learning Outcomes

Chromosome Mutations These mutation alter the structure of one or more chromosomes. There are four types of chromosome mutations: 1)Duplication 2)Deletion 3)Inversion 4)Translocation

Duplication A segment of genes is repeated. Some duplication of genes may have a detrimental effect or be of an advantage.

Deletion A segment of genes becomes detached and the two remaining ends join giving a shorter chromosome lacked the detached genes. Deletion normally has drastic effects on the organism involved.

Inversion A segment of genes is reversed. This results in non-viable gametes.

Translocation A section of one chromosome breaks off and attaches to another chromosome that is not it’s matching partner. Translocation leads to non-viable gametes.

Task Using page 67-69, add diagrams of each type of chromosome mutation to your notes.

Importance of Mutations Mutation is the only source of new variation. New alleles of genes arise. Most mutations are harmful or lethal, but rarely, can be advantageous. Mutations are the raw material of evolution!!!

Polyploidy Polyploidy is the result of an error occurring during gamete formation or cell division and all the matching chromosomes fail to separate. Polyploidy is a mutation where cells receive one or more extra sets of chromosomes.

Think and Discuss Would you ever eat a polyploidy fruit or vegetable? What do you think it would look like/taste like?

Polyploidy in Plants Approximately 50% of plant species are polyploid, due to duplication of entire genomes millions of years ago, in their common ancestors.

Importance of Polyploidy Polyploid plants are larger, have increased seed and fruit size, and higher yields. Polyploid plants with an uneven number of sets of chromosomes are sterile so produce seedless fruit. Advantages are increased vigour, crop quality and resistance to disease.

Examples of Polyploid Banana – a triploid, originated from a cross between two species or wild banana. Bananas are propagated asexually. Potato – a tetraploid, native to South America. Other examples include swede, oil seed rape, wheat and strawberry.