Transcript
GENETIC MUTATION
Asmarinah
Department of Medical Biology
Faculty of Medicine, University of Indonesia
Xeroderma pigmentosum patient(extremely sensitive to sunlight)
DNA - GeneThe gene store genetic information encoded in the sequence of nucleotide pairs in DNA
Inheritance is based on genes that are transmitted from parents to offspring during reproduction with considerable accuracy
MutationIs the heritable changes in the genetic material.
The term mutation refers to (1)change in the genetic material, (2) the process by which the change occurs.
Mutation provides the raw material for evolution. Without mutation, all of genes would exist in only one form and alleles would not exist. Organism would not be able to evolve and adapt to environment changes.
▪ Mutations range in size from a single DNA building block (DNA base) to a large segment of a chromosome.
▪ An organism that exhibits a novel phenotype resulting from a mutation is called a mutant.
* Mutation may occur in any cell and at any stage in the development of a multicellular organism.
- germinal mutation occur in germ-line cell and will be transmitted to progeny This type of mutation is present throughout a person’s life in virtually every cell in the body.
- somatic mutation occur in somatic cell, occur in the DNA of individual cells at some time during a person’s life, and will not be transmitted to the progeny.
Single-site or point mutation within individual genebe classified:
- Substitution In which one or more base-pairs are substituted with other base pairs
- Deletion In which one or more base-pairs are lost
- Insertion In which one or more base-pairs are inserted into sequence
Types of point mutation:
The mutation of a wild-type gene to a form that result ina mutant phenotype forward mutation.
When a second mutation restores the original phenotype,
the process is called reverse mutation.
Reverse mutation may occur in two different ways, 1) by back mutation, a second mutation at the same site
in the gene as the original mutation, restoring the wild type nucleotide sequence,
2) by suppressor mutation, a second mutation at a different location in the genome, which compensates for the effects of the first mutation.
The deletion and insertion of one or two base-pairs within the coding sequence of a gene will alter the codon reading frame (i.e the series of base triplets that specify amino acid during translation) in mRNA. frameshift mutations.
Mutation can alter the sequences of nucleotide pairs in genes, that cause changes in the amino acid sequences of the polypeptides missense mutation.
Mutation that alter the sequences of nucleotide pairs in genes, but can’t cause changes in the amino acid sequences of the polypeptides silent mutation
If the point mutation of base-pairs produce a stop codon (UAA, UAG and UGA) nonsense mutation
Many mutation have no effect on the phenotype of organism neutral mutation.
Most mutation with phenotypically recognizable effects result in decreased gene-product activity or no gene-product activity.
Mutation process and the expression of wild-type and mutant alles
Recessive mutant alleles often result in blocks in metabolic pathway
For example: 5 disorders are caused by autosomal recessive mutation with defect in phenylalanine-tyrosine metabolism:
-Phenylketonuria
-Tyrosinosis
-Tyrosinemia
-Alkaptonuria
-Albinism
Based on the cause of the mutation, there are:
* Spontaneous mutation Occur infrequently, without a known cause. For eukaryotes, mutation rates range from about 10-7 to 10-9 per nucleotide pair per generation Mutation rate per gene varies from about 10-4 to 10-7 per generation
* Induced mutation Resulting from exposure of organism to physical and chemical agents, called mutagens
Mutagenic agent (Mutagen)result in induced mutations. It is classified into:
1. Chemical - alkylating agent, that transfer alkyl group (CH3-, CH3CH2, and so forth) to the bases in DNA Example: Mustard gas [Di-(2-chloroethyl) sulfide] EMS (Ethyl methane sulfonate)
- Basa analogs, that have similar structure to the normal base and are incorporated into DNA during replication Example: 5-Bromouracil (BU) 2-Aminopurin (2-AP)
- Deaminating agent that deaminate the amino groups in bases Example: Nitrous acid (HNO2)
- Hydroxylating agent, that hydroxylase amino groups in the bases caused transition mutation. Example: Hydroxylamine
- Acridin dyes, that intercalate DNA molecule, so doing, they increase the rigidity and alter the conformation of the double helix Example: Proflavin Acridine orange
Some potent chemical mutagens
2. Physical agents - Ionizing radiation High-energy rays collide with atom and cause the release of electron, creating free radical or ion. It also induces gross changes in chromosome structure Examples: X-rays, gamma rays and cosmic rays
- Nonionizing radiation Lower-energy that penetrate only the surface layer of cells and don’t cause ionizations. Example: UV light cause pyrimidine hydrate pyrimidine dimer
3. Transposable Genetic Elements (transposons)
DNA element that can move from site in the genome to another site. The insertion of a transposons will often render the gene nonfunctional.
Three major factors for the occurring of mutation:
1. The accuracy of the DNA replication machinery
2. The efficiency of the mechanisms that have evolved for the repair of damaged DNA.
3. The degree of the exposure to mutagenic agents present in the environment.
The Mechanism of Mutation
1. Tautomerisation in DNA replication process
Tautomerisation is a process in which hydrogen atoms moves from one position to another position in a purine or pyramidine .
Mutation resulting from tautomeric shifts cause: - Transition mutation: replacement of purine with other purine or of pyrimidine to other pyrimidine - Transversion mutation: replacement of purine with pyrimidine and vice versa
Tautomeric forms of the four common bases in DNA
The shift of hydrogen atoms between the number 3 and 4 position of pyrimidine and between the number 1 and 6 position of the purine change their base-pairing potential
Mechanism by which tautomeric shift in the bases in DNA cause mutations
2. Failure in DNA repair process
Consist of 3 steps:a. DNA glycosylase enzyme recognized and then excises the damage bases in DNAb. DNA polymerase fills nucleotide in the gapc. DNA ligase seals the break to complete the repair process
DNA repair mechanisms are classified into:
1. Excision repair
- Light-dependent repair (photoreactivation)
DNA photolyase recognizes and binds to thymine dimmers, and then uses light energy to cleave cross-link
Inherited human disease with DNA mutation (examples) -“Sickle cell anemia” :
Pauling et al., (1949) discovered: substitution of nucleotide A to T that substitute amino acid glutamic acid in the normally hemoglobin (Hb A) to valine (defective hemoglobin (Hb S).
introduced “molecular disease” term
set the foundation of molecular diagnosis
Inherited human disease with defects in DNA repair •Xeroderma Pigmentosum It caused by defect in the repair of UV-induced damaged to DNA
High frequency to skin cancer
Mutation is one of sources for polymorphism
Polymorphism
“many form” : a set of two or more alternative of normal phenotypes
Genetic polymorphism:
The occurrence of two or more allele in a locus in which its frequency is more than 1% in population. Example: ABO and MN blood group
If the alleles with frequencies of less than 1% are called rare variants . Example: O Bombay blood group
▪ Polymorphisms are responsible for many of the normal differences between people such as eye color, hair color, and blood type.
▪ Although many polymorphisms have no negative effects on a person’s health, some of these variations may influence the risk of developing certain disorders.
Forms of genetic polymophism
1. Single Nucleotide Polymorphism (SNP), a polymorphism in DNA sequence consisting of variation in a single base.
Example: Missence mutation that caused by a nucleotide substitution
2. Variable number of tandem repeats (VNTR), a type of DNA polymorphism created by a tandem arrangement of multiple copies of short DNA sequences.
3. Micro satellites (Short Tandem Repeat Polymorphism = STRP)
A polymorphic locus consisting of a variable number of tandem repeated bi-, tri-, or tetra nucleotide units such as (TG)n, (CAA)n, or (GATA)n.
Different numbers of units constitute the different alleles
Gene polymorphism•Occur in 1 in 1000 DNA bp in human genome over 3 million SNPs in the entire human genome
•Is reflected in the diversity of the gene products, such as structural protein, enzymes, channel proteins, receptors, etc.
Use of polymorphism•Medical forensic individual characteristic
•Disease susceptibility, influence drug response
•Genetic relationship (within & between population)
molecular evolution
Genetic Mutation/Polymorphism
can be detected by following techniques:
* RFLP (Restriction Fragment Length Polymorphism)
* PCR (Polymerase Chains Reaction) – RFLP
* PCR – DNA Sequencing
* Southern Blot
11001300
PCR-RFLP method (for diagnosis of sickle cell anemia)
Sequence of PCR product from sperm with low motility
Sequence of PCR product from sperm with normal motility
174
Mutation in exon 6 of VDAC3 gene in sperm with low motility
Posisition 174 : AAG
(Lysine)
Posisition 174 : GAG
(glutamic acid)
PCR-DNA sequencing method:
References:
• Alberts et al., 2008. Molecular Biology of the Cell. 5th ed.
• Snustad & Simmons. 2010. Principles of Genetics . 5td ed.
• Karp. 2005. Cell and Molecular Biology. 4th ed.
• Nussbaum et al. 2001. Thompson & Thompson Genetic Medicine. 6th ed.
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